Literature DB >> 21819456

The copper regulon of the human fungal pathogen Cryptococcus neoformans H99.

Chen Ding1, Jun Yin, Edgar Mauricio Medina Tovar, David A Fitzpatrick, Desmond G Higgins, Dennis J Thiele.   

Abstract

Cryptococcus neoformans is a human fungal pathogen that is the causative agent of cryptococcosis and fatal meningitis in immuno-compromised hosts. Recent studies suggest that copper (Cu) acquisition plays an important role in C. neoformans virulence, as mutants that lack Cuf1, which activates the Ctr4 high affinity Cu importer, are hypo-virulent in mouse models. To understand the constellation of Cu-responsive genes in C. neoformans and how their expression might contribute to virulence, we determined the transcript profile of C. neoformans in response to elevated Cu or Cu deficiency. We identified two metallothionein genes (CMT1 and CMT2), encoding cysteine-rich Cu binding and detoxifying proteins, whose expression is dramatically elevated in response to excess Cu. We identified a new C. neoformans Cu transporter, CnCtr1, that is induced by Cu deficiency and is distinct from CnCtr4 and which shows significant phylogenetic relationship to Ctr1 from other fungi. Surprisingly, in contrast to other fungi, we found that induction of both CnCTR1 and CnCTR4 expression under Cu limitation, and CMT1 and CMT2 in response to Cu excess, are dependent on the CnCuf1 Cu metalloregulatory transcription factor. These studies set the stage for the evaluation of the specific Cuf1 target genes required for virulence in C. neoformans.
© 2011 Blackwell Publishing Ltd.

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Year:  2011        PMID: 21819456      PMCID: PMC3718005          DOI: 10.1111/j.1365-2958.2011.07794.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  96 in total

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Review 2.  Copper in microbial pathogenesis: meddling with the metal.

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Journal:  Biochim Biophys Acta       Date:  2012-02-24

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8.  Cryptococcus neoformans copper detoxification machinery is critical for fungal virulence.

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10.  Exploiting innate immune cell activation of a copper-dependent antimicrobial agent during infection.

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