A spontaneous mutation in DNA polymerase POL3 during in vitro passaging causes a hypermutator phenotype in Cryptococcus species
Open accessAbstract
Passaging of microbes in vitro can lead to the selection of microevolved derivatives with differing properties to their original parent strains. One well characterised instance is the phenotypic differences observed between the series of strains derived from the type strain of the human pathogenic fungus Cryptococcus neoformans. A second case was reported in the close relative Cryptococcus deneoformans, in which a well-studied isolate ATCC 24067 (52D) altered its phenotypic characteristics after in vitro passaging in different laboratories. One of these derivatives, ATCC 24067A, has decreased virulence and also exhibits a hypermutator phenotype, in which the mutation rate is increased compared to wild type. In this study, the molecular basis behind the changes in the lineage of ATCC 24067 was determined by next-generation sequencing of the parent and passaged strain genomes. This analysis resulted in the identification of a point mutation that causes a D270G amino acid substitution within the exonuclease proofreading domain of the DNA polymerase delta subunit encoded by POL3. Complementation with POL3 confirmed that this mutation is responsible for the hypermutator phenotype of this strain. Regeneration of the mutation in C. neoformans, to eliminate the additional mutations present in the ATCC 24067A genetic background, demonstrated that the hypermutator phenotype of the pol3 D270G mutant causes rapid microevolution in vitro but does not result in decreased virulence. These findings indicate that mutator strains can emerge in these pathogenic fungi without conferring a fitness cost, but the subsequent rapid accumulation of mutations can be deleterious.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
A mutation in the proofreading domain of POL3 was shown to confer the hypermutator phenotype.
“a mutation in the proofreading domain of POL3 (encoding the catalytic subunit of DNA polymerase δ) was also shown to confer the hypermutator phenotype31.”
From Treatment strategies for cryptococcal infection: challenges, advances and future outlook (2021) · cites this paper as [31]
A subset of Cryptococcus isolates have been identified as hypermutator strains, which contain mutations in core genes in the DNA mismatch repair pathway, most notably MSH2.
“a subset of Cryptococcus isolates have been identified as hypermutator strains30,31, which contain mutations in core genes in the DNA mismatch repair pathway, most notably MSH2 (refs30,32,33)”
From Treatment strategies for cryptococcal infection: challenges, advances and future outlook (2021) · cites this paper as [31]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Kearse, M., Moir, R., Wilson, A., Stones-Havas, S., Cheung, M., Sturrock, S., Buxton, S., Cooper, A., Markowitz, S., Duran, C., et al. (2012) · Bioinform. · doi:10.1093/bioinformatics/bts199 · Cited by 19,197 · see citing works
Global burden of disease of HIV-associated cryptococcal meningitis: an updated analysis
Rajasingham, R., Smith, R. M., Park, B. J., Jarvis, J. N., Govender, N. P., Chiller, T. M., Denning, D. W., Loyse, A., & Boulware, D. R. (2017) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(17)30243-8 · Cited by 1,861 · see citing works
High Frequency of Hypermutable Pseudomonas aeruginosa in Cystic Fibrosis Lung Infection
Oliver, A., Cantón, R., Campo, P., Baquero, F., & Blázquez, J. (2000) · Science · doi:10.1126/science.288.5469.1251 · Cited by 1,466 · see citing works
High Mutation Frequencies Among Escherichia coli and Salmonella Pathogens
LeClerc, J. E., Li, B., Payne, W. L., & Cebula, T. A. (1996) · Science · doi:10.1126/science.274.5290.1208 · Cited by 818 · see citing works
The Genome of the Basidiomycetous Yeast and Human Pathogen Cryptococcus neoformans
Loftus, B., Fung, E., Roncaglia, P., Rowley, D., Amedeo, P., Bruno, D., Vamathevan, J. J., Miranda, M., Anderson, I., Fraser, J. A., et al. (2005) · Science · doi:10.1126/science.1103773 · Cited by 694 · see citing works
Gene transfer in Cryptococcus neoformans by use of biolistic delivery of DNA
Toffaletti, D. L., Rude, T. H., Johnston, S. A., Durack, D. T., & Perfect, J. R. (1993) · Journal of Bacteriology · doi:10.1128/jb.175.5.1405-1411.1993 · Cited by 488 · see citing works
Systematic Genetic Analysis of Virulence in the Human Fungal Pathogen Cryptococcus neoformans
Liu, O. W., Chun, C. D., Chow, E. D., Chen, C., Madhani, H. D., & Noble, S. M. (2008) · Cell · doi:10.1016/j.cell.2008.07.046 · Cited by 443 · see citing works
Evolution of mutation rates in bacteria
Denamur, É., & Matić, I. (2006) · Molecular Microbiology · doi:10.1111/j.1365-2958.2006.05150.x · Cited by 402 · see citing works
Sexual Cycle of Cryptococcus neoformans var. grubii and Virulence of Congenic a and α Isolates
Nielsen, K., Cox, G. M., Wang, P., Toffaletti, D. L., Perfect, J. R., & Heitman, J. (2003) · Infection and Immunity · doi:10.1128/iai.71.9.4831-4841.2003 · Cited by 383 · see citing works
Hall, B. M., Ma, C.-X., Liang, P., & Singh, K. K. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp253 · Cited by 375 · see citing works
Janbon, G., Ormerod, K. L., Paulet, D., Byrnes, E. J., Yadav, V., Chatterjee, G., Mullapudi, N., Hon, C.-C., Billmyre, R. B., Brunel, F., et al. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004261 · Cited by 369 · see citing works
Self-citationHealey, K. R., Zhao, Y., Perez, W. B., Lockhart, S. R., Sobel, J. D., Farmakiotis, D., Kontoyiannis, D. P., Sanglard, D., Taj-Aldeen, S. J., Alexander, B. D., et al. (2016) · Nature Communications · doi:10.1038/ncomms11128 · Cited by 276 · see citing works
Pathway correcting DNA replication errors in Saccharomyces cerevisiae.
Morrison, A., Johnson, A. L., Johnston, L. H., & Sugino, A. (1993) · The EMBO Journal · doi:10.1002/j.1460-2075.1993.tb05790.x · Cited by 264 · see citing works
Serologic Grouping of Cryptococcus neoformans
Wilson, D. E., Bennett, J. E., & Bailey, J. W. (1968) · Experimental Biology and Medicine · doi:10.3181/00379727-127-32812 · Cited by 222 · see citing works
Tran, H. T., Gordenin, D. A., & Resnick, M. A. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.3.2000 · Cited by 201 · see citing works
Systematic functional profiling of transcription factor networks in Cryptococcus neoformans
Jung, K., Yang, D., Maeng, S., Lee, K.-T., So, Y.-S., Hong, J., Choi, J., Byun, H.-J., Kim, H., Bang, S., et al. (2015) · Nature Communications · doi:10.1038/ncomms7757 · Cited by 200 · see citing works
Franzot, S. P., Mukherjee, J., Cherniak, R., Chen, L.-C., Hamdan, J. S., & Casadevall, A. (1998) · Infection and Immunity · doi:10.1128/iai.66.1.89-97.1998 · Cited by 168 · see citing works
Systematic functional analysis of kinases in the fungal pathogen Cryptococcus neoformans
Lee, K.-T., So, Y.-S., Yang, D., Jung, K.-W., Choi, J., Lee, D., Kwon, H., Jang, J., Wang, L. L., Cha, S., et al. (2016) · Nature Communications · doi:10.1038/ncomms12766 · Cited by 166 · see citing works
Fijałkowska, I. J., & Schaaper, R. M. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.7.2856 · Cited by 160 · see citing works
Jin, Y. H., Obert, R., Burgers, P., Kunkel, T. A., Resnick, M. A., & Gordenin, D. A. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.091095198 · Cited by 158 · see citing works
Mutational landscape of yeast mutator strains
Serero, A., Jubin, C., Loeillet, S., Legoix-Né, P., & Nicolas, A. G. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1314423111 · Cited by 126 · see citing works
Lang, G. I., Parsons, L., & Gammie, A. E. (2013) · G3 Genes Genomes Genetics · doi:10.1534/g3.113.006429 · Cited by 107 · see citing works
Boyce, K. J., Wang, Y., Verma, S., Shakya, V. P. S., Xue, C., & Idnurm, A. (2017) · mBio · doi:10.1128/mbio.00595-17 · Cited by 101 · see citing works
Self-citationRhodes, J., Beale, M. A., Vanhove, M., Jarvis, J. N., Kannambath, S., Simpson, J. A., Ryan, A., Meintjes, G., Harrison, T. S., Fisher, M. C., et al. (2017) · G3 Genes|Genomes|Genetics · doi:10.1534/g3.116.037499 · Cited by 100 · see citing works
Billmyre, R. B., Croll, D., Li, W., Mieczkowski, P., Carter, D. A., Cuomo, C. A., Kronstad, J. W., & Heitman, J. (2014) · mBio · doi:10.1128/mbio.01494-14 · Cited by 90 · see citing works
Magditch, D. A., Liu, T., Xue, C., & Idnurm, A. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002936 · Cited by 85 · see citing works
Self-citationBillmyre, R. B., Clancey, S. A., & Heitman, J. (2017) · eLife · doi:10.7554/elife.28802 · Cited by 79 · see citing works
Serial Isolates ofCryptococcus neoformansfrom Patients with AIDS Differ in Virulence for Mice
Fries, B. C., & Casadevall, A. (1998) · The Journal of Infectious Diseases · doi:10.1086/314521 · Cited by 76 · see citing works
Mutator Suppression and Escape from Replication Error–Induced Extinction in Yeast
Herr, A. J., Ogawa, M., Lawrence, N. A., Williams, L. N., Eggington, J. M., Singh, M., Smith, R. A., & Preston, B. D. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002282 · Cited by 76 · see citing works
Dellière, S., Healey, K., Gits-Muselli, M., Carrara, B., Barbaro, A., Guigue, N., Lecefel, C., Touratier, S., Desnos-Ollivier, M., Perlin, D. S., et al. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.02038 · Cited by 75 · see citing works
Kwon-Chung, K. J., Varma, A., Edman, J. C., & Bennett, J. E. (1992) · Medical Mycology · doi:10.1080/02681219280000081 · Cited by 66 · see citing works
Sullivan, D. J., Haynes, K., Moran, G. P., Shanley, D. B., & Coleman, D. C. (1996) · Journal of Clinical Microbiology · doi:10.1128/jcm.34.7.1739-1744.1996 · Cited by 65 · see citing works
Ianiri, G., & Idnurm, A. (2015) · mBio · doi:10.1128/mbio.02334-14 · Cited by 62 · see citing works
Self-citationA Tetrad Analysis of the Basidiomycete Fungus Cryptococcus neoformans
Idnurm, A. (2010) · Genetics · doi:10.1534/genetics.109.113027 · Cited by 62 · see citing works
Self-citation<i>bz-rates</i>: A Web Tool to Estimate Mutation Rates from Fluctuation Analysis
Gillet-Markowska, A., Louvel, G., & Fischer, G. (2015) · G3 Genes|Genomes|Genetics · doi:10.1534/g3.115.019836 · Cited by 58 · see citing works
Singh, A., Healey, K. R., Yadav, P., Upadhyaya, G., Sachdeva, N., Sarma, S., Kumar, A., Tarai, B., Perlin, D. S., & Chowdhary, A. (2018) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00195-18 · Cited by 56 · see citing works
Blasi, E., Brozzetti, A., Francisci, D., Neglia, R. G., Cardinali, G., Bistoni, F., Vidotto, V., & Baldelli, F. (2001) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s100960100549 · Cited by 53 · see citing works
Byun, S. A., Won, E. J., Kim, M., Lee, W. G., Lee, K., Lee, H. S., Uh, Y., Healey, K. R., Perlin, D. S., Choi, M. J., et al. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01523 · Cited by 51 · see citing works
Convergent microevolution of Cryptococcus neoformans hypervirulence in the laboratory and the clinic
Arras, S. D. M., Ormerod, K. L., Erpf, P. E., Espinosa, M. I., Carpenter, A. C., Blundell, R. D., Stowasser, S. R., Schulz, B. L., Tanurdžić, M., & Fraser, J. A. (2017) · Scientific Reports · doi:10.1038/s41598-017-18106-2 · Cited by 46 · see citing works
Verma, S., & Idnurm, A. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003769 · Cited by 45 · see citing works
Self-citationThe ZIP family zinc transporters support the virulence ofCryptococcus neoformans
Do, E., Hu, G., Caza, M., Kronstad, J. W., & Jung, W. H. (2016) · Medical Mycology · doi:10.1093/mmy/myw013 · Cited by 45 · see citing works
Fusco‐Almeida, A. M., Matsumoto, M. T., Baeza, L. C., Silva, R. B. D. O. E., Kleiner, A. A. P., Melhem, M. D. S. C., & Mendes‐Giannini, M. J. S. (2006) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2006.00128.x · Cited by 44 · see citing works
The Role of Amino Acid Permeases and Tryptophan Biosynthesis in Cryptococcus neoformans Survival
Fernandes, J. D. S., Martho, K. F., Tofik, V., Vallim, M. A., & Pascon, R. C. (2015) · PLoS ONE · doi:10.1371/journal.pone.0132369 · Cited by 43 · see citing works
Phenotypic switching and its implications for the pathogenesis ofCryptococcus neoformans
Jain, N., Guerrero, A., & Fries, B. C. (2006) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2006.00039.x · Cited by 38 · see citing works
Canfield, G. S., Schwingel, J. M., Foley, M. H., Vore, K. L., Boonanantanasarn, K., Gill, A. L., Sutton, M. D., & Gill, S. R. (2012) · Journal of Bacteriology · doi:10.1128/jb.00733-12 · Cited by 38 · see citing works
van Pel, D. M., Stirling, P. C., Minaker, S. W., Sipahimalani, P., & Hieter, P. (2013) · G3 Genes Genomes Genetics · doi:10.1534/g3.112.004754 · Cited by 37 · see citing works
Shor, E., Schuyler, J., & Perlin, D. S. (2019) · mBio · doi:10.1128/mbio.00120-19 · Cited by 19 · see citing works
Chitty, J. L., McMahon, K. L., Blundell, R. D., Koh, Y. Q. A. E., Thompson, M., Robertson, A. A. B., Butler, M. S., Cooper, M. A., Kappler, U., Williams, S. J., et al. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.787994 · Cited by 18 · see citing works
Mahabeer, Y., Chang, C. C., Naidu, D., Dorasamy, A., Lewin, S. R., Ndung’u, T., Moosa, M.-Y., French, M. A., Mlisana, K. P., & Coovadia, Y. M. (2014) · Diagnostic Microbiology and Infectious Disease · doi:10.1016/j.diagmicrobio.2014.09.006 · Cited by 15 · see citing works
Correction: Mutator Suppression and Escape from Replication Error–Induced Extinction in Yeast
Herr, A. J., Ogawa, M., Lawrence, N. A., Williams, L. N., Eggington, J. M., Singh, M., Smith, R. A., & Preston, B. D. (2011) · PLoS Genetics · doi:10.1371/annotation/db1d9553-4ebd-4015-a1cd-c483dbc0d7e5 · Cited by 14 · see citing works
Wollschlaeger, C., Trevijano‐Contador, N., Wang, X., Legrand, M., Zaragoza, Ó., Heitman, J., & Janbon, G. (2014) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2014.09.007 · Cited by 11 · see citing works
Lighting Up Mutation: a New Unbiased System for the Measurement of Microbial Mutation Rates
Boyce, K. J., & Idnurm, A. (2019) · mBio · doi:10.1128/mbio.00740-19 · Cited by 5 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Treatment strategies for cryptococcal infection: challenges, advances and future outlook
Iyer, K. R., Revie, N. M., Fu, C., Robbins, N., & Cowen, L. E. (2021) · Nature Reviews Microbiology · doi:10.1038/s41579-021-00511-0 · Cited by 363 · see citing works
Advances in understanding the evolution of fungal genome architecture
Priest, S. J., Yadav, V., & Heitman, J. (2020) · F1000Research · doi:10.12688/f1000research.25424.1 · Cited by 60 · see citing works
The interplay of phenotype and genotype inCryptococcus neoformansdisease
Altamirano, S., Jackson, K. M., & Nielsen, K. (2020) · Bioscience Reports · doi:10.1042/bsr20190337 · Cited by 46 · see citing works
Mutators Enhance Adaptive Micro-Evolution in Pathogenic Microbes
Boyce, K. J. (2022) · Microorganisms · doi:10.3390/microorganisms10020442 · Cited by 34 · see citing works
Self-citationEpigenetic Regulation of Antifungal Drug Resistance
Patra, S., Raney, M., Pareek, A., & Kaur, R. (2022) · Journal of Fungi · doi:10.3390/jof8080875 · Cited by 33 · see citing works
Short-term evolution strategies for host adaptation and drug escape in human fungal pathogens
Beekman, C. N., & Ene, I. V. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1008519 · Cited by 30 · see citing works
Edwards, H. M., Cogliati, M., Kwenda, G., & Fisher, M. C. (2021) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiab093 · Cited by 18 · see citing works
Recent insights into the evolution of mutation rates in yeast
Melde, R. H., Bao, K. H., & Sharp, N. P. (2022) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2022.101953 · Cited by 14 · see citing works
Distinct evolutionary trajectories following loss of RNA interference in Cryptococcus neoformans
Huang, J. T., Larmore, C. J., Priest, S. J., Xu, Z. Z., Dietrich, F. S., Yadav, V., Magwene, P. M., Sun, S., & Heitman, J. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2416656121 · Cited by 15 · see citing works
Jung, K., Jung, J., & Park, H. Y. (2021) · Journal of Fungi · doi:10.3390/jof7070566 · Cited by 13 · see citing works
Albehaijani, S. H. I., Macreadie, I. G., Morrissey, C. O., & Boyce, K. J. (2022) · JAC-Antimicrobial Resistance · doi:10.1093/jacamr/dlac033 · Cited by 13 · see citing works
Self-citationDrivers of diversification in fungal pathogen populations
Murante, D., & Hogan, D. A. (2024) · PLoS Pathogens · doi:10.1371/journal.ppat.1012430 · Cited by 6 · see citing works
Tsarin, L., & Shcherbakova, P. V. (2025) · Database · doi:10.1093/database/baaf076 · Cited by 3 · see citing works
Paths to pathogenicity: exploring the diversity and evolution of Cryptococcus neoformans
Leinas, J. T., Ruzic, M., & Hilbert, Z. A. (2026) · npj Fungal Science · doi:10.1038/s44512-026-00001-4
- Authors
- Boyce, K. J., Cao, C., Xue, C., & Idnurm, A.
- Affiliations
- RMIT University (AU)
- Rutgers, The State University of New Jersey (US)
- The University of Melbourne (AU)
- Corresponding author
- Boyce, Kylie J.
- Idnurm, Alexander
- Venue
- DNA Repair
- Publisher
- Elsevier BV
- Published
- 2020-02
- Volume
- 86
- Pages
- 102751
- ISSN
- 1568-7856 (ISSN-L)
- 1568-7864
- PMC
- PMC7542539
- OpenAlex
- W2990757339
- Cited by
- 14
- References
- 52
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 2 · 2022: 4 · 2021: 3 · 2020: 3
- FWCI
- 1.90
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- DNA repair (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RMIT Research Repository (RMIT University Library) (submittedVersion)
- Figshare (submittedVersion, cc-by)
- Minerva Access (University of Melbourne) (submittedVersion)
- Funders
- Australian Research Council (FT130100146, LP170100548)
- Topics
- Health Sciences › Medicine › Epidemiology › Fungal Infections and Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
- Keywords
- hypermutator phenotype, DNA polymerase delta, Cryptococcus neoformans, Cryptococcus deneoformans, microevolution, mutator strains, virulence, fungal genome sequencing, complementation
- MeSH terms
- Animals, Cryptococcosis, Cryptococcus neoformans, DNA Polymerase III, Fungal Proteins, Phenotype, Serial Passage, Point Mutation, Sequence Analysis, DNA, Amino Acid Substitution, Mice, High-Throughput Nucleotide Sequencing
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review