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ABSTRACT: Background and objective
Due to contagiousness of pertussis, a rapid and sensitive method for diagnosis is required to initiate the treatment and interrupt its transmission.Materials and methods
To detect B. pertussis strains, we used two real-time PCR targeting IS481 and BP283 sequences and compared factors influencing culture and real-time PCR results.Results
Totally, 779 specimens were collected from patients among which 11 (1.4%) were culture positive. Using IS481 and BP283 primers, 122 (15.6%) and 100 (12.8%) were diagnosed as infected specimens respectively. There were significant relationships between the real-time PCR method for diagnosis of B. pertussis and age, sex and vaccination of patients before sampling.Conclusion
The real-time PCR is superior
SUBMITTER: Nikbin VS
PROVIDER: S-EPMC3895556 | biostudies-literature | 2013 Sep
REPOSITORIES: biostudies-literature