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Survey of Pseudomonas aeruginosa and its phages: de novo peptide sequencing as a novel tool to assess the diversity of worldwide collected viruses
Authors:Pieter-Jan Ceyssens  Jean-Paul Noben  Hans-W Ackermann  Jan Verhaegen  Daniel De Vos  Jean-Paul Pirnay  Maia Merabishvili  Mario Vaneechoutte  rew Chibeu  Guido Volckaert  Rob Lavigne
Institution:Division of Gene Technology, Katholieke Universiteit Leuven, Kasteelpark Arenberg 21, Leuven, Belgium.;
Hasselt University, Biomedical Research Institute and transnational University Limburg, School of Life Sciences, Diepenbeek, Belgium.;
Felix d'Hérelle Reference center for Bacterial Viruses, Department of Medical Biology, Faculty of Medicine, Laval University, Québec, QC G1K 7P4, Canada.;
Division of Experimental Laboratory Medicine, K. U. Leuven, UZ Herestraat 49 box 7003, Leuven, België.;
Hospital Center of the Base-Queen Astrid, Laboratory for Molecular and Cellular Technology, Burn Unit, Bruynstraat 1, B-1120 Neder-over-Heembeek, Belgium.;
Laboratory for Bacteriology Research, Department of Clinical Chemistry, Microbiology and Immunology, Ghent University Hospital, Ghent, Belgium.;
EIBMV, Tbilisi, Georgia.
Abstract:A collection of 15 newly isolated (bacterio)phages infecting the opportunistic pathogen Pseudomonas aeruginosa was established to investigate their global diversity and potential in phage therapy. These phages were sampled in 14 different countries traversing four continents, from both natural environments and hospital sewage. They all display unique DNA and protein profiles and cluster morphologically into six groups within the three major families of the Caudovirales . Extensive host range studies on a library of 122 AFLP-genotyped clinical P. aeruginosa strains (of which 49 were newly isolated at the University Hospital of Leuven, Belgium) showed that the phages lysed 87% of the strains. Infection analysis of outer membrane mutants identified 10 phages as type IV pili-dependent. More detailed information about the evolutionary relatedness of the phages was gathered by de novo peptide sequencing of major virion proteins using tandem Matrix-Assisted Laser Desorption/Ionization Time of Flight technology. Applying this technique for the first time to viruses, seven groups of closely related phages were identified without the need of prior knowledge of genome content and/or electron microscopic imaging. This study demonstrates both the epidemic population structure of P. aeruginosa and the global spread of P. aeruginosa phage species, and points at the resistance of two clinically predominant, widespread P. aeruginosa strains against phage attack.
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