4.6 Article

Integrated conjugative plasmid drives high frequency chromosomal gene transfer in Sulfolobus islandicus

Journal

FRONTIERS IN MICROBIOLOGY
Volume 14, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2023.1114574

Keywords

recombination; gene transfer; conjugative plasmid; Sulfolobus islandicus; archaea; conjugation frequency

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This study investigates a plasmid-mediated mechanism of gene transfer in Sulfolobus islandicus that leads to high frequency recombination within the chromosome. Through genomic analysis, the researchers establish the distribution of recombinant tracts and identify distal non-selected recombination events. This study reveals the molecular factors governing gene transfer and recombination in crenarchaea.
Gene transfer in crenarchaea has been observed within natural and experimental populations of Sulfolobus. However, the molecular factors that govern how gene transfer and recombination manifest themselves in these populations is still unknown. In this study, we examine a plasmid-mediated mechanism of gene transfer in S. islandicus that results in localized high frequency recombination within the chromosome. Through chromosomal marker exchange assays with defined donors and recipients, we find that while bidirectional exchange occurs among all cells, those possessing the integrated conjugative plasmid, pM164, mobilize a nearby locus at a significantly higher frequency when compared to a more distal marker. We establish that traG is essential for this phenotype and that high frequency recombination can be replicated in transconjugants after plasmid transfer. Mapping recombinants through genomic analysis, we establish the distribution of recombinant tracts with decreasing frequency at increasing distance from pM164. We suggest the bias in transfer is a result of an Hfr (high frequency recombination)-like conjugation mechanism in this strain. In addition, we find recombinants containing distal non-selected recombination events, potentially mediated by a different host-encoded marker exchange (ME) mechanism.

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