The Cryptococcus neoformans transcriptome at the site of human meningitis
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.
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https://hdl.handle.net/10161/11059Published Version (Please cite this version)
10.1128/mBio.01087-13Publication Info
Chen, Yuan; Toffaletti, Dena L; Tenor, Jennifer L; Litvintseva, Anastasia P; Fang,
Charles; Mitchell, Thomas G; ... Perfect, John R (2014). The Cryptococcus neoformans transcriptome at the site of human meningitis. mBio, 5(1). 10.1128/mBio.01087-13. Retrieved from https://hdl.handle.net/10161/11059.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Thomas Greenfield Mitchell
Associate Professor Emeritus in Molecular Genetics and Microbiology
Among patients with AIDS, leukemia or other cancers, organ or bone marrow transplants,
and similar immunocompromising risk factors, the incidence of opportunistic mycoses
and the number of different fungal pathogens are increasing dramatically. For many
of these fungi, the definition of a species and the recognition of pathogen are highly
problematic. Conventional methods of identification are based on morphological and
physiological characteristics and are often time-consuming, difficult to int
John Robert Perfect
James B. Duke Distinguished Professor of Medicine
Research in my laboratory focuses around several aspects of medical mycology. We
are investigating antifungal agents (new and old) in animal models of candida and
cryptococcal infections. We have examined clinical correlation of in vitro antifungal
susceptibility testing and with in vivo outcome. Our basic science project examines
the molecular pathogenesis of cryptococcal infections. We have developed a molecular
foundation for C. neoformans, including transformation systems, gene disr
Dena L. Toffaletti
Associate Professor in Medicine
As an investigator in John Perfect's laboratory, I have continued to study the molecular
pathogenesis of Cryptococcus neoformans. We are interested in identifying virulence
genes expressed by the fungus during infection using our rabbit model of cryptococcal
meningitis and during in vitro exposure to the pathological temperature of 37 degrees
C. By PCR differential display, we are identifying genes associated with pathogenesis
of the organism and assessing their effects at the molecular level us
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