产气荚膜梭菌pCW3不断扩大的tcp偶联位点

IF 1.8 4区 生物学 Q3 GENETICS & HEREDITY Plasmid Pub Date : 2021-01-01 DOI:10.1016/j.plasmid.2020.102516
Sarah A. Revitt-Mills, Thomas D. Watts, Dena Lyras, Vicki Adams, Julian I. Rood
{"title":"产气荚膜梭菌pCW3不断扩大的tcp偶联位点","authors":"Sarah A. Revitt-Mills,&nbsp;Thomas D. Watts,&nbsp;Dena Lyras,&nbsp;Vicki Adams,&nbsp;Julian I. Rood","doi":"10.1016/j.plasmid.2020.102516","DOIUrl":null,"url":null,"abstract":"<div><p>The spore-forming, anaerobic Gram positive pathogen <span><em>Clostridium perfringens</em></span><span> encodes many of its disease-causing toxins on closely related conjugative plasmids<span>. Studies of the tetracycline resistance plasmid pCW3 have identified many of the genes involved in conjugative transfer, which are located in the </span></span><em>tcp</em> conjugation locus. Upstream of this locus is an uncharacterised region (the <em>cnaC</em> region) that is highly conserved. This study examined the importance in pCW3 conjugation of several highly conserved proteins encoded in the <em>cnaC</em> region. Conjugative mating studies suggested that the SrtD, TcpN and Dam proteins were required for efficient pCW3 transfer between <em>C. perfringens</em> cells from the same strain background. The requirement of these proteins for conjugation was amplified in matings between <em>C. perfringens</em> cells of different strain backgrounds. Additionally, the putative collagen adhesin protein, CnaC, was only required for the optimal transfer of pCW3 between cells of different strain backgrounds. Based on these studies we postulate that CnaC, SrtD, TcpN and Dam are involved in enhancing the transfer frequency of pCW3. These studies have led to a significant expansion of the <em>tcp</em> conjugation locus, which now encompasses a 19 kb region.</p></div>","PeriodicalId":49689,"journal":{"name":"Plasmid","volume":"113 ","pages":"Article 102516"},"PeriodicalIF":1.8000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.plasmid.2020.102516","citationCount":"8","resultStr":"{\"title\":\"The ever-expanding tcp conjugation locus of pCW3 from Clostridium perfringens\",\"authors\":\"Sarah A. Revitt-Mills,&nbsp;Thomas D. Watts,&nbsp;Dena Lyras,&nbsp;Vicki Adams,&nbsp;Julian I. Rood\",\"doi\":\"10.1016/j.plasmid.2020.102516\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The spore-forming, anaerobic Gram positive pathogen <span><em>Clostridium perfringens</em></span><span> encodes many of its disease-causing toxins on closely related conjugative plasmids<span>. Studies of the tetracycline resistance plasmid pCW3 have identified many of the genes involved in conjugative transfer, which are located in the </span></span><em>tcp</em> conjugation locus. Upstream of this locus is an uncharacterised region (the <em>cnaC</em> region) that is highly conserved. This study examined the importance in pCW3 conjugation of several highly conserved proteins encoded in the <em>cnaC</em> region. Conjugative mating studies suggested that the SrtD, TcpN and Dam proteins were required for efficient pCW3 transfer between <em>C. perfringens</em> cells from the same strain background. The requirement of these proteins for conjugation was amplified in matings between <em>C. perfringens</em> cells of different strain backgrounds. Additionally, the putative collagen adhesin protein, CnaC, was only required for the optimal transfer of pCW3 between cells of different strain backgrounds. Based on these studies we postulate that CnaC, SrtD, TcpN and Dam are involved in enhancing the transfer frequency of pCW3. These studies have led to a significant expansion of the <em>tcp</em> conjugation locus, which now encompasses a 19 kb region.</p></div>\",\"PeriodicalId\":49689,\"journal\":{\"name\":\"Plasmid\",\"volume\":\"113 \",\"pages\":\"Article 102516\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2021-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.plasmid.2020.102516\",\"citationCount\":\"8\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plasmid\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0147619X20300287\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plasmid","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0147619X20300287","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: 8

摘要

产芽孢的厌氧革兰氏阳性病原体产气荚膜梭菌在密切相关的共轭质粒上编码其许多致病毒素。对四环素耐药质粒pCW3的研究已经鉴定出许多参与接合转移的基因,这些基因位于tcp接合位点。该位点的上游是一个高度保守的未表征区域(cnaC区域)。本研究考察了cnaC区域编码的几种高度保守蛋白在pCW3偶联中的重要性。结合研究表明,SrtD、TcpN和Dam蛋白是产气荚膜荚膜菌在相同菌株背景下细胞间高效转移pCW3所需的蛋白。在不同菌株背景的产气荚膜荚膜杆菌细胞间的交配中,这些蛋白的偶联需求被扩增。此外,只有在不同菌株背景的细胞之间,pCW3的最佳转移才需要推定的胶原粘附蛋白CnaC。基于这些研究,我们推测CnaC、SrtD、TcpN和Dam参与了pCW3转移频率的增强。这些研究导致了tcp偶联位点的显著扩展,现在包含了一个19 kb的区域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
The ever-expanding tcp conjugation locus of pCW3 from Clostridium perfringens

The spore-forming, anaerobic Gram positive pathogen Clostridium perfringens encodes many of its disease-causing toxins on closely related conjugative plasmids. Studies of the tetracycline resistance plasmid pCW3 have identified many of the genes involved in conjugative transfer, which are located in the tcp conjugation locus. Upstream of this locus is an uncharacterised region (the cnaC region) that is highly conserved. This study examined the importance in pCW3 conjugation of several highly conserved proteins encoded in the cnaC region. Conjugative mating studies suggested that the SrtD, TcpN and Dam proteins were required for efficient pCW3 transfer between C. perfringens cells from the same strain background. The requirement of these proteins for conjugation was amplified in matings between C. perfringens cells of different strain backgrounds. Additionally, the putative collagen adhesin protein, CnaC, was only required for the optimal transfer of pCW3 between cells of different strain backgrounds. Based on these studies we postulate that CnaC, SrtD, TcpN and Dam are involved in enhancing the transfer frequency of pCW3. These studies have led to a significant expansion of the tcp conjugation locus, which now encompasses a 19 kb region.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 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