Clonal characterisation of Streptococcus pneumoniae strains using MLST and MLVA - Can MLVA improve the

Abstract

Insights

Multilocus sequence typing (MLST) confirmed clonal characteristics of Streptococcus pneumoniae causing invasive pneumococcal disease in the Czech Republic. Multiple-locus variable number tandem repeat analysis (MLVA) showed higher discriminatory power but MLST remains the standard for surveillance.

Area of Science:

  • Microbiology
  • Epidemiology
  • Genetics

Background:

  • Invasive pneumococcal disease (IPD) surveillance is crucial for public health.
  • Understanding the clonal characteristics of Streptococcus pneumoniae (S. pneumoniae) aids in tracking disease spread and vaccine effectiveness.
  • Standardized methods are essential for reliable epidemiological data.

Purpose of the Study:

  • To determine the clonal characteristics of S. pneumoniae strains causing IPD in the Czech Republic in 2017.
  • To compare the utility of multilocus sequence typing (MLST) and multiple-locus variable number tandem repeat analysis (MLVA) for S. pneumoniae clonal assignment.
  • To assess the genetic variability within different S. pneumoniae serotypes.

Main Methods:

  • Utilized 87 S. pneumoniae isolates from the Czech Republic's IPD surveillance program in 2017.
  • Employed multilocus sequence typing (MLST), a global standard for bacterial isolate characterization.
  • Applied multiple-locus variable number tandem repeat analysis (MLVA) as a newly introduced method for clonal analysis.

Main Results:

  • MLST revealed clonal homogeneity for serotypes 1, 9N, 9V, and 22F, and genetic variability for serotypes 4 and 8.
  • A general correlation was observed between MLST and MLVA clonal complex assignments.
  • MLVA demonstrated superior clonal discriminatory power compared to MLST, identifying new MLVA types (MT).

Conclusions:

  • MLST remains the standard method for S. pneumoniae clonal characterization in national and international IPD surveillance.
  • MLVA can serve as a complementary method for rapid identification of clonal relatedness, particularly in local outbreaks.
  • MLVA is more suitable for detecting the emergence and spread of virulent clonal variants.