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PLoS Genet DOI:10.1371/journal.pgen.1002345

Comparative genomic analysis of human fungal pathogens causing paracoccidioidomycosis.

Publication TypeJournal Article
Year of Publication2011
AuthorsDesjardins, CA, Champion, MD, Holder, JW, Muszewska, A, Goldberg, J, Bailão, AM, Brigido, MMacedo, Ferreira, MEliana da, Garcia, AMaria, Grynberg, M, Gujja, S, Heiman, DI, Henn, MR, Kodira, CD, León-Narváez, H, Longo, LVG, Ma, L-J, Malavazi, I, Matsuo, AL, Morais, FV, Pereira, M, Rodríguez-Brito, S, Sakthikumar, S, Salem-Izacc, SM, Sykes, SM, Teixeira, MMelo, Vallejo, MC, Walter, MEmília Ma, Yandava, C, Young, S, Zeng, Q, Zucker, J, Felipe, MSueli, Goldman, GH, Haas, BJ, McEwen, JG, Nino-Vega, G, Puccia, R, San-Blas, G, Soares, CMaria de A, Birren, BW, Cuomo, CA
JournalPLoS Genet
Volume7
Issue10
Pagese1002345
Date Published2011 Oct
ISSN1553-7404
KeywordsCarbohydrate Metabolism, Drug Delivery Systems, Evolution, Molecular, Genome, Fungal, Genome, Mitochondrial, Humans, Multigene Family, Onygenales, Paracoccidioides, Paracoccidioidomycosis, Phylogeny, Protein Kinases, Proteolysis, Repetitive Sequences, Nucleic Acid, Sequence Analysis, DNA
Abstract

Paracoccidioides is a fungal pathogen and the cause of paracoccidioidomycosis, a health-threatening human systemic mycosis endemic to Latin America. Infection by Paracoccidioides, a dimorphic fungus in the order Onygenales, is coupled with a thermally regulated transition from a soil-dwelling filamentous form to a yeast-like pathogenic form. To better understand the genetic basis of growth and pathogenicity in Paracoccidioides, we sequenced the genomes of two strains of Paracoccidioides brasiliensis (Pb03 and Pb18) and one strain of Paracoccidioides lutzii (Pb01). These genomes range in size from 29.1 Mb to 32.9 Mb and encode 7,610 to 8,130 genes. To enable genetic studies, we mapped 94% of the P. brasiliensis Pb18 assembly onto five chromosomes. We characterized gene family content across Onygenales and related fungi, and within Paracoccidioides we found expansions of the fungal-specific kinase family FunK1. Additionally, the Onygenales have lost many genes involved in carbohydrate metabolism and fewer genes involved in protein metabolism, resulting in a higher ratio of proteases to carbohydrate active enzymes in the Onygenales than their relatives. To determine if gene content correlated with growth on different substrates, we screened the non-pathogenic onygenale Uncinocarpus reesii, which has orthologs for 91% of Paracoccidioides metabolic genes, for growth on 190 carbon sources. U. reesii showed growth on a limited range of carbohydrates, primarily basic plant sugars and cell wall components; this suggests that Onygenales, including dimorphic fungi, can degrade cellulosic plant material in the soil. In addition, U. reesii grew on gelatin and a wide range of dipeptides and amino acids, indicating a preference for proteinaceous growth substrates over carbohydrates, which may enable these fungi to also degrade animal biomass. These capabilities for degrading plant and animal substrates suggest a duality in lifestyle that could enable pathogenic species of Onygenales to transfer from soil to animal hosts.

DOI10.1371/journal.pgen.1002345
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/22046142?dopt=Abstract

Alternate JournalPLoS Genet.
PubMed ID22046142
PubMed Central IDPMC3203195
Grant ListHHSN272200900018C / AI / NIAID NIH HHS / United States
HHSN272200900008C / AI / NIAID NIH HHS / United States
HHSN272200900001C / AI / NIAID NIH HHS / United States
HHSN2722009000018C / / PHS HHS / United States
HHSN266200400001C / AO / NIAID NIH HHS / United States
HHSN266200400001C / / PHS HHS / United States