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Alternation between taxonomically divergent hosts is not the major determinant of flavivirus evolution

Flaviviruses display diverse epidemiological and ecological features. Tick-borne and mosquito-borne flaviviruses (TBFV and MBFV, respectively) are important human pathogens that alternate replication in invertebrate vectors and vertebrate hosts. The Flavivirus genus also includes insect-specific vir...

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Autores principales: Pontremoli, Chiara, Forni, Diego, Clerici, Mario, Cagliani, Rachele, Sironi, Manuela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8093920/
https://www.ncbi.nlm.nih.gov/pubmed/33976907
http://dx.doi.org/10.1093/ve/veab040
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author Pontremoli, Chiara
Forni, Diego
Clerici, Mario
Cagliani, Rachele
Sironi, Manuela
author_facet Pontremoli, Chiara
Forni, Diego
Clerici, Mario
Cagliani, Rachele
Sironi, Manuela
author_sort Pontremoli, Chiara
collection PubMed
description Flaviviruses display diverse epidemiological and ecological features. Tick-borne and mosquito-borne flaviviruses (TBFV and MBFV, respectively) are important human pathogens that alternate replication in invertebrate vectors and vertebrate hosts. The Flavivirus genus also includes insect-specific viruses (ISFVs) and viruses with unknown invertebrate hosts. It is generally accepted that viruses that alternate between taxonomically different hosts evolve slowly and that the evolution of MBFVs and TBFVs is dominated by strong constraints, with limited episodes of positive selection. We exploited the availability of flavivirus genomes to test these hypotheses and to compare their rates and patterns of evolution. We estimated the substitution rates of CFAV and CxFV (two ISFVs) and, by taking into account the time-frame of measurement, compared them with those of other flaviviruses. Results indicated that CFAV and CxFV display relatively different substitution rates. However, these data, together with estimates for single-host members of the Flaviviridae family, indicated that MBFVs do not display relatively slower evolution. Conversely, TBFVs displayed some of lowest substitution rates among flaviviruses. Analysis of selective patterns over longer evolutionary time-frames confirmed that MBFVs evolve under strong purifying selection. Interestingly, TBFVs and ISFVs did not show extremely different levels of constraint, although TBFVs alternate among hosts, whereas ISFVs do not. Additional results showed that episodic positive selection drove the evolution of MBFVs, despite their high constraint. Positive selection was also detected on two branches of the TBFVs phylogeny that define the seabird clade. Thus, positive selection was much more common during the evolution of arthropod-borne flaviviruses than previously thought. Overall, our data indicate that flavivirus evolutionary patterns are complex and most likely determined by multiple factors, not limited to the alternation between taxonomically divergent hosts. The frequency of both positive and purifying selection, especially in MBFVs, suggests that a minority of sites in the viral polyprotein experience weak constraint and can evolve to generate new viral phenotypes and possibly promote adaptation to new hosts.
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spelling pubmed-80939202021-05-10 Alternation between taxonomically divergent hosts is not the major determinant of flavivirus evolution Pontremoli, Chiara Forni, Diego Clerici, Mario Cagliani, Rachele Sironi, Manuela Virus Evol Research Article Flaviviruses display diverse epidemiological and ecological features. Tick-borne and mosquito-borne flaviviruses (TBFV and MBFV, respectively) are important human pathogens that alternate replication in invertebrate vectors and vertebrate hosts. The Flavivirus genus also includes insect-specific viruses (ISFVs) and viruses with unknown invertebrate hosts. It is generally accepted that viruses that alternate between taxonomically different hosts evolve slowly and that the evolution of MBFVs and TBFVs is dominated by strong constraints, with limited episodes of positive selection. We exploited the availability of flavivirus genomes to test these hypotheses and to compare their rates and patterns of evolution. We estimated the substitution rates of CFAV and CxFV (two ISFVs) and, by taking into account the time-frame of measurement, compared them with those of other flaviviruses. Results indicated that CFAV and CxFV display relatively different substitution rates. However, these data, together with estimates for single-host members of the Flaviviridae family, indicated that MBFVs do not display relatively slower evolution. Conversely, TBFVs displayed some of lowest substitution rates among flaviviruses. Analysis of selective patterns over longer evolutionary time-frames confirmed that MBFVs evolve under strong purifying selection. Interestingly, TBFVs and ISFVs did not show extremely different levels of constraint, although TBFVs alternate among hosts, whereas ISFVs do not. Additional results showed that episodic positive selection drove the evolution of MBFVs, despite their high constraint. Positive selection was also detected on two branches of the TBFVs phylogeny that define the seabird clade. Thus, positive selection was much more common during the evolution of arthropod-borne flaviviruses than previously thought. Overall, our data indicate that flavivirus evolutionary patterns are complex and most likely determined by multiple factors, not limited to the alternation between taxonomically divergent hosts. The frequency of both positive and purifying selection, especially in MBFVs, suggests that a minority of sites in the viral polyprotein experience weak constraint and can evolve to generate new viral phenotypes and possibly promote adaptation to new hosts. Oxford University Press 2021-04-21 /pmc/articles/PMC8093920/ /pubmed/33976907 http://dx.doi.org/10.1093/ve/veab040 Text en © The Author(s) 2021. 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 (http://creativecommons.org/licenses/by/4.0/ (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 Research Article
Pontremoli, Chiara
Forni, Diego
Clerici, Mario
Cagliani, Rachele
Sironi, Manuela
Alternation between taxonomically divergent hosts is not the major determinant of flavivirus evolution
title Alternation between taxonomically divergent hosts is not the major determinant of flavivirus evolution
title_full Alternation between taxonomically divergent hosts is not the major determinant of flavivirus evolution
title_fullStr Alternation between taxonomically divergent hosts is not the major determinant of flavivirus evolution
title_full_unstemmed Alternation between taxonomically divergent hosts is not the major determinant of flavivirus evolution
title_short Alternation between taxonomically divergent hosts is not the major determinant of flavivirus evolution
title_sort alternation between taxonomically divergent hosts is not the major determinant of flavivirus evolution
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8093920/
https://www.ncbi.nlm.nih.gov/pubmed/33976907
http://dx.doi.org/10.1093/ve/veab040
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