SGI0, a relative of Salmonella genomic islands SGI1 and SGI2, lacking a class 1 integron, found in Proteus mirabilis

IF 1.8 4区 生物学 Q3 GENETICS & HEREDITY Plasmid Pub Date : 2020-01-01 DOI:10.1016/j.plasmid.2019.102453
Claire de Curraize , Eliane Siebor , Catherine Neuwirth , Ruth M. Hall
{"title":"SGI0, a relative of Salmonella genomic islands SGI1 and SGI2, lacking a class 1 integron, found in Proteus mirabilis","authors":"Claire de Curraize ,&nbsp;Eliane Siebor ,&nbsp;Catherine Neuwirth ,&nbsp;Ruth M. Hall","doi":"10.1016/j.plasmid.2019.102453","DOIUrl":null,"url":null,"abstract":"<div><p><span>Several groups of integrative mobilizable elements (IMEs) that harbour a class 1 integron<span> carrying antibiotic resistance genes have been found at the 3′-end of the chromosomal </span></span><em>trmE</em> gene. Here, a new IME, designated SGI0, was found in <em>trmE</em> in the sequenced and assembled genome of a French clinical, multiply antibiotic resistant <em>Proteus mirabilis</em> strain, <em>Pm</em><span>1LENAR. SGI0 shares the same gene content as the backbones of SGI1 and SGI2 (overall 97.6% and 97.7% nucleotide identity, respectively) but it lacks a class 1 integron. However, SGI0 is a mosaic made up of segments with &gt;98.5% identity to SGI1 and SGI2 interspersed with segments sharing 74–95% identity indicating that further diverged backbone types exist and that recombination between them is occurring. The structure of SGI1-V, here re-named SGI-V, which lacks two SGI1 (S023 and S024) backbone genes and includes a group of additional genes in the backbone, was re-examined. In regions shared with SGI1, the backbones shared 97.3% overall identity with the differences distributed in patches with various levels of identity. The class 1 integron is also in a slightly different position with the target site duplication AAATT instead of ACTTG for SGI1 and variants, indicating that it was acquired independently. The </span><em>Pm</em>1LENAR resistance genes are in the chromosome, in Tn<em>7</em> and an IS<em>Ecp1</em>-mobilised segment.</p></div>","PeriodicalId":49689,"journal":{"name":"Plasmid","volume":"107 ","pages":"Article 102453"},"PeriodicalIF":1.8000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.plasmid.2019.102453","citationCount":"10","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plasmid","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0147619X19301295","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: 10

Abstract

Several groups of integrative mobilizable elements (IMEs) that harbour a class 1 integron carrying antibiotic resistance genes have been found at the 3′-end of the chromosomal trmE gene. Here, a new IME, designated SGI0, was found in trmE in the sequenced and assembled genome of a French clinical, multiply antibiotic resistant Proteus mirabilis strain, Pm1LENAR. SGI0 shares the same gene content as the backbones of SGI1 and SGI2 (overall 97.6% and 97.7% nucleotide identity, respectively) but it lacks a class 1 integron. However, SGI0 is a mosaic made up of segments with >98.5% identity to SGI1 and SGI2 interspersed with segments sharing 74–95% identity indicating that further diverged backbone types exist and that recombination between them is occurring. The structure of SGI1-V, here re-named SGI-V, which lacks two SGI1 (S023 and S024) backbone genes and includes a group of additional genes in the backbone, was re-examined. In regions shared with SGI1, the backbones shared 97.3% overall identity with the differences distributed in patches with various levels of identity. The class 1 integron is also in a slightly different position with the target site duplication AAATT instead of ACTTG for SGI1 and variants, indicating that it was acquired independently. The Pm1LENAR resistance genes are in the chromosome, in Tn7 and an ISEcp1-mobilised segment.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
SGI0是沙门氏菌基因组岛SGI1和SGI2的近亲,缺乏1类整合子,发现于变形杆菌中
在染色体trmE基因的3 '端发现了几组含有携带抗生素抗性基因的1类整合子的整合可动元件(IMEs)。在法国临床多重耐抗生素变形杆菌菌株Pm1LENAR的测序和组装基因组中,在trmE中发现了一个新的IME,命名为SGI0。SGI0与SGI1和SGI2的主干基因含量相同(总体核苷酸同源性分别为97.6%和97.7%),但缺少1类整合子。然而,SGI0是由与SGI1和SGI2同源性98.5%的片段组成的马赛克,其中穿插着74-95%同源的片段,表明它们之间存在进一步分化的骨干类型,并且正在发生重组。SGI1- v的结构,在这里被重新命名为SGI-V,缺乏两个SGI1 (S023和S024)骨干基因,在骨干中包括一组额外的基因,被重新检查。在与SGI1共享的区域,主干网总体同一性为97.3%,差异分布在不同同一性水平的斑块上。对于SGI1和变体,1类整合子与目标位点复制AAATT而不是ACTTG的位置也略有不同,表明它是独立获得的。Pm1LENAR抗性基因位于染色体、Tn7和isecp1动员片段中。
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 去求助
来源期刊
Plasmid
Plasmid 生物-遗传学
CiteScore
4.70
自引率
3.80%
发文量
21
审稿时长
53 days
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.
期刊最新文献
miRNA heterologous production in bacteria: A systematic review focusing on the choice of plasmid features and bacterial/prokaryotic microfactory Characterization and functional insights of the novel RC-type plasmid pAnox1 from Anoxybacillus gonensis 05S15 Plasmids affect microindel mutations in Acinetobacter baylyi ADP1 Shedding light on Klebsiella pneumoniae virulence: Engineering of broad host range bioluminescence reporter vectors for transcriptional analysis in drug resistant pathogens. Development of a thermostable Cre/lox-based gene disruption system and in vivo manipulations of the megaplasmid pTT27 in Thermus thermophilus HB27
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1