170 results on '"Michale E. Keeling"'
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2. Immune responses to repetitive adenovirus-mediated gene transfer and restoration of gene expression by cyclophosphamide or etoposide
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William C. Satterfield, Asis K. Sarkar, Stepanie Buchl, Morito Sakaue, Michele Follen, Katsuyuki Hamada, Jack A. Roth, Michale E. Keeling, and Jagannandha Sastry
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Genetic Vectors ,Dose-Response Relationship, Immunologic ,Gene Expression ,Cervix Uteri ,Gene delivery ,Antibodies, Viral ,Adenoviridae ,Viral vector ,Mice ,Immune system ,Gene expression ,medicine ,Animals ,Neutralizing antibody ,Cyclophosphamide ,Etoposide ,Skin ,Mice, Inbred C3H ,biology ,business.industry ,Immunogenicity ,Gene Transfer Techniques ,Obstetrics and Gynecology ,Macaca mulatta ,Virology ,Molecular biology ,Immunoglobulin A ,Lac Operon ,Oncology ,Immunoglobulin G ,biology.protein ,Female ,Antibody ,business ,medicine.drug - Abstract
Background. One major concern about adenoviral vectors for repetitive gene delivery is the induction of an immune response to the vector, thus impeding effective gene transduction. Methods. To assess the immune response to the adenoviral vector, repetitive gene dosing was performed into rhesus monkey cervix and C3H mouse skin using the adenoviral vector carrying the lacZ gene. Three repetitive intracervical injections of adenovirus- lacZ were done in the rhesus monkey at the intervals of 4 weeks. Gene expression on the second and third injection was completely suppressed. Results. Anti-adenovirus IgG levels and neutralizing antibody titers in the rhesus monkey significantly increased after the first injection of adenovirus. In the C3H mouse, neutralizing antibody titers significantly increased after the first injection of adenovirus- lacZ at more than 10 8 plaque-forming unit (PFU). The repetitive expression of lacZ gene in the mouse skin markedly decreased when the second injection is done more than 2 weeks after the first injection. Chronic low-dose treatment with cyclophosphamide or etoposide markedly suppressed neutralizing antibody titers in the mouse serum and restored the gene expression in the mouse skin on the second and third injection. Conclusions. It is suggested that repetitive gene expression by adenovirus-mediated transfer may be reduced by circulating neutralizing antibodies and could be restored by chronic low-dose treatment with cyclophosphamide or etoposide.
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- 2005
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3. Postnatal pre- and postexposure passive immunization strategies: protection of neonatal macaques against oral simian-human immunodeficiency virus challenge
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Bruce J. Bernacky, Lorraine R Hill, P.-L. Li, David C. Montefiori, Hermann Katinger, Robert A. Rasmussen, Shisong Jiang, Regina Hofmann-Lehmann, Ruth M. Ruprecht, Timothy W. Baba, Josef Vlasak, Tahir A. Rizvi, Michale E. Keeling, Gabriela Stiegler, Marshall R. Posner, Russell D. Schmidt, and Lisa A. Cavacini
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chemistry.chemical_classification ,General Veterinary ,Low toxicity ,medicine.drug_class ,Virus transmission ,business.industry ,Simian human immunodeficiency virus ,Human immunodeficiency virus (HIV) ,medicine.disease_cause ,Monoclonal antibody ,medicine.disease ,Virology ,Immunization ,chemistry ,Immunology ,medicine ,Animal Science and Zoology ,Glycoprotein ,business ,Immunodeficiency - Abstract
Simian-human immunodeficiency viruses (SHIV) allow the evaluation of antiviral strategies that target the envelope glycoproteins of the human immunodeficiency virus 1 (HIV-1) in macaques. We previously protected neonates from oral challenge with cell-free SHIV-vpu+ by passive immunization with synergistic human neutralizing monoclonal antibodies (mAbs) (Baba et al., Nat Med 6:200-206, 2000). mAbs were administered prenatally to pregnant dams and postnatally to the neonates. Here, we used solely postnatal or postexposure mAb treatment, thus significantly reducing the amount of mAbs necessary. All neonatal monkeys were also protected with these abbreviated mAb regimens. Our results are directly relevant for humans because we used mAbs that target HIV-1 envelope glycoproteins. Thus, the large-scale use of passive immunization with neutralizing mAbs may be feasible in human neonates. The mAbs, being natural human proteins, can be expected to have low toxicity. Passive immunization has promise to prevent intrapartum as well as milk-borne virus transmission from HIV-1-infected women to their infants.
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- 2002
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4. Postnatal Passive Immunization of Neonatal Macaques with a Triple Combination of Human Monoclonal Antibodies against Oral Simian-Human Immunodeficiency Virus Challenge
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Vladimir Liska, Josef Vlasak, Timothy W. Baba, Gabriela Stiegler, Regina Hofmann-Lehmann, Harold M. McClure, Russell D. Schmidt, Daniel C. Anderson, Beverly A. Smith, Tahir A. Rizvi, Ruth M. Ruprecht, Lori R. Hill, Hermann Katinger, Ting-Chao Chou, Marshall R. Posner, Flavia Ferrantelli, Lisa A. Cavacini, Janet Andersen, Robert A. Rasmussen, David C. Montefiori, Bruce J. Bernacky, Michale E. Keeling, University of Zurich, and Ruprecht, R M
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1109 Insect Science ,medicine.drug_class ,Immunology ,Simian Acquired Immunodeficiency Syndrome ,Administration, Oral ,Biology ,Monoclonal antibody ,medicine.disease_cause ,Microbiology ,Virus ,Acquired immunodeficiency syndrome (AIDS) ,Virology ,Vaccines and Antiviral Agents ,medicine ,Animals ,Humans ,Immunity, Mucosal ,2403 Immunology ,630 Agriculture ,Transmission (medicine) ,2404 Microbiology ,Immunization, Passive ,Antibodies, Monoclonal ,Drug Synergism ,Simian immunodeficiency virus ,medicine.disease ,In vitro ,10187 Department of Farm Animals ,Animals, Newborn ,Immunization ,Insect Science ,2406 Virology ,biology.protein ,570 Life sciences ,biology ,Macaca ,Simian Immunodeficiency Virus ,Antibody - Abstract
To develop prophylaxis against mother-to-child human immunodeficiency virus (HIV) transmission, we established a simian-human immunodeficiency virus (SHIV) infection model in neonatal macaques that mimics intrapartum mucosal virus exposure (T. W. Baba et al., AIDS Res. Hum. Retroviruses 10:351–357, 1994). Using this model, neonates were protected from mucosal SHIV-vpu+challenge by pre- and postnatal treatment with a combination of three human neutralizing monoclonal antibodies (MAbs), F105, 2G12, and 2F5 (Baba et al., Nat. Med. 6:200–206, 2000). In the present study, we used this MAb combination only postnatally, thereby significantly reducing the quantity of antibodies necessary and rendering their potential use in humans more practical. We protected two neonates with this regimen against oral SHIV-vpu+challenge, while four untreated control animals became persistently infected. Thus, synergistic MAbs protect when used as immunoprophylaxis without the prenatal dose. We then determined in vitro the optimal MAb combination against the more pathogenic SHIV89.6P, a chimeric virus encodingenvof the primary HIV89.6. Remarkably, the most potent combination included IgG1b12, which alone does not neutralize SHIV89.6P. We administered the combination of MAbs IgG1b12, 2F5, and 2G12 postnatally to four neonates. One of the four infants remained uninfected after oral challenge with SHIV89.6P, and two infants had no or a delayed CD4+T-cell decline. In contrast, all control animals had dramatic drops in their CD4+T cells by 2 weeks postexposure. We conclude that our triple MAb combination partially protected against mucosal challenge with the highly pathogenic SHIV89.6P. Thus, combination immunoprophylaxis with passively administered synergistic human MAbs may play a role in the clinical prevention of mother-to-infant transmission of HIV type 1.
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- 2001
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5. Evaluation of cellular immune responses in rhesus monkeys subjected to adenovirus-mediated gene transfer into the cervix
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Katsuyuki Hamada, Steven J. Schapiro, Stephanie J. Buchl, K. Jagannadha Sastry, Michele Follen Mitchell, Michale E. Keeling, William C. Satterfield, and Asis K. Sarkar
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Cancer Research ,Cellular immunity ,Time Factors ,Genetic enhancement ,Transgene ,medicine.medical_treatment ,Cervix Uteri ,Biology ,Immunoglobulin G ,Adenoviridae ,Injections ,Immune system ,medicine ,Animals ,Transgenes ,Molecular Biology ,Cervix ,Immunity, Cellular ,Dose-Response Relationship, Drug ,Gene Transfer Techniques ,Gene targeting ,Macaca mulatta ,Cytokine ,medicine.anatomical_structure ,Immunology ,biology.protein ,Molecular Medicine ,Female - Abstract
We reported previously that direct injection of a recombinant adenovirus (rAd), Ad5CMV-beta-gal, into the cervix of the rhesus monkey resulted in efficient beta-galactosidase expression in the cervix within 3 days. In these studies, we also observed the induction of anti-adenovirus (Ad)-specific immunoglobulin G responses after 22 days. In the continuation of evaluating the anti-Ad-specific immune responses resulting from this approach of gene targeting to the cervix, we measured the cellular immune responses. The introduction of Ad5CMV-beta-gal into the cervix by direct injection, but not by the abrasion technique, resulted in the induction of strong proliferative responses against extracts of cells infected with Ad5CMV-beta-gal but not against control uninfected cells. These responses were initially detected at 22 days postinjection and coincided with the abrogation of transgene expression. Significant levels of proliferative responses were maintained foror =83 days. Multiple injections of rAds had no significant enhancing effect on either the level or longevity of the proliferative responses. At 3 days after the injection of Ad5CMV-beta-gal, when the transgene expression in the cervix was clearly evident, proliferative responses against the rAd were not detectable. However, the production of low but significant amounts of interleukin-10, a cytokine characteristic of T helper type 2 responses that promote humoral immune responses, was observed at the 3-day point in these animals. These results suggest that significant differences exist between the kinetics of transgene expression and the priming of specific host immune responses, and that these differences may be important for devising alternate strategies to improve techniques for Ad-mediated gene therapy of cervical cancer.
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- 1999
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6. The 1996 Guide for the Care and Use of Laboratory Animals
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Michale E. Keeling, G.F. Gebhart, J. Derrell Clark, Janet C. Gonder, and Dennis F. Kohn
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World Wide Web ,Text mining ,business.industry ,Medicine ,Animal Science and Zoology ,General Medicine ,business ,General Biochemistry, Genetics and Molecular Biology - Published
- 1997
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7. Genetic structure of three populations of rhesus macaques (Macaca mulatta): Implications for genetic management
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Michale E. Keeling, J. Scheffler, G. S. Manis, W. H. Stone, P. S. Gill, and John Blangero
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Genetics ,education.field_of_study ,Population ,Population genetics ,Biology ,Genetic distance ,Genetic marker ,Genetic variation ,Genetic structure ,Animal Science and Zoology ,Genetic variability ,education ,Inbreeding ,Ecology, Evolution, Behavior and Systematics - Abstract
One of the prime concerns at zoos and at primate breeding facilities is to maintain genetic variability. This can be accomplished by avoiding inbreeding. It is relatively easy to assess genetic variability and the level of inbreeding by using pedigree information and genetic markers. In this study we used genetic markers controlled by 6 independent polymorphic loci (GPI, PGD, CA2, MPI, DIA1, Tf) to ascertain genetic variation in two captive and one wild population of rhesus monkeys. Two other loci ADA and NP were also examined and found to be monomorphic in the three populations. F-statistics and contingency chi-square analyses indicated that there was significant genetic differentiation among the populations. We also found that the mean heterozygosities were very similar in the three populations, in spite of the diverse breeding strategies. These data are important because rhesus monkeys are frequently used for biomedical research; and the genetic markers provide useful information for genetic management of captive colonies of nonhuman primates. © 1992 Wiley-Liss, Inc.
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- 1992
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8. Nonhuman Primates
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Bruce J. Bernacky, Susan V. Gibson, Christian R. Abee, and Michale E. Keeling
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Biology - Published
- 2002
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9. List of Contributors
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Christian R. Abee, Robert J. Adams, Lynn C. Anderson, Keith M. Astrofsky, Henry J. Baker, Kathryn A.L. Bayne, Bonnie V. Beaver, Christine A. Bellezza, Bruce J. Bernacky, Sarah A. Bingel, David W. Brammer, Robert A. Bullis, Clarence E. Chrisp, Charles B. Clifford, Bennett J. Cohen, Patrick W. Concannon, Muriel Davisson, Margaret L. Delano, George J. DeMarco, Thomas M. Donnelly, Robert C. Dysko, Susan Erdman, James G. Fox, Linda K. Fulton, Diane J. Gaertner, James G. Geistfeld, Susan V. Gibson, James A. Goodrich, Brenda Griffin, Thomas E. Hamm, F. Claire Hankenson, John E. Harkness, Jack R. Hessler, William E. Hornbuckle, Robert O. Jacoby, Michale E. Keeling, Dennis F. Kohn, Kathy E. Laber, Steven L. Leary, Stephen I. Levin, J. Russell Lindsey, Neil S. Lipman, Franklin M. Loew, Robert P. Marini, Joy A. Mench, Marian G. Michaels, Scott A. Mischler, Maria R. Moalli, Glenn M. Monastersky, David B. Morton, Kathleen A. Murray, Jean A. Nemzek, Christian E. Newcomer, Dorcas P. O'Rourke, Glen Otto, Lori Palley, Scott E. Perkins, Sulli Popilskis, Fred W. Quimby, Lois Roth, Harry Rozmiarek, Howard G. Rush, Charles G. Sagerström, Evelyn E. Sargent, Terry Wayne Schultz, Juergen Schumacher, Peter A. Schweitzer, John J. Sharp, William R. Shek, Alison C. Smith, Michael K. Stoskopf, Mark A. Suckow, M. Michael Swindle, Bud C. Tennant, Wendy J. Underwood, Gerald L. Van Hoosier, George A. Vogler, Joseph E. Wagner, and Mark T. Whary
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- 2002
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10. Protection of neonatal macaques against experimental SHIV infection by human neutralizing monoclonal antibodies
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Timothy W. Baba, Marshall R. Posner, Russell D. Schmidt, Bruce J. Bernacky, Ruth M. Ruprecht, Agnès-Laurence Chenine, Vladimir Liska, B. A. Smith-Franklin, Michale E. Keeling, Lisa A. Cavacini, Robert A. Rasmussen, Weidong Xu, Tahir A. Rizvi, Lorraine R Hill, David C. Montefiori, Gabriela Stiegler, Josef Vlasak, Regina Hofmann-Lehmann, Harold M. McClure, and Hermann Katinger
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Clinical Biochemistry ,Simian Acquired Immunodeficiency Syndrome ,Administration, Oral ,HIV Infections ,Pilot Projects ,HIV Antibodies ,HIV Envelope Protein gp120 ,Epitope ,Pregnancy ,Pregnancy Complications, Infectious ,Maternal-Fetal Exchange ,AIDS Vaccines ,biology ,Vaccination ,Antibodies, Monoclonal ,Hematology ,HIV Envelope Protein gp41 ,Virus Shedding ,Milk ,Female ,Simian Immunodeficiency Virus ,Antibody ,medicine.drug_class ,Monoclonal antibody ,Gp41 ,Species Specificity ,Immunity ,Neutralization Tests ,medicine ,Animals ,Humans ,Lactation ,Viral shedding ,Linear epitope ,Cesarean Section ,Virus Assembly ,Biochemistry (medical) ,Immunization, Passive ,Infant, Newborn ,HIV ,Delivery, Obstetric ,Virology ,Macaca mulatta ,Infectious Disease Transmission, Vertical ,CD4 Lymphocyte Count ,Disease Models, Animal ,Immunization ,Animals, Newborn ,Immunology ,biology.protein ,Immunity, Maternally-Acquired - Abstract
Neonatal macaques were completely protected against oral challenge with SHIV-vpu+, a simian-human immunodeficiency virus that encodes the envelope gene of a laboratory-adapted HIV strain, by pre- and post-natal treatment with a triple combination of human neutralizing monoclonal antibodies (mAbs). The mAbs were directed either against the CD4 binding site, a glycosylation-dependent gp120 epitope, or against a linear epitope on gp41. This triple combination was highly synergistic in vitro and neutralized primary HIV completely. Subsequently, oral challenge was performed with pathogenic SHIV89.6P, an animal-passaged variant of a chimeric virus that encodes the envelope gene of the primary, dual-tropic HIV89.6. Only post-natal treatment with a similar triple mAb combination was used. One out of 4 mAb-treated infants was completely protected from infection. In the other 3 treated animals, there was a tendency towards lower peak viral RNA loads compared with untreated controls. Two out of 4 mAb-treated infants maintained normal CD4+ T-cell numbers, in contrast to all controls that had steep declines at 2 weeks post-challenge. We conclude that the triple mAb combination significantly protected the neonates, even against mucosal challenge with pathogenic SHIV89.6P. Passively administered synergistic human mAbs may play a role in preventing mother-infant transmission of HIV, both against intrapartum transmission as well as against infection through breast milk. As passive immunization is a tool to assess correlates of immune protection, we conclude that the epitopes recognized by the mAbs in our combinations are important for AIDS vaccine development. Future passive immunization studies may reveal other important conserved epitopes.
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- 2001
11. Passive immunization against oral AIDS virus transmission: an approach to prevent mother-to-infant HIV-1 transmission?
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Timothy W. Baba, Lori R. Hill, Robert A. Rasmussen, Hermann Katinger, Lisa A. Cavacini, Vladimir Liska, Harold M. McClure, Beverly A. Smith, Josef Vlasak, Ting-Chao Chou, Michale E. Keeling, Marshall R. Posner, Gabriela Stiegler, Bruce J. Bernacky, Daniel C. Anderson, David C. Montefiori, Regina Hofmann-Lehmann, Ruth M. Ruprecht, Russell D. Schmidt, and Tahir A. Rizvi
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Male ,medicine.drug_class ,viruses ,HIV Infections ,Monoclonal antibody ,Gp41 ,Virus ,Epitope ,Pregnancy ,medicine ,Animals ,Humans ,Acquired Immunodeficiency Syndrome ,General Veterinary ,biology ,Transmission (medicine) ,Chimera ,Postpartum Period ,Immunization, Passive ,Infant, Newborn ,virus diseases ,Antibodies, Monoclonal ,Virology ,Macaca mulatta ,Infectious Disease Transmission, Vertical ,Disease Models, Animal ,Immunization ,Immunoglobulin G ,Immunology ,biology.protein ,HIV-1 ,Animal Science and Zoology ,Female ,Simian Immunodeficiency Virus ,Antibody ,Postpartum period - Abstract
To develop immunoprophylaxis regimens against mother-to-child human immunodeficiency virus type 1 (HIV-1) transmission, we established a simian-human immunodeficiency virus (SHIV) model in neonatal macaques that mimics intrapartum mucosal virus exposure (T.W. Baba, J. Koch, E.S. Mittler et al: AIDS Res Hum Retroviruses 10:351-357, 1994). We protected four neonates from oral SHIV-vpu+ challenge by ante- and postpartum treatment with a synergistic triple combination of immunoglobulin (Ig) G1 human anti-HIV-1 neutralizing monoclonal antibodies (mAbs) (T.W. Baba, V. Liska, R. Hofmann-Lehmann et al: Nature Med 6:200-206, 2000), which recognize the CD4-binding site of Env, a glycosylation-dependent gp120, or a linear gp41 epitope. Two neonates that received only postpartum mAbs were also protected from oral SHIV-vpu+ challenge, indicating that postpartum treatment alone is sufficient. Next, we evaluated a similar mAb combination against SHIV89.6P, which encodes env of primary HIV89.6. One of four mAb-treated neonates was protected from infection and two maintained normal CD4+ T-cell counts. We conclude that the epitopes recognized by the three mAbs are important determinants for achieving protection. Combination immunoprophylaxis with synergistic mAbs seems promising to prevent maternal HIV-1 transmission in humans.
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- 2001
12. Demography and pedigree structure of an SPF colony of rhesus monkeys (Macaca mulatta)
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Kathryn Mosman, Michale E. Keeling, Carlos Mohamed, Bennett Dyke, Lisa Ludvico, Bruce J. Bernacky, Susan Slifer, W. H. Stone, and Kristina Massey
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Male ,animal diseases ,Population ,Captivity ,Culling ,Biology ,law.invention ,law ,Quarantine ,Animals ,Genetic variability ,Animal Husbandry ,Selection, Genetic ,education ,Ecology, Evolution, Behavior and Systematics ,Selection (genetic algorithm) ,Specific-pathogen-free ,Demography ,education.field_of_study ,Macaca mulatta ,Pedigree ,Specific Pathogen-Free Organisms ,Animals, Domestic ,Animal Science and Zoology ,Female ,Inbreeding - Abstract
The SPF rhesus colony at the M.D. Anderson Cancer Center in Bastrop, Texas, was analyzed with the aim of determining the demographic and genetic effects of stringent selection for virus-free breeders, permanent quarantine, continued surveillance, and culling of animals that show evidence of viral infection. The analysis shows minimal effects on population viability and loss of genetic variability in comparison with the traditionally managed (non-SPF) portion of the population.
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- 2001
13. Human neutralizing monoclonal antibodies of the IgG1 subtype protect against mucosal simian-human immunodeficiency virus infection
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Gabriela Stiegler, Regina Hofmann-Lehmann, Hermann Katinger, Seyoum Ayehunie, Michale E. Keeling, Vladimir Liska, Weidong Xu, Ruth M. Ruprecht, Joel E. Wright, Lisa A. Cavacini, Bruce J. Bernacky, Ting-Chao Chou, Marshall R. Posner, Josef Vlasak, Russell D. Schmidt, Timothy W. Baba, Tahir A. Rizvi, Lorraine R Hill, Yichen Lu, University of Zurich, and Ruprecht, Ruth M
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medicine.drug_class ,animal diseases ,viruses ,Simian Acquired Immunodeficiency Syndrome ,medicine.disease_cause ,Monoclonal antibody ,General Biochemistry, Genetics and Molecular Biology ,Virus ,Immunoglobulin G ,Epitope ,Immunity ,Neutralization Tests ,Pregnancy ,1300 General Biochemistry, Genetics and Molecular Biology ,medicine ,Animals ,Pregnancy Complications, Infectious ,Immunity, Mucosal ,biology ,630 Agriculture ,Chimera ,virus diseases ,Antibodies, Monoclonal ,General Medicine ,Simian immunodeficiency virus ,biology.organism_classification ,Virology ,Macaca mulatta ,Infectious Disease Transmission, Vertical ,10187 Department of Farm Animals ,Lentivirus ,Immunology ,biology.protein ,HIV-1 ,570 Life sciences ,Female ,Simian Immunodeficiency Virus ,Antibody - Abstract
Although maternal human immunodeficiency virus type 1 (HIV-1) transmission occurs during gestation, intrapartum and postpartum (by breast-feeding), 50-70% of all infected children seem to acquire HIV-1 shortly before or during delivery. Epidemiological evidence indicates that mucosal exposure is an important aspect of intrapartum HIV transmission. A simian immunodeficiency virus (SIV) macaque model has been developed that mimics the mucosal exposure that can occur during intrapartum HIV-1 transmission. To develop immunoprophylaxis against intrapartum HIV-1 transmission, we used SHIV-vpu+ (refs. 5,6), a chimeric simian-human virus that encodes the env gene of HIV-IIIB. Several combinations of human monoclonal antibodies against HIV-1 have been identified that neutralize SHIV-vpu+ completely in vitro through synergistic interaction. Here, we treated four pregnant macaques with a triple combination of the human IgG1 monoclonal antibodies F105, 2G12 and 2F5. All four macaques were protected against intravenous SHIV-vpu+ challenge after delivery. The infants received monoclonal antibodies after birth and were challenged orally with SHIV-vpu+ shortly thereafter. We found no evidence of infection in any infant during 6 months of follow-up. This demonstrates that IgG1 monoclonal antibodies protect against mucosal lentivirus challenge in neonates. We conclude that epitopes recognized by the three monoclonal antibodies are important determinants for achieving substantial protection, thus providing a rational basis for AIDS vaccine development.
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- 2000
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14. Oral transmission of primate lentiviruses
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Harold M. McClure, Ruth M. Ruprecht, Vladimir Liska, Nancy B. Ray, Timothy W. Baba, Tahir A. Rizvi, Michael Murphey-Corb, Bruce J. Bernacky, Michale E. Keeling, Janet Andersen, and Louis N. Martin
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viruses ,Simian Acquired Immunodeficiency Syndrome ,Viremia ,Biology ,Simian ,medicine.disease_cause ,Virus ,Viral Proteins ,medicine ,Immunology and Allergy ,Animals ,Seroconversion ,Cloning, Molecular ,Transmission (medicine) ,Vaccination ,Age Factors ,Immunization, Passive ,Mouth Mucosa ,Simian immunodeficiency virus ,biology.organism_classification ,medicine.disease ,Virology ,Macaca mulatta ,Infectious Diseases ,Lentivirus ,Immunology ,Simian Immunodeficiency Virus ,Viral disease - Abstract
Oral transmission of human immunodeficiency virus type 1 (HIV-1) is well documented in children who become infected postnatally through breast milk. In contrast, epidemiologic surveys have yielded conflicting data regarding oral HIV-1 transmission among adults, even though case reports have described seroconversion and the development of AIDS in adults whose only risk was oral-genital contact. To study oral virus transmission in primate models, we exposed rhesus macaques of various ages to cell-free simian immunodeficiency virus (SIV), including uncloned and molecularly cloned viruses. In neonates, viremia and AIDS developed after nontraumatic oral exposure to several SIV strains. Furthermore, chimeric simian human immunodeficiency viruses containing the HIV-1 envelope can also cross intact upper gastrointestinal mucosal surfaces in neonates. In adult macaques, infection and AIDS have resulted from well-controlled, nontraumatic, experimental oral exposure to different strains of SIV. These findings have implications for the risks of HIV-1 transmission during oral-genital contact.
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- 1999
15. Special Report: The 1996 Guide for the Care and Use of Laboratory Animals
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J. Derrell, Clark, Gerald F., Gebhart, Janet C., Gonder, Michale E., Keeling, and Dennis F., Kohn
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- 1997
16. Establishing Specific Pathogen-Free (SPF) Nonhuman Primate Colonies
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William R. Voss, Michale E. Keeling, and Stephanie J. Buchl
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biology ,viruses ,Xenotransplantation ,medicine.medical_treatment ,General Medicine ,Disease ,Simian ,Simian immunodeficiency virus ,medicine.disease ,biology.organism_classification ,medicine.disease_cause ,Virology ,General Biochemistry, Genetics and Molecular Biology ,Immunodeficiency Syndrome ,Acquired immunodeficiency syndrome (AIDS) ,Simian retrovirus ,medicine ,Animal Science and Zoology ,Specific-pathogen-free - Abstract
Nonhuman primates continue to make significant contributions to human health through their role in comparative biomedical research in vaccine development, toxicology, teratogenesis, reproduction, xenotransplantation, and infectious diseases along with their therapy (Schmidt 1972; Eichberg 1989; Dormont and others 1990; Kalter and Heberling 1995). With today's growing sophistication in research and technology there is a demand for a comparably high-quality animal model that was foreseen in 1972 (Neurauter and Goodwin 1972). In 1988, it became apparent there would be a significant future need for retrovirusand herpes B virus-free monkeys to enable investigators to fully develop a promising simian immunodeficiency virus (SIV) monkey model (StahlHennig and others 1990). Several of the retroviruses that infect rhesus monkeys have the same biological characteristics as HIV (human immunodeficiency virus) (Lerche and others 1994). Simian retrovirus infection in rhesus monkeys is widespread and in an experimental setting produces many of the same diseases as HIV in humans. Simian retroviruses cause neoplasia, leukemias, neurological disease, and immunodeficiency syndrome in nonhuman primates (Lerche and others 1991; Daniel and others 1984, 1985; Letvin and others 1985; Lowenstine and others 1986; Murphey-Corb and others 1986; Chakrabarti and others 1987). Many of the domestic rhesus production colonies were naturally infected with simian retroviruses that would confound experimental data relevant to AIDS research. There was an obvious need to establish a sustainable resource of rhesus monkeys free of simian retroviruses (Lerche and others 1994). In concert with the mission of the National Center for Research Resources (NCRR), of the National Institutes of Health (NIH) and as part of the AIDS animal model program, a new initiative was launched to assist the development of self-propagating specific-pathogen-free (SPF) breeding populations of rhesus monkeys. The driving force behind creating SPF rhesus monkey colonies was AIDS, which was
- Published
- 1997
17. What Is Your Diagnosis?
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Lorraine R Hill, Bruce J. Bernacky, John D Hazle, Roger E. Price, and Michale E. Keeling
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General Veterinary ,biology ,business.industry ,Periosteal reaction ,Anatomy ,medicine.disease ,biology.organism_classification ,Skull ,Rhesus macaque ,Frontal bone ,medicine.anatomical_structure ,Hematoma ,Medicine ,Soft tissue mass ,business - Published
- 2000
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18. Decision analysis for developing programs of psychological well-being: A bias-for-action approach
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Patricia L. Alford, Molly A. Bloomsmith, and Michale E. Keeling
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Action (philosophy) ,Management science ,Psychological well-being ,Evidential reasoning approach ,Psychology ,Decision analysis - Published
- 1991
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19. Human Monoclonal Antibodies Protect Neonatal and Adult Rhesus Monkeys from Mucosal or Parenteral Immunodeficiency Virus Exposure
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Russell D. Schmidt, Bruce J. Bernacky, Vladimir Liska, Lisa A. Cavacini, Timothy W. Baba, Josef Vlasak, Hermann Katinger, Tahir A. Rizvi, Marshall R. Posner, Ruth M. Ruprecht, Michale E. Keeling, and Regina Hoffman-Lehmann
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medicine.drug_class ,business.industry ,Pediatrics, Perinatology and Child Health ,Immunology ,medicine ,Monoclonal antibody ,business ,Virology ,Immunodeficiency virus - Abstract
Human Monoclonal Antibodies Protect Neonatal and Adult Rhesus Monkeys from Mucosal or Parenteral Immunodeficiency Virus Exposure
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- 1999
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20. Veterinary perspectives of infertility in male great apes
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Michale E. Keeling
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Infertility ,Veterinary medicine ,Gonorrhea ,Disease ,Mycoplasma ,Biology ,medicine.disease ,medicine.disease_cause ,Male infertility ,stomatognathic system ,medicine ,Psychogenic disease ,Animal Science and Zoology ,Syphilis ,Differential diagnosis ,Ecology, Evolution, Behavior and Systematics - Abstract
Diagnosis and therapy of infertility in male great apes is not extensively documented. Current suspicion that male infertility is a significant cause of reproductive failure in captive populations of great apes prompted this discussion of veterinary andrology in the ape. The differential diagnosis of infertility in the great ape must include consideration of the numerous pathways of psychoendocrine disease. We must develop methods of preventing and treating neurogenic as well as organic causes of infertility. The rationale for classifying problems of subfertility as primary testicular failure, secondary testicular failure, and normal testicular function is presented along with a current list of pharmacological compounds used to treat infertility. Specific pathological conditions and infections of the male reproductive tract that the veterinary clinician should be familiar with are presented. The implications of syphilis, gonorrhea, chlamydial urethritis, genital herpes, and Mycoplasma infection in the great ape are reviewed. The immunological aspects of male ape infertility and therapeutic regimens that may have application are briefly discussed. Our broadening responsibilities to enhance the successful breeding of apes in captivity dictate that the veterinary clinician expand his knowledge and ability to treat male infertility.
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- 1982
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21. Lipolytic Peptides in Mammalian Stomach and Choroid Plexus
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Bettye Hollins, Michale E. Keeling, Daniel Rudman, Diane H. Houser, Alejandro E. Del Rio, and Thomas J. Bixler
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Adipose tissue ,Acetates ,Acetone ,Guinea pig ,Acetic acid ,chemistry.chemical_compound ,Endocrinology ,Adrenocorticotropic Hormone ,medicine ,Animals ,Chymotrypsin ,Lipolysis ,biology ,Abomasum ,Chromatography, Ion Exchange ,Trypsin ,Adipose Tissue ,chemistry ,Biochemistry ,Sephadex ,Choroid Plexus ,Cats ,biology.protein ,Choroid plexus ,Chickens ,medicine.drug - Abstract
Acetone powders of porcine stomach stimulated lipolysis in the rabbit’s adipose tissue at a concentration of 1000 μg/ml. By extraction with glacial acetic acid, fractional precipitation with organic solvents, gel filtration and ion exchange chromatography, the lipolytic activity was concentrated 1000 times. This activity was destroyed by trypsin and by chymotrypsin. The porcine stomach lipolytic factor, apparently a peptide with molecular weight 1000–3500 (as indicated by volume of elution from Sephadex G-25), stimulated lipolysis in adipose tissues of rabbit, rat, hamster, guinea pig, cat and opossum, but not in that of the chicken. Lipolytic activity with similar properties was found in omassum and abomassum of bovine stomach, and in leporine, cavian, canine and simian stomach. Acetone powder of bovine choroid plexus was also active at 1000 μg/ral on adipose tissue of the rabbit. The lipolytic activity was concentrated 100-fold by extraction with glacial acetic acid, fractional precipitation with organi...
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- 1971
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22. Biological Activity of an Encephalitogenic Fragment in the Monkey
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Sarah S. McKneally, Michale E. Keeling, Raymond Shapira, Robert F. Kibler, and Peter K. Re
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biology ,Experimental allergic ,Chemistry ,Encephalomyelitis ,Tryptic peptide ,Biological activity ,Cell Biology ,medicine.disease ,Biochemistry ,Myelin basic protein ,Sephadex ,medicine ,biology.protein ,Tyrosine ,Molecular Biology ,Carboxymethylcellulose chromatography - Abstract
A 45-residue encephalitogenic fragment of myelin basic protein has been prepared by extraction of acetone-ether defatted Rhesus monkey brain at pH 3.5 followed by Sephadex G-50 and carboxymethylcellulose chromatography. A ninhydrin-stained tryptic peptide map showed it to be free of contamination. A dose of 1.5 mg per animal produced the classical clinical and histological changes of experimental allergic encephalomyelitis 3 to 4 weeks after challenge in three out of three Rhesus monkeys. This fragment contains the region around tyrosine 69 which is encephalitogenic in the rabbit but does not contain the other active region of the molecule.
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- 1972
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23. Rev/RRE-Independent Mason–Pfizer Monkey Virus Constitutive Transport Element-Dependent Propagation of SIVmac239 Vectors Using a Single Round of Replication Assay
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Kathy A. Lew, Russell D. Schmidt, Tahir A. Rizvi, and Michale E. Keeling
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viruses ,Genetic Vectors ,Biology ,Regulatory Sequences, Nucleic Acid ,medicine.disease_cause ,Virus Replication ,Genes, env ,Virus ,chemistry.chemical_compound ,Virology ,Chlorocebus aethiops ,medicine ,Animals ,Humans ,Enhancer ,Gene ,Cell Line, Transformed ,COS cells ,virus diseases ,rev Gene Products, Human Immunodeficiency Virus ,Simian immunodeficiency virus ,In vitro ,Gene cassette ,Gene Products, rev ,chemistry ,HIV-1 ,Simian Immunodeficiency Virus ,Mason-Pfizer monkey virus ,DNA ,HeLa Cells - Abstract
In a step toward creating live-attenuated or DNA subunit vaccines for AIDS, the replication of simian immunodeficiency virus (SIV) was studied independently of the Rev and RRE (Rev-responsive element) regulatory system, over a single round. To accomplish this, the env gene of an SIV vector was made defective by the insertion of a SV40 promoter/enhancer hygromycin B phosphotransferase gene cassette. Using this vector as the backbone, molecular clones of SIV were generated that contained a mutated Rev, Rev(−), a deleted RRE, RRE(−), or both, Rev(−)RRE(−). It has been shown recently that human immunodeficiency virus type 1 (HIV-1) Rev and RRE functions can be replaced in vitro by a cis -acting sequence, constitutive transport element (CTE), from simian type D retroviruses. To determine whether such a cis -acting element from Mason–Pfizer monkey virus (MPMV) would substitute for SIV Rev and RRE functions, the MPMV CTE was inserted either into the Nef ORF or at the junction of vpx and vpr of our Rev(−), RRE(−), and Rev(−)RRE(−) SIV molecular clones. Cell-free viral stocks harvested from Cos cells following transfections of these molecular clones revealed that these stocks were infectious over a single round of replication; however, their replication was attenuated 16-fold compared to that of wild-type virus. In addition, our experiments revealed that CTE functions in a position-dependent manner such that its insertion at the junction of vpx and vpr attenuated SIV replication 8- to 12-fold compared to the attenuation observed when it was inserted in the nef region. Our results demonstrate that MPMV CTE is capable of substituting for SIV Rev and RRE functions, resulting in an attenuated ability to produce infectious virus.
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24. Electroejaculation of the great apes
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David E. Martin, Harold Warner, and Michale E. Keeling
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Atropine ,Male ,medicine.medical_specialty ,business.industry ,Biomedical Engineering ,Rectum ,Cell Count ,Hominidae ,Anesthesia, General ,Electroejaculation ,Spermatozoa ,Electric Stimulation ,Surgery ,Physical medicine and rehabilitation ,Phenothiazines ,Semen ,medicine ,Animals ,Ejaculation ,business ,Promazine ,Penis - Abstract
The scientific literature concerning electroejaculation of simian primates contains many reports of successful collection of seminal fluid through electrostimulation with penile and rectal electrodes. In none of these reports is there a sufficient discussion of the important electrical parameters involved, such as the amplitude and density of electric current and the impedance of the electrode/tissue interface. Without such information it is difficult, if not impossible, for investigators in other laboratories to duplicate the stimulation regimen successfully and without injury to the animal. This assumes even greater importance when such techniques are considered for application to human beings.
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- 1974
25. Helping east meet west. Review ofanimal models: Assessing the scope of their use in biomedical research, edited by Junichi Kawamata and Edward C. Melby, Jr. New York, Alan R. Liss, Inc., 1987, 398 pp, $65.00
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Michale E. Keeling
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Scope (project management) ,Library science ,Animal Science and Zoology ,Environmental ethics ,Sociology ,Ecology, Evolution, Behavior and Systematics - Published
- 1989
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26. Birth of a Lowland Gorilla (Gorilla gorilla gorilla) at the Yerkes Regional Primate Research Center
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Kenton E. Riddle, Jimmy Roberts, and Michale E. Keeling
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biology ,biology.animal ,Lowland gorilla ,Zoology ,Gorilla ,Primate - Published
- 1973
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27. Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
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Vicente C. Quintanilla, Cecilia R Giulivi, Donna F. Kusewitt, Jimi L. Brandon, Fernando Benavides, Jean Jaubert, Kirstin F. Barnhart, Irma B. Gimenez-Conti, Nancy W. Otto, Catherine Ross-Inta, John DiGiovanni, Claudio J. Conti, Carlos J. Perez, Jean-Louis Guénet, Isabelle Aubin, The University of Texas M.D. Anderson Cancer Center [Houston], Graduate School of Biomedical Sciences [Houston], The University of Texas Health Science Center at Houston (UTHealth)-The University of Texas M.D. Anderson Cancer Center [Houston], Génétique de la souris - Mouse Genetics, Institut Pasteur [Paris] (IP), Michale E. Keeling Center for Comparative Medicine and Research [Bastrop, Texas], School of Veterinary Medicine [Univ California Davis] (VetMed - UC Davis), University of California [Davis] (UC Davis), University of California (UC)-University of California (UC), Génétique fonctionnelle de la Souris, Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS), Supported by National Institutes of Health grant CA90922 (C.J.C.), Department of Health and Human Services/National Cancer Institute grants P30 CA016672 (F.B. and D.F. K.) and P30 ES007784 (I.G.C.), and funding from Autism Speaks (C.G.)., We thank the Research Animal Support Facility-Smithville for their assistance with the maintenance of the mouse strains. We also thank Kevin Lin for statistical analyses, the Histology and Tissue Processing Facility Core for the IHC, and the Molecular Biology Facility Core for DNA sequencing., We are grateful to Brenda Webb (Michale E. Keeling Center) for her excellent technical skills with blood sampling. We thank Qin Sun (BCM Medical Genetics Laboratories) for the plasma amino acid analysis and ASS liver activity assays., Institut Pasteur [Paris], School of Veterinary Medicine [UC Davis], University of California-University of California, and Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS)
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Male ,MESH: Disease Models, Animal ,Cerebellum ,MESH: Mice, Mutant Strains ,Developmental Disabilities ,Argininosuccinate synthase ,MESH: Sodium Benzoate / pharmacology ,MESH: Mice, Knockout ,Immunoenzyme Techniques ,Mice ,0302 clinical medicine ,Cell Movement ,Sodium Benzoate ,Hyperammonemia ,MESH: Animals ,MESH: Syndrome ,MESH: Cell Movement ,Growth Disorders ,Mice, Knockout ,Citrullinemia ,0303 health sciences ,biology ,MESH: Developmental Disabilities / etiology ,Syndrome ,MESH: Arginine / pharmacology ,MESH: Mutation, Missense / genetics ,MESH: Hyperammonemia / etiology ,Phenotype ,MESH: Citrullinemia / etiology ,3. Good health ,medicine.anatomical_structure ,Urea cycle ,MESH: Argininosuccinate Synthase / physiology ,Female ,medicine.symptom ,medicine.medical_specialty ,Ataxia ,Urea cycle disorder ,Blotting, Western ,Mutation, Missense ,Argininosuccinate Synthase ,MESH: Developmental Disabilities / drug therapy ,Arginine ,Nitric Oxide ,MESH: Hyperammonemia / drug therapy ,MESH: Phenotype ,Pathology and Forensic Medicine ,03 medical and health sciences ,MESH: Mice, Inbred C57BL ,Internal medicine ,MESH: Growth Disorders / etiology ,medicine ,Animals ,Humans ,MESH: Blotting, Western ,MESH: Growth Disorders / drug therapy ,Allele ,MESH: Immunoenzyme Techniques ,MESH: Mice ,Alleles ,030304 developmental biology ,MESH: Humans ,MESH: Alleles ,medicine.disease ,MESH: Cerebellum / abnormalities ,Mice, Mutant Strains ,MESH: Male ,Mice, Inbred C57BL ,Disease Models, Animal ,[SDV.GEN.GA]Life Sciences [q-bio]/Genetics/Animal genetics ,Endocrinology ,biology.protein ,MESH: Nitric Oxide / metabolism ,MESH: Female ,MESH: Citrullinemia / drug therapy ,030217 neurology & neurosurgery ,Regular Articles - Abstract
International audience; Citrullinemia type I (CTLN1, OMIM# 215700) is an inherited urea cycle disorder that is caused by an argininosuccinate synthetase (ASS) enzyme deficiency. In this report, we describe two spontaneous hypomorphic alleles of the mouse Ass1 gene that serve as an animal model of CTLN1. These two independent mouse mutant alleles, also described in patients affected with CTLN1, interact to produce a range of phenotypes. While some mutant mice died within the first week after birth, others survived but showed severe retardation during postnatal development as well as alopecia, lethargy, and ataxia. Notable pathological findings were similar to findings in human CTLN1 patients and included citrullinemia and hyperammonemia along with delayed cerebellar development, epidermal hyperkeratosis, and follicular dystrophy. Standard treatments for CTLN1 were effective in rescuing the phenotype of these mutant mice. Based on our studies, we propose that defective cerebellar granule cell migration secondary to disorganization of Bergmann glial cell fibers cause cerebellar developmental delay in the hyperammonemic and citrullinemic brain, pointing to a possible role for nitric oxide in these processes. These mouse mutations constitute a suitable model for both mechanistic and preclinical studies of CTLN1 and other hyperammonemic encephalopathies and, at the same time, underscore the importance of complementing knockout mutations with hypomorphic mutations for the generation of animal models of human genetic diseases.
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- 2010
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28. Genetic Factors and Orofacial Motor Learning Selectively Influence Variability in Central Sulcus Morphology in Chimpanzees (Pan troglodytes)
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Oliver Coulon, William D. Hopkins, Steven J. Schapiro, Mary Catherine Mareno, Kendall Davidek, Lindsay M. Mahovetz, Michelle M. Autrey, Adrien Meguerditchian, Sarah M. Pope, Institute for Advanced Studies - Aix-Marseille University (IMéRA), Institute of Language, Communication and the Brain (ILCB), Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS), Laboratoire des Sciences de l'Information et des Systèmes (LSIS), Centre National de la Recherche Scientifique (CNRS)-Arts et Métiers Paristech ENSAM Aix-en-Provence-Université de Toulon (UTLN)-Aix Marseille Université (AMU), Station de Primatologie, CNRS, UPS846, 13790 Rousset, France, Centre National de la Recherche Scientifique (CNRS), Laboratoire de psychologie cognitive (LPC), Centre National de la Recherche Scientifique (CNRS)-Aix Marseille Université (AMU), Station de primatologie (SP), Georgia State University, University System of Georgia (USG), Michale E. Keeling Center for Comparative Medicine and Research, The University of Texas Health Science Center at Houston (UTHealth), University of Texas-Pan, ANR-16-CONV-0002,ILCB,ILCB: Institute of Language Communication and the Brain(2016), and Aix Marseille Université (AMU)-Université de Toulon (UTLN)-Arts et Métiers Paristech ENSAM Aix-en-Provence-Centre National de la Recherche Scientifique (CNRS)
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0301 basic medicine ,Male ,Pan troglodytes ,central sulcus ,Troglodytes ,Sound production ,heritability ,03 medical and health sciences ,0302 clinical medicine ,chimpanzee ,Neuroplasticity ,medicine ,Animals ,Animal communication ,orofacial movements ,Research Articles ,Mouth ,Neuronal Plasticity ,language ,biology ,General Neuroscience ,Motor Cortex ,vocal learning ,Genetic Variation ,Anatomy ,biology.organism_classification ,Central sulcus ,Animal Communication ,030104 developmental biology ,medicine.anatomical_structure ,[SCCO.PSYC]Cognitive science/Psychology ,Vocal learning ,Female ,Psychology ,Motor learning ,Neuroscience ,030217 neurology & neurosurgery ,Psychomotor Performance ,Motor cortex - Abstract
Captive chimpanzees (Pan troglodytes) have been shown to learn the use of novel attention-getting (AG) sounds to capture the attention of humans as a means of requesting or drawing their attention to a desired object or food. There are significant individual differences in the use of AG sounds by chimpanzees and, here, we examined whether changes in cortical organization of the central sulcus (CS) were associated with AG sound production. MRI scans were collected from 240 chimpanzees, including 122 that reliably produced AG sounds and 118 that did not. For each subject, the depth of CS was quantified along the superior–inferior plane with specific interest in the inferior portion corresponding to the region of the motor cortex where the mouth and orofacial movements are controlled. Results indicated that CS depth in the inferior, but not superior, portion was significantly greater in chimpanzees that reliably produced AG sounds compared with those who did not. Quantitative genetic analyses indicated that overall CS surface area and depth were significantly heritable, particularly in the superior regions, but less so in the inferior and central portions. Further, heritability in CS depth was altered as a function of acquisition of AG sounds. The collective results suggest that learning to produce AG sounds resulted in region-specific cortical reorganization within the inferior portion of the CS, a finding previously undocumented in chimpanzees or any nonhuman primate.SIGNIFICANCE STATEMENTRecent studies in chimpanzees (Pan troglodytes) have shown that some can learn to produce novel sounds by configuring different orofacial movement patterns and these sounds are used in communicatively relevant contexts. Here, we examined the neuromorphological correlates in the production of these sounds in chimpanzees. We show that chimpanzees that have learned to produce these sounds show significant differences in central sulcus (CS) morphology, particularly in the inferior region. We further show that overall CS morphology and regions within the superior portion are significantly heritable, whereas central and inferior portions of the CS are not. The collective findings suggest chimpanzees exhibit cortical plasticity in regions of the brain that were central to the emergence of speech functions in humans.
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- 2017
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29. Social networks in primates: Smart and tolerant species have more efficient networks
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Barbara Tiddi, Bernard Thierry, Linda M. Fedigan, Nicolas Claidière, Odile Petit, Andrew Whiten, Mackenzie L. Bergstrom, Marine Levé, Claudia Fichtel, Eugenia Polizzi di Sorrentino, Sarah F. Brosnan, Christèle Borgeaud, Erica van de Waal, Andrew J. J. MacIntosh, Lydia M. Hopper, Anna Viktoria Schnoell, Margaret C. Crofoot, Cédric Sueur, Mary Catherine Mareno, Marie Pelé, Cristian Pasquaretta, Département Ecologie, Physiologie et Ethologie (DEPE-IPHC), Institut Pluridisciplinaire Hubert Curien (IPHC), Université de Strasbourg (UNISTRA)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), School of Psychology, University of St Andrew, Kyoto University [Kyoto], Department of Anthropology at the University of Calgary, Université de Neuchâtel (UNINE), Georgia State University, University System of Georgia (USG), Department of Anthropology, University of California, Courant Research Centre Geobiology, Georg-August-University [Göttingen], Michale E. Keeling Center for Comparative Medicine and Research, The University of Texas Health Science Center at Houston (UTHealth), University of St Andrews. School of Psychology and Neuroscience, University of St Andrews. ‘Living Links to Human Evolution’ Research Centre, University of St Andrews. Institute of Behavioural and Neural Sciences, and University of St Andrews. Centre for Social Learning & Cognitive Evolution
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Male ,Theoretical computer science ,BF Psychology ,Group-size ,Modularity (biology) ,Intelligence ,BF ,Biology ,social network primates ,Neocortex size ,Basic Behavioral and Social Science ,Models, Biological ,Article ,Social support ,Models ,Phénomènes atmosphériques ,ddc:570 ,Behavioral and Social Science ,Behavioural ecology ,Social evolution ,Animal behaviour ,Animals ,Humans ,Information flow (information theory) ,Social Behavior ,Consequences ,Behavior ,Multidisciplinary ,Natural selection ,Behavior, Animal ,Animal ,Lemur ,Community structure ,Brain ,Social Support ,Cognition ,Haplorhini ,Social learning ,Biological ,Cooperation ,GN ,[SDE]Environmental Sciences ,Female ,Centrality ,Organization ,Decision-making - Abstract
Network optimality has been described in genes, proteins and human communicative networks. In the latter, optimality leads to the efficient transmission of information with a minimum number of connections. Whilst studies show that differences in centrality exist in animal networks with central individuals having higher fitness, network efficiency has never been studied in animal groups. Here we studied 78 groups of primates (24 species).We found that group size and neocortex ratio were correlated with network efficiency. Centralisation (whether several individuals are central in the group) and modularity (how a group is clustered) had opposing effects on network efficiency, showing that tolerant species have more efficient networks. Such network properties affecting individual fitness could be shaped by natural selection. Our results are in accordance with the social brain and cultural intelligence hypotheses, which suggest that the importance of network efficiency and information flow through social learning relates to cognitive abilities., SCOPUS: ar.j, info:eu-repo/semantics/published
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- 2014
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30. Identification of the social and cognitive processes underlying human cumulative culture
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Kevin N. Laland, Bernard Thierry, Lewis G. Dean, Rachel L. Kendal, Steven J. Schapiro, Centre for Social Learning and Cognitive Evolution, University of St Andrews [Scotland], Centre for the Coevolution of Biology and Culture, Durham University, Michale E. Keeling Center for Comparative Medicine and Research, The University of Texas Health Science Center at Houston (UTHealth), Département Ecologie, Physiologie et Ethologie (DEPE-IPHC), Institut Pluridisciplinaire Hubert Curien (IPHC), Université Louis Pasteur - Strasbourg I-Centre National de la Recherche Scientifique (CNRS)-Université Louis Pasteur - Strasbourg I-Centre National de la Recherche Scientifique (CNRS), Université de Strasbourg (UNISTRA)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), Université Louis Pasteur - Strasbourg I-Centre National de la Recherche Scientifique (CNRS), and Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)
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MESH: Imitative Behavior ,MESH: Cognition ,MESH: Pan troglodytes ,Altruism ,Cognition ,Mental Processes ,0302 clinical medicine ,MESH: Cultural Evolution ,MESH: Animals ,Sociocultural evolution ,Problem Solving ,MESH: Mental Processes ,MESH: Teaching ,media_common ,Multidisciplinary ,MESH: Altruism ,[SDV.NEU.PC]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Psychology and behavior ,Communication ,05 social sciences ,MESH: Interpersonal Relations ,Child, Preschool ,[SDE]Environmental Sciences ,Female ,Identification (biology) ,MESH: Communication ,Imitation ,Psychology ,MESH: Social Behavior ,Cognitive psychology ,MESH: Problem Solving ,Pan troglodytes ,media_common.quotation_subject ,050105 experimental psychology ,03 medical and health sciences ,Interpersonal relationship ,Reward ,Cultural Evolution ,MESH: Cebus ,Animals ,Cebus ,Humans ,Learning ,Interpersonal Relations ,0501 psychology and cognitive sciences ,Social Behavior ,MESH: Reward ,MESH: Humans ,Extramural ,Teaching ,MESH: Child, Preschool ,Imitative Behavior ,MESH: Learning ,MESH: Female ,030217 neurology & neurosurgery - Abstract
Acquire and Share Few would argue with the stance that human social cognition supports an unequaled capacity to acquire knowledge and to share it with others. Dean et al. (p. 1114 ; see the Perspective by Kurzban and Barrett ) compared the extent to which these social and cognitive psychological processes can be elicited in children, capuchins, and chimpanzees through the use of a three-level puzzlebox task. Incentivized by improving rewards, 3- to 4-year-old children progressed from the first to the third level by imitating observed actions, taught other members of their social group how to solve the problem, and shared the rewards obtained. By contrast, neither the capuchins nor chimpanzees, very few of which ever reached the third level, exhibited these charactertistics.
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- 2012
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31. Long term impacts of early social environment on chimpanzee white matter.
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Mulholland MM, Hecht E, Wesley MJ, and Hopkins WD
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- Animals, Female, Male, Social Behavior, Gray Matter diagnostic imaging, Brain diagnostic imaging, Anisotropy, Pan troglodytes physiology, White Matter diagnostic imaging, Diffusion Tensor Imaging methods, Social Environment
- Abstract
Early adverse rearing conditions are known to have deleterious consequences on social behavior, cognition, and brain development of both human and nonhuman primates. We analyzed archival diffusion tensor imaging (DTI) data from mother- (MR) or nursery-reared (NR) chimpanzees and used support vector machine learning to determine whether we could retrospectively classify chimpanzees as MR or NR based on white matter fractional anisotropy (FA) decades after their rearing experiences. A significant proportion of chimpanzees were correctly classified as MR and NR based on white matter fractional anisotropy (76.32%; p = 0.004). Voxel-based morphometry revealed that MR chimpanzees had increased FA in the splenium/isthmus of the corpus collosum and premotor cortex, while NR chimpanzees had increased FA in the thalamic region, cuneus, and lateral genu of the corpus collosum (p < 0.01). A subset of the NR chimpanzees participated in early social interventions, but unlike gray matter, these interventions do not explain misclassification based on white matter. These findings suggest that nursery rearing has long-term effects on both gray and white matter, but that early interventions may ameliorate the effects on gray matter only. Future research should investigate the effectiveness and relative contributions of combined social, cognitive, and nutritional interventions on brain development in nonhuman primates., Competing Interests: Declarations. Competing interests: The authors declare no competing interests., (© 2024. The Author(s).)
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- 2024
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32. Diversity of Campylobacter spp. circulating in a rhesus macaque ( Macaca mulatta ) breeding colony using culture and molecular methods.
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Bacon RL, Hodo CL, Wu J, Welch S, Nickodem C, Vinasco J, Threadgill D, Gray SB, Norman KN, and Lawhon SD
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- Animals, Monkey Diseases microbiology, Campylobacter coli genetics, Campylobacter coli drug effects, Campylobacter coli isolation & purification, Male, Campylobacter genetics, Campylobacter classification, Campylobacter isolation & purification, Campylobacter drug effects, Female, Drug Resistance, Multiple, Bacterial genetics, Diarrhea microbiology, Diarrhea veterinary, Feces microbiology, Prevalence, Genetic Variation, Genotype, Macaca mulatta, Campylobacter Infections microbiology, Campylobacter Infections veterinary, Whole Genome Sequencing, Campylobacter jejuni genetics, Campylobacter jejuni drug effects, Campylobacter jejuni isolation & purification, Campylobacter jejuni classification, Anti-Bacterial Agents pharmacology
- Abstract
Campylobacter jejuni and Campylobacter coli represent the leading causes of bacterial gastroenteritis in humans, and infections can produce post-infectious irritable bowel syndrome (PI-IBS). Rhesus macaques ( Macaca mulatta ) (RM) are similarly susceptible to acute campylobacteriosis and represent a potential model of PI-IBS. We characterized the Campylobacter species circulating in an RM breeding colony using culture, qPCR, and whole genome sequencing (WGS). We also compared the C. jejuni and C. coli prevalence in RM as detected with qPCR versus culture and identified risk factors for bacteria presence and intestinal disease. Culture of 275 samples yielded C. coli (103) and C. jejuni (8), of which 21.6% were resistant to quinolones and 3.6% were resistant to macrolides. Multidrug-resistant isolates were obtained exclusively from animals exhibiting diarrhea or with histologically confirmed chronic enterocolitis. WGS revealed a non-clonal population of Campylobacter spp. Genotypic predictions of resistance were excellent except for aminoglycosides. All sequenced isolates contained genes for all subunits of cytolethal distending toxin. qPCR detected a prevalence of 45.9% for C. coli and 29.6% for C. jejuni . The quantity of either bacteria was significantly higher ( P < 0.05) in animals with intestinal disease compared to healthy animals, though only young age was significantly associated with the presence of Campylobacter sp. or intestinal disease. Significantly more C. jejuni positive animals were detected with qPCR than with culture. These results provide a comprehensive characterization of Campylobacter spp. circulating in a breeding colony of RM in the United States and suggest that qPCR is superior for the detection of C. jejuni in RM., Importance: Gastrointestinal disease is one of the most common reasons for hospitalization in non-human primate colonies and accounts for over one-third of non-research related euthanasia. In rhesus macaques, this manifests as both acute diarrhea and chronic enterocolitis (CE), a syndrome of chronic diarrhea resulting in poor weight gain or weight loss which is minimally responsive to treatment. Campylobacter spp. are major causes of acute enterocolitis in rhesus macaques and may predispose individuals to the development of CE, similar to post-infectious irritable bowel syndrome in humans. Despite these concerns, there are few studies characterizing Campylobacter in rhesus macaque colonies, in particular utilizing whole genome sequencing and assessing findings with respect to the health status of the host. Our findings provide insight into Campylobacter strains circulating in rhesus macaque colonies, which can improve clinical monitoring, assist in treatment decisions, and provide new avenues of investigation into campylobacteriosis as a catalyst for CE., Competing Interests: The authors declare no conflict of interest.
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- 2024
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33. Development of an operational trap for collection, killing, and preservation of triatomines (Hemiptera: Reduviidae): the kissing bug kill trap.
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Hamer GL, Fimbres-Macias JP, Juarez JG, Downs CH, Carbajal E, Melo M, Garza DY, Killets KC, Wilkerson GK, Carrera-Treviño R, Corona-Barrera E, Tello-Campa AA, Rojas-Mesta MR, Borden JH, Banfield MG, and Hamer SA
- Subjects
- Animals, Triatoma, Texas, Mexico, Triatominae, Insect Vectors, Chagas Disease transmission, Insect Control instrumentation, Insect Control methods
- Abstract
Surveillance of triatomines or kissing bugs (Hemiptera: Reduviidae: Triatominae), the insect vectors of Trypanosoma cruzi, a Chagas disease agent, is hindered by the lack of an effective trap. To develop a kissing bug trap, we made iterative improvements over 3 years on a basic design resulting in 7 trap prototypes deployed across field sites in Texas, United States and Northern Mexico, yielding the capture of 325 triatomines of 4 species (Triatoma gerstaeckeri [Stål], T. sanguisuga [LeConte], T. neotomae [Neiva], and T. rubida [Uhler]). We began in 2019 with vertical transparent tarpaulin panel traps illuminated with artificial light powered by AC current, which were successful in autonomous trapping of flying triatomines, but were expensive, labor-intensive, and fragile. In 2020, we switched to white LED lights powered by a solar cell. We tested a scaled-down version of the vertical panel traps, a commercial cross-vane trap, and a multiple-funnel trap. The multiple-funnel traps captured 2.6× more kissing bugs per trap-day than cross-vane traps and approached the performance of the vertical panel traps in number of triatomines captured, number of triatomines per trap-day and triatomines per arthropod bycatch. Multiple-funnel traps required the least labor, were more durable, and had the highest triatomines per day per cost. Propylene glycol in the collection cups effectively preserved captured triatomines allowing for molecular detection of T. cruzi. The trapping experiments established dispersal patterns for the captured species. We conclude that multiple-funnel traps with solar-powered LED lights should be considered for adoption as surveillance and potentially mass-trapping management tools for triatomines., (© The Author(s) 2024. Published by Oxford University Press on behalf of Entomological Society of America. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.)
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- 2024
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34. Serial 'deep-sampling' PCR of fragmented DNA reveals the wide range of Trypanosoma cruzi burden among chronically infected hosts and allows accurate monitoring of parasite load following treatment.
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White BE, Hodo CL, Hamer SA, Saunders AB, Laucella SA, Hall DB, and Tarleton RL
- Abstract
Infection with the protozoan parasite Trypanosoma cruzi is generally well-controlled by host immune responses, but appears to be rarely eliminated. The resulting persistent, low-level infection results in cumulative tissue damage with the greatest impact generally in the heart in the form of chagasic cardiomyopathy. The relative success in immune control of T. cruzi infection usually averts acute phase death but has the negative consequence that the low-level presence of T. cruzi in hosts is challenging to detect unequivocally. Thus, it is difficult to identify those who are actively infected and, as well, problematic to gauge the impact of treatment, particularly in the evaluation of the relative efficacy of new drugs. In this study we employ DNA fragmentation and high numbers of replicate PCR reaction ('deep-sampling') to extend the quantitative range of detecting T. cruzi in blood by at least 3 orders of magnitude relative to current protocols. When combined with sampling blood at multiple time points, deep sampling of fragmented DNA allowed for detection of T. cruzi in all infected hosts in multiple host species. In addition, we provide evidence for a number of characteristics not previously rigorously quantified in the population of hosts with naturally acquired T. cruzi infection, including, a > 6-log variation between chronically infected individuals in the stable parasite levels, a continuing decline in parasite load during the second and third years of infection in some hosts, and the potential for parasite load to change dramatically when health conditions change. Although requiring strict adherence to contamination-prevention protocols and significant resources, deep-sampling PCR provides an important new tool for assessing new therapies and for addressing long-standing questions in T. cruzi infection and Chagas disease.
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- 2024
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35. ECG Features in Orthotopic Cardiac Xenotransplantation: Comparisons With Published Literature.
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Mitchell CB, Simmons J, Neal SJ, Cleveland DC, Bar-Cohen Y, and Cleveland JD
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- Animals, Swine, Humans, Heterografts, Transplantation, Heterologous methods, Transplantation, Heterologous adverse effects, Heart Transplantation, Electrocardiography methods
- Abstract
Introduction: Although there is a plethora of literature on electrocardiographic changes following cardiac allotransplantation, there is little in the field of cardiac xenotransplantation. The only published literature to date is that of the first pig-to-human cardiac xenotransplantation. Here we take a close look at the electrocardiographic parameters in four non-human primate recipients of orthotopic cardiac xenotransplantation to develop baseline metrics for comparison., Methods: Orthotopic cardiac xenotransplantion was carried out in four non-human primate recipients. Electrocardiographic parameters were followed at various intervals using an internal hemodynamic monitoring system (DSI) as well as a standard 12-lead electrocardiogram (ECG). ECG intervals were then compared to published literature on porcine ECG intervals and pig-to-human cardiac xenotransplantation., Results: There were no significant differences observed between timepoints for HR, PR, QRS, QT, or QTc after cardiac xenotransplantation for each animal subject. ECG parameters were statistically similar to those of in situ mini-pig hearts in the literature. ECG parameters from the DSI on average were shorter than those from a traditional ECG, however, DSI parameters were consistent over time., Conclusion: These results demonstrate the possibility of conduction health for genetically engineered porcine donor hearts following cardiac xenotransplantation. Ongoing work to compare the results of an ECG in a porcine donor heart before and after implantation into a NHP is necessary to better characterize variables that may be at play in the function of the conduction system., (© 2024 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
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- 2024
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36. Comparative analysis of the chimpanzee and human brain superficial structural connectivities.
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Chauvel M, Pascucci M, Uszynski I, Herlin B, Mangin JF, Hopkins WD, and Poupon C
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- Animals, Humans, Diffusion Tensor Imaging, Neural Pathways anatomy & histology, Male, Species Specificity, Female, Image Processing, Computer-Assisted, Connectome, Pan troglodytes anatomy & histology, Brain anatomy & histology, Brain diagnostic imaging, White Matter anatomy & histology, White Matter diagnostic imaging
- Abstract
Diffusion MRI tractography (dMRI) has fundamentally transformed our ability to investigate white matter pathways in the human brain. While long-range connections have extensively been studied, superficial white matter bundles (SWMBs) have remained a relatively underexplored aspect of brain connectivity. This study undertakes a comprehensive examination of SWMB connectivity in both the human and chimpanzee brains, employing a novel combination of empirical and geometric methodologies to classify SWMB morphology in an objective manner. Leveraging two anatomical atlases, the Ginkgo Chauvel chimpanzee atlas and the Ginkgo Chauvel human atlas, comprising respectively 844 and 1375 superficial bundles, this research focuses on sparse representations of the morphology of SWMBs to explore the little-understood superficial connectivity of the chimpanzee brain and facilitate a deeper understanding of the variability in shape of these bundles. While similar, already well-known in human U-shape fibers were observed in both species, other shapes with more complex geometry such as 6 and J shapes were encountered. The localisation of the different bundle morphologies, putatively reflecting the brain gyrification process, was different between humans and chimpanzees using an isomap-based shape analysis approach. Ultimately, the analysis aims to uncover both commonalities and disparities in SWMBs between chimpanzees and humans, shedding light on the evolution and organization of these crucial neural structures., (© 2024. The Author(s).)
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- 2024
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37. Evolutionary scaling and cognitive correlates of primate frontal cortex microstructure.
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Stimpson CD, Smaers JB, Raghanti MA, Phillips KA, Jacobs B, Hopkins WD, Hof PR, and Sherwood CC
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- Animals, Neuropil, Species Specificity, Motor Cortex physiology, Motor Cortex anatomy & histology, Prefrontal Cortex physiology, Prefrontal Cortex anatomy & histology, Male, Biological Evolution, Cognition physiology, Primates anatomy & histology, Frontal Lobe physiology, Frontal Lobe anatomy & histology
- Abstract
Investigating evolutionary changes in frontal cortex microstructure is crucial to understanding how modifications of neuron and axon distributions contribute to phylogenetic variation in cognition. In the present study, we characterized microstructural components of dorsolateral prefrontal cortex, orbitofrontal cortex, and primary motor cortex from 14 primate species using measurements of neuropil fraction and immunohistochemical markers for fast-spiking inhibitory interneurons, large pyramidal projection neuron subtypes, serotonergic innervation, and dopaminergic innervation. Results revealed that the rate of evolutionary change was similar across these microstructural variables, except for neuropil fraction, which evolves more slowly and displays the strongest correlation with brain size. We also found that neuropil fraction in orbitofrontal cortex layers V-VI was associated with cross-species variation in performance on experimental tasks that measure self-control. These findings provide insight into the evolutionary reorganization of the primate frontal cortex in relation to brain size scaling and its association with cognitive processes., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
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- 2024
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38. The Integration of Veterinary Medicine and Behavioral Management in the Care of Captive Pigtail Macaques ( Macaca nemestrina ).
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Toscano JE, Hart SA, and Malinowski CM
- Abstract
The Washington National Primate Research Center (WaNPRC) maintains the largest domestic breeding colony of pigtail macaques ( Macaca nemestrina ) in the United States, with animals housed in small to medium-sized social groups. As part of the animal care plan, a programmatic framework is utilized, which integrates clinical care with socialization considerations for nonhuman primates (NHPs). This framework encompasses the following areas: (1) socialization in the clinical setting; (2) positive reinforcement training (PRT); (3) measures to ensure proper identification and medication distribution; and (4) in-group treatments. The success of this framework is demonstrated by the high socialization rate for hospitalized animals (99.5% social pairing success), with the majority of clinical cases (95%) being treated in social groups. Ultimately, this framework seeks to buffer stressors when animals require clinical care or husbandry manipulations. Taken together, the above components foster an environment that provides a comprehensive approach to NHP medical and behavioral management.
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- 2024
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39. Development of an engineered extracellular vesicles-based vaccine platform for combined delivery of mRNA and protein to induce functional immunity.
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Luo X, McAndrews KM, Arian KA, Morse SJ, Boeker V, Kumbhar SV, Hu Y, Mahadevan KK, Church KA, Chitta S, Ryujin NT, Hensel J, Dai J, Dowlatshahi DP, Sugimoto H, Kirtley ML, LeBleu VS, Shalapour S, Simmons JH, and Kalluri R
- Subjects
- Animals, Mice, Female, SARS-CoV-2 immunology, Spike Glycoprotein, Coronavirus immunology, Spike Glycoprotein, Coronavirus genetics, Humans, Cell Line, Tumor, Melanoma immunology, Melanoma therapy, Lipids chemistry, Lipids administration & dosage, Liposomes, Extracellular Vesicles immunology, COVID-19 Vaccines administration & dosage, COVID-19 Vaccines immunology, Cancer Vaccines administration & dosage, Cancer Vaccines immunology, RNA, Messenger administration & dosage, COVID-19 prevention & control, COVID-19 immunology, Ovalbumin immunology, Ovalbumin administration & dosage, Mice, Inbred C57BL, Nanoparticles administration & dosage, Nanoparticles chemistry
- Abstract
mRNA incorporated in lipid nanoparticles (LNPs) became a new class of vaccine modality for induction of immunity against COVID-19 and ushered in a new era in vaccine development. Here, we report a novel, easy-to-execute, and cost effective engineered extracellular vesicles (EVs)-based combined mRNA and protein vaccine platform (EV
X-M+P vaccine) and explore its utility in proof-of-concept immunity studies in the settings of cancer and infectious disease. As a first example, we engineered EVs, natural nanoparticle carriers shed by all cells, to contain ovalbumin mRNA and protein (EVOvaM+P vaccine) to serve as cancer vaccine against ovalbumin-expressing melanoma tumors. EVOvaM+P administration to mice with established melanoma tumors resulted in tumor regression associated with effective humoral and adaptive immune responses. As a second example, we generated engineered EVs that contain Spike (S) mRNA and protein to serve as a combined mRNA and protein vaccine (EVSpikeM+P vaccine) against SARS-CoV-2 infection. EVSpikeM+P vaccine administration in mice and baboons elicited robust production of neutralizing IgG antibodies against RBD (receptor binding domain) of S protein and S protein specific T cell responses. Our proof-of-concept study describes a new platform with an ability for rapid development of combination mRNA and protein vaccines employing EVs for deployment against cancer and other diseases., Competing Interests: Declaration of competing interest MD Anderson Cancer Center and RK have filed patent applications and patents issued in the area of exosome biology, and some of them are licensed to PranaX, Inc. for non-cancer related use. MD Anderson and RK hold equity in PranaX and RK serves as an advisor on non-cancer related matters., (Copyright © 2024. Published by Elsevier B.V.)- Published
- 2024
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40. Longitudinal Baboon ( Papio anubis ) Neutrophil to Lymphocyte Ratio (NLR), and Correlations with Monthly Sedation Rate and Within-Group Sedation Order.
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Neal SJ, Schapiro SJ, and Magden ER
- Abstract
Neutrophil to lymphocyte ratio (NLR) is a simple marker of stress and inflammation, but there is limited research regarding NLR in nonhuman primates (NHPs), with studies showing associations with longevity, certain medical conditions, and stressful circumstances. Here, we examined baboon NLR longitudinally, and as a function of health parameters. We also examined whether NLR was affected by sedation rate, as well as the order of sedation within a group, given that sedation events during clinical and research practices can induce stress in NHPs. While older adult and geriatric baboon NLR did not differ longitudinally, juvenile and young adult NLR tended to increase, primarily driven by increases in females. Additionally, baboons sedated later within a group showed significantly higher NLRs than those sedated earlier in the process. However, baboons with higher sedation rates per month showed lower NLRs. These data indicate that NLR may be dysregulated in different ways as a function of different types of stress, with sedation order (i.e., acute stress) causing pathological increases in NLR, and sedation rate over time (i.e., chronic stress) causing decreases. Importantly, we propose that NLR, a routinely obtained veterinary measure, has potential utility as a welfare indicator of stress resulting from clinical and research practices, as well as a measure that can inform behavioral management practices and interventions.
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- 2024
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41. Nursery- vs. Mother-Reared Baboons: Reproductive Success and Health Parameters.
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Neal SJ, Schapiro SJ, Lambeth SP, and Magden ER
- Abstract
There is a plethora of data demonstrating the deleterious consequences of nursery rearing in nonhuman primates (NHPs). However, baboon studies report varying consequences of nursery rearing, from no differences in reproduction and sociality to moderate differences in social cognition and abnormal behavior. We compared health and reproductive parameters in a large sample (N= 231) of mother-reared (MR) and nursery-reared (NR) captive olive baboons housed at the Keeling Center for Comparative Medicine and Research, Texas. MR baboons had higher neutrophil-to-lymphocyte ratios and heart rates than NR baboons. Rearing was not a significant predictor of body condition score or body weight ( p > 0.20), and MR and NR individuals did not differ in the level of wounding observed ( p > 0.70). The proportion of successful births across NR and MR females was also not significantly different ( p > 0.70), nor were rates of maternal neglect and infant death. These data suggest minimal differences in health and reproductive parameters across rearing statuses in baboons housed at this facility. In conjunction with previous research that also seems to show minimal differences as a function of rearing in baboons, but directly contrast with data in other NHP species, these data suggest that baboons may be more robust against deleterious effects of abnormal rearing conditions than other NHP species.
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- 2024
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42. The uniqueness of human vulnerability to brain aging in great ape evolution.
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Vickery S, Patil KR, Dahnke R, Hopkins WD, Sherwood CC, Caspers S, Eickhoff SB, and Hoffstaedter F
- Subjects
- Humans, Animals, Male, Female, Hominidae, Gray Matter, Adult, Aged, Magnetic Resonance Imaging, Middle Aged, Aging physiology, Biological Evolution, Brain, Pan troglodytes
- Abstract
Aging is associated with progressive gray matter loss in the brain. This spatially specific, morphological change over the life span in humans is also found in chimpanzees, and the comparison between these great ape species provides a unique evolutionary perspective on human brain aging. Here, we present a data-driven, comparative framework to explore the relationship between gray matter atrophy with age and recent cerebral expansion in the phylogeny of chimpanzees and humans. In humans, we show a positive relationship between cerebral aging and cortical expansion, whereas no such relationship was found in chimpanzees. This human-specific association between strong aging effects and large relative cortical expansion is particularly present in higher-order cognitive regions of the ventral prefrontal cortex and supports the "last-in-first-out" hypothesis for brain maturation in recent evolutionary development of human faculties.
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- 2024
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43. Thyroblastoma in a rhesus macaque (Macaca mulatta): A case report.
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Greenberg J, Wiener DJ, Buchl SJ, and Hensel ME
- Subjects
- Animals, Male, Female, Macaca mulatta, Monkey Diseases pathology, Monkey Diseases diagnosis, Thyroid Neoplasms veterinary, Thyroid Neoplasms pathology, Thyroid Neoplasms diagnosis
- Abstract
In this report, we describe the gross, histopathology, and immunohistochemical findings of a thyroblastoma that arose in the right lobe of the thyroid gland in a 2-month-old rhesus macaque (Macaca mulatta)., (© 2024 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
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- 2024
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44. Chimpanzees (Pan troglodytes) with better task-based delay of gratification skills are rated as less impulsive, more agreeable, and smarter.
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Hopkins WD, Cox CM, Latzman RD, and Beran MJ
- Subjects
- Animals, Male, Female, Behavior, Animal physiology, Self-Control, Individuality, Age Factors, Sex Factors, Pan troglodytes, Delay Discounting physiology, Impulsive Behavior physiology, Personality physiology
- Abstract
Delay of gratification and inhibitory control are generally considered measures of self-control. In humans, individual differences in measures of self-control are associated with a host of behavioral, neurological, cognitive, and health-related outcomes. Self-control is not unique to humans and has been demonstrated in a variety of nonhuman species using a variety of paradigms. In this study, the effect of sex and age on delay of gratification performance, as measured by the hybrid delay task, was tested in a sample of 88 chimpanzees. Additionally, whether individual differences in hybrid delay task performance were associated with different aspects of personality was examined in this study. Contrary to reports in human subjects, geriatric male chimpanzees were found to perform more efficiently than adult males, while no age differences were found between geriatric and adult females. Indeed, delay of gratification efficiency was positively associated with age in males and negatively associated with age in females. Chimpanzees that performed more efficiently on the hybrid delay task were also found to be rated as more intelligent, more extraverted, and less impulsive. These findings suggest that objective measures of efficiency in delay of gratification tasks are associated with different dimensions of personality, which have some overlapping construct validity. (PsycInfo Database Record (c) 2024 APA, all rights reserved).
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- 2024
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45. Phylogenetic differences in the morphology and shape of the central sulcus in great apes and humans: implications for the evolution of motor functions.
- Author
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Foubet O, Mangin JF, Sun ZY, Sherwood CC, and Hopkins WD
- Subjects
- Animals, Humans, Male, Female, Adult, Hand physiology, Hand anatomy & histology, Young Adult, Pongo pygmaeus anatomy & histology, Pongo pygmaeus physiology, Species Specificity, Pongo abelii anatomy & histology, Pongo abelii physiology, Biological Evolution, Pan troglodytes anatomy & histology, Pan troglodytes physiology, Gorilla gorilla anatomy & histology, Gorilla gorilla physiology, Magnetic Resonance Imaging, Phylogeny, Motor Cortex anatomy & histology, Motor Cortex physiology, Motor Cortex diagnostic imaging, Hominidae anatomy & histology, Hominidae physiology
- Abstract
The central sulcus divides the primary motor and somatosensory cortices in many anthropoid primate brains. Differences exist in the surface area and depth of the central sulcus along the dorso-ventral plane in great apes and humans compared to other primate species. Within hominid species, there are variations in the depth and aspect of their hand motor area, or knob, within the precentral gyrus. In this study, we used post-image analyses on magnetic resonance images to characterize the central sulcus shape of humans, chimpanzees (Pan troglodytes), gorillas (Gorilla gorilla), and orangutans (Pongo pygmaeus and Pongo abelii). Using these data, we examined the morphological variability of central sulcus in hominids, focusing on the hand region, a significant change in human evolution. We show that the central sulcus shape differs between great ape species, but all show similar variations in the location of their hand knob. However, the prevalence of the knob location along the dorso-ventral plane and lateralization differs between species and the presence of a second ventral motor knob seems to be unique to humans. Humans and orangutans exhibit the most similar and complex central sulcus shapes. However, their similarities may reflect divergent evolutionary processes related to selection for different positional and habitual locomotor functions., (© The Author(s) 2024. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.)
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- 2024
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46. Neutrophil to lymphocyte ratio in captive olive baboons (Papio anubis): The effects of age, sex, rearing, stress, and pregnancy.
- Author
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Neal SJ, Achorn AM, Schapiro SJ, Hopkins WD, and Simmons JH
- Subjects
- Animals, Female, Male, Pregnancy, Age Factors, Sex Factors, Papio anubis genetics, Papio anubis physiology, Neutrophils, Lymphocytes, Stress, Physiological
- Abstract
In apes and humans, neutrophil to lymphocyte ratio (NLR) can be used as a predictive indicator of a variety of clinical conditions, longevity, and physiological stress. In chimpanzees specifically, NLR systematically varies with age, rearing, sex, and premature death, indicating that NLR may be a useful diagnostic tool in assessing primate health. To date, just one very recent study has investigated NLR in old world monkeys and found lower NLR in males and nursery-reared individuals, as well as a negative relationship between NLR and disease outcomes. Given that baboons are increasingly used as research models, we aimed to characterize NLR in baboons by providing descriptive data and examinations of baboon NLR heritability, and of the relationships between NLR, age, rearing, and sex in 387 olive baboons (Papio anubis) between 6 months and 19 years of age. We found that (1) mother-reared baboons had higher NLRs than nursery-reared baboons; (2) females had higher NLRs than males; and (3) there was a quadratic relationship between NLR and age, such that middle-aged individuals had the highest NLR values. We also examined NLR as a function of transport to a new facility using a subset of the data. Baboons exhibited significantly higher transport NLRs compared to routine exam NLRs. More specifically, adult baboons had higher transport NLRs than routine NLRs, whereas juveniles showed no such difference, suggesting that younger animals may experience transport stress differently than older animals. We also found that transport NLR was heritable, whereas routine NLR was not, possibly suggesting that stress responses (as indicated in NLR) have a strong genetic component. Consistent with research in humans and chimpanzees, these findings suggest that NLR varies with important biological and life history variables and that NLR may be a useful health biomarker in baboons., (© 2024 Wiley Periodicals LLC.)
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- 2024
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47. Whole-genome sequences of Campylobacter coli and Campylobacter jejuni isolates from rhesus macaques ( Macaca mulatta ) with and without intestinal disease.
- Author
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Bacon RL, Norman KN, Nickodem CA, Vinasco JA, Gray SB, Hodo CL, and Lawhon SD
- Abstract
Campylobacter jejuni or Campylobacter coli infection can lead to post-infectious irritable bowel syndrome in humans and may produce a similar syndrome in rhesus macaques ( Macaca mulatta ). We report the complete genomes of 8 C . jejuni isolates and 103 C . coli isolates obtained from rhesus macaques with and without intestinal disease., Competing Interests: The authors declare no conflict of interest.
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- 2024
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48. Structurally divergent and recurrently mutated regions of primate genomes.
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Mao Y, Harvey WT, Porubsky D, Munson KM, Hoekzema K, Lewis AP, Audano PA, Rozanski A, Yang X, Zhang S, Yoo D, Gordon DS, Fair T, Wei X, Logsdon GA, Haukness M, Dishuck PC, Jeong H, Del Rosario R, Bauer VL, Fattor WT, Wilkerson GK, Mao Y, Shi Y, Sun Q, Lu Q, Paten B, Bakken TE, Pollen AA, Feng G, Sawyer SL, Warren WC, Carbone L, and Eichler EE
- Subjects
- Animals, Humans, Base Sequence, Biological Evolution, Sequence Analysis, DNA, Genomic Structural Variation, Genome, Primates classification, Primates genetics
- Abstract
We sequenced and assembled using multiple long-read sequencing technologies the genomes of chimpanzee, bonobo, gorilla, orangutan, gibbon, macaque, owl monkey, and marmoset. We identified 1,338,997 lineage-specific fixed structural variants (SVs) disrupting 1,561 protein-coding genes and 136,932 regulatory elements, including the most complete set of human-specific fixed differences. We estimate that 819.47 Mbp or ∼27% of the genome has been affected by SVs across primate evolution. We identify 1,607 structurally divergent regions wherein recurrent structural variation contributes to creating SV hotspots where genes are recurrently lost (e.g., CARD, C4, and OLAH gene families) and additional lineage-specific genes are generated (e.g., CKAP2, VPS36, ACBD7, and NEK5 paralogs), becoming targets of rapid chromosomal diversification and positive selection (e.g., RGPD gene family). High-fidelity long-read sequencing has made these dynamic regions of the genome accessible for sequence-level analyses within and between primate species., Competing Interests: Declaration of interests E.E.E. is a scientific advisory board (SAB) member of Variant Bio, Inc., (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)
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- 2024
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49. Perspectives on SARS-CoV-2 Cases in Zoological Institutions.
- Author
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Nederlof RA, de la Garza MA, and Bakker J
- Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections in a zoological institution were initially reported in March 2020. Since then, at least 94 peer-reviewed cases have been reported in zoos worldwide. Among the affected animals, nonhuman primates, carnivores, and artiodactyls appear to be most susceptible to infection, with the Felidae family accounting for the largest number of reported cases. Clinical symptoms tend to be mild across taxa; although, certain species exhibit increased susceptibility to disease. A variety of diagnostic tools are available, allowing for initial diagnostics and for the monitoring of infectious risk. Whilst supportive therapy proves sufficient in most cases, monoclonal antibody therapy has emerged as a promising additional treatment option. Effective transmission of SARS-CoV-2 in some species raises concerns over potential spillover and the formation of reservoirs. The occurrence of SARS-CoV-2 in a variety of animal species may contribute to the emergence of variants of concern due to altered viral evolutionary constraints. Consequently, this review emphasizes the need for effective biosecurity measures and surveillance strategies to prevent and control SARS-CoV-2 infections in zoological institutions.
- Published
- 2024
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50. Abundant triatomines in Texas dog kennel environments: Triatomine collections, infection with Trypanosoma cruzi, and blood feeding hosts.
- Author
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Busselman RE, Curtis-Robles R, Meyers AC, Zecca IB, Auckland LD, Hodo CL, Christopher D, Saunders AB, and Hamer SA
- Subjects
- Animals, Dogs, Humans, Cats, Texas epidemiology, Insect Vectors parasitology, Chickens, Mammals, Trypanosoma cruzi genetics, Chagas Disease epidemiology, Chagas Disease veterinary, Chagas Disease parasitology, Triatoma parasitology
- Abstract
Triatomine insects are vectors of the protozoan parasite Trypanosoma cruzi- the causative agent of Chagas disease. Chagas disease is endemic to Latin America and the southern United States and can cause severe cardiac damage in infected mammals, ranging from chronic disease to sudden death. Identifying interactions among triatomines, T. cruzi discrete typing units (DTUs), and blood feeding hosts is necessary to understand parasite transmission dynamics and effectively protect animal and human health. Through manual insect trapping efforts, kennel staff collections, and with the help of a trained scent detection dog, we collected triatomines from 10 multi-dog kennels across central and south Texas over a one-year period (2018-2019) and tested a subset to determine their T. cruzi infection status and identify the primary bloodmeal hosts. We collected 550 triatomines, including Triatoma gerstaeckeri (n = 515), Triatoma lecticularia (n = 15), Triatoma sanguisuga (n = 6), and Triatoma indictiva (n = 2), with an additional 10 nymphs and 2 adults unable to be identified to species. The trained dog collected 42 triatomines, including nymphs, from areas not previously considered vector habitat by the kennel owners. Using qPCR, we found a T. cruzi infection prevalence of 47 % (74/157), with T. lecticularia individuals more likely to be infected with T. cruzi than other species. Infected insects harbored two T. cruzi discrete typing units: TcI (64 %), TcIV (23 %), and mixed TcI/TcIV infections (13 %). Bloodmeal host identification was successful in 50/149 triatomines, revealing the majority (74 %) fed on a dog (Canis lupus), with other host species including humans (Homo sapiens), raccoons (Procyon lotor), chickens (Gallus gallus), wild pig (Sus scrofa), black vulture (Coragyps atratus), cat (Felis catus), and curve-billed thrasher (Toxostoma curviostre). Given the frequency of interactions between dogs and infected triatomines in these kennel environments, dogs may be an apt target for future vector control and T. cruzi intervention efforts., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Author(s). Published by Elsevier B.V. All rights reserved.)
- Published
- 2024
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