4.1 Article

Evolution and dissemination of L and M plasmid lineages carrying antibiotic resistance genes in diverse Gram-negative bacteria

期刊

PLASMID
卷 113, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.plasmid.2020.102528

关键词

IncL; IncM; L/M plasmids; Evolution; Antibiotic resistance

资金

  1. MRC-NSFC DETECTIVE project [MR/S013660/1]
  2. MRC [MR/S013660/1] Funding Source: UKRI

向作者/读者索取更多资源

Conjugative, broad host-range plasmids of the L/M complex, associated with antibiotic resistance, have been found in Gram-negative bacteria causing human infections and persisting in hospital environments. Accurate typing of these plasmids is crucial for tracing their clinical and global dissemination in epidemiological studies. The complex has been divided into L, M1, and M2 subtypes, but further investigation reveals additional diversity within the group, with distinct lineages evolving through genetic recombination and acquisition of antibiotic resistance genes.
Conjugative, broad host-range plasmids of the L/M complex have been associated with antibiotic resistance since the 1970s. They are found in Gram-negative bacterial genera that cause human infections and persist in hospital environments. It is crucial that these plasmids are typed accurately so that their clinical and global dissemination can be traced in epidemiological studies. The L/M complex has previously been divided into L, M1 and M2 subtypes. However, those types do not encompass all diversity seen in the group. Here, we have examined 148 complete L/M plasmid sequences in order to understand the diversity of the complex and trace the evolution of distinct lineages. The backbone sequence of each plasmid was determined by removing translocatable genetic elements and reversing their effects in silico. The sequence identities of replication regions and complete backbones were then considered for typing. This supported the distinction of L and M plasmids and revealed that there are five L and eight M types, where each type is comprised of further sub-lineages that are distinguished by variation in their backbone and translocatable element content. Regions containing antibiotic resistance genes in L and M sub-lineages have often formed by initial rare insertion events, followed by insertion of other trans locatable elements within the inceptive element. As such, islands evolve in situ to contain genes conferring resistance to multiple antibiotics. In some cases, different plasmid sub-lineages have acquired the same or related resistance genes independently. This highlights the importance of these plasmids in acting as vehicles for the dissemination of emerging resistance genes. Materials are provided here for typing plasmids of the L/M complex from complete sequences or draft genomes. This should enable rapid identification of novel types and facilitate tracking the evolution of existing lineages.

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