{"title":"Variation in the plasmid backbone and dif module content of R3-T33 Acinetobacter plasmids","authors":"Stephanie J. Ambrose, Ruth M. Hall","doi":"10.1016/j.plasmid.2024.102722","DOIUrl":null,"url":null,"abstract":"<div><p>The predominant type of plasmids found in <em>Acinetobacter</em> species encode a Rep_3 initiation protein and many of these carry their accessory genes in <em>dif</em> modules. Here, available sequences of the 14 members of the group of Rep_3 plasmids typed as R3-T33, using a threshold of 95% identity in the <em>repA</em> gene, were compiled and compared. These plasmids were from various <em>Acinetobacter</em> species. The p<em>dif</em> sites were identified allowing the backbone and <em>dif</em> modules to be defined. As for other Rep_3 plasmids carrying <em>dif</em> modules, orfX encoding a protein of unknown function was found downstream of <em>repA</em> followed by a p<em>dif</em> site in the orientation XerC binding site–spacer–XerD binding site. Most backbones (<em>n</em> = 12) also included <em>mobA</em> and <em>mobC</em> genes but the two plasmids with the most diverged <em>repA</em> and orfX genes had different backbone contents. Although the gene content of the plasmid backbone was largely conserved, extensive recombinational exchange was detected and only two small groups carried identical or nearly identical backbones. Individual plasmids were associated with 1 to 13 <em>dif</em> modules. Many different <em>dif</em> modules were identified, including ones containing antibiotic or chromate resistance genes and several toxin/antitoxin gene pairs. In some cases, modules carrying the same genes were significantly diverged. Generally, the orientation of the p<em>dif</em> sites alternated such that C modules (XerC binding sites internal) alternated with D modules (XerD binding sites internal). However, fusions of two <em>dif</em> modules via mutational inactivation or loss of a p<em>dif</em> site were also detected.</p></div>","PeriodicalId":49689,"journal":{"name":"Plasmid","volume":"129 ","pages":"Article 102722"},"PeriodicalIF":1.8000,"publicationDate":"2024-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0147619X24000027/pdfft?md5=e5d925dcad79fa60e75605f3964b2f92&pid=1-s2.0-S0147619X24000027-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plasmid","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0147619X24000027","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0
Abstract
The predominant type of plasmids found in Acinetobacter species encode a Rep_3 initiation protein and many of these carry their accessory genes in dif modules. Here, available sequences of the 14 members of the group of Rep_3 plasmids typed as R3-T33, using a threshold of 95% identity in the repA gene, were compiled and compared. These plasmids were from various Acinetobacter species. The pdif sites were identified allowing the backbone and dif modules to be defined. As for other Rep_3 plasmids carrying dif modules, orfX encoding a protein of unknown function was found downstream of repA followed by a pdif site in the orientation XerC binding site–spacer–XerD binding site. Most backbones (n = 12) also included mobA and mobC genes but the two plasmids with the most diverged repA and orfX genes had different backbone contents. Although the gene content of the plasmid backbone was largely conserved, extensive recombinational exchange was detected and only two small groups carried identical or nearly identical backbones. Individual plasmids were associated with 1 to 13 dif modules. Many different dif modules were identified, including ones containing antibiotic or chromate resistance genes and several toxin/antitoxin gene pairs. In some cases, modules carrying the same genes were significantly diverged. Generally, the orientation of the pdif sites alternated such that C modules (XerC binding sites internal) alternated with D modules (XerD binding sites internal). However, fusions of two dif modules via mutational inactivation or loss of a pdif site were also detected.
期刊介绍:
Plasmid publishes original research on genetic elements in all kingdoms of life with emphasis on maintenance, transmission and evolution of extrachromosomal elements. Objects of interest include plasmids, bacteriophages, mobile genetic elements, organelle DNA, and genomic and pathogenicity islands.