SGI1家族整合可移动元件能否克服IncA和IncC质粒对IncC质粒施加的进入排斥?

IF 1.8 4区 生物学 Q3 GENETICS & HEREDITY Plasmid Pub Date : 2022-09-01 DOI:10.1016/j.plasmid.2022.102654
Stephanie J. Ambrose, Ruth M. Hall
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引用次数: 1

摘要

虽然IncC和IncA质粒是相容的,但它们彼此之间存在高度排斥。在这里,我们研究了供体中SGI1家族元素的存在是否可以克服IncC质粒或受体中IncC质粒所施加的IncC质粒的排斥。整合可移动元件SGI1及其多种变体形式向新宿主的转移依赖于IncC或IncA质粒提供的转移机制。SGI1元件包括动员系统的决定因素和三个编码转运蛋白同源物的基因,包括TraG。完整的IncA质粒或受体中的IncC质粒对完整的IncC质粒的排斥作用并未因供体中的SGI1元素而得到改善。然而,SGI的转移不受影响,这表明形成了一个功能性的交配装置。受体中仅存在质粒衍生的eexC或eexA基因,这对传入的IncC质粒产生了高水平的排斥,这被供体中的SGI1变体所克服。因此,SGI仅影响入口排除,其他质粒特征必须影响质粒排除的其他途径。
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Can SGI1 family integrative mobilizable elements overcome entry exclusion exerted by IncA and IncC plasmids on IncC plasmids?

Though IncC and IncA plasmids are compatible, they exert high level exclusion on one another. Here, the question of whether the presence of an SGI1 family element in the donor can overcome the exclusion of an IncC plasmid exerted by an IncC or IncA plasmid in the recipient was investigated. The transfer of the integrative mobilizable element SGI1 and its many variant forms into a new host is dependent on transfer machinery supplied by IncC or IncA plasmids. SGI1 elements include the determinants of a mobilization system and three genes that encode homologues of transfer proteins including TraG. Exclusion of a complete IncC plasmid by a complete IncA or IncC plasmid in the recipient was not ameliorated by an SGI1 element in the donor. However, transfer of the SGI was unaffected indicating that a functional mating apparatus was formed. The presence of only the plasmid-derived eexC or eexA gene in the recipient exerted high level exclusion on an incoming IncC plasmid and this was overcome by an SGI1 variant in the donor. Hence, the SGI affects only entry exclusion and additional plasmid features must influence other routes to plasmid exclusion.

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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.
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