Distinct Streptococcus pneumoniae cause invasive disease in Papua New Guinea

Kate C Mellor1, Stephanie Lo1, Mition Yoannes2

  • 1Parasites and Microbes, Wellcome Sanger Institute, Hinxton, UK.

Microbial Genomics
|July 11, 2022
PubMed

Insights

Whole genome sequencing revealed diverse Streptococcus pneumoniae strains causing childhood invasive disease in Papua New Guinea before PCV13 introduction. Pre-vaccine strains showed varied antimicrobial resistance, with vaccine serotypes being more multidrug-resistant.

Area of Science:

  • Microbiology
  • Genomics
  • Epidemiology

Background:

  • Streptococcus pneumoniae is a major cause of childhood illness and death in Papua New Guinea.
  • Understanding the pneumococcal population before widespread vaccination is crucial for monitoring vaccine impact.

Purpose of the Study:

  • To characterize the diversity of S. pneumoniae causing invasive disease in young children in PNG using whole genome sequencing.
  • To establish a baseline of pneumococcal population structure, serotypes, and antimicrobial resistance prior to PCV13 introduction.

Main Methods:

  • Whole genome sequencing of 174 S. pneumoniae isolates from invasive disease cases in PNG (1989-2014).
  • Analysis of genetic diversity, serotype distribution, antimicrobial resistance profiles, and comparison with global isolates.
  • Identification of Global Pneumococcal Sequence Clusters (GPSCs) and unique PNG lineages.

Main Results:

  • A diverse S. pneumoniae population was identified, with 45 unique GPSCs, including lineages not previously reported globally.
  • Non-PCV13 serotypes were prevalent (52%) in meningitis cases. Over one-third of isolates exhibited antimicrobial resistance.
  • Isolates with PCV13 serotypes were significantly more likely to be multidrug-resistant (MDR) than non-vaccine serotype isolates.

Conclusions:

  • The pre-PCV13 pneumococcal population in PNG was diverse, with unique lineages and significant antimicrobial resistance.
  • PCV13 serotypes were associated with higher rates of multidrug resistance, highlighting potential impacts on resistance patterns post-vaccination.
  • Continued genomic surveillance is essential to track serotype replacement and antimicrobial resistance trends following PCV13 implementation.

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