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2. Testing of Cryogenic Photomultiplier Tubes for the MicroBooNE Experiment

Author

Briese, T., Bugel, L., Conrad, J. M., Fournier, M., Ignarra, C., Jones, B. J. P., Katori, T., Navarrete-Perez, R., Nienaber, P., McDonald, T., Musolf, B., Prakash, A., Shockley, E., Smidt, T., Swanson, K., and Toups, M.

Subjects
Physics - Instrumentation and Detectors, High Energy Physics - Experiment
Abstract

The MicroBooNE detector, to be located on axis in the Booster Neutrino Beamline (BNB) at the Fermi National Accelerator Laboratory (Fermilab), consists of two main components: a large liquid argon time projection chamber (LArTPC), and a light collection system. Thirty 8-inch diameter Hamamatsu R5912-02mod cryogenic photomultiplier tubes (PMTs) will detect the scintillation light generated in the liquid argon (LAr). This article first describes the MicroBooNE PMT performance test procedures, including how the light collection system functions in the detector, and the design of the PMT base. The design of the cryogenic test stand is then discussed, and finally the results of the cryogenic tests are reported., Comment: 17 pages, 14 figures, submitted to JINST

Published
2013
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5. The relationships between West Nile and Kunjin viruses.

Author

Scherret, J. H., Poidinger, M., Mackenzie, J. S., Broom, A. K., Deubel, V., Lipkin, W. I., Briese, T., Gould, E. A., and Hall, R. A.

Subjects
yellow-fever virus, nucleotide-sequence, encephalitis-virus, molecular characterization, nonstructural proteins, monoclonal-antibodies, cross-neutralization, secondary structure, genetic-analysis, genomic rna
Abstract

Until recently, West Nile (WN) and Kunjin (KUN) viruses were classified as distinct types in the Flavivirus genus. However, genetic and antigenic studies on isolates of these two viruses indicate that the relationship between them is more complex. To better define this relationship, we performed sequence analyses on 32 isolates of KUN virus and 28 isolates of WN virus from different geographic areas, including a WN isolate from the recent outbreak in New York. Sequence comparisons showed that the KUN virus isolates from Australia were tightly grouped but that the WN virus isolates exhibited substantial divergence and could be differentiated into four distinct groups. KUN virus isolates from Australia were antigenically homologous and distinct from the WN isolates and a Malaysian KUN virus. Our results suggest that KUN and WN viruses comprise a group of closely related viruses that can be differentiated into subgroups on the basis of genetic and antigenic analyses.

Published
2001

8. Anteromedial rotatory knee instability – much more than the medial collateral ligament

Author

Herbst, E, Peez, C, Muhmann, R, Wermers, J, Briese, T, Glasbrenner, J, Raschke, MJ, and Kittl, C

Subjects
musculoskeletal diseases, medial collateral ligament, instability, ddc: 610, ACL, Medicine and health, knee, anteromedial, musculoskeletal system, human activities
Abstract

Objectives: Most studies on the medial knee structures focused on valgus or posteromedial rotatory instability, while there is a lack of data regarding anteromedial rotatory knee instability (AMRI). Thus, the aim of this study was to investigate the biomechanical contribution of medial sided anatomical [for full text, please go to the a.m. URL]

Published
2021
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10. Molecular Biology of Borna Disease Virus

Author

Briese, T., Lipkin, W. I., de la Torre, J. C., Capron, A., editor, Compans, R. W., editor, Cooper, M., editor, Koprowski, H., editor, McConnell, I., editor, Melchers, F., editor, Oldstone, M., editor, Olsnes, S., editor, Potter, M., editor, Saedler, H., editor, Vogt, P. K., editor, Wagner, H., editor, Wilson, I., editor, Koprowski, Hilary, editor, and Lipkin, W. Ian, editor

Published
1995
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12. Taxonomic update of phylum Negarnaviricota (Riboviria: Orthornavirae), including the large orders Bunyavirales and Mononegavirales

Author

Kuhn J.H., Adkins S., Agwanda B.R., Al Kubrusli R., Alkhovsky S.V., Amarasinghe G.K., Avsic-Zupanc T., Ayllon M.A., Bahl J., Balkema-Buschmann A., Ballinger M.J., Basler C.F., Bavari S., Beer M., Bejerman N., Bennett A.J., Bente D.A., Bergeron E., Bird B.H., Blair C.D., Blasdell K.R., Blystad D.-R., Bojko J., Borth W.B., Bradfute S., Breyta R., Briese T., Brown P.A., Brown J.K., Buchholz U.J., Buchmeier M.J., Bukreyev A., Burt F., Buttner C., Calisher C.H., Cao M., Casas I., Chandran K., Charrel R.N., Cheng Q., Chiaki Y., Chiapello M., Choi I.-R., Ciuffo M., Clegg J.C.S., Crozier I., Dal Bo E., de la Torre J.C., de Lamballerie X., de Swart R.L., Debat H., Dheilly N.M., Di Cicco E., Di Paola N., Di Serio F., Dietzgen R.G., Digiaro M., Dolnik O., Drebot M.A., Drexler J.F., Dundon W.G., Duprex W.P., Durrwald R., Dye J.M., Easton A.J., Ebihara H., Elbeaino T., Ergunay K., Ferguson H.W., Fooks A.R., Forgia M., Formenty P.B.H., Franova J., Freitas-Astua J., Fu J., Furl S., Gago-Zachert S., Gao G.F., Garcia M.L., Garcia-Sastre A., Garrison A.R., Gaskin T., Gonzalez J.-P.J., Griffiths A., Goldberg T.L., Groschup M.H., Gunther S., Hall R.A., Hammond J., Han T., Hepojoki J., Hewson R., Hong J., Hong N., Hongo S., Horie M., Hu J.S., Hu T., Hughes H.R., Huttner F., Hyndman T.H., Ilyas M., Jalkanen R., Jiang D., Jonson G.B., Junglen S., Kadono F., Kaukinen K.H., Kawate M., Klempa B., Klingstrom J., Kobinger G., Koloniuk I., Kondo H., Koonin E.V., Krupovic M., Kubota K., Kurath G., Laenen L., Lambert A.J., Langevin S.L., Lee B., Lefkowitz E.J., Leroy E.M., Li S., Li L., Li J., Liu H., Lukashevich I.S., Maes P., de Souza W.M., Marklewitz M., Marshall S.H., Marzano S.-Y.L., Massart S., McCauley J.W., Melzer M., Mielke-Ehret N., Miller K.M., Ming T.J., Mirazimi A., Mordecai G.J., Muhlbach H.-P., Muhlberger E., Naidu R., Natsuaki T., Navarro J.A., Netesov S.V., Neumann G., Nowotny N., Nunes M.R.T., Olmedo-Velarde A., Palacios G., Pallas V., Palyi B., Papa A., Paraskevopoulou S., Park A.C., Parrish C.R., Patterson D.A., Pauvolid-Correa A., Paweska J.T., Payne S., Peracchio C., Perez D.R., Postler T.S., Qi L., Radoshitzky S.R., Resende R.O., Reyes C.A., Rima B.K., Luna G.R., Romanowski V., Rota P., Rubbenstroth D., Rubino L., Runstadler J.A., Sabanadzovic S., Sall A.A., Salvato M.S., Sang R., Sasaya T., Schulze A.D., Schwemmle M., Shi M., Shi X., Shi Z., Shimomoto Y., Shirako Y., Siddell S.G., Simmonds P., Sironi M., Smagghe G., Smither S., Song J.-W., Spann K., Spengler J.R., Stenglein M.D., Stone D.M., Sugano J., Suttle C.A., Tabata A., Takada A., Takeuchi S., Tchouassi D.P., Teffer A., Tesh R.B., Thornburg N.J., Tomitaka Y., Tomonaga K., Tordo N., Torto B., Towner J.S., Tsuda S., Tu C., Turina M., Tzanetakis I.E., Uchida J., Usugi T., Vaira A.M., Vallino M., van den Hoogen B., Varsani A., Vasilakis N., Verbeek M., von Bargen S., Wada J., Wahl V., Walker P.J., Wang L.-F., Wang G., Wang Y., Waqas M., Wei T., Wen S., Whitfield A.E., Williams J.V., Wolf Y.I., Wu J., Xu L., Yanagisawa H., Yang C., Yang Z., Zerbini F.M., Zhai L., Zhang Y.-Z., Zhang S., Zhang J., Zhang Z., and Zhou X.

Subjects
Virus classification, Negative-stranded RNA viruses
Abstract

In March 2021, following the annual International Committee on Taxonomy of Viruses (ICTV) ratifcation vote on newly proposed taxa, the phylum Negarnaviricota was amended and emended. The phylum was expanded by four families (Aliusviridae, Crepuscuviridae, Myriaviridae, and Natareviridae), three subfamilies (Alpharhabdovirinae, Betarhabdovirinae, and Gammarhabdovirinae), 42 genera, and 200 species. Thirty-nine species were renamed and/ or moved and seven species were abolished. This article presents the updated taxonomy of Negarnaviricota as now accepted by the ICTV

Published
2021

24. Early probiotic supplementation and the risk of celiac disease in children at genetic risk

Author

Uusitalo, U. (Ulla), Aronsson, C. A. (Carin Andren), Liu, X. (Xiang), Kurppa, K. (Kalle), Yang, J. (Jimin), Liu, E. (Edwin), Skidmore, J. (Jennifer), Winkler, C. (Christiane), Rewers, M. J. (Marian J.), Hagopian, W. A. (William A.), She, J.-X. (Jin-Xiong), Toppari, J. (Jorma), Ziegler, A.-G. (Anette-G), Akolkar, B. (Beena), Norris, J. M. (Jill M.), Virtanen, S. M. (Suvi M.), Krischer, J. P. (Jeffrey P.), Agardh, D. (Daniel), Rewers, M. (Marian), Bautista, K. (Kimberly), Baxter, J. (Judith), Felipe-Morales, D. (Daniel), Driscoll, K. (Kimberly), Frohnert, B. I. (Brigitte, I), Gallant, M. (Marisa), Gesualdo, P. (Patricia), Hoffman, M. (Michelle), Karban, R. (Rachel), Norris, J. (Jill), Steck, A. (Andrea), Waugh, K. (Kathleen), Simell, O. G. (Olli G.), Adamsson, A. (Annika), Ahonen, S. (Suvi), Akerlund, M. (Mari), Hekkala, A. (Anne), Holappa, H. (Henna), Hyoty, H. (Heikki), Ikonen, A. (Anni), Ilonen, J. (Jorma), Jaminki, S. (Sinikka), Jokipuu, S. (Sanna), Karlsson, L. (Leena), Kahonen, M. (Miia), Knip, M. (Mikael), Koivikko, M.-L. (Minna-Liisa), Koreasalo, M. (Mirva), Kytola, J. (Jarita), Latva-aho, T. (Tiina), Lindfors, K. (Katri), Lonnrot, M. (Maria), Mantymaki, E. (Elina), Mattila, M. (Markus), Multasuo, K. (Katja), Mykkanenv, T. (Teija), Niininen, T. (Titha), Niinisto, S. (Sari), Nyblom, M. (Mia), Oikarinen, S. (Sami), Ollikainen, P. (Paula), Pohjola, S. (Sirpa), Rajala, P. (Petra), Rautanen, J. (Jenna), Riikonen, A. (Anne), Romo, M. (Minna), Ruohonen, S. (Suvi), Simell, S. (Satu), Sjoberg, M. (Maija), Stenius, A. (Aino), Tossavainen, P. (Paivi), Vaha-Makila, M. (Mari), Vainionpaa, S. (Sini), Varjonen, E. (Eeva), Veijola, R. (Riitta), Viinikangas, I. (Irene), Schatz, D. (Desmond), Hopkins, D. (Diane), Steed, L. (Leigh), Bryant, J. (Jennifer), Silvis, K. (Katherine), Haller, M. (Michael), Gardiner, M. (Melissa), Mclndoe, R. (Richard), Sharma, A. (Ashok), Anderson, S. W. (Stephen W.), Jacobsen, L. (Laura), Marks, J. (John), Towe, P. D. (P. D.), Ziegler, A. G. (Anette G.), Bonifacio, E. (Ezio), D'Angelo, M. (Miryam), Gavrisan, A. (Anita), Gezginci, C. (Cigdem), Heublein, A. (Anja), Hoffmann, V. (Verena), Hummel, S. (Sandra), Keimer, A. (Andrea), Knopff, A. (Annette), Koch, C. (Charlotte), Koletzko, S. (Sibylle), Ramminger, C. (Claudia), Roth, R. (Roswith), Scholz, M. (Marlon), Stock, J. (Joanna), Warncke, K. (Katharina), Wendel, L. (Lorena), Lernmark, A. (Ake), Ask, M. (Maria), Bremer, J. (Jenny), Cilio, C. (Corrado), Ericson-Hallstrom, E. (Emelie), Fors, A. (Annika), Fransson, L. (Lina), Gard, T. (Thomas), Bennet, R. (Rasmus), Hansen, M. (Monika), Hyberg, S. (Susanne), Jisser, H. (Hanna), Johansen, F. (Fredrik), Jonsdottir, B. (Berglind), Jovic, S. (Silvija), Larsson, H. E. (Helena Elding), Lindstrom, M. (Marielle), Lundgren, M. (Markus), Manson-Martinez, M. (Maria), Markan, M. (Maria), Melin, J. (Jessica), Mestan, Z. (Zeliha), Nilsson, C. (Caroline), Ottosson, K. (Karin), Rahmati, K. (Kobra), Ramelius, A. (Anita), Salami, F. (Falastin), Sjoberg, A. (Anette), Sjoberg, B. (Birgitta), Torn, C. (Carina), Wallin, A. (Anne), Wimar, A. (Asa), Aberg, S. (Sofie), Killian, M. (Michael), Crouch, C. C. (Claire Cowen), Akramoff, A. (Ashley), Chavoshi, M. (Masumeh), Dunson, K. (Kayleen), Hervey, R. (Rachel), Lyons, R. (Rachel), Meyer, A. (Arlene), Mulenga, D. (Denise), Radtke, J. (Jared), Romancik, M. (Matei), Schmitt, D. (Davey), Schwabe, J. (Julie), Zink, S. (Sarah), Becker, D. (Dorothy), Franciscus, M. (Margaret), Smith, M. D. (Maryellen Dalmagro-Elias), Daftary, A. (Ashi), Klein, M. B. (Mary Beth), Yates, C. (Chrystal), Austin-Gonzalez, S. (Sarah), Avendano, M. (Maryouri), Baethke, S. (Sandra), Brown, R. (Rasheedah), Burkhardt, B. (Brant), Butterworth, M. (Martha), Clasen, J. (Joanna), Cuthbertson, D. (David), Eberhard, C. (Christopher), Fiske, S. (Steven), Garmeson, J. (Jennifer), Gowda, V. (Veena), Heyman, K. (Kathleen), Hsiao, B. (Belinda), Karges, C. (Christina), Laras, F. P. (Francisco Perez), Lee, H.-S. (Hye-Seung), Li, Q. (Qian), Liu, S. (Shu), Lynch, K. (Kristian), Maguire, C. (Colleen), Malloy, J. (Jamie), McCarthy, C. (Cristina), Merrell, A. (Aubrie), Meulemans, S. (Steven), Parikh, H. (Hemang), Quigley, R. (Ryan), Remedios, C. (Cassandra), Shaffer, C. (Chris), Smith, L. (Laura), Smith, S. (Susan), Sulman, N. (Noah), Tamura, R. (Roy), Tewey, D. (Dena), Toth, M. (Michael), Vehik, K. (Kendra), Vijayakandipan, P. (Ponni), Wood, K. (Keith), Abbondondolo, M. (Michael), Ballard, L. (Lori), Hadley, D. (David), McLeod, W. (Wendy), Yu, L. (Liping), Miao, D. (Dongmei), Bingley, P. (Polly), Williams, A. (Alistair), Chandler, K. (Kyla), Ball, O. (Olivia), Kelland, I. (Ilana), Grace, S. (Sian), Hagopian, W. (William), Erlich, H. (Henry), Mack, S. J. (Steven J.), Fear, A. L. (Anna Lisa), Ke, S. (Sandra), Mulholland, N. (Niveen), Bourcier, K. (Kasia), Briese, T. (Thomas), Johnson, S. B. (Suzanne Bennett), and Triplett, E. (Eric)

Subjects
dietary supplements, probiotics, infant formula, celiac disease, celiac disease autoimmunity
Abstract

Probiotics are linked to positive regulatory effects on the immune system. The aim of the study was to examine the association between the exposure of probiotics via dietary supplements or via infant formula by the age of 1 year and the development of celiac disease autoimmunity (CDA) and celiac disease among a cohort of 6520 genetically susceptible children. Use of probiotics during the first year of life was reported by 1460 children. Time-to-event analysis was used to examine the associations. Overall exposure of probiotics during the first year of life was not associated with either CDA (n = 1212) (HR 1.15; 95%CI 0.99, 1.35; p = 0.07) or celiac disease (n = 455) (HR 1.11; 95%CI 0.86, 1.43; p = 0.43) when adjusting for known risk factors. Intake of probiotic dietary supplements, however, was associated with a slightly increased risk of CDA (HR 1.18; 95%CI 1.00, 1.40; p = 0.043) compared to children who did not get probiotics. It was concluded that the overall exposure of probiotics during the first year of life was not associated with CDA or celiac disease in children at genetic risk.

Published
2019

30. Nipah virus ecology and infection dynamics in its bat reservoir, Pteropus medius, in Bangladesh

Author

Epstein, J.H., primary, Anthony, S.J., additional, Islam, A., additional, Kilpatrick, A.M., additional, Khan, S. Ali, additional, Ross, N., additional, Smith, I., additional, Barr, J., additional, Zambrana-Torrelio, C., additional, Tao, Y., additional, Quan, P.L., additional, Olival, K., additional, Gurley, E., additional, Hossain, M.J., additional, Field, H.E., additional, Fielder, M., additional, Briese, T., additional, Rahman, M., additional, Crameri, G., additional, Wang, L.-F., additional, Luby, S., additional, Lipkin, W.I., additional, and Daszak, P., additional

Published
2016
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31. Methods, Quality Control and Specimen Management in an International Multi-Center Investigation of Type 1 Diabetes: TEDDY

Author

Vehik, K., Fiske, S.W., Logan, C.A., Agardh, D., Cilio, C.M., Hagopian, W., Simell, O., Roivainen, M., She, J.X., Briese, T., Oikarinen, S., Hyoty, H., Ziegler, A.-G., Rewers, M., Lernmark, A., Akolkar, B., Krischer, J.P., and Burkhardt, B.R.

Subjects
Quality Control, Adolescent, Infant, Newborn, Infant, Article, Specimen Handling, Feces, Diabetes Mellitus, Type 1, Child, Preschool, Data Integrity, Stool Sample Preservation, Rna, Biomarker Stability, Metabolic Biomarkers, T-cell Viability, Humans, Longitudinal Studies, RNA, Messenger, Child, Autoantibodies, Biological Specimen Banks
Abstract

BACKGROUND: The vast array and quantity of longitudinal samples collected in The Environmental Determinants of Diabetes in the Young study present a series of challenges in terms of quality control procedures and data validity. To address this, pilot studies have been conducted to standardize and enhance both biospecimen collection and sample obtainment in terms of autoantibody collection, stool sample preservation, RNA, biomarker stability, metabolic biomarkers and T-cell viability. RESEARCH DESIGN AND METHODS: The Environmental Determinants of Diabetes in the Young is a multicentre, international prospective study (n = 8677) designed to identify environmental triggers of type 1 diabetes (T1D) in genetically at-risk children from ages 3 months until 15 years. The study is conducted through six primary clinical centres located in four countries. RESULTS: As of May 2012, over three million biological samples and 250 million total data points have been collected, which will be analysed to assess autoimmunity status, presence of inflammatory biomarkers, genetic factors, exposure to infectious agents, dietary biomarkers and other potentially important environmental exposures in relation to autoimmunity and progression to T1D. CONCLUSIONS: Detailed procedures were utilized to standardize both data harmonization and management when handling a large quantity of longitudinal samples obtained from multiple locations. In addition, a description of the available specimens is provided that serve as an invaluable repository for the elucidation of determinants in T1D focusing on autoantibody concordance and harmonization, transglutaminase autoantibody, inflammatory biomarkers (T-cells), genetic proficiency testing, RNA lab internal quality control testing, infectious agents (monitoring cross-contamination, virus preservation and nasal swab collection validity) and HbA1c testing.

Published
2013

32. Testing of cryogenic photomultiplier tubes for the MicroBooNE experiment

Author

Briese, T, primary, Bugel, L, additional, Conrad, J M, additional, Fournier, M, additional, Ignarra, C, additional, Jones, B J P, additional, Katori, T, additional, Navarrete-Perez, R, additional, Nienaber, P, additional, McDonald, T, additional, Musolf, B, additional, Prakash, A, additional, Shockley, E, additional, Smidt, T, additional, Swanson, K, additional, and Toups, M, additional

Published
2013
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37. Genetic Analysis of Israel Acute Paralysis Virus: Distinct Clusters Are Circulating in the United States

Author

Palacios, G., primary, Hui, J., additional, Quan, P. L., additional, Kalkstein, A., additional, Honkavuori, K. S., additional, Bussetti, A. V., additional, Conlan, S., additional, Evans, J., additional, Chen, Y. P., additional, vanEngelsdorp, D., additional, Efrat, H., additional, Pettis, J., additional, Cox-Foster, D., additional, Holmes, E. C., additional, Briese, T., additional, and Lipkin, W. I., additional

Published
2008
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47. Nosocomial outbreak of novel arenavirus infection, southern Africa.

Author

Paweska JT, Sewlall NH, Ksiazek TG, Blumberg LH, Hale MJ, Lipkin WI, Weyer J, Nichol ST, Rollin PE, McMullan LK, Paddock CD, Briese T, Mnyaluza J, Dinh TH, Mukonka V, Ching P, Duse A, Richards G, de Jong G, and Cohen C

Abstract

A nosocomial outbreak of disease involving 5 patients, 4 of whom died, occurred in South Africa during September-October 2008. The first patient had been transferred from Zambia to South Africa for medical management. Three cases involved secondary spread of infection from the first patient, and 1 was a tertiary infection. A novel arenavirus was identified. The source of the first patient's infection remains undetermined. [ABSTRACT FROM AUTHOR]

Published
2009
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49. Penicillin-binding proteins of penicillin-susceptible and -resistant pneumococci: immunological relatedness of altered proteins and changes in peptides carrying the beta-lactam binding site

Author

Hakenbeck, R, Ellerbrok, H, Briese, T, Handwerger, S, and Tomasz, A

Abstract

There are several major differences between the penicillin-binding proteins (PBPs) of highly penicillin-resistant and -susceptible strains of pneumococci. The highest-molecular-size PBP 1a (98 kilodaltons [kDa]) of susceptible pneumococci is not detectable in resistant bacteria. Instead, resistant strains contain a PBP of smaller size: 92 and 94 kDa in South African strains 8249 and A95210, respectively, and 96 kDa in New Guinea strain 2955 (S. Zighelboim and A. Tomasz, Antimicrob. Agents Chemother. 17:434-442, 1980). Using antibodies prepared against PBP 1a of penicillin-susceptible pneumococci, we demonstrated that these anomalous-sized proteins in the resistant strains are immunologically related to PBP 1a of penicillin-susceptible bacteria. A second difference between the PBP patterns of strain 8249 and the susceptible pneumococci is that the 78-kDa PBP 2b is not detectable by the radioactive penicillin binding assay in the resistant strain. Using antibodies prepared against PBP 2b of susceptible cells, we demonstrated the presence of PBP 2b in membrane preparations from strain 8249 cells. Thus, the poor detection of this PBP appears to be related to its greatly decreased affinity for the antibiotic molecule. We also compared the patterns of penicillin-labeled peptides derived from PBPs of resistant and susceptible cells during partial proteolysis by V8 protease. Several changes were observable in small peptides carrying the beta-lactam binding site generated from the high Mr (PBP 1a-related) binding proteins. In contrast, no differences in the pattern of penicillin-labeled peptides were seen when the pattern of PBP 2a of susceptible pneumococci was compared with the peptide pattern of PBP 2a from resistant strains. One of the resistant isolates (strain 2955) also had a PBP 3 with a higher-than-normal molecular weight. This protein gave strong positive reaction with antibodies against PBP 3 of susceptible cells. Examination of the pattern of penicilloyl peptides generated from the susceptible and resistant PBP 3s during partial proteolysis revealed only differences which seem to reside distant from the beta-lactam binding site.

Published
1986
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50. State of knowledge and data gaps of middle east respiratory syndrome coronavirus (MERS-CoV) in humans

Author

Abdallat, M. M., Abroug, F., Al Dhahry, S. H. S., Alhajri, M. M., Al-Hakeem, R., Al Hosani, F. I., Al Qasrawi, S. M. A., Al-Romaihi, H. E., Assiri, A., Baillie, J. K., Ben Embarek, P. K., Ben Salah, A., Blümel, B., Briese, T., Buchholz, U., Cognat, S. B. F., Defang, G. N., La Rocque, S., Donatelli, I., Drosten, C., Drury, P. A., Eremin, S. R., Ferguson, N. M., Fontanet, A., Formenty, P. B. H., Fouchier, R. A. M., Gao, C. Q., Garcia, E., Gerber, S. I., Guery, B., Haagmans, B. L., Haddadin, A. J., Hardiman, M. C., Lisa Hensley, Hugonnet, S. A. L., Hui, D. S. C., Isla, N., Karesh, W. B., Koopmans, M., Kuehne, A., Lipkin, W. I., Mafi, A. R., Malik, M., Manuguerra, J. -C, Memish, Z., Mounts, A. W., Mumford, E., Opoka, L., Osterhaus, A., John Oxenford, C., Pang, J., Pebody, R., Peiris, J. S. M., Jay Plotkin, B., Poumerol, G., Reusken, C., Rezza, G., Roth, C. E., Shindo, N., Shumate, A. M., Siwula, M., Slim, A., Smallwood, C., Werf, S., Kerkhove, M. D., and Zambon, M.

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