R.F. Benson

Centers for Disease Control and Prevention, Atlanta, Michigan, United States

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Publications (1)2.48 Total impact

  • Source
    J.H. Helbig · R.F. Benson · C Pelaz · E Jacobs · P.C. Lück
    [Show abstract] [Hide abstract]
    ABSTRACT: To validate identification methods for Legionella pneumophila strains that cannot be serotyped into the known serogroups and to characterize their antigenic diversity. Fifty L. pneumophila strains that could not be serogrouped, but which had been confirmed as L. pneumophila by mip gene sequencing, were further identified phenotypically. We used (i) MONOFLUO anti-Legionella Staining Reagent (Bio-Rad) (50/50), (ii) an in-house prepared immunoblot assay for the detection of L. pneumophila- specific Mip protein epitope (50/50), (iii) fatty acid analysis using the Microbial Identifications System (MIDI) (47/50) and (iv) Oxoid agglutination tests (44/50). The serological diversity was further characterized by testing with five serogroup-cross-reactive monoclonal antibodies, resulting in nine phenons. The division of L. pneumophila into 15 serogroups does not reflect the serogroup heterogeneity. Results of these tests indicate that there are more serogroups. MONOFLUO anti-Legionella Staining Reagent is the only commercially available tool for identifying atypical strains of L. pneumophila. If necessary for epidemiological purposes, the antigenic heterogeneity of these strains can be analysed by monoclonal antibodies.
    Preview · Article · Feb 2007 · Journal of Applied Microbiology

Publication Stats

24 Citations
2.48 Total Impact Points


  • 2007
    • Centers for Disease Control and Prevention
      • Division of Bacterial Diseases
      Atlanta, Michigan, United States