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Genetic Characteristics of Porcine Hemagglutinating Encephalomyelitis Coronavirus: Identification of Naturally Occurring Mutations Between 1970 and 2015

Porcine hemagglutinating encephalomyelitis virus (PHEV) is a Betacoronavirus characterized by neurological symptoms and a worldwide prevalence. Although PHEV is one of the earliest discovered porcine coronaviruses, it remains poorly studied. The full-length genome of the earliest PHEV strain collect...

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Autores principales: Bahoussi, Amina Nawal, Guo, Yan-Yan, Shi, Rui-Zhu, Wang, Pei-Hua, Li, Ya-Qian, Wu, Chang-Xin, Xing, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8971845/
https://www.ncbi.nlm.nih.gov/pubmed/35369458
http://dx.doi.org/10.3389/fmicb.2022.860851
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author Bahoussi, Amina Nawal
Guo, Yan-Yan
Shi, Rui-Zhu
Wang, Pei-Hua
Li, Ya-Qian
Wu, Chang-Xin
Xing, Li
author_facet Bahoussi, Amina Nawal
Guo, Yan-Yan
Shi, Rui-Zhu
Wang, Pei-Hua
Li, Ya-Qian
Wu, Chang-Xin
Xing, Li
author_sort Bahoussi, Amina Nawal
collection PubMed
description Porcine hemagglutinating encephalomyelitis virus (PHEV) is a Betacoronavirus characterized by neurological symptoms and a worldwide prevalence. Although PHEV is one of the earliest discovered porcine coronaviruses, it remains poorly studied. The full-length genome of the earliest PHEV strain collected in 1970 in the United States (PHEV/67 N/US/1970) was determined in October 2020. Using this virus as a prototype, we comparatively analyzed all available PHEV full-length sequences during 1970–2015. In phylogenetic trees based on PHEV full-length or spike glycoprotein open reading frame genomic sequences, PHEV/67 N/US/1970 was sorted into a clade different from that of viruses isolated in the United States in 2015. Intriguingly, United States and Belgium viruses isolated in 2015 and 2005, respectively, revealed multiple deletion mutation patterns compared to the strain PHEV/67 N/US/1970, leading to a truncated or a non-functional NS2A coding region. In addition, the genomic similarity analysis showed a hypervariability of the spike glycoprotein coding region, which can affect at least eight potential linear B cell epitopes located in the spike glycoprotein. This report indicates that PHEVs in the United States underwent a significant genetic drift, which might influence PHEV surveillance in other countries.
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spelling pubmed-89718452022-04-02 Genetic Characteristics of Porcine Hemagglutinating Encephalomyelitis Coronavirus: Identification of Naturally Occurring Mutations Between 1970 and 2015 Bahoussi, Amina Nawal Guo, Yan-Yan Shi, Rui-Zhu Wang, Pei-Hua Li, Ya-Qian Wu, Chang-Xin Xing, Li Front Microbiol Microbiology Porcine hemagglutinating encephalomyelitis virus (PHEV) is a Betacoronavirus characterized by neurological symptoms and a worldwide prevalence. Although PHEV is one of the earliest discovered porcine coronaviruses, it remains poorly studied. The full-length genome of the earliest PHEV strain collected in 1970 in the United States (PHEV/67 N/US/1970) was determined in October 2020. Using this virus as a prototype, we comparatively analyzed all available PHEV full-length sequences during 1970–2015. In phylogenetic trees based on PHEV full-length or spike glycoprotein open reading frame genomic sequences, PHEV/67 N/US/1970 was sorted into a clade different from that of viruses isolated in the United States in 2015. Intriguingly, United States and Belgium viruses isolated in 2015 and 2005, respectively, revealed multiple deletion mutation patterns compared to the strain PHEV/67 N/US/1970, leading to a truncated or a non-functional NS2A coding region. In addition, the genomic similarity analysis showed a hypervariability of the spike glycoprotein coding region, which can affect at least eight potential linear B cell epitopes located in the spike glycoprotein. This report indicates that PHEVs in the United States underwent a significant genetic drift, which might influence PHEV surveillance in other countries. Frontiers Media S.A. 2022-03-18 /pmc/articles/PMC8971845/ /pubmed/35369458 http://dx.doi.org/10.3389/fmicb.2022.860851 Text en Copyright © 2022 Bahoussi, Guo, Shi, Wang, Li, Wu and Xing. 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 Microbiology
Bahoussi, Amina Nawal
Guo, Yan-Yan
Shi, Rui-Zhu
Wang, Pei-Hua
Li, Ya-Qian
Wu, Chang-Xin
Xing, Li
Genetic Characteristics of Porcine Hemagglutinating Encephalomyelitis Coronavirus: Identification of Naturally Occurring Mutations Between 1970 and 2015
title Genetic Characteristics of Porcine Hemagglutinating Encephalomyelitis Coronavirus: Identification of Naturally Occurring Mutations Between 1970 and 2015
title_full Genetic Characteristics of Porcine Hemagglutinating Encephalomyelitis Coronavirus: Identification of Naturally Occurring Mutations Between 1970 and 2015
title_fullStr Genetic Characteristics of Porcine Hemagglutinating Encephalomyelitis Coronavirus: Identification of Naturally Occurring Mutations Between 1970 and 2015
title_full_unstemmed Genetic Characteristics of Porcine Hemagglutinating Encephalomyelitis Coronavirus: Identification of Naturally Occurring Mutations Between 1970 and 2015
title_short Genetic Characteristics of Porcine Hemagglutinating Encephalomyelitis Coronavirus: Identification of Naturally Occurring Mutations Between 1970 and 2015
title_sort genetic characteristics of porcine hemagglutinating encephalomyelitis coronavirus: identification of naturally occurring mutations between 1970 and 2015
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8971845/
https://www.ncbi.nlm.nih.gov/pubmed/35369458
http://dx.doi.org/10.3389/fmicb.2022.860851
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