4.5 Article

Antibiograms and Randomly Amplified Polymorphic DNA-Polymerase Chain Reactions (RAPD-PCR) as Epidemiological Markers of Gonorrhea

Journal

JOURNAL OF CLINICAL LABORATORY ANALYSIS
Volume 24, Issue 1, Pages 31-37

Publisher

WILEY
DOI: 10.1002/jcla.20355

Keywords

Neissseria gonorrhoeae; gonorrhea; gyrase A; RAPD-PCR

Funding

  1. Mahidol University

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The development of antimicrobial resistance of Neisseria gonorrhoeae arising from wide dissemination of resistant clones is a major global health problem. In this study, a total of 235 isolates of N. gonorrhoeae isolated from patients of Bangrak Hospital were tested for their antibiotic susceptibilities to penicillin, norfloxacin, ofloxacin, ciprofloxacin, spectinomycin, and ceftriaxone. Mutation (Ser-91) in the quinolone resistance determining regions of gyrA and random amplification of the polymorphic DNA polymerase chain reaction (RAPD-PCR) were examined from 145 isolates. Among these, 55 isolates were obtained during January-March 2000, 46 isolates during January-March 2002, and 44 isolates during October-December 2002. The occurrence of combination resistance between penicillin and quinolone was 20% in January-March 2000, which was increased to 57.8% during the period of October-December 2002 (P<0.0001). Mutation of Ser-91 in gyrA could be directly linked with the resistance or declining of susceptibility to ciprofloxacin. Using RAPD-PCR, we could classify the 145 isolates into 4 and 5 groups by primers D11344 (5'-AGTGAATTCGCGGTGAGATGCCA-3') and D8635 (5'-GAGCGGCCAAAGGGAG-CA GAC-3'), respectively. Combination of the data obtained from these two primers produced 11 fingerprint groups. Our findings conclude that monitoring of the Ser-91 mutation of gyrA and RAPD-PCR methods are most useful for epidemiological screening. J. Clin. Lab. Anal. 24:31-37, 2010. (C) 2010 Wiley-Liss, Inc.

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