{"title":"Capture of armA by a novel ISCR element, ISCR28","authors":"","doi":"10.1016/j.ijantimicag.2024.107250","DOIUrl":null,"url":null,"abstract":"<div><p>IS<em>CR28</em> is a fully functional and active member of the IS<em>91</em>-like family of insertion sequences. IS<em>CR28</em> is 1,708-bp long and contains a 1,293-bp long putative open reading frame that codes a transposase. Sixty IS<em>CR28</em>-containing sequences from GenBank generated 27 non-repeat genetic contexts, all of which represented naturally occurring biological events that had occurred in a wide range of gram-negative organisms. Insertion of IS<em>CR28</em> into target DNA preferred the presence of a 5′-GXXT-3′ sequence at its <em>ter</em>IS (replication terminator) end. Loss of the first 4 bp of its <em>ori</em>IS (origin of replication) likely caused IS<em>CR28</em> to be trapped in IS<em>Apl1</em>-based transposons or similar structures. Loss of <em>ter</em>IS and fusion with a mobile element upstream likely promoted co-transfer of IS<em>CR28</em> and the downstream resistance genes. <em>ArmA</em> and its downstream intact IS<em>CR28</em> can be excised from recombinant pKD46 plasmids forming circular intermediates, further elucidating its activity as a transposase.</p></div>","PeriodicalId":13818,"journal":{"name":"International Journal of Antimicrobial Agents","volume":null,"pages":null},"PeriodicalIF":4.9000,"publicationDate":"2024-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0924857924001687/pdfft?md5=7b5af124c9a24f66939d9e1be08f9d5b&pid=1-s2.0-S0924857924001687-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Antimicrobial Agents","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0924857924001687","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0
Abstract
ISCR28 is a fully functional and active member of the IS91-like family of insertion sequences. ISCR28 is 1,708-bp long and contains a 1,293-bp long putative open reading frame that codes a transposase. Sixty ISCR28-containing sequences from GenBank generated 27 non-repeat genetic contexts, all of which represented naturally occurring biological events that had occurred in a wide range of gram-negative organisms. Insertion of ISCR28 into target DNA preferred the presence of a 5′-GXXT-3′ sequence at its terIS (replication terminator) end. Loss of the first 4 bp of its oriIS (origin of replication) likely caused ISCR28 to be trapped in ISApl1-based transposons or similar structures. Loss of terIS and fusion with a mobile element upstream likely promoted co-transfer of ISCR28 and the downstream resistance genes. ArmA and its downstream intact ISCR28 can be excised from recombinant pKD46 plasmids forming circular intermediates, further elucidating its activity as a transposase.
期刊介绍:
The International Journal of Antimicrobial Agents is a peer-reviewed publication offering comprehensive and current reference information on the physical, pharmacological, in vitro, and clinical properties of individual antimicrobial agents, covering antiviral, antiparasitic, antibacterial, and antifungal agents. The journal not only communicates new trends and developments through authoritative review articles but also addresses the critical issue of antimicrobial resistance, both in hospital and community settings. Published content includes solicited reviews by leading experts and high-quality original research papers in the specified fields.