PsrP, a Protective Pneumococcal Antigen, Is Highly Prevalent in Children with Pneumonia and Is Strongly Associated with Clonal Type
Author(s) -
Carmen MuñozAlmagro,
Laura Selva,
Carlos J. Sánchez,
Cristina Esteva,
Mariona Fernández de Sevilla,
Román Pallarés,
Carlos J. Orihuela
Publication year - 2010
Publication title -
clinical and vaccine immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.649
H-Index - 77
eISSN - 1556-6811
pISSN - 1556-679X
DOI - 10.1128/cvi.00271-10
Subject(s) - medicine , serotype , pneumonia , biology , immunology
Invasive pneumococcal disease (IPD) is a major health problem worldwide. Due to ongoing serotype replacement, current efforts are focused in an attempt to identify the pneumococcal antigens that could be used in a next-generation multivalent protein vaccine. The objective of our study was to use real-time PCR to determine the distribution and clonal type variability of PsrP, a protective pneumococcal antigen, among pneumococcal isolates from children with IPD or healthy nasopharyngeal carriers.psrP was detected in 52.4% of the 441 strains tested. While no differences were determined when the prevalence ofpsrP in colonizing strains (n = 89) versus that in all invasive strains (n = 352) was compared, a strong trend was observed when the prevalence ofpsrP in all pneumonia isolates (n = 209) and colonizing isolates (P = 0.067) was compared, and a significant difference was observed when the prevalence in all pneumonia isolates and those causing bacteremia (n = 76) was compared (P = 0.001). An age-dependent distribution ofpsrP was also observed, with the incidence ofpsrP being the greatest in strains isolated from children >2 years of age (P = 0.02). Strikingly, the presence ofpsrP within a serotype was highly dependent on the clonotype, with all isolates of invasive clones such as clonal complex 306 carryingpsrP (n = 88), whereas for sequence type 304, only 1 of 19 isolates carriedpsrP ; moreover, this was inversely correlated with antibiotic susceptibility. This finding suggests that inclusion ofpsrP in a vaccine formulation would not target resistant strains. We conclude thatpsrP is highly prevalent in strains that cause IPD but is most prevalent in strains isolated from older children with pneumonia. These data support the potential use of PsrP as one component in a multivalent protein-based vaccine.
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