Multi-serotype pneumococcal nasopharyngeal carriage prevalence in vaccine naïve Nepalese children, assessed using

Rama Kandasamy1, Meeru Gurung2, Anushil Thapa2

  • 1Oxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom; NIHR Oxford Biomedical Research Centre, Oxford, United Kingdom.

Plos One
|February 3, 2015
PubMed

Insights

Most young children in Nepal carry multiple pneumococcal serotypes, highlighting the need for effective vaccines. This study used advanced molecular methods to understand pneumococcal carriage before vaccine introduction.

Area of Science:

  • Microbiology
  • Epidemiology
  • Vaccinology

Background:

  • Invasive pneumococcal disease (IPD) is a significant cause of mortality in young children, particularly in low-resource settings.
  • Nasopharyngeal carriage studies are crucial for understanding the prevalence of Streptococcus pneumoniae serotypes.
  • Data on concurrent carriage of multiple pneumococcal serotypes are limited.

Purpose of the Study:

  • To determine the prevalence and serotype distribution of nasopharyngeal pneumococcal carriage in healthy Nepalese children before pneumococcal conjugate vaccine (PCV) introduction.
  • To utilize a microarray-based molecular serotyping method to detect multi-serotype carriage.

Main Methods:

  • A cross-sectional study was conducted on 600 healthy children (6 weeks to 24 months) in the Kathmandu Valley, Nepal (May-October 2012).
  • Nasopharyngeal swabs were cultured, and DNA extracts were analyzed using a molecular serotyping microarray.
  • The microarray identified the relative abundance of multiple pneumococcal serotypes.

Main Results:

  • Typeable pneumococci were found in 49.5% of samples (297/600).
  • Multi-serotype carriage was observed in 20.2% of positive samples (67/297).
  • Serotypes targeted by the 13-valent PCV were present in 44.4% of samples with typeable pneumococci.

Conclusions:

  • Molecular serotyping reveals a substantial prevalence of pneumococcal co-colonization in young children in Nepal.
  • This approach provides a more accurate understanding of vaccine efficacy against carriage and replacement dynamics post-PCV introduction.
  • Continued surveillance using this method is recommended to monitor serotype and genotype replacement after PCV implementation.