A Genome-Scale Metabolic Model of Cryptosporidium hominis

The apicomplexan Cryptosporidium is a protozoan parasite of humans and other mammals. Cryptosporidium species cause acute gastroenteritis and diarrheal disease in healthy humans and animals, and cause life‐threatening infection in immunocompromised individuals such as people with AIDS. The parasite...

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Veröffentlicht in:Chemistry & biodiversity 2010-05, Vol.7 (5), p.1026-1039
Hauptverfasser: Vanee, Niti, Roberts, Seth B., Fong, Stephen S., Manque, Patricio, Buck, Gregory A.
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container_end_page 1039
container_issue 5
container_start_page 1026
container_title Chemistry & biodiversity
container_volume 7
creator Vanee, Niti
Roberts, Seth B.
Fong, Stephen S.
Manque, Patricio
Buck, Gregory A.
description The apicomplexan Cryptosporidium is a protozoan parasite of humans and other mammals. Cryptosporidium species cause acute gastroenteritis and diarrheal disease in healthy humans and animals, and cause life‐threatening infection in immunocompromised individuals such as people with AIDS. The parasite has a one‐host life cycle and commonly invades intestinal epithelial cells. The current genome annotation of C. hominis, the most serious human pathogen, predicts 3884 genes of which ca. 1581 have predicted functional annotations. Using a combination of bioinformatics analysis, biochemical evidence, and high‐throughput data, we have constructed a genome‐scale metabolic model of C. hominis. The model is comprised of 213 gene‐associated enzymes involved in 540 reactions among the major metabolic pathways and provides a link between the genotype and the phenotype of the organism, making it possible to study and predict behavior based upon genome content. This model was also used to analyze the two life stages of the parasite by integrating the stage‐specific proteomic data for oocyst and sporozoite stages. Overall, this model provides a computational framework to systematically study and analyze various functional behaviors of C. hominis with respect to its life cycle and pathogenicity.
doi_str_mv 10.1002/cbdv.200900323
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Cryptosporidium species cause acute gastroenteritis and diarrheal disease in healthy humans and animals, and cause life‐threatening infection in immunocompromised individuals such as people with AIDS. The parasite has a one‐host life cycle and commonly invades intestinal epithelial cells. The current genome annotation of C. hominis, the most serious human pathogen, predicts 3884 genes of which ca. 1581 have predicted functional annotations. Using a combination of bioinformatics analysis, biochemical evidence, and high‐throughput data, we have constructed a genome‐scale metabolic model of C. hominis. The model is comprised of 213 gene‐associated enzymes involved in 540 reactions among the major metabolic pathways and provides a link between the genotype and the phenotype of the organism, making it possible to study and predict behavior based upon genome content. This model was also used to analyze the two life stages of the parasite by integrating the stage‐specific proteomic data for oocyst and sporozoite stages. 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subjects Cryptosporidium
Cryptosporidium - genetics
Cryptosporidium - metabolism
Cryptosporidium hominis
Dysentery - parasitology
Gastroenteritis - parasitology
Genome, Protozoan
Genome-scale metabolic model
Genotype
Humans
Metabolic models
Metabolic Networks and Pathways
Metabolome
Models, Biological
Phenotype
Proteome
Protozoan Proteins - genetics
Protozoan Proteins - metabolism
title A Genome-Scale Metabolic Model of Cryptosporidium hominis
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