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PMID: 12748267 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Lysogeny and bacteriophage host range within the Burkholderia cepacia complex.

Journal of medical microbiology ·Vol. 52 ·No. Pt 6 ·2003-06-00 ·Pages 483-490

Langley R, Kenna DT, Vandamme P, Ure R, Govan JRW

Abstract

The Burkholderia cepacia complex comprises a group of nine closely related species that have emerged as life-threatening pulmonary pathogens in immunocompromised patients, particularly individuals with cystic fibrosis or chronic granulomatous disease. Attempts to explain the genomic plasticity, adaptability and virulence of the complex have paid little attention to bacteriophages, particularly the potential contribution of lysogenic conversion and transduction. In this study, lysogeny was observed in 10 of 20 representative strains of the B. cepacia complex. Three temperate phages and five lytic phages isolated from soils, river sediments or the plant rhizosphere were chosen for further study. Six phages exhibited T-even morphology and two were lambda-like. The host range of individual phages, when tested against 66 strains of the B. cepacia complex and a representative panel of other pseudomonads, was not species-specific within the B. cepacia complex and, in some phages, included Burkholderia gladioli and Pseudomonas aeruginosa. These new data indicate a potential role for phages of the B. cepacia complex in the evolution of these soil bacteria as pathogens of plants, humans and animals, and as novel therapeutic agents.

MeSH Terms
Bacteriophages/isolation & purification,pathogenicity,physiology,ultrastructure Burkholderia cepacia/physiology,virology Humans Lysogeny/physiology Microscopy, Electron Plants/virology Soil Microbiology
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Langley Ross
Department of Medical Microbiology, University of Edinburgh, Teviot Place, Edinburgh EH8 9AG, UK 2Laboratorium voor Mikrobiologie, Faculteit Wetenschappen, Universiteit Gent, K. L. Ledeganckstraat 35, B-9000 Gent, Belgium#dReceived 11 October 2002 Accepted 12 February 2003.
Kenna Dervla T
Department of Medical Microbiology, University of Edinburgh, Teviot Place, Edinburgh EH8 9AG, UK 2Laboratorium voor Mikrobiologie, Faculteit Wetenschappen, Universiteit Gent, K. L. Ledeganckstraat 35, B-9000 Gent, Belgium#dReceived 11 October 2002 Accepted 12 February 2003.
Vandamme Peter
Department of Medical Microbiology, University of Edinburgh, Teviot Place, Edinburgh EH8 9AG, UK 2Laboratorium voor Mikrobiologie, Faculteit Wetenschappen, Universiteit Gent, K. L. Ledeganckstraat 35, B-9000 Gent, Belgium#dReceived 11 October 2002 Accepted 12 February 2003.
Ure Rebecca
Department of Medical Microbiology, University of Edinburgh, Teviot Place, Edinburgh EH8 9AG, UK 2Laboratorium voor Mikrobiologie, Faculteit Wetenschappen, Universiteit Gent, K. L. Ledeganckstraat 35, B-9000 Gent, Belgium#dReceived 11 October 2002 Accepted 12 February 2003.
Govan John R W
Department of Medical Microbiology, University of Edinburgh, Teviot Place, Edinburgh EH8 9AG, UK 2Laboratorium voor Mikrobiologie, Faculteit Wetenschappen, Universiteit Gent, K. L. Ledeganckstraat 35, B-9000 Gent, Belgium#dReceived 11 October 2002 Accepted 12 February 2003.
Article Info
Journal
Journal of medical microbiology
Abbr.
J Med Microbiol
ISSN
0022-2615
Published
2003-06-00
Pages
483-490
Language
English
Region
England
NLM ID
0224131
Subset
IM
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