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通过接合性拟杆菌四环素抗性元件促进IncP β R751衍生物从均匀拟杆菌染色体转移至大肠杆菌受体菌。

Facilitated transfer of IncP beta R751 derivatives from the chromosome of Bacteroides uniformis to Escherichia coli recipients by a conjugative Bacteroides tetracycline resistance element.

作者信息

Shoemaker N B, Salyers A A

出版信息

J Bacteriol. 1987 Jul;169(7):3160-7. doi: 10.1128/jb.169.7.3160-3167.1987.

Abstract

The broad-host-range IncP beta plasmid R751 can mobilize itself from Escherichia coli to Bacteroides spp, but it is not maintained in Bacteroides spp. If R751 carries the Bacteroides transposon Tn4351, it can be integrated into the Bacteroides chromosome. Previously we showed that R751, integrated in the chromosome of Bacteroides uniformis, cannot mobilize itself out of B. uniformis into E. coli or isogenic B. uniformis strains. In this report, we showed that if the Bacteroides conjugative tetracycline resistance element Tcr ERL was coresident with the R751 insertion in B. uniformis, derivatives of R751 were transferred to E. coli, where they were recovered as plasmids. The most common derivatives were R751::Tn4351 and R751::IS4351, but some strains transferred R751 derivatives, containing additional DNA segments ranging in size from 10 to 23 kilobases. These DNA inserts cross-hybridized with chromosomal DNA from B. uniformis which did not carry the Tcr ERL element. Therefore, the inserts appeared to be segments of the wild-type B. uniformis chromosome and were not associated with the Tcr ERL element. The transfer of integrated R751 from B. uniformis was independent of the RecA phenotype of the E. coli recipients and did not appear to be due to transfer of B. uniformis chromosomal DNA, followed by RecA-dependent recombination between homologous IS4351 sequences to form the resultant R751 plasmid derivatives. Consistent with this, no transfer of Tn4351 (associated with the cointegrated R751) from B. uniformis donors to isogenic B. uniformis recipients was detected (< 10(-8)). Our data support the hypothesis that R751 excises from the B. uniformis chromosome by recombination involving flanking Tn4351 or IS4351 sequences and forms nonreplicating circles. The mobilization of these circular forms out of B. uniformis to E.coli is then facilitated by the Tcr ERL element.

摘要

广宿主范围的IncPβ质粒R751能够将自身从大肠杆菌转移至拟杆菌属,但它在拟杆菌属中无法维持。如果R751携带拟杆菌转座子Tn4351,它就能整合到拟杆菌染色体中。此前我们发现,整合在单形拟杆菌染色体中的R751无法将自身从单形拟杆菌转移至大肠杆菌或同基因的单形拟杆菌菌株中。在本报告中,我们发现,如果拟杆菌接合型四环素抗性元件Tcr ERL与R751在单形拟杆菌中的插入片段共存,R751的衍生物会转移至大肠杆菌,并以质粒形式回收。最常见的衍生物是R751::Tn4351和R751::IS4351,但一些菌株转移的R751衍生物含有额外的DNA片段,大小在10至23千碱基之间。这些DNA插入片段与未携带Tcr ERL元件的单形拟杆菌染色体DNA发生交叉杂交。因此,这些插入片段似乎是野生型单形拟杆菌染色体的片段,与Tcr ERL元件无关。整合在单形拟杆菌中的R751的转移与大肠杆菌受体的RecA表型无关,似乎也不是由于单形拟杆菌染色体DNA的转移,随后同源IS4351序列之间发生RecA依赖性重组形成最终的R751质粒衍生物。与此一致的是,未检测到Tn4351(与共整合的R751相关)从单形拟杆菌供体转移至同基因的单形拟杆菌受体(<10^(-8))。我们的数据支持这样的假设,即R751通过涉及侧翼Tn4351或IS4351序列的重组从单形拟杆菌染色体上切除,形成非复制性环状物。然后,Tcr ERL元件促进这些环状物从单形拟杆菌转移至大肠杆菌。

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