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Rare Detection of Bordetella pertussis Pertactin-Deficient Strains in Argentina. | LitMetric

AI Article Synopsis

  • Pertussis resurgence is linked to decreased vaccine immunity and bacteria adapting to evade vaccine protection, particularly in countries using the acellular pertussis vaccine.
  • Genetic analysis of B. pertussis isolates from Buenos Aires indicates a high prevalence of a specific allelic profile, with very few pertactin-deficient strains present since the adoption of whole-cell vaccines.
  • The findings imply that the presence of pertactin-deficient strains may be influenced by the widespread use of the acellular vaccine in other regions, necessitating further research in places like Argentina that primarily utilize whole-cell vaccines.

Article Abstract

Pertussis resurgence had been attributed to waning vaccine immunity and Bordetella pertussis adaptation to escape vaccine-induced immunity. Circulating bacteria differ genotypically from strains used in production of pertussis vaccine. Pertactin-deficient strains are highly prevalent in countries that use acellular vaccine (aP), suggesting strong aP-imposed selection of circulating bacteria. To corroborate this hypothesis, systematic studies on pertactin prevalence of infection in countries using whole-cell vaccine are needed. We provide pertussis epidemiologic data and molecular characterization of B. pertussis isolates from Buenos Aires, Argentina, during 2000-2017. This area used primary vaccination with whole-cell vaccine. Since 2002, pertussis case incidences increased at regular 4-year outbreaks; most cases were in infants <1 year of age. Of the B. pertussis isolates analyzed, 90.6% (317/350) contained the ptxP3-ptxA1-prn2-fim3-2 allelic profile. Immunoblotting and sequencing techniques detected only the 2 pertactin-deficient isolates. The low prevalence of pertactin-deficient strains in Argentina suggests that loss of pertactin gene expression might be driven by aP vaccine.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6810201PMC
http://dx.doi.org/10.3201/eid2511.190329DOI Listing

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