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Intranasal infection by SARS-CoV-2 Omicron variants can induce inflammatory brain damage in newly weaned hamsters

Children infected by SARS-CoV-2 Omicron variant may develop neurological complications. To study the pathogenesis in the growing brain, we intranasally challenged newly-weaned or mature hamsters with SARS-CoV-2 Omicron BA.2, BA.5, or Delta variant. Omicron BA.2 and Delta infection produced a signifi...

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Autores principales: Li, Can, Song, Wenchen, Chan, Jasper Fuk-Woo, Chen, Yanxia, Liu, Feifei, Ye, Zhanhong, Lam, Alvin Hiu-Chung, Cai, Jianpiao, Lee, Andrew Chak-Yiu, Wong, Bosco Ho-Yin, Chu, Hin, Lung, David Christopher, Sridhar, Siddharth, Chen, Honglin, Zhang, Anna Jin-Xia, Yuen, Kwok-Yung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10262819/
https://www.ncbi.nlm.nih.gov/pubmed/37122119
http://dx.doi.org/10.1080/22221751.2023.2207678
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author Li, Can
Song, Wenchen
Chan, Jasper Fuk-Woo
Chen, Yanxia
Liu, Feifei
Ye, Zhanhong
Lam, Alvin Hiu-Chung
Cai, Jianpiao
Lee, Andrew Chak-Yiu
Wong, Bosco Ho-Yin
Chu, Hin
Lung, David Christopher
Sridhar, Siddharth
Chen, Honglin
Zhang, Anna Jin-Xia
Yuen, Kwok-Yung
author_facet Li, Can
Song, Wenchen
Chan, Jasper Fuk-Woo
Chen, Yanxia
Liu, Feifei
Ye, Zhanhong
Lam, Alvin Hiu-Chung
Cai, Jianpiao
Lee, Andrew Chak-Yiu
Wong, Bosco Ho-Yin
Chu, Hin
Lung, David Christopher
Sridhar, Siddharth
Chen, Honglin
Zhang, Anna Jin-Xia
Yuen, Kwok-Yung
author_sort Li, Can
collection PubMed
description Children infected by SARS-CoV-2 Omicron variant may develop neurological complications. To study the pathogenesis in the growing brain, we intranasally challenged newly-weaned or mature hamsters with SARS-CoV-2 Omicron BA.2, BA.5, or Delta variant. Omicron BA.2 and Delta infection produced a significantly lower viral load in the lung tissues of newly-weaned than mature hamsters despite comparable histopathological damages. Newly-weaned hamsters had higher brain viral load, significantly increased cerebrospinal fluid concentration of TNF-α and CXCL10 and inflammatory damages including mild meningitis and parenchymal vascular congestion, despite sparse expression of nucleocapsid antigen in brain cells. Furthermore, 63.6% (28/44) of all SARS-CoV-2 infected newly-weaned hamsters showed microgliosis in olfactory bulb (OB), cerebral cortex, and hippocampus. In infected mature hamsters, microgliosis was observed mainly in OB and olfactory cortex of 35.3% (12/34) of their brains. Neuronal degeneration was found in 75% (33/44) of newly-weaned hamsters affecting multiple regions including OB, olfactory cortex, midbrain cortex, and hippocampus, while such changes were mainly observed in the hippocampus of mature hamsters. Importantly, similar brain histopathology was also observed in Omicron BA.5-infected newly-weaned hamsters. Our study suggested that SARS-CoV-2 may affect the brain at a young age. This kind of brain involvement and histological changes are not virus variant or subvariant specific. Incidentally, a moderate amount of eosinophilic infiltration was observed in the mucosa of nasal turbinate and trachea of newly-weaned hamsters infected by Omicron BA.2 and BA.5 but not Delta variant. This histological finding is consistent with the higher incidence of laryngotracheobronchitis in young children infected by the Omicron variant. SUMMARY: Intranasal infection of newly-weaned Syrian hamsters by SARS-CoV-2 Omicron variants can lead to brain inflammation and neuron degeneration with detectable low level of viral load and sparse expression of viral nucleoprotein.
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spelling pubmed-102628192023-06-15 Intranasal infection by SARS-CoV-2 Omicron variants can induce inflammatory brain damage in newly weaned hamsters Li, Can Song, Wenchen Chan, Jasper Fuk-Woo Chen, Yanxia Liu, Feifei Ye, Zhanhong Lam, Alvin Hiu-Chung Cai, Jianpiao Lee, Andrew Chak-Yiu Wong, Bosco Ho-Yin Chu, Hin Lung, David Christopher Sridhar, Siddharth Chen, Honglin Zhang, Anna Jin-Xia Yuen, Kwok-Yung Emerg Microbes Infect Coronaviruses Children infected by SARS-CoV-2 Omicron variant may develop neurological complications. To study the pathogenesis in the growing brain, we intranasally challenged newly-weaned or mature hamsters with SARS-CoV-2 Omicron BA.2, BA.5, or Delta variant. Omicron BA.2 and Delta infection produced a significantly lower viral load in the lung tissues of newly-weaned than mature hamsters despite comparable histopathological damages. Newly-weaned hamsters had higher brain viral load, significantly increased cerebrospinal fluid concentration of TNF-α and CXCL10 and inflammatory damages including mild meningitis and parenchymal vascular congestion, despite sparse expression of nucleocapsid antigen in brain cells. Furthermore, 63.6% (28/44) of all SARS-CoV-2 infected newly-weaned hamsters showed microgliosis in olfactory bulb (OB), cerebral cortex, and hippocampus. In infected mature hamsters, microgliosis was observed mainly in OB and olfactory cortex of 35.3% (12/34) of their brains. Neuronal degeneration was found in 75% (33/44) of newly-weaned hamsters affecting multiple regions including OB, olfactory cortex, midbrain cortex, and hippocampus, while such changes were mainly observed in the hippocampus of mature hamsters. Importantly, similar brain histopathology was also observed in Omicron BA.5-infected newly-weaned hamsters. Our study suggested that SARS-CoV-2 may affect the brain at a young age. This kind of brain involvement and histological changes are not virus variant or subvariant specific. Incidentally, a moderate amount of eosinophilic infiltration was observed in the mucosa of nasal turbinate and trachea of newly-weaned hamsters infected by Omicron BA.2 and BA.5 but not Delta variant. This histological finding is consistent with the higher incidence of laryngotracheobronchitis in young children infected by the Omicron variant. SUMMARY: Intranasal infection of newly-weaned Syrian hamsters by SARS-CoV-2 Omicron variants can lead to brain inflammation and neuron degeneration with detectable low level of viral load and sparse expression of viral nucleoprotein. Taylor & Francis 2023-06-12 /pmc/articles/PMC10262819/ /pubmed/37122119 http://dx.doi.org/10.1080/22221751.2023.2207678 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Coronaviruses
Li, Can
Song, Wenchen
Chan, Jasper Fuk-Woo
Chen, Yanxia
Liu, Feifei
Ye, Zhanhong
Lam, Alvin Hiu-Chung
Cai, Jianpiao
Lee, Andrew Chak-Yiu
Wong, Bosco Ho-Yin
Chu, Hin
Lung, David Christopher
Sridhar, Siddharth
Chen, Honglin
Zhang, Anna Jin-Xia
Yuen, Kwok-Yung
Intranasal infection by SARS-CoV-2 Omicron variants can induce inflammatory brain damage in newly weaned hamsters
title Intranasal infection by SARS-CoV-2 Omicron variants can induce inflammatory brain damage in newly weaned hamsters
title_full Intranasal infection by SARS-CoV-2 Omicron variants can induce inflammatory brain damage in newly weaned hamsters
title_fullStr Intranasal infection by SARS-CoV-2 Omicron variants can induce inflammatory brain damage in newly weaned hamsters
title_full_unstemmed Intranasal infection by SARS-CoV-2 Omicron variants can induce inflammatory brain damage in newly weaned hamsters
title_short Intranasal infection by SARS-CoV-2 Omicron variants can induce inflammatory brain damage in newly weaned hamsters
title_sort intranasal infection by sars-cov-2 omicron variants can induce inflammatory brain damage in newly weaned hamsters
topic Coronaviruses
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10262819/
https://www.ncbi.nlm.nih.gov/pubmed/37122119
http://dx.doi.org/10.1080/22221751.2023.2207678
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