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Temporal and coevolutionary analyses reveal the events driving the emergence and circulation of human mamastroviruses

Characterized by high genetic diversity, broad host range, and resistance to adverse conditions, coupled with recent reports of neurotropic astroviruses circulating in humans, mamastroviruses pose a threat to public health. The current astrovirus classification system based on host source prevents d...

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Autores principales: Perez, Lester J., Forberg, Kenn, Cloherty, Gavin A., Berg, Michael G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10262812/
https://www.ncbi.nlm.nih.gov/pubmed/37222427
http://dx.doi.org/10.1080/22221751.2023.2217942
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author Perez, Lester J.
Forberg, Kenn
Cloherty, Gavin A.
Berg, Michael G.
author_facet Perez, Lester J.
Forberg, Kenn
Cloherty, Gavin A.
Berg, Michael G.
author_sort Perez, Lester J.
collection PubMed
description Characterized by high genetic diversity, broad host range, and resistance to adverse conditions, coupled with recent reports of neurotropic astroviruses circulating in humans, mamastroviruses pose a threat to public health. The current astrovirus classification system based on host source prevents determining whether strains with distinct tropism or virulence are emerging. By using integrated phylogeny, we propose a standardized demarcation of species and genotypes, with reproducible cut-off values that reconcile the pairwise sequence distribution, genetic distances between lineages, and the topological reconstruction of the Mamastrovirus genus. We further define the various links established by co-evolution and resolve the dynamics of transmission chains to identify host-jump events and the sources from which different mamastrovirus species circulating in humans have emerged. We observed that recombination is relatively infrequent and restricted to within genotypes. The well-known “human” astrovirus, defined here as mamastrovirus species 7, has co-speciated with humans, while there have been two additional host-jumps into humans from distinct hosts. Newly defined species 6 genotype 2, linked to severe gastroenteritis in children, resulted from a marmot to human jump taking place ∼200 years ago while species 6 genotype 7 (MastV-Sp6Gt7), linked to neurological disease in immunocompromised patients, jumped from bovines only ∼50 years ago. Through demographic reconstruction, we determined that the latter reached coalescent viral population growth only 20 years ago and is evolving at a much higher evolutionary rate than other genotypes infecting humans. This study constitutes mounting evidence of MastV-Sp6Gt7 active circulation and highlights the need for diagnostics capable of detecting it.
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spelling pubmed-102628122023-06-15 Temporal and coevolutionary analyses reveal the events driving the emergence and circulation of human mamastroviruses Perez, Lester J. Forberg, Kenn Cloherty, Gavin A. Berg, Michael G. Emerg Microbes Infect Research Article Characterized by high genetic diversity, broad host range, and resistance to adverse conditions, coupled with recent reports of neurotropic astroviruses circulating in humans, mamastroviruses pose a threat to public health. The current astrovirus classification system based on host source prevents determining whether strains with distinct tropism or virulence are emerging. By using integrated phylogeny, we propose a standardized demarcation of species and genotypes, with reproducible cut-off values that reconcile the pairwise sequence distribution, genetic distances between lineages, and the topological reconstruction of the Mamastrovirus genus. We further define the various links established by co-evolution and resolve the dynamics of transmission chains to identify host-jump events and the sources from which different mamastrovirus species circulating in humans have emerged. We observed that recombination is relatively infrequent and restricted to within genotypes. The well-known “human” astrovirus, defined here as mamastrovirus species 7, has co-speciated with humans, while there have been two additional host-jumps into humans from distinct hosts. Newly defined species 6 genotype 2, linked to severe gastroenteritis in children, resulted from a marmot to human jump taking place ∼200 years ago while species 6 genotype 7 (MastV-Sp6Gt7), linked to neurological disease in immunocompromised patients, jumped from bovines only ∼50 years ago. Through demographic reconstruction, we determined that the latter reached coalescent viral population growth only 20 years ago and is evolving at a much higher evolutionary rate than other genotypes infecting humans. This study constitutes mounting evidence of MastV-Sp6Gt7 active circulation and highlights the need for diagnostics capable of detecting it. Taylor & Francis 2023-06-12 /pmc/articles/PMC10262812/ /pubmed/37222427 http://dx.doi.org/10.1080/22221751.2023.2217942 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-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial 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 Research Article
Perez, Lester J.
Forberg, Kenn
Cloherty, Gavin A.
Berg, Michael G.
Temporal and coevolutionary analyses reveal the events driving the emergence and circulation of human mamastroviruses
title Temporal and coevolutionary analyses reveal the events driving the emergence and circulation of human mamastroviruses
title_full Temporal and coevolutionary analyses reveal the events driving the emergence and circulation of human mamastroviruses
title_fullStr Temporal and coevolutionary analyses reveal the events driving the emergence and circulation of human mamastroviruses
title_full_unstemmed Temporal and coevolutionary analyses reveal the events driving the emergence and circulation of human mamastroviruses
title_short Temporal and coevolutionary analyses reveal the events driving the emergence and circulation of human mamastroviruses
title_sort temporal and coevolutionary analyses reveal the events driving the emergence and circulation of human mamastroviruses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10262812/
https://www.ncbi.nlm.nih.gov/pubmed/37222427
http://dx.doi.org/10.1080/22221751.2023.2217942
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