Evidence map›Paper›PMID 37818721›Full record

ArticleMedical mycology2023

Cryptococcus neoformans requires the TVF1 gene for thermotolerance and virulence.

Keigo Ueno, Akiko Nagamori, Nahoko Oniyama Honkyu, Michiyo Kataoka, Kiminori Shimizu, Yun C Chang, Kyung J Kwon-Chung, Yoshitsugu Miyazaki

Abstract read
In one paragraph

Article in Medical mycology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Lack of an atypical PDR transporter generates an immunogenicbioRxiv : the preprint server for biology · 2025
    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

8 authors.

Keigo UenoDepartment of Fungal Infection, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.ORCID 0000-0003-0671-0049
Akiko NagamoriDepartment of Fungal Infection, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Nahoko Oniyama HonkyuDepartment of Fungal Infection, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Michiyo KataokaDepartment of Pathology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Kiminori ShimizuDepartment of Biological Science and Technology, Tokyo University of Science, Tokyo 125-8585, Japan.ORCID 0000-0001-5966-976X
Yun C ChangMolecular Microbiology Section, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
Kyung J Kwon-ChungMolecular Microbiology Section, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
Yoshitsugu MiyazakiDepartment of Fungal Infection, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.

Funding

Japan Agency for Medical Research and Development JP23fk0108679Ministry of Education, Culture, Sports, Science and Technology 20K07507Ministry of Health, Labor and Welfare 22HA2001NIAIDNIH
6 · The paper itself

Abstract

Cryptococcus neoformans is the primary causative agent of cryptococcosis. Since C. neoformans thrives in environments and its optimal growth temperature is 25-30°C, it needs to adapt to heat stress in order to cause infection in mammalian hosts. In this study, we aimed to investigate the role of an uncharacterized gene, CNAG_03308. Although the CNAG_03308 deletion strain grew as well as the parent strain KN99, it produced yeast cells with abnormal morphology at 37°C and failed to propagate at 39°C. Furthermore, the deletion strain exhibited slower growth at 37°C in the presence of congo red, which is a cell wall stressor. When cultured at 39°C, the deletion strain showed strong staining with fluorescent probes for cell wall chitin and chitosan, including FITC-labeled wheat germ agglutinin, Eosin Y, and calcofluor white. The transmission electron microscopy of the deletion strain revealed a thickened inner layer of the cell wall containing chitin and chitosan under heat stress. This cell-surface altered deletion strain induced dendritic cells to secrete more interleukin (IL)-6 and IL-23 than the control strains under heat stress. In a murine infection study, C57BL/6 mice infected with the deletion strain exhibited lower mortality and lower fungal burden in the lungs and brain compared to those infected with the control strains. Based on these findings, we concluded that CNAG_03308 gene is necessary for C. neoformans to adapt to heat stress both in vitro and in the host environment. Therefore, we designated the CNAG_03308 gene as TVF1, which stands for thermotolerance and virulence-related factor 1.

Indexed as

ChitosanCryptococcosisCryptococcus neoformansThermotoleranceAnimalsChitinFungal ProteinsMammalsMiceMice, Inbred C57BLVirulenceChitinChitosanFungal Proteinsantigenicitycell wall integrityCryptococcus neoformansthermotolerancevirulence

Identifiers

PMID37818721
PMCPMC10565887

What Socratic holds

Textmetadata
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.