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mcr-8 通过质粒杂交与 bla 或 tmexCD1-toprJ1 共同转移。

Co-transfer of mcr-8 with bla or tmexCD1-toprJ1 by plasmid hybridisation.

机构信息

College of Veterinary Medicine, China Agricultural University, Beijing, China; College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, China.

College of Veterinary Medicine, China Agricultural University, Beijing, China.

出版信息

Int J Antimicrob Agents. 2022 Aug;60(2):106619. doi: 10.1016/j.ijantimicag.2022.106619. Epub 2022 Jun 16.

Abstract

Carbapenems, tigecycline and colistin are three important antimicrobial agents for the treatment of clinical infections caused by multidrug-resistant Enterobacteriaceae. Here we characterised the formation of hybrid plasmids containing mcr-8 and bla or tmexCD1-toprJ1 that could confer resistance to colistin and carbapenems or tigecycline. More specifically, these clinically important genes could be co-transferred through IS26- and ltrA-mediated plasmid fusion to clinical isolates during conjugation under single drug (colistin) selection, following which the recipient strains became carbapenem- or tigecycline-resistant. The transferability and stability of these hybrid multidrug resistance (MDR) plasmids depend on the bacterial host and the presence of antibiotics. Further evolution and adaptation of these hybrid plasmids may facilitate their emergence and spread, which is of great concern for clinical therapy.

摘要

碳青霉烯类、替加环素和黏菌素是治疗多重耐药肠杆菌科引起的临床感染的三种重要抗菌药物。在这里,我们描述了含有 mcr-8 和 bla 或 tmexCD1-toprJ1 的杂交质粒的形成,这些质粒可以赋予对黏菌素和碳青霉烯类药物或替加环素的耐药性。更具体地说,这些临床上重要的基因可以通过 IS26 和 ltrA 介导的质粒融合在单一药物(黏菌素)选择下的接合过程中共同转移到临床分离株中,随后受体菌株对碳青霉烯类或替加环素产生耐药性。这些杂交多药耐药(MDR)质粒的可转移性和稳定性取决于细菌宿主和抗生素的存在。这些杂交质粒的进一步进化和适应可能会促进它们的出现和传播,这对临床治疗非常关注。

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