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ICEA of Mycoplasma agalactiae: a new family of self‐transmissible integrative elements that confers conjugative properties to the recipient strain
Authors:Emilie Dordet Frisoni  Marc Serge Marenda  Eveline Sagné  Laurent Xavier Nouvel  Romain Guérillot  Philippe Glaser  Alain Blanchard  Florence Tardy  Pascal Sirand‐Pugnet  Eric Baranowski  Christine Citti
Institution:1. INRA, UMR 1225, IHAP, , 31076 Toulouse, France;2. Université de Toulouse, INP, ENVT, UMR1225, IHAP, , 31076 Toulouse, France;3. University of Melbourne, Department of Veterinary Science, , Melbourne, Vic., 3030 Australia;4. Institut Pasteur, Unité de Biologie des Bactéries pathogènes à Gram‐positif, , 75724 Paris, France;5. CNRS UMR 3525, , 75005 Paris, France;6. Université Pierre et Marie Curie, , 75005 Paris, France;7. INRA, UMR 1332 de Biologie du Fruit et Pathologie, , F‐33140 Villenave d'Ornon, France;8. Université de Bordeaux, UMR 1332 de Biologie du Fruit et Pathologie, , F‐33140 Villenave d'Ornon, France;9. Anses, Laboratoire de Lyon, UMR Mycoplasmoses des Ruminants, , 69364 Lyon Cedex 07, France;10. Université de Lyon, VetAgro Sup, UMR Mycoplasmoses des Ruminants, , 69280 Marcy L'Etoile, France
Abstract:Horizontal gene transfer (HGT) is a major force of microbial evolution but was long thought to be marginal in mycoplasmas. In silico detection of exchanged regions and of loci encoding putative Integrative Conjugative Elements (ICE) in several mycoplasma genomes challenged this view, raising the prospect of these simple bacteria being able to conjugate. Using the model pathogen Mycoplasma agalactiae, we demonstrated for the first time that one of these elements, ICEA, is indeed self‐transmissible. As a hallmark of conjugative processes, ICEA transfers were DNase resistant and required viable cells. ICEA acquisition conferred ICE‐negative strains with the new ability to conjugate, allowing the spread of ICEA. Analysis of transfer‐deficient mutants indicated that this process requires an ICEA‐encoded lipoprotein of unknown function, CDS14. Formation of a circular extrachromosomal intermediate and the subsequent chromosomal integration of ICEA involved CDS22, an ICEA‐encoded product distantly related to the ISLre2 transposase family. Remarkably, ICEA has no specific or no preferential integration site, often resulting in gene disruptions. Occurrence of functional mycoplasma ICE offers these bacteria with a means for HGT, a phenomenon with far‐reaching implications given their minute‐size genome and the number of species that are pathogenic for a broad host‐range.
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