13 results on '"Gurfield N"'
Search Results
2. Vesicular Stomatitis Virus Detected in Biting Midges and Black Flies during the 2023 Outbreak in Southern California.
- Author
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Scroggs SLP, Swanson DA, Steele TD, Hudson AR, Reister-Hendricks LM, Gutierrez J, Shults P, McGregor BL, Taylor CE, Davis TM, Lamberski N, Phair KA, Howard LL, McConnell NE, Gurfield N, Drolet BS, Pelzel-McCluskey AM, and Cohnstaedt LW
- Subjects
- Animals, California epidemiology, Cattle, Horses, RNA, Viral genetics, Ceratopogonidae virology, Simuliidae virology, Disease Outbreaks, Insect Vectors virology, Vesicular stomatitis New Jersey virus genetics, Vesicular stomatitis New Jersey virus isolation & purification, Vesicular Stomatitis virology, Vesicular Stomatitis epidemiology
- Abstract
Vesicular stomatitis (VS) is a viral disease that affects horses, cattle, and swine that is transmitted by direct contact and hematophagous insects. In 2023, a multi-state outbreak of vesicular stomatitis New Jersey virus (VSNJV) occurred in California, Nevada, and Texas, infecting horses, cattle, and rhinoceros. To identify possible insect vectors, we conducted insect surveillance at various locations in San Diego County, CA, including at a wildlife park. CO
2 baited traps set from mid-May to mid-August 2023 collected 2357 Culicoides biting midges and 1215 Simulium black flies, which are insect genera implicated in VSNJV transmission. Insects were pooled by species, location, and date, then tested for viral RNA. Nine RNA-positive pools of Culicoides spp. and sixteen RNA-positive pools of Simulium spp were detected. Infectious virus was detected by cytopathic effect in 96% of the RNA-positive pools. This is the first report of VSNJV in wild-caught C. bergi , C. freeborni , C. occidentalis , S. argus , S. hippovorum , and S. tescorum. The vector competency of these species for VSNJV has yet to be determined but warrants examination. Active vector surveillance and testing during disease outbreaks increases our understanding of the ecology and epidemiology of VS and informs vector control efforts.- Published
- 2024
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- View/download PDF
3. Exploring the value of a global gene drive project registry.
- Author
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Taitingfong RI, Triplett C, Vásquez VN, Rajagopalan RM, Raban R, Roberts A, Terradas G, Baumgartner B, Emerson C, Gould F, Okumu F, Schairer CE, Bossin HC, Buchman L, Campbell KJ, Clark A, Delborne J, Esvelt K, Fisher J, Friedman RM, Gronvall G, Gurfield N, Heitman E, Kofler N, Kuiken T, Kuzma J, Manrique-Saide P, Marshall JM, Montague M, Morrison AC, Opesen CC, Phelan R, Piaggio A, Quemada H, Rudenko L, Sawadogo N, Smith R, Tuten H, Ullah A, Vorsino A, Windbichler N, Akbari OS, Long K, Lavery JV, Evans SW, Tountas K, and Bloss CS
- Subjects
- Registries, Data Collection, Gene Drive Technology
- Published
- 2023
- Full Text
- View/download PDF
4. Wastewater sequencing reveals early cryptic SARS-CoV-2 variant transmission.
- Author
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Karthikeyan S, Levy JI, De Hoff P, Humphrey G, Birmingham A, Jepsen K, Farmer S, Tubb HM, Valles T, Tribelhorn CE, Tsai R, Aigner S, Sathe S, Moshiri N, Henson B, Mark AM, Hakim A, Baer NA, Barber T, Belda-Ferre P, Chacón M, Cheung W, Cresini ES, Eisner ER, Lastrella AL, Lawrence ES, Marotz CA, Ngo TT, Ostrander T, Plascencia A, Salido RA, Seaver P, Smoot EW, McDonald D, Neuhard RM, Scioscia AL, Satterlund AM, Simmons EH, Abelman DB, Brenner D, Bruner JC, Buckley A, Ellison M, Gattas J, Gonias SL, Hale M, Hawkins F, Ikeda L, Jhaveri H, Johnson T, Kellen V, Kremer B, Matthews G, McLawhon RW, Ouillet P, Park D, Pradenas A, Reed S, Riggs L, Sanders A, Sollenberger B, Song A, White B, Winbush T, Aceves CM, Anderson C, Gangavarapu K, Hufbauer E, Kurzban E, Lee J, Matteson NL, Parker E, Perkins SA, Ramesh KS, Robles-Sikisaka R, Schwab MA, Spencer E, Wohl S, Nicholson L, McHardy IH, Dimmock DP, Hobbs CA, Bakhtar O, Harding A, Mendoza A, Bolze A, Becker D, Cirulli ET, Isaksson M, Schiabor Barrett KM, Washington NL, Malone JD, Schafer AM, Gurfield N, Stous S, Fielding-Miller R, Garfein RS, Gaines T, Anderson C, Martin NK, Schooley R, Austin B, MacCannell DR, Kingsmore SF, Lee W, Shah S, McDonald E, Yu AT, Zeller M, Fisch KM, Longhurst C, Maysent P, Pride D, Khosla PK, Laurent LC, Yeo GW, Andersen KG, and Knight R
- Subjects
- Humans, RNA, Viral analysis, RNA, Viral genetics, Sequence Analysis, RNA, COVID-19 epidemiology, COVID-19 transmission, COVID-19 virology, SARS-CoV-2 classification, SARS-CoV-2 genetics, SARS-CoV-2 isolation & purification, Wastewater virology, Wastewater-Based Epidemiological Monitoring
- Abstract
As SARS-CoV-2 continues to spread and evolve, detecting emerging variants early is critical for public health interventions. Inferring lineage prevalence by clinical testing is infeasible at scale, especially in areas with limited resources, participation, or testing and/or sequencing capacity, which can also introduce biases
1-3 . SARS-CoV-2 RNA concentration in wastewater successfully tracks regional infection dynamics and provides less biased abundance estimates than clinical testing4,5 . Tracking virus genomic sequences in wastewater would improve community prevalence estimates and detect emerging variants. However, two factors limit wastewater-based genomic surveillance: low-quality sequence data and inability to estimate relative lineage abundance in mixed samples. Here we resolve these critical issues to perform a high-resolution, 295-day wastewater and clinical sequencing effort, in the controlled environment of a large university campus and the broader context of the surrounding county. We developed and deployed improved virus concentration protocols and deconvolution software that fully resolve multiple virus strains from wastewater. We detected emerging variants of concern up to 14 days earlier in wastewater samples, and identified multiple instances of virus spread not captured by clinical genomic surveillance. Our study provides a scalable solution for wastewater genomic surveillance that allows early detection of SARS-CoV-2 variants and identification of cryptic transmission., (© 2022. The Author(s).)- Published
- 2022
- Full Text
- View/download PDF
5. Wastewater sequencing uncovers early, cryptic SARS-CoV-2 variant transmission.
- Author
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Karthikeyan S, Levy JI, De Hoff P, Humphrey G, Birmingham A, Jepsen K, Farmer S, Tubb HM, Valles T, Tribelhorn CE, Tsai R, Aigner S, Sathe S, Moshiri N, Henson B, Mark AM, Hakim A, Baer NA, Barber T, Belda-Ferre P, Chacón M, Cheung W, Cresini ES, Eisner ER, Lastrella AL, Lawrence ES, Marotz CA, Ngo TT, Ostrander T, Plascencia A, Salido RA, Seaver P, Smoot EW, McDonald D, Neuhard RM, Scioscia AL, Satterlund AM, Simmons EH, Abelman DB, Brenner D, Bruner JC, Buckley A, Ellison M, Gattas J, Gonias SL, Hale M, Hawkins F, Ikeda L, Jhaveri H, Johnson T, Kellen V, Kremer B, Matthews G, McLawhon RW, Ouillet P, Park D, Pradenas A, Reed S, Riggs L, Sanders A, Sollenberger B, Song A, White B, Winbush T, Aceves CM, Anderson C, Gangavarapu K, Hufbauer E, Kurzban E, Lee J, Matteson NL, Parker E, Perkins SA, Ramesh KS, Robles-Sikisaka R, Schwab MA, Spencer E, Wohl S, Nicholson L, Mchardy IH, Dimmock DP, Hobbs CA, Bakhtar O, Harding A, Mendoza A, Bolze A, Becker D, Cirulli ET, Isaksson M, Barrett KMS, Washington NL, Malone JD, Schafer AM, Gurfield N, Stous S, Fielding-Miller R, Garfein RS, Gaines T, Anderson C, Martin NK, Schooley R, Austin B, MacCannell DR, Kingsmore SF, Lee W, Shah S, McDonald E, Yu AT, Zeller M, Fisch KM, Longhurst C, Maysent P, Pride D, Khosla PK, Laurent LC, Yeo GW, Andersen KG, and Knight R
- Abstract
As SARS-CoV-2 continues to spread and evolve, detecting emerging variants early is critical for public health interventions. Inferring lineage prevalence by clinical testing is infeasible at scale, especially in areas with limited resources, participation, or testing/sequencing capacity, which can also introduce biases. SARS-CoV-2 RNA concentration in wastewater successfully tracks regional infection dynamics and provides less biased abundance estimates than clinical testing. Tracking virus genomic sequences in wastewater would improve community prevalence estimates and detect emerging variants. However, two factors limit wastewater-based genomic surveillance: low-quality sequence data and inability to estimate relative lineage abundance in mixed samples. Here, we resolve these critical issues to perform a high-resolution, 295-day wastewater and clinical sequencing effort, in the controlled environment of a large university campus and the broader context of the surrounding county. We develop and deploy improved virus concentration protocols and deconvolution software that fully resolve multiple virus strains from wastewater. We detect emerging variants of concern up to 14 days earlier in wastewater samples, and identify multiple instances of virus spread not captured by clinical genomic surveillance. Our study provides a scalable solution for wastewater genomic surveillance that allows early detection of SARS-CoV-2 variants and identification of cryptic transmission.
- Published
- 2022
- Full Text
- View/download PDF
6. Outbreak of human infections with uncommon Salmonella serotypes linked to pet bearded dragons, 2012-2014.
- Author
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Kiebler CA, Bottichio L, Simmons L, Basler C, Klos R, Gurfield N, Roberts E, Kimura A, Lewis LS, Bird K, Stiles F, Schlater LK, Lantz K, Edling T, and Barton Behravesh C
- Subjects
- Adolescent, Adult, Aged, Animals, Carrier State, Child, Child, Preschool, Disease Outbreaks, Female, Humans, Infant, Infant, Newborn, Male, Middle Aged, Salmonella Infections transmission, Wisconsin, Young Adult, Lizards microbiology, Pets, Salmonella classification, Salmonella Infections microbiology, Zoonoses
- Abstract
Reptiles are one of the fastest growing sectors in the United States pet industry. Reptile-associated salmonellosis (RAS) continues to be an important public health problem, especially among children. We investigated an outbreak of human Salmonella infections resulting from serotypes Cotham and Kisarawe, predominately occurring among children. An outbreak of illnesses was identified in persons with exposure to pet bearded dragon lizards. Human and animal health officials, in cooperation with the pet industry, conducted epidemiologic, traceback and laboratory investigations. Onsite sampling was conducted at two US breeding facilities, one foreign breeding facility, and a large pet retail chain. A total of 166 patients in 36 states were identified with illness onset dates from 02/2012-06/2014. The median patient age was 3 years (range, <1-79 years), 57% were aged ≤5 years, and 37% were aged ≤1 year. Forty-four patients (37%) were hospitalized, predominantly children. Sampling at breeding facilities and a national pet store chain resulted in isolation of outbreak serotypes at each facility; isolation proportions ranged from 2%-24% of samples collected at each facility.Epidemiologic, microbiologic and traceback evidence linked an outbreak of uncommon Salmonella serotypes to contact with pet bearded dragons. The high proportion of infants involved in this outbreak highlights the need to educate owners about the risk of RAS in children and the potential for household contamination by pet reptiles or their habitats. Strategies should be developed to improve breeding practices, biosecurity and monitoring protocols to reduce Salmonella in the pet reptile trade., (© 2020 Blackwell Verlag GmbH.)
- Published
- 2020
- Full Text
- View/download PDF
7. An amplicon-based sequencing framework for accurately measuring intrahost virus diversity using PrimalSeq and iVar.
- Author
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Grubaugh ND, Gangavarapu K, Quick J, Matteson NL, De Jesus JG, Main BJ, Tan AL, Paul LM, Brackney DE, Grewal S, Gurfield N, Van Rompay KKA, Isern S, Michael SF, Coffey LL, Loman NJ, and Andersen KG
- Subjects
- Genetic Variation, Sequence Analysis, RNA, Genomics methods, West Nile virus genetics, Zika Virus genetics
- Abstract
How viruses evolve within hosts can dictate infection outcomes; however, reconstructing this process is challenging. We evaluate our multiplexed amplicon approach, PrimalSeq, to demonstrate how virus concentration, sequencing coverage, primer mismatches, and replicates influence the accuracy of measuring intrahost virus diversity. We develop an experimental protocol and computational tool, iVar, for using PrimalSeq to measure virus diversity using Illumina and compare the results to Oxford Nanopore sequencing. We demonstrate the utility of PrimalSeq by measuring Zika and West Nile virus diversity from varied sample types and show that the accumulation of genetic diversity is influenced by experimental and biological systems.
- Published
- 2019
- Full Text
- View/download PDF
8. Endosymbiont interference and microbial diversity of the Pacific coast tick, Dermacentor occidentalis , in San Diego County, California.
- Author
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Gurfield N, Grewal S, Cua LS, Torres PJ, and Kelley ST
- Abstract
The Pacific coast tick, Dermacentor occidentalis Marx, is found throughout California and can harbor agents that cause human diseases such as anaplasmosis, ehrlichiosis, tularemia, Rocky Mountain spotted fever and rickettsiosis 364D. Previous studies have demonstrated that nonpathogenic endosymbiotic bacteria can interfere with Rickettsia co-infections in other tick species. We hypothesized that within D. occidentalis ticks, interference may exist between different nonpathogenic endosymbiotic or nonendosymbiotic bacteria and Spotted Fever group Rickettsia (SFGR). Using PCR amplification and sequencing of the romp A gene and intergenic region we identified a cohort of SFGR-infected and non-infected D. occidentalis ticks collected from San Diego County. We then amplified a partial segment of the 16S rRNA gene and used next-generation sequencing to elucidate the microbiomes and levels of co-infection in the ticks. The SFGR R. philipii str. 364D and R. rhipicephali were detected in 2.3% and 8.2% of the ticks, respectively, via romp A sequencing. Interestingly, next generation sequencing revealed an inverse relationship between the number of Francisella- like endosymbiont (FLE) 16S rRNA sequences and Rickettsia 16S rRNA sequences within individual ticks that is consistent with partial interference between FLE and SFGR infecting ticks. After excluding the Rickettsia and FLE endosymbionts from the analysis, there was a small but significant difference in microbial community diversity and a pattern of geographic isolation by distance between collection locales. In addition, male ticks had a greater diversity of bacteria than female ticks and ticks that weren't infected with SFGR had similar microbiomes to canine skin microbiomes. Although experimental studies are required for confirmation, our findings are consistent with the hypothesis that FLEs and, to a lesser extent, other bacteria, interfere with the ability of D. occidentalis to be infected with certain SFGR. The results also raise interesting possibilities about the effects of putative vertebrate hosts on the tick microbiome., Competing Interests: The authors declare there are no competing interests.
- Published
- 2017
- Full Text
- View/download PDF
9. Rapid bilateral intraocular cocktail sampling method for West Nile virus detection in dead corvids.
- Author
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Lim AK, Dunne G, and Gurfield N
- Subjects
- Animals, Peptides, Population Surveillance, Predictive Value of Tests, West Nile Fever diagnosis, West Nile Fever epidemiology, West Nile Fever veterinary, Aqueous Humor virology, Crows virology, West Nile virus isolation & purification
- Abstract
Corvids can be a sensitive indicator for West Nile virus (WNV) prevalence and are a component of many WNV surveillance programs. An improved sampling procedure using a bilateral intraocular cocktail (BIC) was developed for testing corvid carcasses for WNV. This new procedure was substantially faster than harvesting internal organs, required less specialized equipment and training, and yielded excellent diagnostic sensitivity.
- Published
- 2009
- Full Text
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10. Local veterinary diagnostic laboratory, a model for the one health initiative.
- Author
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Dunne G and Gurfield N
- Subjects
- Animal Diseases epidemiology, Animal Diseases microbiology, Animals, California epidemiology, Clinical Laboratory Techniques veterinary, Communicable Diseases epidemiology, Communicable Diseases microbiology, Communicable Diseases veterinary, Community Health Services methods, Community Health Services organization & administration, Humans, Local Government, Sentinel Surveillance veterinary, Animal Welfare, Interinstitutional Relations, Laboratories, Public Health Administration methods, Public Health Practice
- Abstract
The San Diego County Animal Disease Diagnostic Laboratory (ADDL) is unique in its emphasis on protecting both human and animal health in San Diego County, and its use of interagency and community collaboration to create strong, effective public health programs. This article describes the ADDL core programs of avian and vector-borne disease surveillance, rabies testing, and animal abuse investigations and uses selected case studies to illustrate the need for a local veterinary diagnostic laboratory to safeguard the health of humans and animals. The ADDL serves as a role model for other local communities to develop vital public health partnerships to ensure a healthier community.
- Published
- 2009
- Full Text
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11. Discrimination between Francisella tularensis and Francisella-like endosymbionts when screening ticks by PCR.
- Author
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Kugeler KJ, Gurfield N, Creek JG, Mahoney KS, Versage JL, and Petersen JM
- Subjects
- Animals, Francisella genetics, Francisella isolation & purification, Francisella tularensis genetics, Francisella tularensis isolation & purification, Molecular Sequence Data, Sequence Analysis, DNA, Species Specificity, Symbiosis, Tularemia microbiology, Tularemia transmission, Francisella classification, Francisella tularensis classification, Polymerase Chain Reaction methods, Ticks microbiology
- Abstract
The presence of Francisella-like endosymbionts in tick species known to transmit tularemia poses a potential diagnostic problem for laboratories that screen tick samples by PCR for Francisella tularensis. Tick samples initially considered positive for F. tularensis based on standard 16S rRNA gene PCR were found to be positive only for Francisella-like endosymbionts using a multitarget F. tularensis TaqMan assay (ISFtu2, tul4, and iglC) and 16S rRNA gene sequencing. Specificity of PCR-based diagnostics for F. tularensis should be carefully evaluated with appropriate specimen types prior to diagnostic use.
- Published
- 2005
- Full Text
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12. Equine placental teratoma.
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Gurfield N and Benirschke K
- Subjects
- Animals, Female, Histocytochemistry veterinary, Horses, Placenta Diseases pathology, Pregnancy, Teratoma pathology, Horse Diseases pathology, Placenta Diseases veterinary, Teratoma veterinary
- Abstract
The placenta from a 300-day-gestational age, female, Arabian equine fetus was examined. Multifocal to coalescing, 0.5- to 4-cm-diameter, white, smooth nodules covered 50% of the placenta. Microscopic evaluation of the nodules revealed undifferentiated germ cells and a haphazard arrangement of immature, mesenchymal stroma, cartilage, squamous cornifying epithelium, scattered ducts and secretory acini lined by cuboidal to columnar epithelium, and mineralized foci. No umbilicus, arrangement about an axial skeleton, or organized polarity of structures was present. The lesion was diagnosed as a placental teratoma, a lesion not reported in species other than man.
- Published
- 2003
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13. Genomic diversity of Bartonella henselae isolates from domestic cats from Japan, the USA and France by pulsed-field gel electrophoresis.
- Author
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Maruyama S, Kasten RW, Boulouis HJ, Gurfield NA, Katsube Y, and Chomel BB
- Subjects
- Animals, Bartonella henselae classification, Bartonella henselae isolation & purification, Cat-Scratch Disease microbiology, Cats, Cluster Analysis, DNA, Bacterial genetics, Electrophoresis, Gel, Pulsed-Field veterinary, France, Genetic Variation genetics, Genome, Bacterial, Japan, Phylogeny, Polymerase Chain Reaction veterinary, United States, Bartonella henselae genetics, Cat Diseases microbiology, Cat-Scratch Disease veterinary
- Abstract
The genomic DNA diversity of 27 Bartonella henselae and three B. clarridgeiae isolates from 18 domestic cats from Japan, the USA and France was investigated by pulsed-field gel electrophoresis (PFGE) with NotI, AscI and SmaI restriction enzymes. A great diversity of genomic patterns was found for all B. henselae, but none for B. clarridgeiae isolates. The DNA size of B. henselae and B. clarridgeiae isolates were 1.7-2.9 and 1.7Mbp, respectively. All 13 Japanese cat isolates were identified as B. henselae type I. Furthermore, three of the four Japanese cats harbored genetically different B. henselae type I isolates, suggesting for the first time co-infection with various type I isolates. One French cat and one American cat were co-infected with B. henselae and B. clarridgeiae. B. henselae type I and type II were mainly grouped in two different clusters by PFGE using SmaI endonuclease in the dendrogram.
- Published
- 2001
- Full Text
- View/download PDF
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