Do not let perfect be the enemy of good: the current reality of Bordetella testing
Diagnosis of is made by using polymerase chain reaction (PCR) to detect insertion sequence 481 (IS ). However, IS is found in both and . In a recent study, Cole et al. (Microbiol Spectr 12:e00783-24. https://doi.org/10.1128/spectrum.00783-24) compared the accuracy of assays performed at two differen...
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Veröffentlicht in: | Microbiology spectrum 2025-01, Vol.13 (1), p.e0221024 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Diagnosis of
is made by using polymerase chain reaction (PCR) to detect insertion sequence 481 (IS
). However, IS
is found in both
and
. In a recent study, Cole et al. (Microbiol Spectr 12:e00783-24. https://doi.org/10.1128/spectrum.00783-24) compared the accuracy of assays performed at two different commercial laboratories that used IS
as a molecular target against a multiplex PCR assay performed at the Centers for Disease Control and Prevention (CDC) that can differentiate the different
species. The results demonstrated that the overall agreement among the assays from the commercial laboratories and the CDC was 85%. Only a small percentage (1.4%) of specimens positive for IS
were identified as
. This study suggests that PCR tests using IS
as a target provide reliable diagnosis for pertussis. However, end users should recognize the limitations of PCR testing for pertussis including the inability to differentiate and monitor transmission of non-pertussis
species. |
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ISSN: | 2165-0497 2165-0497 |
DOI: | 10.1128/spectrum.02210-24 |