Anthropogenic Transmission of SARS-CoV-2 from Humans to Lions, Singapore, 2021
In Singapore, 10 captive lions tested positive for SARS-CoV-2 by real-time PCR. Genomic analyses of nanopore sequencing confirmed human-to-animal transmission of the SARS-CoV-2 Delta variant. Viral genomes from the lions and zookeeper shared a unique spike protein substitution, S:A1016V. Widespread...
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Published in | Emerging infectious diseases Vol. 29; no. 12; pp. 2550 - 2553 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Atlanta
U.S. National Center for Infectious Diseases
01.12.2023
Centers for Disease Control and Prevention |
Subjects | |
Online Access | Get full text |
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Summary: | In Singapore, 10 captive lions tested positive for SARS-CoV-2 by real-time PCR. Genomic analyses of nanopore sequencing confirmed human-to-animal transmission of the SARS-CoV-2 Delta variant. Viral genomes from the lions and zookeeper shared a unique spike protein substitution, S:A1016V. Widespread SARS-CoV-2 transmission among humans can increase the likelihood of anthroponosis. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Author contributions: C.L., J.O., and W.K.W. conducted the molecular diagnostic tests; Y.C.A.I. performed the nanopore sequencing for viral genome assembly. Y.C.A.I and A.T. performed data analyses. The figures and the manuscript draft were prepared by Y.C.A.I. with input from C.J.F. Study initiation and guidance was by K.B.H.E, and supervised by C.J.F., S.F.C., Y.H.H., and K.B.H.E. Y.C.A.I. wrote the manuscript and all authors contributed to the manuscript editing process, approved the final version for publication, and declared that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The ethical handling of animal subjects during the course of this research has been supervised and approved by National Parks Board, Singapore. |
ISSN: | 1080-6040 1080-6059 |
DOI: | 10.3201/eid2912.221916 |