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IS 重组多药耐药大肠杆菌菌株中的质粒。

IS Reorganizes Plasmids in a Multidrug-Resistant Escherichia coli Strain.

机构信息

College of Veterinary Medicine, Henan Agricultural Universitygrid.108266.b, Zhengzhou, China.

West China Hospital, Sichuan University, Chengdu, China.

出版信息

Microbiol Spectr. 2021 Oct 31;9(2):e0050321. doi: 10.1128/Spectrum.00503-21. Epub 2021 Oct 6.

Abstract

The aims of this study were to elucidate the role of IS in plasmid reorganization and to analyze biological characteristics of cointegrates derived from different daughter plasmids. The genetic profiles of plasmids in Escherichia coli strain C21 and its transconjugants were characterized by conjugation, S1 nuclease pulsed-field gel electrophoresis (S1-PFGE), Southern hybridization, whole-genome sequencing (WGS) analysis, and PCR. The traits of cointegrates were characterized by conjugation and stability assays. -bearing IncI2 pC21-1 and nonresistant IncI1 pC21-3, as conjugative helper plasmids, were fused with nonconjugative -bearing IncN-X1 pC21-2, generating cointegrates pC21-F1 and pC21-F2. Similarly, pC21-1 and pC21-3 were fused with nonconjugative IncF33:A-:B- pHB37-2 from another E. coli strain to generate cointegrates pC21-F3 and pC21-F4 under experimental conditions. Four cointegrates were further conjugated into the E. coli strain J53 recipient at high conjugation frequencies, ranging from 2.8 × 10 to 3.2 × 10. The formation of pC21-F1 and pC21-F4 was the result of host- and ISmediated reactions and occurred at high fusion frequencies of 9.9 × 10 and 2.1 × 10, respectively. Knockout of RecA resulted in a 100-fold decrease in the frequency of plasmid reorganization. The phenomenon of cointegrate pC21-F2 and its daughter plasmids coexisting in transconjugants was detected for the first time in plasmid stability experiments. IS-- was excised from cointegrate pC21-F2 through a circular intermediate at a very low frequency, which was experimentally observed. To the best of our knowledge, this is the first report of IS-mediated fusion between plasmids with different replicons. This study provides insight into the formation and evolution of cointegrate plasmids under different drug selection pressures, which can promote the dissemination of MDR plasmids. The increasing resistance to β-lactams and aminoglycoside antibiotics, mainly due to extended-spectrum β-lactamases (ESBLs) and 16S rRNA methylase genes, is becoming a serious problem in Gram-negative bacteria. Plasmids, as the vehicles for resistance gene capture and horizontal gene transfer, serve a key role in terms of antibiotic resistance emergence and transmission. IS, present in many antibiotic-resistant plasmids from Gram-negative bacteria, plays a critical role in the spread, clustering, and reorganization of resistance determinant-encoding plasmids and in plasmid reorganization through replicative transposition mechanisms and homologous recombination. However, the role of IS, present in many MDR plasmids, in the formation of cointegrates remains unclear. Here, we investigated experimentally the intermolecular recombination of IS, which occurred with high frequencies and led to the formation of conjugative MDR cointegrates and facilitated the cotransfer of and , and we further uncovered the significance of IS in the formation of cointegrates and the common features of IS-driven cointegration of plasmids.

摘要

本研究旨在阐明 IS 在质粒重排中的作用,并分析来自不同子质粒的杂种质粒的生物学特性。通过接合、S1 核酸酶脉冲场凝胶电泳(S1-PFGE)、Southern 杂交、全基因组测序(WGS)分析和 PCR,对大肠杆菌 C21 菌株及其转导子中质粒的遗传特征进行了表征。杂种质粒的特性通过接合和稳定性测定进行了表征。作为可接合的辅助质粒,携带 IncI2 pC21-1 和非耐药 IncI1 pC21-3 与非可接合的携带 IncN-X1 pC21-2 融合,生成杂种质粒 pC21-F1 和 pC21-F2。同样,将 pC21-1 和 pC21-3 与来自另一种大肠杆菌菌株的非可接合的 IncF33:A-:B- pHB37-2 融合,在实验条件下生成杂种质粒 pC21-F3 和 pC21-F4。四个杂种质粒以高接合频率(范围为 2.8×10 到 3.2×10)进一步接合到大肠杆菌 J53 受体中。pC21-F1 和 pC21-F4 的形成是宿主和 IS 介导的反应的结果,融合频率分别高达 9.9×10 和 2.1×10。RecA 的敲除导致质粒重排频率降低 100 倍。在质粒稳定性实验中,首次检测到杂种质粒 pC21-F2 及其子质粒在转导子中共存的现象。通过环形中间产物,IS--从杂种质粒 pC21-F2 中以非常低的频率被切除,这在实验中得到了观察。据我们所知,这是第一个报告 IS 介导的具有不同复制子的质粒之间的融合。本研究深入了解了在不同药物选择压力下杂种质粒的形成和进化,这有助于推动 MDR 质粒的传播。β-内酰胺类和氨基糖苷类抗生素的耐药性不断增加,主要是由于超广谱β-内酰胺酶(ESBLs)和 16S rRNA 甲基酶基因,这在革兰氏阴性菌中已成为一个严重的问题。质粒作为耐药基因捕获和水平基因转移的载体,在抗生素耐药性的出现和传播中起着关键作用。IS 存在于革兰氏阴性菌中许多抗生素耐药质粒中,在耐药决定簇编码质粒的传播、聚类和重排以及通过复制转座机制和同源重组进行质粒重排中发挥关键作用。然而,存在于许多 MDR 质粒中的 IS 在杂种质粒形成中的作用仍不清楚。在这里,我们通过实验研究了 IS 之间的分子间重组,这种重组发生的频率很高,导致可接合的多药耐药杂种质粒的形成,并促进了 和 的共转移,我们进一步揭示了 IS 在杂种质粒形成中的意义以及 IS 驱动质粒共整合的共同特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa50/8510248/bdb5fdf2eeda/spectrum.00503-21-f001.jpg

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