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      Isolation and characterization of phi AB2: a novel bacteriophage of Acinetobacter baumannii.

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          Abstract

          Multidrug-resistant strains of Acinetobacter baumannii (MDRAB) are increasingly being reported worldwide. Bacteriophage therapy is a potential alternative treatment for MDR bacterial infections. Although A. baumannii infection has been experimentally treated with phages, no MDRAB-specific phage has been characterized. In this study, 10 phages with differing host ranges and lysis efficacy for MDRAB were isolated; one of these, phi AB2, was further studied. Electron microscopy revealed phi AB2 to have an isometric head (60 nm), a short tail (diameter, 9 nm; length, 11 nm) and a double-stranded DNA genome--which was resistant to digestion with several restriction endonucleases--estimated to be 40 kb by pulsed-field gel electrophoresis. Partial genome sequencing of a 2.1 kb region gave sequences resembling the tubular proteins A and B of Pseudomonas aeruginosa phage LKA1. These data suggest that phi AB2 resembles phi KMV-like phages and is a new member of the Podoviridae family. It exhibited rapid adsorption (>99% adsorbed in 8 min), a short latent period (<10 min) and a large burst size (ca. 200); moreover, it was capable of infecting a wide spectrum of A. baumannii strains, causing virtually complete lysis, indicating that phi AB2 may be a good candidate as a therapeutic/disinfectant agent to control nosocomial infections caused by MDRAB.

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          Author and article information

          Journal
          Res Microbiol
          Research in microbiology
          Elsevier BV
          1769-7123
          0923-2508
          May 2010
          : 161
          : 4
          Affiliations
          [1 ] Institute of Microbiology Immunology and Molecular Medicine, Tzu Chi University, Hualien 970, Taiwan. ntlin@mail.tcu.edu.tw
          Article
          S0923-2508(10)00077-X
          10.1016/j.resmic.2010.03.007
          20385229
          c25dc68f-9f9b-44df-a6a0-5918d6fc0482
          (c) 2010 Elsevier Masson SAS. All rights reserved.
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