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

Citation
Jr. Dillon et al., A PCR assay for discriminating Neisseria gonorrhoeae beta-lactamase-producing plasmids, MOL CELL PR, 13(2), 1999, pp. 89-92
Citations number
12
Categorie Soggetti
Molecular Biology & Genetics
Journal title
MOLECULAR AND CELLULAR PROBES
ISSN journal
08908508 → ACNP
Volume
13
Issue
2
Year of publication
1999
Pages
89 - 92
Database
ISI
SICI code
0890-8508(199904)13:2<89:APAFDN>2.0.ZU;2-S
Abstract
Oligonucleotide primers were developed for use in polymerase chain reaction (PCR) assays to differentiate three related, epidemic beta-lactamase-produ cing plasmids of Neisseria gonorrhoeae-the Asia-(7426 bp), Africa-(5599 bp) and Toronto-(5154 bp) type plasmids. One-hundred and two N. gonorrhoeae is olates with different plasmid profiles were tested-16 isolates carried the Asia plasmid, 41 isolates contained the Africa plasmid, 16 isolates contain ed the Toronto plasmid and 29 isolates contained no beta-lactamase-producin g plasmids. Most (101/102) isolates also carried the gonococcal cryptic pla smid, 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 usefu l for rapidly detecting the presence of gonococcal beta-lactamase-producing plasmids in clinical samples and discriminating them for epidemiological t yping. (C) 1999 Academic Press.