Abstract
Epidemiological investigations of bacterial infections are generally based on multiple phenotypic markers that are often difficult to verify. A more general and reliable method is genomic DNA analysis by restriction endonucleases. However, the commonly used endonucleases produce too many fragments for correct separation by agarose electrophoresis. In contrast, simple electrophoretic patterns are obtained after genomic DNA digestion by low-frequency-cleavage restriction endonucleases and pulsed-field gel electrophoresis, making it easier to compare numerous strains from the same species. This technique was used to investigate an Acinetobacter calcoaceticus outbreak in a urologic department and bronchial colonization of artificially ventilated patients by Pseudomonas aeruginosa in an intensive care unit. The method allowed a clear distinction between epidemic and self-contaminating strains in these different epidemiological situations.
MeSH Terms
Acinetobacter/classification,genetics
Acinetobacter Infections/epidemiology,microbiology
Cross Infection/epidemiology,microbiology
DNA Restriction Enzymes
DNA, Bacterial/analysis
Deoxyribonucleases, Type II Site-Specific
Disease Outbreaks
Electrophoresis, Agar Gel
Humans
Pseudomonas Infections/epidemiology,microbiology
Pseudomonas aeruginosa/classification,genetics
Restriction Mapping
Chemicals
DNA, Bacterial
DNA Restriction Enzymes
endodeoxyribonuclease XBAI
CCCGGG-specific type II deoxyribonucleases
Deoxyribonucleases, Type II Site-Specific
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Allardet-Servent A
Faculté de Médecine, Institut National de la Santé et de la Recherche Médicale, Montpellier-Nîmes, France.
Bouziges N
Carles-Nurit M J
Bourg G
Gouby A
Ramuz M
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