Predicting potential SARS-CoV-2 spillover and spillback in animals

被引:1
作者
Tan, Zi Hian [1 ]
Yong, Kian Yan [1 ]
Shu, Jian-Jun [1 ]
机构
[1] Nanyang Technol Univ, Sch Mech & Aerosp Engn, 50 Nanyang Ave, Singapore 639798, Singapore
关键词
SARS-CoV-2; Outbreak; Human-to-animal and animal-to-human transmissions; Spillover and spillback; Infectious disease; MULTIPLE SEQUENCE ALIGNMENT; INFECTION; HOST; BATS;
D O I
10.1016/j.jmii.2024.01.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: The COVID-19 pandemic is spreading rapidly around the world, causing countries to impose lockdowns and efforts to develop vaccines on a global scale. However, human-to-animal and animal-to-human transmission cannot be ignored, as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) can spread rapidly in farmed and wild animals. This could create a worrying cycle of SARS-CoV-2 spillover from humans to animals and spillback of new strains back into humans, rendering vaccines ineffective. Method: This study provides a key indicator of animals that may be potential susceptible hosts for SARS-CoV-2 and coronavirus infections by analysing the phylogenetic distance between host angiotensin-converting enzyme 2 and the coronavirus spike protein. Crucially, our analysis identifies animals that are at elevated risk from a spillover and spillback incident. Results: One group of animals has been identified as potentially susceptible to SARS-CoV-2 by harbouring a parasitic coronavirus spike protein similar to the SARS-CoV-2 spike protein. These animals may serve as amplification hosts in spillover events from zoonotic reservoirs. This group consists of a mixture of animals infected internally and naturally: minks, dogs, cats, tigers. Additionally, no internal or natural infections have been found in masked palm civet. Conclusion: Tracing interspecies transmission in multi-host environments based solely on in vitro and in vivo examinations of animal susceptibility or serology is a time-consuming task. This approach allows rapid identification of high-risk animals to prioritize research and assessment of the risk of zoonotic disease transmission in the environment. It is a tool to rapidly identify zoonotic species that may cause outbreaks or participate in expansion cycles of coexistence with their hosts. This prevents the spread of coronavirus infections between species, preventing spillover and spillback incidents from occurring. Copyright (c) 2024, Taiwan Society of Microbiology. Published by Elsevier Taiwan LLC. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/bync-nd/4.0/).
引用
收藏
页码:225 / 237
页数:13
相关论文
共 42 条
[1]   TMPRSS2 and furin are both essential for proteolytic activation of SARS-CoV-2 in human airway cells [J].
Bestle, Dorothea ;
Heindl, Miriam Ruth ;
Limburg, Hannah ;
Thuy Van Lam Van ;
Pilgram, Oliver ;
Moulton, Hong ;
Stein, David A. ;
Hardes, Kornelia ;
Eickmann, Markus ;
Dolnik, Olga ;
Rohde, Cornelius ;
Klenk, Hans-Dieter ;
Garten, Wolfgang ;
Steinmetzer, Torsten ;
Boettcher-Friebertshaeuser, Eva .
LIFE SCIENCE ALLIANCE, 2020, 3 (09)
[2]   Broad host range of SARS-CoV-2 predicted by comparative and structural analysis of ACE2 in vertebrates [J].
Damas, Joana ;
Hughes, Graham M. ;
Keough, Kathleen C. ;
Painter, Corrie A. ;
Persky, Nicole S. ;
Corbo, Marco ;
Hiller, Michael ;
Koepfli, Klaus-Peter ;
Pfenning, Andreas R. ;
Zhao, Huabin ;
Genereux, Diane P. ;
Swofford, Ross ;
Pollard, Katherine S. ;
Ryder, Oliver A. ;
Nweeia, Martin T. ;
Lindblad-Toh, Kerstin ;
Teeling, Emma C. ;
Karlsson, Elinor K. ;
Lewin, Harris A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2020, 117 (36) :22311-22322
[3]   Nextflow enables reproducible computational workflows [J].
Di Tommaso, Paolo ;
Chatzou, Maria ;
Floden, Evan W. ;
Prieto Barja, Pablo ;
Palumbo, Emilio ;
Notredame, Cedric .
NATURE BIOTECHNOLOGY, 2017, 35 (04) :316-319
[4]   UFBoot2: Improving the Ultrafast Bootstrap Approximation [J].
Diep Thi Hoang ;
Chernomor, Olga ;
von Haeseler, Arndt ;
Minh, Bui Quang ;
Le Sy Vinh .
MOLECULAR BIOLOGY AND EVOLUTION, 2018, 35 (02) :518-522
[5]   MUSCLE: multiple sequence alignment with high accuracy and high throughput [J].
Edgar, RC .
NUCLEIC ACIDS RESEARCH, 2004, 32 (05) :1792-1797
[6]   Transmission of SARS-CoV-2 in free-ranging white-tailed deer in the United States [J].
Feng, Aijing ;
Bevins, Sarah ;
Chandler, Jeff ;
DeLiberto, Thomas J. ;
Ghai, Ria ;
Lantz, Kristina ;
Lenoch, Julianna ;
Retchless, Adam ;
Shriner, Susan ;
Tang, Cynthia Y. ;
Tong, Suxiang Sue ;
Torchetti, Mia ;
Uehara, Anna ;
Wan, Xiu-Feng .
NATURE COMMUNICATIONS, 2023, 14 (01)
[7]   Virus Variation Resource - improved response to emergent viral outbreaks [J].
Hatcher, Eneida L. ;
Zhdanov, Sergey A. ;
Bao, Yiming ;
Blinkova, Olga ;
Nawrocki, Eric P. ;
Ostapchuck, Yuri ;
Schaffer, Alejandro A. ;
Brister, J. Rodney .
NUCLEIC ACIDS RESEARCH, 2017, 45 (D1) :D482-D490
[8]   A Multibasic Cleavage Site in the Spike Protein of SARS-CoV-2 Is Essential for Infection of Human Lung Cells [J].
Hoffmann, Markus ;
Kleine-Weber, Hannah ;
Poehlmann, Stefan .
MOLECULAR CELL, 2020, 78 (04) :779-+
[9]   Animal and translational models of SARS-CoV-2 infection and COVID-19 [J].
Johansen, M. D. ;
Irving, A. ;
Montagutelli, X. ;
Tate, M. D. ;
Rudloff, I ;
Nold, M. F. ;
Hansbro, N. G. ;
Kim, R. Y. ;
Donovan, C. ;
Liu, G. ;
Faiz, A. ;
Short, K. R. ;
Lyons, J. G. ;
McCaughan, G. W. ;
Gorrell, M. D. ;
Cole, A. ;
Moreno, C. ;
Couteur, D. ;
Hesselson, D. ;
Triccas, J. ;
Neely, G. G. ;
Gamble, J. R. ;
Simpson, S. J. ;
Saunders, B. M. ;
Oliver, B. G. ;
Britton, W. J. ;
Wark, P. A. ;
Nold-Petry, C. A. ;
Hansbro, P. M. .
MUCOSAL IMMUNOLOGY, 2020, 13 (06) :877-891
[10]  
Kalyaanamoorthy S, 2017, NAT METHODS, V14, P587, DOI [10.1038/NMETH.4285, 10.1038/nmeth.4285]