Cargando…

The Omicron Variant BA.1.1 Presents a Lower Pathogenicity than B.1 D614G and Delta Variants in a Feline Model of SARS-CoV-2 Infection

Omicron (B.1.1.529) is the most recent SARS-CoV-2 variant of concern, which emerged in late 2021 and rapidly achieved global predominance by early 2022. In this study, we compared the infection dynamics, tissue tropism, and pathogenesis and pathogenicity of SARS-CoV-2 D614G (B.1), Delta (B.1.617.2),...

Descripción completa

Detalles Bibliográficos
Autores principales: Martins, Mathias, do Nascimento, Gabriela M., Nooruzzaman, Mohammed, Yuan, Fangfeng, Chen, Chi, Caserta, Leonardo C., Miller, Andrew D., Whittaker, Gary R., Fang, Ying, Diel, Diego G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9472624/
https://www.ncbi.nlm.nih.gov/pubmed/36000850
http://dx.doi.org/10.1128/jvi.00961-22
_version_ 1784789340000354304
author Martins, Mathias
do Nascimento, Gabriela M.
Nooruzzaman, Mohammed
Yuan, Fangfeng
Chen, Chi
Caserta, Leonardo C.
Miller, Andrew D.
Whittaker, Gary R.
Fang, Ying
Diel, Diego G.
author_facet Martins, Mathias
do Nascimento, Gabriela M.
Nooruzzaman, Mohammed
Yuan, Fangfeng
Chen, Chi
Caserta, Leonardo C.
Miller, Andrew D.
Whittaker, Gary R.
Fang, Ying
Diel, Diego G.
author_sort Martins, Mathias
collection PubMed
description Omicron (B.1.1.529) is the most recent SARS-CoV-2 variant of concern, which emerged in late 2021 and rapidly achieved global predominance by early 2022. In this study, we compared the infection dynamics, tissue tropism, and pathogenesis and pathogenicity of SARS-CoV-2 D614G (B.1), Delta (B.1.617.2), and Omicron BA.1.1 (B.1.1.529) variants in a highly susceptible feline model of infection. Although D614G- and Delta-inoculated cats became lethargic and showed increased body temperatures between days 1 and 3 postinfection (pi), Omicron-inoculated cats remained subclinical and, similar to control animals, gained weight throughout the 14-day experimental period. Intranasal inoculation of cats with D614G- and the Delta variants resulted in high infectious virus shedding in nasal secretions (up to 6.3 log(10) TCID(50).Ml(−1)), whereas strikingly lower level of viruses shedding (<3.1 log(10) TCID(50).Ml(−1)) was observed in Omicron-inoculated animals. In addition, tissue distribution of the Omicron variant was markedly reduced in comparison to the D614G and Delta variants, as evidenced by lower in situ viral RNA detection, in situ viral immunofluorescence staining, and viral loads in tissues on days 3, 5, and 14 pi. Nasal turbinate, trachea, and lung were the main—but not the only—sites of replication for all three viral variants. However, only scarce virus staining and lower viral titers suggest lower levels of viral replication in tissues from Omicron-infected animals. Notably, while D614G- and Delta-inoculated cats presented pneumonia, histologic examination of the lungs from Omicron-infected cats revealed mild to modest inflammation. Together, these results demonstrate that the Omicron variant BA.1.1 is less pathogenic than D614G and Delta variants in a highly susceptible feline model. IMPORTANCE The SARS-CoV-2 Omicron (B.1.1.529) variant of concern emerged in South Africa late in 2021 and rapidly spread across the world causing a significant increase in the number of infections. Importantly, this variant was also associated with an increased risk of reinfections. However, the number of hospitalizations and deaths due to COVID-19 did not follow the same trends. These early observations suggested effective protection conferred by immunizations and/or overall lower virulence of the highly mutated variant virus. In this study we present novel evidence demonstrating that the Omicron BA.1.1 variant of concern presents a lower pathogenicity when compared to D614G- or Delta variants in cats. Clinical, virological, and pathological evaluations revealed lower disease severity, viral replication, and lung pathology in Omicron-infected cats when compared with D614G and Delta variant inoculated animals, confirming that Omicron BA.1.1 is less pathogenic in a highly susceptible feline model of infection.
format Online
Article
Text
id pubmed-9472624
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-94726242022-09-15 The Omicron Variant BA.1.1 Presents a Lower Pathogenicity than B.1 D614G and Delta Variants in a Feline Model of SARS-CoV-2 Infection Martins, Mathias do Nascimento, Gabriela M. Nooruzzaman, Mohammed Yuan, Fangfeng Chen, Chi Caserta, Leonardo C. Miller, Andrew D. Whittaker, Gary R. Fang, Ying Diel, Diego G. J Virol Pathogenesis and Immunity Omicron (B.1.1.529) is the most recent SARS-CoV-2 variant of concern, which emerged in late 2021 and rapidly achieved global predominance by early 2022. In this study, we compared the infection dynamics, tissue tropism, and pathogenesis and pathogenicity of SARS-CoV-2 D614G (B.1), Delta (B.1.617.2), and Omicron BA.1.1 (B.1.1.529) variants in a highly susceptible feline model of infection. Although D614G- and Delta-inoculated cats became lethargic and showed increased body temperatures between days 1 and 3 postinfection (pi), Omicron-inoculated cats remained subclinical and, similar to control animals, gained weight throughout the 14-day experimental period. Intranasal inoculation of cats with D614G- and the Delta variants resulted in high infectious virus shedding in nasal secretions (up to 6.3 log(10) TCID(50).Ml(−1)), whereas strikingly lower level of viruses shedding (<3.1 log(10) TCID(50).Ml(−1)) was observed in Omicron-inoculated animals. In addition, tissue distribution of the Omicron variant was markedly reduced in comparison to the D614G and Delta variants, as evidenced by lower in situ viral RNA detection, in situ viral immunofluorescence staining, and viral loads in tissues on days 3, 5, and 14 pi. Nasal turbinate, trachea, and lung were the main—but not the only—sites of replication for all three viral variants. However, only scarce virus staining and lower viral titers suggest lower levels of viral replication in tissues from Omicron-infected animals. Notably, while D614G- and Delta-inoculated cats presented pneumonia, histologic examination of the lungs from Omicron-infected cats revealed mild to modest inflammation. Together, these results demonstrate that the Omicron variant BA.1.1 is less pathogenic than D614G and Delta variants in a highly susceptible feline model. IMPORTANCE The SARS-CoV-2 Omicron (B.1.1.529) variant of concern emerged in South Africa late in 2021 and rapidly spread across the world causing a significant increase in the number of infections. Importantly, this variant was also associated with an increased risk of reinfections. However, the number of hospitalizations and deaths due to COVID-19 did not follow the same trends. These early observations suggested effective protection conferred by immunizations and/or overall lower virulence of the highly mutated variant virus. In this study we present novel evidence demonstrating that the Omicron BA.1.1 variant of concern presents a lower pathogenicity when compared to D614G- or Delta variants in cats. Clinical, virological, and pathological evaluations revealed lower disease severity, viral replication, and lung pathology in Omicron-infected cats when compared with D614G and Delta variant inoculated animals, confirming that Omicron BA.1.1 is less pathogenic in a highly susceptible feline model of infection. American Society for Microbiology 2022-08-24 /pmc/articles/PMC9472624/ /pubmed/36000850 http://dx.doi.org/10.1128/jvi.00961-22 Text en Copyright © 2022 American Society for Microbiology. https://doi.org/10.1128/ASMCopyrightv2All Rights Reserved (https://doi.org/10.1128/ASMCopyrightv2) . https://doi.org/10.1128/ASMCopyrightv2This article is made available via the PMC Open Access Subset for unrestricted noncommercial re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Pathogenesis and Immunity
Martins, Mathias
do Nascimento, Gabriela M.
Nooruzzaman, Mohammed
Yuan, Fangfeng
Chen, Chi
Caserta, Leonardo C.
Miller, Andrew D.
Whittaker, Gary R.
Fang, Ying
Diel, Diego G.
The Omicron Variant BA.1.1 Presents a Lower Pathogenicity than B.1 D614G and Delta Variants in a Feline Model of SARS-CoV-2 Infection
title The Omicron Variant BA.1.1 Presents a Lower Pathogenicity than B.1 D614G and Delta Variants in a Feline Model of SARS-CoV-2 Infection
title_full The Omicron Variant BA.1.1 Presents a Lower Pathogenicity than B.1 D614G and Delta Variants in a Feline Model of SARS-CoV-2 Infection
title_fullStr The Omicron Variant BA.1.1 Presents a Lower Pathogenicity than B.1 D614G and Delta Variants in a Feline Model of SARS-CoV-2 Infection
title_full_unstemmed The Omicron Variant BA.1.1 Presents a Lower Pathogenicity than B.1 D614G and Delta Variants in a Feline Model of SARS-CoV-2 Infection
title_short The Omicron Variant BA.1.1 Presents a Lower Pathogenicity than B.1 D614G and Delta Variants in a Feline Model of SARS-CoV-2 Infection
title_sort omicron variant ba.1.1 presents a lower pathogenicity than b.1 d614g and delta variants in a feline model of sars-cov-2 infection
topic Pathogenesis and Immunity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9472624/
https://www.ncbi.nlm.nih.gov/pubmed/36000850
http://dx.doi.org/10.1128/jvi.00961-22
work_keys_str_mv AT martinsmathias theomicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT donascimentogabrielam theomicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT nooruzzamanmohammed theomicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT yuanfangfeng theomicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT chenchi theomicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT casertaleonardoc theomicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT millerandrewd theomicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT whittakergaryr theomicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT fangying theomicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT dieldiegog theomicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT martinsmathias omicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT donascimentogabrielam omicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT nooruzzamanmohammed omicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT yuanfangfeng omicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT chenchi omicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT casertaleonardoc omicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT millerandrewd omicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT whittakergaryr omicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT fangying omicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection
AT dieldiegog omicronvariantba11presentsalowerpathogenicitythanb1d614ganddeltavariantsinafelinemodelofsarscov2infection