Mismatch Repair of DNA Replication Errors Contributes to Microevolution in the Pathogenic Fungus Cryptococcus neoformans
Related Experiment Video
Updated: Mar 1, 2026

Biolistic Transformation of a Fluorescent Tagged Gene into the Opportunistic Fungal Pathogen Cryptococcus neoformans
Published on: March 19, 2015
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.
Abstract:
The ability to adapt to a changing environment provides a selective advantage to microorganisms. In the case of many pathogens, a large change in their environment occurs when they move from a natural setting to a setting within a human host and then during the course of disease development to various locations within that host. Two clinical isolates of the human fungal pathogen Cryptococcus neoformans were identified from a collection of environmental and clinical strains that exhibited a mutator phenotype, which is a phenotype which provides the ability to change rapidly due to the accumulation of DNA mutations at high frequency. Whole-genome analysis of these strains revealed mutations in MSH2 of the mismatch repair pathway, and complementation confirmed that these mutations are responsible for the mutator phenotype. Comparison of mutation frequencies in deletion strains of eight mismatch repair pathway genes in C. neoformans showed that the loss of three of them, MSH2, MLH1, and PMS1, results in an increase in mutation rates. Increased mutation rates enable rapid microevolution to occur in these strains, generating phenotypic variations in traits associated with the ability to grow in vivo, in addition to allowing rapid generation of resistance to antifungal agents. Mutation of PMS1 reduced virulence, whereas mutation of MSH2 or MLH1 had no effect on the level of virulence. These findings thus support the hypothesis that this pathogenic fungus can take advantage of a mutator phenotype in order to cause disease but that it can do so only in specific pathways that lead to a mutator trait without a significant tradeoff in fitness.IMPORTANCE Fungi account for a large number of infections that are extremely difficult to treat; superficial fungal infections affect approximately 1.7 billion (25%) of the general population worldwide, and systemic fungal diseases result in an unacceptably high mortality rate. How fungi adapt to their hosts is not fully understood. This research investigated the role of changes to DNA sequences in adaption to the host environment and the ability to cause disease in Cryptococcus neoformans, one of the world's most common and most deadly fungal pathogens. The study results showed that microevolutionary rates are enhanced in either clinical isolates or in gene deletion strains with msh2 mutations. This gene has similar functions in regulating the rapid emergence of antifungal drug resistance in a distant fungal relative of C. neoformans, the pathogen Candida glabrata Thus, microevolution resulting from enhanced mutation rates may be a common contributor to fungal pathogenesis.
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.
Related Concept Videos
Mismatch Repair
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
Mismatch Repair
Genome Copying Errors
Viral Mutations
Nucleotide Excision Repair
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
Nucleotide Excision Repair

