{"title":"Comprehensive analysis of the composition and distribution of anti-phage defense systems in <i>Vibrio</i> genomes.","authors":"Xue-Feng Xu, Xing-Kun Jin, Yan Shi, Zhe Zhao","doi":"10.16288/j.yczz.24-290","DOIUrl":null,"url":null,"abstract":"<p><p>The long-term co-evolution between bacteria and their viruses (bacteriophages) drives the diversification of anti-phage defense systems. As key members of marine ecosystems, <i>Vibrio</i> species are known for their large and complex genomes. To investigate the composition and distribution of anti-phage defense systems in <i>Vibrio</i> genomes, we collect 242 representative genomes from the GTDB and NCBI databases. Using bioinformatics tools (including Defense Finder), we analyze the anti-phage defense systems encoded by these genomes and identify a total of 108 distinct systems, including GAPS, dGTPase, RM systems, etc. We observe significant variation in defense capabilities among different <i>Vibrio</i> strains: five strains encode more than 20 defense systems, highlighting their high defense potential, while over 30 strains encode five or fewer defense systems. Notably, we find no known defense systems in '<i>Vibrio katoptron</i>'. Furthermore, we note that the diversity of defense systems varies among <i>Vibrio</i> clades, with the Cholerae clade exhibiting the highest entropy in its defense systems. We conduct a detailed analysis of the composition, structure, and functional mechanisms of these defense systems. Although <i>Vibrio</i> species exhibit a complex and diverse array of anti-phage defense systems, the specific functions of many remain unknown. Given the complexity of <i>Vibrio</i> genomes, we suggest that numerous potential defense systems are yet to be discovered. This study provides a comprehensive overview of the genomic characteristics of <i>Vibrio</i> defense systems, laying a foundation for future research into the interactions and evolutionary dynamics between <i>Vibrio</i> and bacteriophages.</p>","PeriodicalId":35536,"journal":{"name":"遗传","volume":"47 9","pages":"1057-1068"},"PeriodicalIF":0.0000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"遗传","FirstCategoryId":"1091","ListUrlMain":"https://doi.org/10.16288/j.yczz.24-290","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
The long-term co-evolution between bacteria and their viruses (bacteriophages) drives the diversification of anti-phage defense systems. As key members of marine ecosystems, Vibrio species are known for their large and complex genomes. To investigate the composition and distribution of anti-phage defense systems in Vibrio genomes, we collect 242 representative genomes from the GTDB and NCBI databases. Using bioinformatics tools (including Defense Finder), we analyze the anti-phage defense systems encoded by these genomes and identify a total of 108 distinct systems, including GAPS, dGTPase, RM systems, etc. We observe significant variation in defense capabilities among different Vibrio strains: five strains encode more than 20 defense systems, highlighting their high defense potential, while over 30 strains encode five or fewer defense systems. Notably, we find no known defense systems in 'Vibrio katoptron'. Furthermore, we note that the diversity of defense systems varies among Vibrio clades, with the Cholerae clade exhibiting the highest entropy in its defense systems. We conduct a detailed analysis of the composition, structure, and functional mechanisms of these defense systems. Although Vibrio species exhibit a complex and diverse array of anti-phage defense systems, the specific functions of many remain unknown. Given the complexity of Vibrio genomes, we suggest that numerous potential defense systems are yet to be discovered. This study provides a comprehensive overview of the genomic characteristics of Vibrio defense systems, laying a foundation for future research into the interactions and evolutionary dynamics between Vibrio and bacteriophages.
期刊介绍:
Hereditas is a national academic journal sponsored by the Institute of Genetics and Developmental Biology of the Chinese Academy of Sciences and the Chinese Society of Genetics and published by Science Press. It is a Chinese core journal and a Chinese high-quality scientific journal. The journal mainly publishes innovative research papers in the fields of genetics, genomics, cell biology, developmental biology, biological evolution, genetic engineering and biotechnology; new technologies and new methods; monographs and reviews on hot issues in the discipline; academic debates and discussions; experience in genetics teaching; introductions to famous geneticists at home and abroad; genetic counseling; information on academic conferences at home and abroad, etc. Main columns: review, frontier focus, research report, technology and method, resources and platform, experimental operation guide, genetic resources, genetics teaching, scientific news, etc.