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Epidemiological Evidence for Fecal-Oral Transmission of Murine Kobuvirus
BACKGROUND: Murine Kobuvirus (MuKV) is a novel picornavirus of the genus Kobuvirus, and was first identified in the feces of murine rodents in the USA in 2011. There is limited information on the transmission route of MuKV. Thus, we conducted a study to investigate virus detection rates in fecal, se...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062591/ https://www.ncbi.nlm.nih.gov/pubmed/35517645 http://dx.doi.org/10.3389/fpubh.2022.865605 |
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author | Gao, Yuhan He, Wenqiao Fu, Jiaqi Li, Yongzhi He, Huan Chen, Qing |
author_facet | Gao, Yuhan He, Wenqiao Fu, Jiaqi Li, Yongzhi He, Huan Chen, Qing |
author_sort | Gao, Yuhan |
collection | PubMed |
description | BACKGROUND: Murine Kobuvirus (MuKV) is a novel picornavirus of the genus Kobuvirus, and was first identified in the feces of murine rodents in the USA in 2011. There is limited information on the transmission route of MuKV. Thus, we conducted a study to investigate virus detection rates in fecal, serum, throat, and lung tissue samples from murine rodents. RESULTS: A total of 413 fecal samples, 385 lung samples, 269 throat swab samples, and 183 serum samples were collected from 413 murine rodents (Rattus norvegicus, Rattus tanezumi, and Rattus rattus) captured in urban Shenzhen. Kobuviruses were detected via RT-PCR. Only fecal samples were positive, with prevalence rates of 34.9% in Rattus norvegicus and 29.4% in Rattus tanezumi. Phylogenetic analysis based on partial 3D and complete VP1 sequence regions indicated that all of the MuKV sequences obtained belonged to Aichivirus A, and were genetically closely related to other MuKVs reported in China, Hungary, and the USA. Twenty-eight full-length MuKV sequences were acquired. Phylogenetic analysis of two sequences randomly selected from the two species (SZ59 and SZ171) indicated that they shared very high nucleotide and amino acid identity with one another (94.0 and 99.3%, respectively), and comparison with human Kobuvirus revealed amino acid identity values of ~80%. Additionally, a sewage-derived sequence shared high similarity with the rat-derived sequences identified in this study, with respective nucleotide and amino acid identity values from 86.5 and 90.7% to 87.2 and 91.1%. CONCLUSION: The results of the current study provide evidence that murine Kobuvirus is transmitted via the fecal-oral route. |
format | Online Article Text |
id | pubmed-9062591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90625912022-05-04 Epidemiological Evidence for Fecal-Oral Transmission of Murine Kobuvirus Gao, Yuhan He, Wenqiao Fu, Jiaqi Li, Yongzhi He, Huan Chen, Qing Front Public Health Public Health BACKGROUND: Murine Kobuvirus (MuKV) is a novel picornavirus of the genus Kobuvirus, and was first identified in the feces of murine rodents in the USA in 2011. There is limited information on the transmission route of MuKV. Thus, we conducted a study to investigate virus detection rates in fecal, serum, throat, and lung tissue samples from murine rodents. RESULTS: A total of 413 fecal samples, 385 lung samples, 269 throat swab samples, and 183 serum samples were collected from 413 murine rodents (Rattus norvegicus, Rattus tanezumi, and Rattus rattus) captured in urban Shenzhen. Kobuviruses were detected via RT-PCR. Only fecal samples were positive, with prevalence rates of 34.9% in Rattus norvegicus and 29.4% in Rattus tanezumi. Phylogenetic analysis based on partial 3D and complete VP1 sequence regions indicated that all of the MuKV sequences obtained belonged to Aichivirus A, and were genetically closely related to other MuKVs reported in China, Hungary, and the USA. Twenty-eight full-length MuKV sequences were acquired. Phylogenetic analysis of two sequences randomly selected from the two species (SZ59 and SZ171) indicated that they shared very high nucleotide and amino acid identity with one another (94.0 and 99.3%, respectively), and comparison with human Kobuvirus revealed amino acid identity values of ~80%. Additionally, a sewage-derived sequence shared high similarity with the rat-derived sequences identified in this study, with respective nucleotide and amino acid identity values from 86.5 and 90.7% to 87.2 and 91.1%. CONCLUSION: The results of the current study provide evidence that murine Kobuvirus is transmitted via the fecal-oral route. Frontiers Media S.A. 2022-04-19 /pmc/articles/PMC9062591/ /pubmed/35517645 http://dx.doi.org/10.3389/fpubh.2022.865605 Text en Copyright © 2022 Gao, He, Fu, Li, He and Chen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Public Health Gao, Yuhan He, Wenqiao Fu, Jiaqi Li, Yongzhi He, Huan Chen, Qing Epidemiological Evidence for Fecal-Oral Transmission of Murine Kobuvirus |
title | Epidemiological Evidence for Fecal-Oral Transmission of Murine Kobuvirus |
title_full | Epidemiological Evidence for Fecal-Oral Transmission of Murine Kobuvirus |
title_fullStr | Epidemiological Evidence for Fecal-Oral Transmission of Murine Kobuvirus |
title_full_unstemmed | Epidemiological Evidence for Fecal-Oral Transmission of Murine Kobuvirus |
title_short | Epidemiological Evidence for Fecal-Oral Transmission of Murine Kobuvirus |
title_sort | epidemiological evidence for fecal-oral transmission of murine kobuvirus |
topic | Public Health |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062591/ https://www.ncbi.nlm.nih.gov/pubmed/35517645 http://dx.doi.org/10.3389/fpubh.2022.865605 |
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