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Selective events at individual sites underlie the evolution of monkeypox virus clades

In endemic regions (West Africa and the Congo Basin), the genetic diversity of monkeypox virus (MPXV) is geographically structured into two major clades (Clades I and II) that differ in virulence and host associations. Clade IIb is closely related to the B.1 lineage, which is dominating a worldwide...

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Autores principales: Molteni, Cristian, Forni, Diego, Cagliani, Rachele, Arrigoni, Federica, Pozzoli, Uberto, De Gioia, Luca, Sironi, Manuela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10256197/
https://www.ncbi.nlm.nih.gov/pubmed/37305708
http://dx.doi.org/10.1093/ve/vead031
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author Molteni, Cristian
Forni, Diego
Cagliani, Rachele
Arrigoni, Federica
Pozzoli, Uberto
De Gioia, Luca
Sironi, Manuela
author_facet Molteni, Cristian
Forni, Diego
Cagliani, Rachele
Arrigoni, Federica
Pozzoli, Uberto
De Gioia, Luca
Sironi, Manuela
author_sort Molteni, Cristian
collection PubMed
description In endemic regions (West Africa and the Congo Basin), the genetic diversity of monkeypox virus (MPXV) is geographically structured into two major clades (Clades I and II) that differ in virulence and host associations. Clade IIb is closely related to the B.1 lineage, which is dominating a worldwide outbreak initiated in 2022. Lineage B.1 has however accumulated mutations of unknown significance that most likely result from apolipoprotein B mRNA editing catalytic polypeptide-like 3 (APOBEC3) editing. We applied a population genetics—phylogenetics approach to investigate the evolution of MPXV during historical viral spread in Africa and to infer the distribution of fitness effects. We observed a high preponderance of codons evolving under strong purifying selection, particularly in viral genes involved in morphogenesis and replication or transcription. However, signals of positive selection were also detected and were enriched in genes involved in immunomodulation and/or virulence. In particular, several genes showing evidence of positive selection were found to hijack different steps of the cellular pathway that senses cytosolic DNA. Also, a few selected sites in genes that are not directly involved in immunomodulation are suggestive of antibody escape or other immune-mediated pressures. Because orthopoxvirus host range is primarily determined by the interaction with the host immune system, we suggest that the positive selection signals represent signatures of host adaptation and contribute to the different virulence of Clade I and II MPXVs. We also used the calculated selection coefficients to infer the effects of mutations that define the predominant human MPXV1 (hMPXV1) lineage B.1, as well as the changes that have been accumulating during the worldwide outbreak. Results indicated that a proportion of deleterious mutations were purged from the predominant outbreak lineage, whose spread was not driven by the presence of beneficial changes. Polymorphic mutations with a predicted beneficial effect on fitness are few and have a low frequency. It remains to be determined whether they have any significance for ongoing virus evolution.
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spelling pubmed-102561972023-06-10 Selective events at individual sites underlie the evolution of monkeypox virus clades Molteni, Cristian Forni, Diego Cagliani, Rachele Arrigoni, Federica Pozzoli, Uberto De Gioia, Luca Sironi, Manuela Virus Evol Rapid Communication In endemic regions (West Africa and the Congo Basin), the genetic diversity of monkeypox virus (MPXV) is geographically structured into two major clades (Clades I and II) that differ in virulence and host associations. Clade IIb is closely related to the B.1 lineage, which is dominating a worldwide outbreak initiated in 2022. Lineage B.1 has however accumulated mutations of unknown significance that most likely result from apolipoprotein B mRNA editing catalytic polypeptide-like 3 (APOBEC3) editing. We applied a population genetics—phylogenetics approach to investigate the evolution of MPXV during historical viral spread in Africa and to infer the distribution of fitness effects. We observed a high preponderance of codons evolving under strong purifying selection, particularly in viral genes involved in morphogenesis and replication or transcription. However, signals of positive selection were also detected and were enriched in genes involved in immunomodulation and/or virulence. In particular, several genes showing evidence of positive selection were found to hijack different steps of the cellular pathway that senses cytosolic DNA. Also, a few selected sites in genes that are not directly involved in immunomodulation are suggestive of antibody escape or other immune-mediated pressures. Because orthopoxvirus host range is primarily determined by the interaction with the host immune system, we suggest that the positive selection signals represent signatures of host adaptation and contribute to the different virulence of Clade I and II MPXVs. We also used the calculated selection coefficients to infer the effects of mutations that define the predominant human MPXV1 (hMPXV1) lineage B.1, as well as the changes that have been accumulating during the worldwide outbreak. Results indicated that a proportion of deleterious mutations were purged from the predominant outbreak lineage, whose spread was not driven by the presence of beneficial changes. Polymorphic mutations with a predicted beneficial effect on fitness are few and have a low frequency. It remains to be determined whether they have any significance for ongoing virus evolution. Oxford University Press 2023-05-20 /pmc/articles/PMC10256197/ /pubmed/37305708 http://dx.doi.org/10.1093/ve/vead031 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Rapid Communication
Molteni, Cristian
Forni, Diego
Cagliani, Rachele
Arrigoni, Federica
Pozzoli, Uberto
De Gioia, Luca
Sironi, Manuela
Selective events at individual sites underlie the evolution of monkeypox virus clades
title Selective events at individual sites underlie the evolution of monkeypox virus clades
title_full Selective events at individual sites underlie the evolution of monkeypox virus clades
title_fullStr Selective events at individual sites underlie the evolution of monkeypox virus clades
title_full_unstemmed Selective events at individual sites underlie the evolution of monkeypox virus clades
title_short Selective events at individual sites underlie the evolution of monkeypox virus clades
title_sort selective events at individual sites underlie the evolution of monkeypox virus clades
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10256197/
https://www.ncbi.nlm.nih.gov/pubmed/37305708
http://dx.doi.org/10.1093/ve/vead031
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