1994
DOI: 10.1136/jcp.47.4.353
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Polymerase chain reaction for screening clinical isolates of corynebacteria for the production of diphtheria toxin.

Abstract: Aims-To assess the performance of the polymerase chain reaction (PCR) when used to screen rapidly large numbers of corynebacteria for toxin production; and to determine the incidence of false positive PCR results with non-toxigenic Corynebacterium diphtheriae isolates. Methods-Eighty seven recent British isolates of corynebacteria were assayed by PCR. All isolates were assayed from both blood and telilurite agar within a five day period. Thirty three non-toxigenic isolates of C diphtheriae from six countries w… Show more

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Cited by 79 publications
(70 citation statements)
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“…The isolate was also consistent for C. diphtheriae using cellular fatty acid composition analysis (1). PCR detection of the diphtheria tox gene was positive for both the 248-bp fragment and the complete tox gene (7,13). The modified Elek test (8), used to determine production of the diphtheria toxin, was positive after 24 h of incubation.…”
Section: Case Reportmentioning
confidence: 99%
“…The isolate was also consistent for C. diphtheriae using cellular fatty acid composition analysis (1). PCR detection of the diphtheria tox gene was positive for both the 248-bp fragment and the complete tox gene (7,13). The modified Elek test (8), used to determine production of the diphtheria toxin, was positive after 24 h of incubation.…”
Section: Case Reportmentioning
confidence: 99%
“…However, data are not yet sufficient for PCR to be accepted as a criterion for laboratory confirmation. PCR may be used with caution because some isolates of C. diphtheriae present toxin genes but fail to express a biologically active toxin (Pallen et al 1994, Efstratiou et al 1998, 2000.…”
Section: Laboratory Diagnosismentioning
confidence: 99%
“…The toxigenicity of C. diphtheriae strains was confirmed by the Elek test, by polymerase chain reaction (PCR) using a primer pair targeted to a portion of fragment A of tox gene (PCR-DTA; 258 bp) and by the "goldstandard" Vero cell cytotoxicity assay (Pallen et al 1994, Efstratiou et al 1998 (Table).…”
Section: Methodsmentioning
confidence: 99%