Serotype 3 is a common serotype causing invasive pneumococcal disease in children less than 5 years old, as

L Selva1, P Ciruela, C Esteva

  • 1Molecular Microbiology Department, Hospital Universitari Sant Joan de Déu, Passeig Sant Joan de Déu, 2, 08950, Esplugues de Llobregat, Barcelona, Spain.

Insights

Molecular methods like real-time PCR detect more pneumococcal serotypes in children with invasive pneumococcal disease (IPD) than traditional culture. Serotype 3 is significantly underdiagnosed by culture, highlighting its importance in pediatric IPD.

Area of Science:

  • * Pediatric Infectious Diseases
  • * Microbiology and Molecular Diagnostics
  • * Vaccine Preventable Diseases Epidemiology

Background:

  • * Streptococcus pneumoniae causes invasive pneumococcal disease (IPD), with serotype 3 frequently associated with severe illness in adults.
  • * Serotype 3 is notably underrepresented in pediatric IPD cases identified through standard bacterial culture methods.
  • * Accurate serotype distribution is crucial for effective vaccine strategies and understanding disease burden in children.

Purpose of the Study:

  • * To determine the serotype distribution of pediatric IPD using molecular methods, including culture-negative cases.
  • * To compare the efficacy of bacterial culture versus real-time polymerase chain reaction (PCR) in identifying pneumococcal serotypes in pediatric IPD.
  • * To assess the impact of diagnostic method on theoretical vaccine coverage rates.

Main Methods:

  • * Retrospective study of children under 5 years with IPD admitted to two hospitals in Catalonia, Spain (2007-2009).
  • * Implementation of sequential real-time multiplex polymerase chain reaction (PCR) alongside routine culture methods for detection and serotyping.
  • * Analysis of 257 IPD episodes, including pneumonia, meningitis, and bacteremia.

Main Results:

  • * Real-time PCR detected 66.5% of IPD cases exclusively, while culture identified only 33.5%.
  • * Culture-detected serotypes were primarily 1 (26.7%) and 19A (25.6%); PCR detected serotypes 1 (19.8%) and 3 (18.1%).
  • * Theoretical coverage by PCV13 was significantly lower for PCR-detected (60.2%) versus culture-detected (87.2%) episodes, indicating underdiagnosis of key serotypes like 3 by culture.

Conclusions:

  • * Multiplex real-time PCR is a valuable tool for comprehensive IPD surveillance studies in children.
  • * Bacterial culture significantly underdiagnoses serotype 3 in pediatric IPD, despite its association with serious disease.
  • * Accurate molecular diagnostics are essential for precise epidemiological assessment and informing pediatric vaccination policies.