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Constructing Mutants in Serotype 1 Streptococcus pneumoniae strain 519/43
Published on: September 11, 2020
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.
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.
Abstract:
Streptococcus pneumoniae is a key contributor to childhood morbidity and mortality in Papua New Guinea (PNG). For the first time, whole genome sequencing of 174 isolates has enabled detailed characterisation of diverse S. pneumoniae causing invasive disease in young children in PNG, 1989-2014. This study captures the baseline S. pneumoniae population prior to the introduction of 13-valent pneumococcal conjugate vaccine (PCV13) into the national childhood immunisation programme in 2014. Relationships amongst lineages, serotypes and antimicrobial resistance traits were characterised, and the population was viewed in the context of a global collection of isolates. The analyses highlighted adiverse S. pneumoniae population associated with invasive disease in PNG, with 45 unique Global Pneumococcal Sequence Clusters (GPSCs) observed amongst the 174 isolates reflecting multiple lineages observed in PNG that have not been identified in other geographic locations. The majority of isolates were from children with meningitis, of which 52% (n=72) expressed non-PCV13 serotypes. Over a third of isolates were predicted to be resistant to at least one antimicrobial. PCV13 serotype isolates had 10.1 times the odds of being multidrug-resistant (MDR) compared to non-vaccine serotype isolates, and no isolates with GPSCs unique to PNG were MDR. Serotype 2 was the most commonly identified serotype; we identified a highly clonal cluster of serotype 2 isolates unique to PNG, and a distinct second cluster indicative of long-distance transmission. Ongoing surveillance, including whole-genome sequencing, is needed to ascertain the impact of the national PCV13 programme upon the S. pneumoniae population, including serotype replacement and antimicrobial resistance traits.
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