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The Diversity of the CRISPR-Cas System and Prophages Present in the Genome Reveals the Co-evolution of Bifidobacterium pseudocatenulatum and Phages

Diverse CRISPR-Cas systems constitute an indispensable part of the bacterial adaptive immune system against viral infections. However, to escape from this immune system, bacteriophages have also evolved corresponding anti-defense measures. We investigated the diversity of CRISPR-Cas systems and the...

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Autores principales: Wang, Gang, Liu, Qian, Pei, Zhangming, Wang, Linlin, Tian, Peijun, Liu, Zhenmin, Zhao, Jianxin, Zhang, Hao, Chen, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264901/
https://www.ncbi.nlm.nih.gov/pubmed/32528454
http://dx.doi.org/10.3389/fmicb.2020.01088
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author Wang, Gang
Liu, Qian
Pei, Zhangming
Wang, Linlin
Tian, Peijun
Liu, Zhenmin
Zhao, Jianxin
Zhang, Hao
Chen, Wei
author_facet Wang, Gang
Liu, Qian
Pei, Zhangming
Wang, Linlin
Tian, Peijun
Liu, Zhenmin
Zhao, Jianxin
Zhang, Hao
Chen, Wei
author_sort Wang, Gang
collection PubMed
description Diverse CRISPR-Cas systems constitute an indispensable part of the bacterial adaptive immune system against viral infections. However, to escape from this immune system, bacteriophages have also evolved corresponding anti-defense measures. We investigated the diversity of CRISPR-Cas systems and the presence of prophages in the genomes of 66 Bifidobacterium pseudocatenulatum strains. Our findings revealed a high occurrence of complete CRISPR-Cas systems (62%, 41/66) in the B. pseudocatenulatum genomes. Subtypes I-C, I-U and II-A, were found to be widespread in this species. No significant association was found between the number of bacterial CRISPR spacers and its host’s age. This study on prophages within B. pseudocatenulatum genomes revealed that prophage genes related to distinct functional modules became degraded at different levels, indicating that these prophages were not likely to enter lytic cycle spontaneously. Further, the evolutionary analysis of prophages in this study revealed that they might be derived from different phage ancestors. Notably, self-targeting phenomenon within B. pseudocatenulatum and Anti-CRISPR (Acr) coding genes in prophages was observed. Overall, our results indicate that the competition between B. pseudocatenulatum and phages is a major driving factor for the genomic diversity of both partners.
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spelling pubmed-72649012020-06-10 The Diversity of the CRISPR-Cas System and Prophages Present in the Genome Reveals the Co-evolution of Bifidobacterium pseudocatenulatum and Phages Wang, Gang Liu, Qian Pei, Zhangming Wang, Linlin Tian, Peijun Liu, Zhenmin Zhao, Jianxin Zhang, Hao Chen, Wei Front Microbiol Microbiology Diverse CRISPR-Cas systems constitute an indispensable part of the bacterial adaptive immune system against viral infections. However, to escape from this immune system, bacteriophages have also evolved corresponding anti-defense measures. We investigated the diversity of CRISPR-Cas systems and the presence of prophages in the genomes of 66 Bifidobacterium pseudocatenulatum strains. Our findings revealed a high occurrence of complete CRISPR-Cas systems (62%, 41/66) in the B. pseudocatenulatum genomes. Subtypes I-C, I-U and II-A, were found to be widespread in this species. No significant association was found between the number of bacterial CRISPR spacers and its host’s age. This study on prophages within B. pseudocatenulatum genomes revealed that prophage genes related to distinct functional modules became degraded at different levels, indicating that these prophages were not likely to enter lytic cycle spontaneously. Further, the evolutionary analysis of prophages in this study revealed that they might be derived from different phage ancestors. Notably, self-targeting phenomenon within B. pseudocatenulatum and Anti-CRISPR (Acr) coding genes in prophages was observed. Overall, our results indicate that the competition between B. pseudocatenulatum and phages is a major driving factor for the genomic diversity of both partners. Frontiers Media S.A. 2020-05-26 /pmc/articles/PMC7264901/ /pubmed/32528454 http://dx.doi.org/10.3389/fmicb.2020.01088 Text en Copyright © 2020 Wang, Liu, Pei, Wang, Tian, Liu, Zhao, Zhang and Chen. http://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
Wang, Gang
Liu, Qian
Pei, Zhangming
Wang, Linlin
Tian, Peijun
Liu, Zhenmin
Zhao, Jianxin
Zhang, Hao
Chen, Wei
The Diversity of the CRISPR-Cas System and Prophages Present in the Genome Reveals the Co-evolution of Bifidobacterium pseudocatenulatum and Phages
title The Diversity of the CRISPR-Cas System and Prophages Present in the Genome Reveals the Co-evolution of Bifidobacterium pseudocatenulatum and Phages
title_full The Diversity of the CRISPR-Cas System and Prophages Present in the Genome Reveals the Co-evolution of Bifidobacterium pseudocatenulatum and Phages
title_fullStr The Diversity of the CRISPR-Cas System and Prophages Present in the Genome Reveals the Co-evolution of Bifidobacterium pseudocatenulatum and Phages
title_full_unstemmed The Diversity of the CRISPR-Cas System and Prophages Present in the Genome Reveals the Co-evolution of Bifidobacterium pseudocatenulatum and Phages
title_short The Diversity of the CRISPR-Cas System and Prophages Present in the Genome Reveals the Co-evolution of Bifidobacterium pseudocatenulatum and Phages
title_sort diversity of the crispr-cas system and prophages present in the genome reveals the co-evolution of bifidobacterium pseudocatenulatum and phages
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264901/
https://www.ncbi.nlm.nih.gov/pubmed/32528454
http://dx.doi.org/10.3389/fmicb.2020.01088
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