Mismatch Repair of DNA Replication Errors Contributes to Microevolution in the Pathogenic Fungus Cryptococcus

Kylie J Boyce1, Yina Wang2, Surbhi Verma3

  • 1School of BioSciences, University of Melbourne, Parkville, Victoria, Australia kboyce@unimelb.edu.au alexander.idnurm@unimelb.edu.au.

Mbio
|June 1, 2017
PubMed

Insights

Cryptococcus neoformans utilizes a mutator phenotype, driven by DNA mismatch repair gene mutations, to rapidly adapt and cause disease. This enhanced mutation rate aids in antifungal resistance and virulence, crucial for fungal pathogenesis.

Area of Science:

  • Microbiology
  • Genetics
  • Pathogenesis

Background:

  • Microorganisms adapt to environmental changes, a critical factor for pathogens transitioning to host environments.
  • Cryptococcus neoformans, a major fungal pathogen, faces significant environmental shifts during infection.
  • The mutator phenotype, characterized by high-frequency DNA mutations, facilitates rapid adaptation.

Purpose of the Study:

  • To investigate the role of DNA mismatch repair genes in the mutator phenotype of Cryptococcus neoformans.
  • To determine how enhanced mutation rates influence fungal adaptation, virulence, and antifungal resistance.
  • To understand the evolutionary strategies employed by C. neoformans during host colonization and disease progression.

Main Methods:

  • Whole-genome analysis of clinical isolates exhibiting a mutator phenotype.
  • Identification and confirmation of mutations in the MSH2 mismatch repair gene.
  • Comparative analysis of mutation rates in deletion strains of eight mismatch repair pathway genes (MSH2, MLH1, PMS1).

Main Results:

  • Mutations in MSH2 were identified as responsible for the mutator phenotype in clinical C. neoformans isolates.
  • Loss of MSH2, MLH1, or PMS1 significantly increased mutation rates.
  • Increased mutation rates facilitated rapid microevolution, enhancing traits for in vivo growth and antifungal resistance, though PMS1 mutation reduced virulence.

Conclusions:

  • C. neoformans leverages a mutator phenotype, specifically through mutations in mismatch repair genes, to adapt and cause disease.
  • This microevolutionary strategy allows for rapid acquisition of advantageous traits like antifungal resistance without significant fitness costs.
  • Enhanced mutation rates likely represent a common mechanism contributing to fungal pathogenesis across different species.

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