Abstract

Antibiotic resistance gene transfer mediated by plasmids is a matter of concern for public health, but permissive environments supporting plasmid dissemination are still quite difficult to identify. Lately, we have reported a molecular approach based on quantitative PCR (qPCR) to monitor the fate of the IncP-1β plasmid pB10 in natural microbial communities maintained in microcosms. Such plasmid transfer experiments were carried out with 13 different environmental matrices, and demonstrated that the transfer of the conjugative-proficient plasmid pB10 in complex environments is relatively rare and is strongly matrix dependent. An attempt to link the microbial community structure and the matrix permissiveness showed that TTGE analysis is not resolutive enough to point out common features among comparable communities supporting pB10 transfer. However, an estimation of the IncP-1α/IncP-1β plasmids abundance by qPCR demonstrated that pB10 transfer tends to be supported by environmental matrices exhibiting a higher content of IncP-1 plasmids. We suggest that the relative abundance of IncP-1 plasmids in a given microbial community reflects its permissiveness to the transfer of plasmids belonging to the same incompatibility group, which prevails over transfer limitation due to a phenomenon known as superinfection immunity.

Highlights

  • Bacteria have evolved various adaptive mechanisms allowing them to deal with the constraints imposed by their ever-changing local environments

  • MICROBIAL COMMUNITY STRUCTURE AND TRANSFER OF pB10 In the first instance, we hypothesized that depending on its structure, the microbial community involved as recipient could be responsible for the efficiency of the pB10 dissemination in a given matrix

  • In order to highlight the involvement of particular community members, we compared the bacterial community structures of different but related microcosm samples, as well as their ability to support pB10 transfer

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Summary

Introduction

Bacteria have evolved various adaptive mechanisms allowing them to deal with the constraints imposed by their ever-changing local environments. The bacterial genetic flexibility is associated with mobile genetic elements that seem to play a significant role in acquiring and sharing new genes, enabling bacteria to improve their fitness under local stresses. In this respect, the dissemination of resistance genes that followed (and still follows) the use and consumption of antibiotics is just a dramatic illustration of such adaptability (Davies, 1995, 2007; Davies and Davies, 2010; Wiedenbeck and Cohan, 2011). It could be argued that resistant bacteria hosting mobile genetic elements could accumulate in some environments that are not necessarily permissive to horizontal gene transfer

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