The Cryptococcus neoformans transcriptome at the site of human meningitis

dc.contributor.author

Chen, Yuan

dc.contributor.author

Toffaletti, Dena L

dc.contributor.author

Tenor, Jennifer L

dc.contributor.author

Litvintseva, Anastasia P

dc.contributor.author

Fang, Charles

dc.contributor.author

Mitchell, Thomas G

dc.contributor.author

McDonald, Tami R

dc.contributor.author

Nielsen, Kirsten

dc.contributor.author

Boulware, David R

dc.contributor.author

Bicanic, Tihana

dc.contributor.author

Perfect, John R

dc.contributor.editor

Dromer, Françoise

dc.date.accessioned

2015-12-03T19:25:57Z

dc.date.issued

2014-02-04

dc.description.abstract

Cryptococcus neoformans is the leading cause of fungal meningitis worldwide. Previous studies have characterized the cryptococcal transcriptome under various stress conditions, but a comprehensive profile of the C. neoformans transcriptome in the human host has not been attempted. Here, we extracted RNA from yeast cells taken directly from the cerebrospinal fluid (CSF) of two AIDS patients with cryptococcal meningitis prior to antifungal therapy. The patients were infected with strains of C. neoformans var. grubii of molecular type VNI and VNII. Using RNA-seq, we compared the transcriptional profiles of these strains under three environmental conditions (in vivo CSF, ex vivo CSF, and yeast extract-peptone-dextrose [YPD]). Although we identified a number of differentially expressed genes, single nucleotide variants, and novel genes that were unique to each strain, the overall expression patterns of the two strains were similar under the same environmental conditions. Specifically, yeast cells obtained directly from each patient's CSF were more metabolically active than cells that were incubated ex vivo in CSF. Compared with growth in YPD, some genes were identified as significantly upregulated in both in vivo and ex vivo CSF, and they were associated with genes previously recognized for contributing to pathogenicity. For example, genes with known stress response functions, such as RIM101, ENA1, and CFO1, were regulated similarly in the two clinical strains. Conversely, many genes that were differentially regulated between the two strains appeared to be transporters. These findings establish a platform for further studies of how this yeast survives and produces disease. © 2014 Chen et al.

dc.identifier.eissn

2150-7511

dc.identifier.issn

2161-2129

dc.identifier.uri

https://hdl.handle.net/10161/11059

dc.publisher

American Society for Microbiology

dc.relation.ispartof

mBio

dc.relation.isversionof

10.1128/mBio.01087-13

dc.title

The Cryptococcus neoformans transcriptome at the site of human meningitis

dc.type

Journal article

duke.contributor.orcid

Perfect, John R|0000-0002-6606-9460|0000-0003-3465-5518

pubs.issue

1

pubs.organisational-group

Basic Science Departments

pubs.organisational-group

Clinical Science Departments

pubs.organisational-group

Duke

pubs.organisational-group

Medicine

pubs.organisational-group

Medicine, Infectious Diseases

pubs.organisational-group

Molecular Genetics and Microbiology

pubs.organisational-group

School of Medicine

pubs.publication-status

Published

pubs.volume

5

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
mBio-5-e01087-13-2014.pdf
Size:
1.19 MB
Format:
Adobe Portable Document Format
Description:
Published version