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Genomics and High-Resolution Typing Confirm Predominant Clonal Evolution down to a Microevolutionary Scale in Trypanosoma cruzi

Trypanosoma cruzi, the agent of Chagas disease, is a paradigmatic case of the predominant clonal evolution (PCE) model, which states that the impact of genetic recombination in pathogens’ natural populations is not sufficient to suppress a persistent phylogenetic signal at all evolutionary scales. I...

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Autores principales: Tibayrenc, Michel, Ayala, Francisco J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281314/
https://www.ncbi.nlm.nih.gov/pubmed/32397142
http://dx.doi.org/10.3390/pathogens9050356
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author Tibayrenc, Michel
Ayala, Francisco J.
author_facet Tibayrenc, Michel
Ayala, Francisco J.
author_sort Tibayrenc, Michel
collection PubMed
description Trypanosoma cruzi, the agent of Chagas disease, is a paradigmatic case of the predominant clonal evolution (PCE) model, which states that the impact of genetic recombination in pathogens’ natural populations is not sufficient to suppress a persistent phylogenetic signal at all evolutionary scales. In spite of indications for occasional recombination and meiosis, recent genomics and high-resolution typing data in T. cruzi reject the counterproposal that PCE does not operate at lower evolutionary scales, within the evolutionary units (=near-clades) that subdivide the species. Evolutionary patterns in the agent of Chagas disease at micro- and macroevolutionary scales are strikingly similar (“Russian doll pattern”), suggesting gradual, rather than saltatory evolution.
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spelling pubmed-72813142020-06-19 Genomics and High-Resolution Typing Confirm Predominant Clonal Evolution down to a Microevolutionary Scale in Trypanosoma cruzi Tibayrenc, Michel Ayala, Francisco J. Pathogens Concept Paper Trypanosoma cruzi, the agent of Chagas disease, is a paradigmatic case of the predominant clonal evolution (PCE) model, which states that the impact of genetic recombination in pathogens’ natural populations is not sufficient to suppress a persistent phylogenetic signal at all evolutionary scales. In spite of indications for occasional recombination and meiosis, recent genomics and high-resolution typing data in T. cruzi reject the counterproposal that PCE does not operate at lower evolutionary scales, within the evolutionary units (=near-clades) that subdivide the species. Evolutionary patterns in the agent of Chagas disease at micro- and macroevolutionary scales are strikingly similar (“Russian doll pattern”), suggesting gradual, rather than saltatory evolution. MDPI 2020-05-08 /pmc/articles/PMC7281314/ /pubmed/32397142 http://dx.doi.org/10.3390/pathogens9050356 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Concept Paper
Tibayrenc, Michel
Ayala, Francisco J.
Genomics and High-Resolution Typing Confirm Predominant Clonal Evolution down to a Microevolutionary Scale in Trypanosoma cruzi
title Genomics and High-Resolution Typing Confirm Predominant Clonal Evolution down to a Microevolutionary Scale in Trypanosoma cruzi
title_full Genomics and High-Resolution Typing Confirm Predominant Clonal Evolution down to a Microevolutionary Scale in Trypanosoma cruzi
title_fullStr Genomics and High-Resolution Typing Confirm Predominant Clonal Evolution down to a Microevolutionary Scale in Trypanosoma cruzi
title_full_unstemmed Genomics and High-Resolution Typing Confirm Predominant Clonal Evolution down to a Microevolutionary Scale in Trypanosoma cruzi
title_short Genomics and High-Resolution Typing Confirm Predominant Clonal Evolution down to a Microevolutionary Scale in Trypanosoma cruzi
title_sort genomics and high-resolution typing confirm predominant clonal evolution down to a microevolutionary scale in trypanosoma cruzi
topic Concept Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281314/
https://www.ncbi.nlm.nih.gov/pubmed/32397142
http://dx.doi.org/10.3390/pathogens9050356
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