Evidence map›Paper›PMID 40839773›Full record

ArticleGenetics2025

Distinct routes to thermotolerance in the fungal pathogen Cryptococcus neoformans.

Mara J W Schwiesow, Leah A Farinella, Marina Ruzic, Jake T Leinas, Nels C Elde, Zoë A Hilbert

Abstract read
In one paragraph

Article in Genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Set202 is a histone lysine methyltransferase that enablesbioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Thermal adaptation crosstalk with azole response through lncRNA inbioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Mara J W SchwiesowDepartment of Human Genetics, The University of Utah, Salt Lake City, UT 84112, United States.ORCID 0000-0003-1245-1354
Leah A FarinellaDepartment of Biology, Boston College, Chestnut Hill, MA 02467, United States.
Marina RuzicDepartment of Biology, Boston College, Chestnut Hill, MA 02467, United States.
Jake T LeinasDepartment of Biology, Boston College, Chestnut Hill, MA 02467, United States.
Nels C EldeDepartment of Human Genetics, The University of Utah, Salt Lake City, UT 84112, United States.
Zoë A HilbertDepartment of Human Genetics, The University of Utah, Salt Lake City, UT 84112, United States.ORCID 0000-0002-3833-6912

Funding

Evolutionary innovations from host-microbe interactionsR35GM134936 · NIGMS · UNIVERSITY OF UTAH · PI ELDE, NELS C. · 2020 to 2024
$1.7M
Boston CollegeBurroughs Wellcome FundHelen Hay Whitney FoundationNIGMS NIH HHS R35 GM134936NIH HHS R35GM134936Pathogenesis of Infectious Disease
6 · The paper itself

Abstract

Increasing temperatures associated with climate change have the potential for far-reaching impacts on human health and disease vectors, including fungal pathogens. Pathogenic fungi inhabit a wide range of environments across the world, and their ranges have been slowly expanding in recent decades due, in part, to climate change. Despite these links between increasing temperature and higher prevalence of fungal disease, the direct effects of rising environmental temperatures on the evolution of pathogenic fungi remain unclear. In this study, we investigated how increasing temperatures drive adaptive evolution in the human fungal pathogen Cryptococcus neoformans. First, we performed serial passages of a C. neoformans environmental isolate with gradual changes in temperature over the course of 38 days. Through this approach, we identified several distinct thermally adapted isolates with competitive growth advantages over the parental strain at high temperatures. We then characterized the phenotypic and genetic changes acquired in these evolved isolates, which included alteration of cell size, colony morphology, and, notably, antifungal resistance. Our genetic analyses further revealed distinct genes that facilitate thermoadaptation in different populations-identifying new molecular players in the regulation of this trait and revealing that there are multiple independent routes to gaining thermotolerance. These results highlight the remarkable flexibility of fungi to adapt rapidly to new environments and raise pressing questions about the impacts of rising environmental temperatures on the future of infectious diseases and human health.

Indexed as

Cryptococcus neoformansThermotoleranceAdaptation, PhysiologicalClimate ChangeCryptococcosisHumansPhenotypeTemperatureexperimental evolutionfungithermotolerance

Identifiers

PMID40839773
PMCPMC12606428

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.