Going through phages: a computational approach to revealing the role of prophage in Staphylococcus aureus.

Access Microbiology Pub Date : 2023-06-16 eCollection Date: 2023-01-01 DOI:10.1099/acmi.0.000424
Tyrome Sweet, Suzanne Sindi, Mark Sistrom
{"title":"Going through phages: a computational approach to revealing the role of prophage in <i>Staphylococcus aureus</i>.","authors":"Tyrome Sweet, Suzanne Sindi, Mark Sistrom","doi":"10.1099/acmi.0.000424","DOIUrl":null,"url":null,"abstract":"<p><p>Prophages have important roles in virulence, antibiotic resistance, and genome evolution in <i>Staphylococcus aureus</i> . Rapid growth in the number of sequenced <i>S. aureus</i> genomes allows for an investigation of prophage sequences at an unprecedented scale. We developed a novel computational pipeline for phage discovery and annotation. We combined PhiSpy, a phage discovery tool, with VGAS and PROKKA, genome annotation tools to detect and analyse prophage sequences in nearly 10 011  <i>S</i> . <i>aureus</i> genomes, discovering thousands of putative prophage sequences with genes encoding virulence factors and antibiotic resistance. To our knowledge, this is the first large-scale application of PhiSpy on a large-scale set of genomes (10 011  <i>S</i> . <i>aureus</i> ). Determining the presence of virulence and resistance encoding genes in prophage has implications for the potential transfer of these genes/functions to other bacteria via transduction and thus can provide insight into the evolution and spread of these genes/functions between bacterial strains. While the phage we have identified may be known, these phages were not necessarily known or characterized in <i>S. aureus</i> and the clustering and comparison we did for phage based on their gene content is novel. Moreover, the reporting of these genes with the <i>S. aureus</i> genomes is novel.</p>","PeriodicalId":6956,"journal":{"name":"Access Microbiology","volume":"5 6","pages":"acmi000424"},"PeriodicalIF":0.0000,"publicationDate":"2023-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10323782/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Access Microbiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1099/acmi.0.000424","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Prophages have important roles in virulence, antibiotic resistance, and genome evolution in Staphylococcus aureus . Rapid growth in the number of sequenced S. aureus genomes allows for an investigation of prophage sequences at an unprecedented scale. We developed a novel computational pipeline for phage discovery and annotation. We combined PhiSpy, a phage discovery tool, with VGAS and PROKKA, genome annotation tools to detect and analyse prophage sequences in nearly 10 011  S . aureus genomes, discovering thousands of putative prophage sequences with genes encoding virulence factors and antibiotic resistance. To our knowledge, this is the first large-scale application of PhiSpy on a large-scale set of genomes (10 011  S . aureus ). Determining the presence of virulence and resistance encoding genes in prophage has implications for the potential transfer of these genes/functions to other bacteria via transduction and thus can provide insight into the evolution and spread of these genes/functions between bacterial strains. While the phage we have identified may be known, these phages were not necessarily known or characterized in S. aureus and the clustering and comparison we did for phage based on their gene content is novel. Moreover, the reporting of these genes with the S. aureus genomes is novel.

Abstract Image

Abstract Image

Abstract Image

穿越噬菌体:揭示金黄色葡萄球菌噬菌体作用的计算方法。
噬菌体在金黄色葡萄球菌的毒力、抗生素耐药性和基因组进化中发挥着重要作用。金黄色葡萄球菌基因组测序数量的快速增长使噬菌体序列的研究达到了前所未有的规模。我们开发了一种用于噬菌体发现和注释的新型计算管道。我们将噬菌体发现工具 PhiSpy 与基因组注释工具 VGAS 和 PROKKA 相结合,检测并分析了近 10 011 个金黄色葡萄球菌基因组中的噬菌体序列,发现了数千个带有编码毒力因子和抗生素耐药性基因的假定噬菌体序列。据我们所知,这是 PhiSpy 在大规模基因组(10 011 个金黄色葡萄球菌)中的首次大规模应用。确定噬菌体中是否存在毒力和抗药性编码基因对这些基因/功能通过转导转移到其他细菌的可能性有影响,因此可以深入了解这些基因/功能在细菌菌株之间的进化和传播。虽然我们发现的噬菌体可能是已知的,但这些噬菌体在金黄色葡萄球菌中并不一定是已知的或有特征的,我们根据基因含量对噬菌体进行的聚类和比较是新颖的。此外,这些基因与金黄色葡萄球菌基因组的报告也是新颖的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信