Reduced airborne transmission of SARS-CoV-2 BA.1 Omicron virus in Syrian hamsters
JRP and VJM are supported by the Intramural Research Program of the National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH). The authors report no other conflict of interest. Since the start of the COVID-19 pandemic, Severe Acute Respiratory Syndrome Corona...
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Published in | PLOS Pathogens Vol. 18; no. 12; p. e1010970 |
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Main Authors | , , , , , , , , , |
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Abstract | JRP and VJM are supported by the Intramural Research Program of the National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH). The authors report no other conflict of interest. Since the start of the COVID-19 pandemic, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) has caused hundreds of millions of infections worldwide with more than 6.5 million confirmed deaths. Transmission of SARS-CoV-2 can be established by detection of viral RNA, RNA replication intermediates, viable infectious virus, or seroconversion, with the latter two metrics being the most stringent. Since January 2021, the National Institutes of Health SARS-CoV-2 Assessment of Variant Evolution (SAVE) initiative has evaluated the transmission potential of SARS-CoV-2 variants in Syrian hamsters [16]. [...]it is possible that the changes in the spike protein of Omicron affect and reduce stability of the virus in the infected hosts. |
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AbstractList | JRP and VJM are supported by the Intramural Research Program of the National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH).
The authors report no other conflict of interest.
Since the start of the COVID-19 pandemic, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) has caused hundreds of millions of infections worldwide with more than 6.5 million confirmed deaths.
Transmission of SARS-CoV-2 can be established by detection of viral RNA, RNA replication intermediates, viable infectious virus, or seroconversion, with the latter two metrics being the most stringent.
Since January 2021, the National Institutes of Health SARS-CoV-2 Assessment of Variant Evolution (SAVE) initiative has evaluated the transmission potential of SARS-CoV-2 variants in Syrian hamsters [16].
[...]it is possible that the changes in the spike protein of Omicron affect and reduce stability of the virus in the infected hosts. JRP and VJM are supported by the Intramural Research Program of the National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH). The authors report no other conflict of interest. Since the start of the COVID-19 pandemic, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) has caused hundreds of millions of infections worldwide with more than 6.5 million confirmed deaths. Transmission of SARS-CoV-2 can be established by detection of viral RNA, RNA replication intermediates, viable infectious virus, or seroconversion, with the latter two metrics being the most stringent. Since January 2021, the National Institutes of Health SARS-CoV-2 Assessment of Variant Evolution (SAVE) initiative has evaluated the transmission potential of SARS-CoV-2 variants in Syrian hamsters [16]. [...]it is possible that the changes in the spike protein of Omicron affect and reduce stability of the virus in the infected hosts. |
Audience | Academic |
Author | Tamarand L. Darling Michael S. Diamond John Franks Adrianus C. M. Boon Yoshihiro Kawaoka Vincent J. Munster Peter J. Halfmann Julia R. Port Dan H. Barouch Richard J. Webby |
AuthorAffiliation | 5 Department of Infectious Diseases, St. Jude Children’s Research Hospital, Memphis, Tennessee, United States of America 4 Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, Wisconsin, United States of America 11 The Research Center for Global Viral Diseases, National Center for Global Health and Medicine Research Institute, Tokyo, Japan 10 Department of Virology, Institute of Medical Science, University of Tokyo, Tokyo, Japan 2 Department of Pathology and Immunology Washington University School of Medicine in St. Louis, Missouri, United States of America 7 Ragon Institute of MGH, MIT, and Harvard, Cambridge, Massachusetts, United States of America Boston Children’s Hospital, UNITED STATES 1 Department of Medicine, Washington University School of Medicine in St. Louis, Missouri, United States of America 8 Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of He |
AuthorAffiliation_xml | – name: 5 Department of Infectious Diseases, St. Jude Children’s Research Hospital, Memphis, Tennessee, United States of America – name: 10 Department of Virology, Institute of Medical Science, University of Tokyo, Tokyo, Japan – name: 11 The Research Center for Global Viral Diseases, National Center for Global Health and Medicine Research Institute, Tokyo, Japan – name: 3 Department of Microbiology, Washington University School of Medicine in St. Louis, Missouri, United States of America – name: 8 Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana, United States of America – name: 1 Department of Medicine, Washington University School of Medicine in St. Louis, Missouri, United States of America – name: 2 Department of Pathology and Immunology Washington University School of Medicine in St. Louis, Missouri, United States of America – name: 4 Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, Wisconsin, United States of America – name: 9 The Andrew M. and Jane M. Bursky Center for Human Immunology and Immunotherapy Programs, Washington University School of Medicine. St. Louis, Missouri, United States of America – name: 7 Ragon Institute of MGH, MIT, and Harvard, Cambridge, Massachusetts, United States of America – name: Boston Children’s Hospital, UNITED STATES – name: 6 Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States of America |
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CitedBy_id | crossref_primary_10_1016_j_ebiom_2023_104677 crossref_primary_10_1038_s41467_023_38783_0 crossref_primary_10_1038_s41467_023_42796_0 crossref_primary_10_1128_jvi_00851_23 crossref_primary_10_1128_jvi_02217_24 crossref_primary_10_1128_spectrum_04717_22 crossref_primary_10_1128_jvi_00628_23 crossref_primary_10_1038_s41467_023_42346_8 crossref_primary_10_1038_s44298_023_00012_2 crossref_primary_10_1126_sciadv_adp1290 crossref_primary_10_1126_sciadv_ads2927 crossref_primary_10_7717_peerj_16420 crossref_primary_10_1080_01919512_2025_2474479 crossref_primary_10_3389_fimmu_2024_1427284 crossref_primary_10_3390_v16010089 crossref_primary_10_1038_s44298_025_00092_2 crossref_primary_10_1016_j_celrep_2024_114076 crossref_primary_10_1038_s41467_025_55938_3 |
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Copyright | COPYRIGHT 2022 Public Library of Science 2022 Boon et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2022 Boon et al 2022 Boon et al |
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Notes | SourceType-Scholarly Journals-1 ObjectType-Commentary-1 content type line 14 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 I have read the journal’s policy and the authors of this manuscript have the following competing interests: D.H.B is a co-inventor on provisional vaccine patents (63/121,482; 63/133,969; 63/135,182). The Boon laboratory has received unrelated funding support in sponsored research agreements from AI Therapeutics, GreenLight Biosciences Inc., and Nano targeting & Therapy Biopharma Inc. The Boon laboratory has received funding support from AbbVie Inc., for the commercial development of SARS-CoV-2 mAb. M.S.D. is a consultant for Inbios, Vir Biotechnology, Senda Biosciences, and Carnival Corporation, on the Scientific Advisory Boards of Moderna and Immunome, and has licensed mucosal vaccine technology to Bharat Biotech and Ocugen. The Diamond laboratory has received unrelated funding support in sponsored research agreements from Vir Biotechnology, Kaleido, and Emergent BioSolutions and past support from Moderna not related to these studies. The authors report no other conflict of interest. |
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Nature doi: 10.1038/s41586-022-04442-5 |
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SubjectTerms | Airborne infection Allergies Animal experimentation Animal models in research Animals Biology (General) Biology and Life Sciences Conflicts of interest Coronaviruses COVID-19 Cricetinae Disease transmission Funding Hamsters Immunologic diseases. Allergy Infectious diseases Influenza Intermediates Laboratories Medical research Medicine and health sciences Medicine, Experimental Mesocricetus Methods Mutation Opinion Pandemics Physiological aspects Proteins QH301-705.5 R&D RC581-607 Research & development Research and Analysis Methods Respiratory Aerosols and Droplets SARS-CoV-2 Seroconversion Severe acute respiratory syndrome coronavirus 2 Spike protein Vaccines Viral diseases Viruses |
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Title | Reduced airborne transmission of SARS-CoV-2 BA.1 Omicron virus in Syrian hamsters |
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