Integrative and conjugative elements in streptococci can act as vectors for plasmids and translocatable units integrated via IS1216E.

Int J Antimicrob Agents

State Key Laboratory for Animal Disease Control and Prevention, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, 150069, China. Electronic address:

Published: May 2023

AI Article Synopsis

  • Mobile genetic elements (MGEs) play a key role in spreading antibiotic resistance, but the specific contributions of integrative and conjugative elements (ICEs) in this process are not fully understood.
  • In this study, researchers identified a new translocatable unit (TU) and a non-conjugative plasmid that carry antibiotic resistance genes, as well as a new ICE, which can facilitate the transfer of these elements between bacteria.
  • The study demonstrated that ICEs can act as vectors for non-conjugative elements, enhancing their transfer among bacteria and potentially increasing the spread of antibiotic resistance in clinical settings.

Article Abstract

Mobile genetic elements (MGEs), such as integrative and conjugative elements (ICEs), plasmids and translocatable units (TUs), are important drivers for the spread of antibiotic resistance. Although ICEs have been reported to support the spread of plasmids among different bacteria, their role in mobilizing resistance plasmids and TUs has not yet been fully explored. In this study, a novel TU bearing optrA, a novel non-conjugative plasmid p5303-cfrD carrying cfr(D) and a new member of the ICESa2603 family, ICESg5301 were identified in streptococci. Polymerase chain reaction (PCR) assays revealed that three different types of cointegrates can be formed by IS1216E-mediated cointegration between the three different MGEs, including ICESg5301::p5303-cfrD::TU, ICESg5301::p5303-cfrD, and ICESg5301::TU. Conjugation assays showed that ICEs carrying p5303-cfrD and/or TU successfully transferred into recipient strains, thereby confirming that ICEs can serve as vectors for other non-conjugative MGEs, such as TUs and p5303-cfrD. As neither the TU nor plasmid p5303-cfrD can spread on their own between different bacteria, their integration into an ICE via IS1216E-mediated cointegrate formation not only increases the plasticity of ICEs, but also furthers the dissemination of plasmids and TUs carrying oxazolidinone resistance genes.

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Source
http://dx.doi.org/10.1016/j.ijantimicag.2023.106793DOI Listing

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