A PCR assay for discriminating Neisseria gonorrhoeae β-lactamase-producing plasmids

被引:32
作者
Dillon, JR
Li, H
Yeung, KH
Aman, TA
机构
[1] Univ Ottawa, Dept Biochem Microbiol & Immunol, Ottawa, ON K1H 8M5, Canada
[2] Univ Ottawa, Dept Biol, Ottawa, ON K1H 8M5, Canada
[3] Hlth Canada, Ottawa, ON K1A 0L2, Canada
关键词
Neisseria gonorrhoeae; PCR; beta-lactamase-producing plasmids; DNA sequence; diagnostic test;
D O I
10.1006/mcpr.1998.0216
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Oligonucleotide primers were developed for use in polymerase chain reaction (PCR) assays to differentiate three related, epidemic beta-lactamase-producing plasmids of Neisseria gonorrhoeae-the Asia-(7426 bp), Africa-(5599 bp) and Toronto-(5154 bp) type plasmids. One-hundred and two N. gonorrhoeae isolates with different plasmid profiles were tested-16 isolates carried the Asia plasmid, 41 isolates contained the Africa plasmid, 16 isolates contained the Toronto plasmid and 29 isolates contained no beta-lactamase-producing plasmids. Most (101/102) isolates also carried the gonococcal cryptic plasmid, while 27/102 and 44/102 isolates carried either the transfer plasmid or the tetM-containing plasmids, respectively. The assay was 100% sensitive and specific for identifying the correct plasmid type. This assay is useful for rapidly detecting the presence of gonococcal beta-lactamase-producing plasmids in clinical samples and discriminating them for epidemiological typing. (C) 1999 Academic Press.
引用
收藏
页码:89 / 92
页数:4
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