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Genomic erosion and horizontal gene transfer shape functional differences of the ExlA toxin in Pseudomonas spp.
Job, Viviana; Gomez-Valero, Laura; Renier, Adèle; Rusniok, Christophe; Bouillot, Stephanie; Chenal-Francisque, Viviane; Gueguen, Erwan; Adrait, Annie; Robert-Genthon, Mylène; Jeannot, Katy; Panchev, Peter; Elsen, Sylvie; Fauvarque, Marie-Odile; Couté, Yohann; Buchrieser, Carmen; Attrée, Ina.
  • Job V; Université Grenoble Alpes, Institute of Structural Biology, Bacterial Pathogenesis and Cellular Responses Team, UMR5075 CNRS, IRIG, CEA, Grenoble, France.
  • Gomez-Valero L; Institut Pasteur, Université de Paris, CNRS UMR 6047, Unité Biologie des Bactéries Intracellulaires, 75015 Paris, France.
  • Renier A; Université Grenoble Alpes, Institute of Structural Biology, Bacterial Pathogenesis and Cellular Responses Team, UMR5075 CNRS, IRIG, CEA, Grenoble, France.
  • Rusniok C; Institut Pasteur, Université de Paris, CNRS UMR 6047, Unité Biologie des Bactéries Intracellulaires, 75015 Paris, France.
  • Bouillot S; Université Grenoble Alpes, Institute of Structural Biology, Bacterial Pathogenesis and Cellular Responses Team, UMR5075 CNRS, IRIG, CEA, Grenoble, France.
  • Chenal-Francisque V; Institut Pasteur, Université de Paris, CNRS UMR 6047, Unité Biologie des Bactéries Intracellulaires, 75015 Paris, France.
  • Gueguen E; University of Lyon, Université Lyon 1, INSA de Lyon, CNRS UMR 5240 Microbiologie Adaptation et Pathogénie, Lyon, France.
  • Adrait A; Université Grenoble Alpes, INSERM, CEA, UMR BioSanté U1292, Grenoble, France.
  • Robert-Genthon M; Université Grenoble Alpes, Institute of Structural Biology, Bacterial Pathogenesis and Cellular Responses Team, UMR5075 CNRS, IRIG, CEA, Grenoble, France.
  • Jeannot K; Centre National de Référence de la Résistance aux Antibiotiques, Laboratoire de Bactériologie, Centre Hospitalier Universitaire Jean Minjoz, UMR6249 CNRS, Université de Bourgogne-Franche Comté, Besançon, France.
  • Panchev P; Université Grenoble Alpes, Institute of Structural Biology, Bacterial Pathogenesis and Cellular Responses Team, UMR5075 CNRS, IRIG, CEA, Grenoble, France.
  • Elsen S; Université Grenoble Alpes, Institute of Structural Biology, Bacterial Pathogenesis and Cellular Responses Team, UMR5075 CNRS, IRIG, CEA, Grenoble, France.
  • Fauvarque MO; Université Grenoble Alpes, INSERM, CEA, UMR BioSanté U1292, Grenoble, France.
  • Couté Y; Université Grenoble Alpes, INSERM, CEA, UMR BioSanté U1292, Grenoble, France.
  • Buchrieser C; CNRS, CEA, FR2048, Grenoble, France.
  • Attrée I; Institut Pasteur, Université de Paris, CNRS UMR 6047, Unité Biologie des Bactéries Intracellulaires, 75015 Paris, France.
iScience ; 25(7): 104596, 2022 Jul 15.
Article en En | MEDLINE | ID: mdl-35789842
ABSTRACT
Two-partner secretion (TPS) is widespread in the bacterial world. The pore-forming TPS toxin ExlA of Pseudomonas aeruginosa is conserved in pathogenic and environmental Pseudomonas. While P. chlororaphis and P. entomophila displayed ExlA-dependent killing, P. putida did not cause damage to eukaryotic cells. ExlA proteins interacted with epithelial cell membranes; however, only ExlA Pch induced the cleavage of the adhesive molecule E-cadherin. ExlA proteins participated in insecticidal activity toward the larvae of Galleria mellonella and the fly Drosophila melanogaster. Evolutionary analyses demonstrated that the differences in the C-terminal domains are partly due to horizontal movements of the operon within the genus Pseudomonas. Reconstruction of the evolutionary history revealed the complex horizontal acquisitions. Together, our results provide evidence that conserved TPS toxins in environmental Pseudomonas play a role in bacteria-insect interactions and discrete differences in CTDs may determine their specificity and mode of action toward eukaryotic cells.
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