Genotypic and Phenotypic Methods for the Investigation of a Nosocomial Legionella pneumophila Outbreak and Efficacy of Control Measures

To determine the source of a nosocomial outbreak of Legionella pneumophila serogroup 1 infection and the efficacy of control measures, clinical and environmental isolates were characterized by molecular subtyping and disease surveillance was conducted. The outbreak involved 32 cases (relative risk,...

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Published in:The Journal of infectious diseases Vol. 166; no. 1; pp. 22 - 30
Main Authors: Struelens, Marc J., Maes, Nicole, Rost, Francis, Deplano, Ariane, Jacobs, Frédérique, Liesnard, Corinne, Bornstein, Nicole, Grimont, Francine, Lauwers, Sabine, McIntyre, Michael P., Serruys, Elisabeth
Format: Journal Article
Language:English
Published: Chicago, IL The University of Chicago Press 01-07-1992
University of Chicago Press
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Summary:To determine the source of a nosocomial outbreak of Legionella pneumophila serogroup 1 infection and the efficacy of control measures, clinical and environmental isolates were characterized by molecular subtyping and disease surveillance was conducted. The outbreak involved 32 cases (relative risk, 4.0; P < .001 vs. previous period). Water colonization with L. pneumophila serogroup 1 and patients' exposure to faucet use incriminated the water system as the environmental source. Monoclonal antibody typing showed that patient isolates belonged mainly to type Pontiac and water isolates mainly to type Bellingham (P < .001). By four genotypic techniques, outbreak-related isolates from patients and the water system were found to be clonally related and distinct from control strains (P < .001). Heat and UV light treatment of the water system showed a protective efficacy of 88% (95% confidence interval, 75%–94%). These findings indicate that phenotypic variation may interfere with monoclonal antibody typing of legionellae and that waterborne legionellosis can be controlled by physical disinfection.
Bibliography:ark:/67375/HXZ-946X2MB8-F
Reprints or correspondence: Dr. M. J. Struelens, Laboratoire de Microbiologic, Hôpital Erasme 808, Route de Lennik, 1070 Bruxelles, Belgium.
Present affiliation: Department of Microbiology, Wexham Park Hospital, Slough, United Kingdom.
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ISSN:0022-1899
1537-6613
DOI:10.1093/infdis/166.1.22