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Comparative Study
. 2014 May;21(5):636-40.
doi: 10.1128/CVI.00760-13. Epub 2014 Mar 5.

Serodiagnosis as adjunct assay for pertussis infection in São Paulo, Brazil

Affiliations
Comparative Study

Serodiagnosis as adjunct assay for pertussis infection in São Paulo, Brazil

Lourdes R A Vaz-de-Lima et al. Clin Vaccine Immunol. 2014 May.

Abstract

Pertussis remains an important public health problem in many countries despite extensive immunization. Cultures and real-time PCR (RT-PCR) assays are the recommended pertussis diagnostic tests, but they lack sensitivity at the later stage of the disease. This study introduces the IgG anti-pertussis toxin enzyme-linked immunosorbent assay (PT ELISA) in our routine diagnosis to improve disease burden estimation. Serum samples and nasopharyngeal swabs (n = 503) were collected at the same time from patients presenting with cough illness suspected of being pertussis and tested by the PT ELISA and culture and/or RT-PCR, respectively. Patients were separated into three age groups: group 1, <1 year (n = 260; mean age, 3 months), group 2, 1 to 6 years (n = 81; mean age, 3 years), and group 3, ≥7 years (n = 162; mean age, 26 years). The times (means) from cough onset to specimen collection were 16, 24, and 26 days, respectively. In group 1, 83 (82.2%) of 101 positive cases were positive for pertussis by culture/RT-PCR, while 40 (39.6%) tested positive by PT ELISA. In group 2, 6 (19.4%) of 31 positive cases were culture/RT-PCR positive, and 29 (93.6%) were seropositive. In group 3, 13 (13.8%) of 94 positive cases were positive by culture/RT-PCR and 91 (96.8%) were positive by serology. Culture/RT-PCR detected more cases of pertussis in infants (P < 0.0001), whereas the PT ELISA detected more cases in adolescents and adults (P < 0.0001). The timing between cough onset and specimen collection or recent vaccination may have partially affected our results. Serology is a suitable, cost-effective, and complementary pertussis diagnostic tool, especially among older children, adolescents, and adults during the later disease phase.

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Figures

FIG 1
FIG 1
Proportion of positive pertussis cases diagnosed by culture and/or RT-PCR, PT ELISA, and combined assays, stratified by age. m, months; y, years.
FIG 2
FIG 2
Proportion of positive cases diagnosed by culture and/or RT-PCR and PT ELISA stratified by time since cough onset in weeks (w). The total number of subjects per time point was used as the denominator. (A) Analysis based on time of symptoms for all reported cases; (B) cases separated by age groups: group 1 (<1 year), group 2 (1 to 6 years), and group 3 (≥7 years).

References

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