TY - JOUR
T1 - Experimental re-infected cats do not transmit SARS-CoV-2
AU - Gaudreault, Natasha N.
AU - Carossino, Mariano
AU - Morozov, Igor
AU - Trujillo, Jessie D.
AU - Meekins, David A.
AU - Madden, Daniel W.
AU - Cool, Konner
AU - Artiaga, Bianca Libanori
AU - McDowell, Chester
AU - Bold, Dashzeveg
AU - Balaraman, Velmurugan
AU - Kwon, Taeyong
AU - Ma, Wenjun
AU - Henningson, Jamie
AU - Wilson, Dennis W.
AU - Wilson, William C.
AU - Balasuriya, Udeni B.R.
AU - García-Sastre, Adolfo
AU - Richt, Juergen A.
N1 - Funding Information:
for this study was provided through grants from NBAF Transition Funds from the State of Kansas, the NIAID Centers of Excellence for Influenza Research and Surveillance under contract number HHSN 272201400006C, the National Institute of General Medical Sciences (NIGMS) of the National Institutes of Health under award number P20GM130448, and the Department of Homeland Security Center of Excellence for Emerging and Zoonotic Animal Diseases under grant number HSHQDC 16-A-B0006 to JAR. This study was also partially supported by the Louisiana State University, School of Veterinary Medicine start-up fund (PG 002165) to UBRB and the US Department of Agriculture, Agricultural Research Service (58-32000-009-00D) to WCW, by the Center for Research for Influenza Pathogenesis (CRIP), a NIAID supported Center of Excellence for Influenza Research and Surveillance (CEIRS, contract # HHSN272201400008C), and by the generous support of the JPB Foundation, the Open Philanthropy Project (research grant 2020-215611 [5384]) and anonymous donors to AG-S. We thank the staff of KSU Biosecurity Research Institute, the histological laboratory at the Kansas State Veterinary Diagnostic Laboratory, the CMG staff and Sabarish Indran, Gleyder Roman-Sosa, Yonghai Li, and Emily Gilbert-Esparza at KSU. We also thank the staff at the Histology and Immunohistochemistry section of the Louisiana Animal Disease Diagnostic Laboratory (LADDL) for assistance with this study. The SARS-CoV-2 strain USA-WA1/2020 was obtained through BEI Resources (catalogue # NR-52281). Mention of trade names or commercial products in this publication is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the US Department of Agriculture. USDA is an equal opportunity provider and employer.
Publisher Copyright:
© 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.
PY - 2021
Y1 - 2021
N2 - SARS-CoV-2 is the causative agent of COVID-19 and responsible for the current global pandemic. We and others have previously demonstrated that cats are susceptible to SARS-CoV-2 infection and can efficiently transmit the virus to naïve cats. Here, we address whether cats previously exposed to SARS-CoV-2 can be re-infected with SARS-CoV-2. In two independent studies, SARS-CoV-2-infected cats were re-challenged with SARS-CoV-2 at 21 days post primary challenge (DPC) and necropsies performed at 4, 7 and 14 days post-secondary challenge (DP2C). Sentinels were co-mingled with the re-challenged cats at 1 DP2C. Clinical signs were recorded, and nasal, oropharyngeal, and rectal swabs, blood, and serum were collected and tissues examined for histologic lesions. Viral RNA was transiently shed via the nasal, oropharyngeal and rectal cavities of the re-challenged cats. Viral RNA was detected in various tissues of re-challenged cats euthanized at 4 DP2C, mainly in the upper respiratory tract and lymphoid tissues, but less frequently and at lower levels in the lower respiratory tract when compared to primary SARS-CoV-2 challenged cats at 4 DPC. Viral RNA and antigen detected in the respiratory tract of the primary SARS-CoV-2 infected cats at early DPCs were absent in the re-challenged cats. Naïve sentinels co-housed with the re-challenged cats did not shed virus or seroconvert. Together, our results indicate that cats previously infected with SARS-CoV-2 can be experimentally re-infected with SARS-CoV-2; however, the levels of virus shed was insufficient for transmission to co-housed naïve sentinels. We conclude that SARS-CoV-2 infection in cats induces immune responses that provide partial, non-sterilizing immune protection against re-infection.
AB - SARS-CoV-2 is the causative agent of COVID-19 and responsible for the current global pandemic. We and others have previously demonstrated that cats are susceptible to SARS-CoV-2 infection and can efficiently transmit the virus to naïve cats. Here, we address whether cats previously exposed to SARS-CoV-2 can be re-infected with SARS-CoV-2. In two independent studies, SARS-CoV-2-infected cats were re-challenged with SARS-CoV-2 at 21 days post primary challenge (DPC) and necropsies performed at 4, 7 and 14 days post-secondary challenge (DP2C). Sentinels were co-mingled with the re-challenged cats at 1 DP2C. Clinical signs were recorded, and nasal, oropharyngeal, and rectal swabs, blood, and serum were collected and tissues examined for histologic lesions. Viral RNA was transiently shed via the nasal, oropharyngeal and rectal cavities of the re-challenged cats. Viral RNA was detected in various tissues of re-challenged cats euthanized at 4 DP2C, mainly in the upper respiratory tract and lymphoid tissues, but less frequently and at lower levels in the lower respiratory tract when compared to primary SARS-CoV-2 challenged cats at 4 DPC. Viral RNA and antigen detected in the respiratory tract of the primary SARS-CoV-2 infected cats at early DPCs were absent in the re-challenged cats. Naïve sentinels co-housed with the re-challenged cats did not shed virus or seroconvert. Together, our results indicate that cats previously infected with SARS-CoV-2 can be experimentally re-infected with SARS-CoV-2; however, the levels of virus shed was insufficient for transmission to co-housed naïve sentinels. We conclude that SARS-CoV-2 infection in cats induces immune responses that provide partial, non-sterilizing immune protection against re-infection.
KW - COVID-19
KW - SARS-CoV-2
KW - cats
KW - re-infection
KW - transmission
UR - http://www.scopus.com/inward/record.url?scp=85103815571&partnerID=8YFLogxK
U2 - 10.1080/22221751.2021.1902753
DO - 10.1080/22221751.2021.1902753
M3 - Article
C2 - 33704016
AN - SCOPUS:85103815571
SN - 2222-1751
VL - 10
SP - 638
EP - 650
JO - Emerging Microbes and Infections
JF - Emerging Microbes and Infections
IS - 1
ER -