Nh. Birkebaek et al., BORDETELLA-PERTUSSIS DIAGNOSED BY POLYMERASE CHAIN-REACTION, APMIS. Acta pathologica, microbiologica et immunologica Scandinavica, 102(4), 1994, pp. 291-294
The object of this work was to test the polymerase chain reaction (PCR
) for demonstration of Bordetella pertussis (BP) in nasopharyngeal sec
retions. The method was applied to patients with recently diagnosed pe
rtussis, as verified by BP culture. In order to test the sensitivity a
nd specificity of PCR for the diagnosis of BP, we used known concentra
tions of BP, Bordetella parapertussis and Bordetella bronchiseptica in
aqueous solutions. PCR was furthermore carried out on species of bact
eria that might be isolated from the nasopharynx. The applicability of
PCR to patient specimens was tested in 25 patients in whose nasophary
ngeal secretions BP had been demonstrated after 4-7 days of culture. T
he detection limit of PCR in aqueous solution was 1-2 BP bacteria per
reaction tube. PCR was 100% specific for BP, showing no response with
other Bordetella species or other bacteria known to colonize the nasop
harynx. Of 25 patient specimens, 16 were PCR-positive 4-7 days after t
he positive primary culture had been established; only 5 out of 13 pat
ient specimens were positive by repeated conventional nasopharyngeal c
ulture at that time. We conclude that PCR is a possible alternative to
culture for the demonstration of BP, as PCR is considerably faster th
an culture and might be more sensitive.