Use of arbitrary primer PCR to type Clostridium difficile and comparison of results with those by immunoblot typing

Author:

Killgore G E1,Kato H1

Affiliation:

1. Nosocomial Pathogens Laboratory Branch, Centers for Disease Control and Prevention, Atlanta, Georgia 30333.

Abstract

An arbitrarily primed PCR (AP-PCR) assay was used to type Clostridium difficile isolates from a hospital outbreak of antibiotic-associated diarrhea. Forty-one isolates were separated into nine groups, with 66% falling into one group; no other group contained more than 10%. Comparison of AP-PCR grouping with that when the immunoblot technique was used showed agreement for 33 of 34 isolates typed by both techniques, and AP-PCR grouped seven isolates that were not typeable by immunoblotting.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference16 articles.

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2. DNA amplification fingerprinting using very short arbitrary oligonucleotide primers;Caetano-Anolles G.;Bio/Technology,1991

3. Development of a rapid and efficient restriction endonuclease analysis typing system for Clostridiumn difficile and correlation with other typing systems;Clabots C. R.;J. Clin. Microbiol.,1993

4. Restriction endonuclease analysis of nosocomial isolates of Clostridium difficile;Devlin H. R.;J. Clin. Microbiol.,1987

5. Clostridium difficile and its cytotoxin in feces of patients with antimicrobial agent-associated diarrhea and miscellaneous conditions;George W. L.;J. Clin. Microbiol.,1982

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