Variation of the Mycobacterium tuberculosis PE_PGRS 33 gene among clinical isolates

Sarah Talarico1, M Donald Cave, Carl F Marrs

  • 1Epidemiology Department, School of Public Health, University of Michigan, 109 S. Observatory Street, Ann Arbor, MI 48109-2029, USA.

Insights

Genetic diversity in the PE_PGRS 33 gene of Mycobacterium tuberculosis was analyzed in 123 clinical isolates. Significant variations were found, supporting its role in immune evasion and antigenic variation.

Area of Science:

  • Microbiology
  • Genetics
  • Immunology

Background:

  • The PE_PGRS 33 gene in Mycobacterium tuberculosis is implicated in antigenic variation and immune system evasion.
  • Previous studies noted genetic differences in PE_PGRS 33 between reference strains, but variation in clinical isolates remained unevaluated.

Purpose of the Study:

  • To investigate the genetic diversity of the PE_PGRS 33 gene in clinical Mycobacterium tuberculosis isolates.
  • To understand the genetic basis of PE_PGRS 33's role in antigenic variation and immune evasion.

Main Methods:

  • PCR and DNA sequencing were used to analyze the PE_PGRS 33 gene.
  • 123 clinical Mycobacterium tuberculosis isolates from a population-based study were examined.

Main Results:

  • 68.3% of isolates (84/123) exhibited sequence variations in the PE_PGRS 33 gene compared to the H37Rv strain.
  • Twenty-five distinct variations were identified, including insertions, deletions, and single-nucleotide polymorphisms (synonymous and nonsynonymous).
  • Polymorphisms in the PE_PGRS 33 gene appear to shift along evolutionary lineages.

Conclusions:

  • The study reveals significant genetic diversity within the PE_PGRS 33 gene among clinical Mycobacterium tuberculosis isolates.
  • This genetic variation supports the proposed role of PE_PGRS 33 in antigenic variation and host immune system evasion.
  • Further research into the functional implications of PE_PGRS 33 diversity in clinical settings is warranted.

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