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Revealing parasite influence in metabolic pathways in Apicomplexa infected patients
BACKGROUND: As an obligate intracellular parasite, Apicomplexa interacts with the host in the special living environment, competing for energy and nutrients from the host cells by manipulating the host metabolism. Previous studies of host-parasite interaction mainly focused on using cellular and bio...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3024860/ https://www.ncbi.nlm.nih.gov/pubmed/21172048 http://dx.doi.org/10.1186/1471-2105-11-S11-S13 |
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author | Xu, Tao Ping, Jie Yu, Yao Yu, Fudong Yu, Yongtao Hao, Pei Li, Xuan |
author_facet | Xu, Tao Ping, Jie Yu, Yao Yu, Fudong Yu, Yongtao Hao, Pei Li, Xuan |
author_sort | Xu, Tao |
collection | PubMed |
description | BACKGROUND: As an obligate intracellular parasite, Apicomplexa interacts with the host in the special living environment, competing for energy and nutrients from the host cells by manipulating the host metabolism. Previous studies of host-parasite interaction mainly focused on using cellular and biochemical methods to investigate molecular functions in metabolic pathways of parasite infected hosts. Computational approaches taking advantage of high-throughput biological data and topology of metabolic pathways have a great potential in revealing the details and mechanism of parasites-to-host interactions. A new analytical method was designed in this work to study host-parasite interactions in human cells infected with Plasmodium falciparum and Cryptosporidium parvum. RESULTS: We introduced a new method that analyzes the host metabolic pathways in divided parts: host specific subpathways and host-parasite common subpathways. Upon analysis on gene expression data from cells infected by Plasmodium falciparum or Cryptosporidium parvum, we found: (i) six host-parasite common subpathways and four host specific subpathways were significantly altered in plasmodium infected human cells; (ii) plasmodium utilized fatty acid biosynthesis and elongation, and Pantothenate and CoA biosynthesis to obtain nutrients from host environment; (iii) in Cryptosporidium parvum infected cells, most of the host-parasite common enzymes were down-regulated, whereas the host specific enzymes up-regulated; (iv) the down-regulation of common subpathways in host cells might be caused by competition for the substrates and up-regulation of host specific subpathways may be stimulated by parasite infection. CONCLUSION: Results demonstrated a significantly coordinated expression pattern between the two groups of subpathways. The method helped expose the impact of parasite infection on host cell metabolism, which was previously concealed in the pathway enrichment analysis. Our approach revealed detailed subpathways and metabolic information are important to the symbiosis in two kinds of the apicomplex parasites, and highlighted its significance in research and understanding of parasite-host interactions. |
format | Text |
id | pubmed-3024860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30248602011-01-22 Revealing parasite influence in metabolic pathways in Apicomplexa infected patients Xu, Tao Ping, Jie Yu, Yao Yu, Fudong Yu, Yongtao Hao, Pei Li, Xuan BMC Bioinformatics Research BACKGROUND: As an obligate intracellular parasite, Apicomplexa interacts with the host in the special living environment, competing for energy and nutrients from the host cells by manipulating the host metabolism. Previous studies of host-parasite interaction mainly focused on using cellular and biochemical methods to investigate molecular functions in metabolic pathways of parasite infected hosts. Computational approaches taking advantage of high-throughput biological data and topology of metabolic pathways have a great potential in revealing the details and mechanism of parasites-to-host interactions. A new analytical method was designed in this work to study host-parasite interactions in human cells infected with Plasmodium falciparum and Cryptosporidium parvum. RESULTS: We introduced a new method that analyzes the host metabolic pathways in divided parts: host specific subpathways and host-parasite common subpathways. Upon analysis on gene expression data from cells infected by Plasmodium falciparum or Cryptosporidium parvum, we found: (i) six host-parasite common subpathways and four host specific subpathways were significantly altered in plasmodium infected human cells; (ii) plasmodium utilized fatty acid biosynthesis and elongation, and Pantothenate and CoA biosynthesis to obtain nutrients from host environment; (iii) in Cryptosporidium parvum infected cells, most of the host-parasite common enzymes were down-regulated, whereas the host specific enzymes up-regulated; (iv) the down-regulation of common subpathways in host cells might be caused by competition for the substrates and up-regulation of host specific subpathways may be stimulated by parasite infection. CONCLUSION: Results demonstrated a significantly coordinated expression pattern between the two groups of subpathways. The method helped expose the impact of parasite infection on host cell metabolism, which was previously concealed in the pathway enrichment analysis. Our approach revealed detailed subpathways and metabolic information are important to the symbiosis in two kinds of the apicomplex parasites, and highlighted its significance in research and understanding of parasite-host interactions. BioMed Central 2010-12-14 /pmc/articles/PMC3024860/ /pubmed/21172048 http://dx.doi.org/10.1186/1471-2105-11-S11-S13 Text en Copyright ©2010 Hao et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Xu, Tao Ping, Jie Yu, Yao Yu, Fudong Yu, Yongtao Hao, Pei Li, Xuan Revealing parasite influence in metabolic pathways in Apicomplexa infected patients |
title | Revealing parasite influence in metabolic pathways in Apicomplexa infected patients |
title_full | Revealing parasite influence in metabolic pathways in Apicomplexa infected patients |
title_fullStr | Revealing parasite influence in metabolic pathways in Apicomplexa infected patients |
title_full_unstemmed | Revealing parasite influence in metabolic pathways in Apicomplexa infected patients |
title_short | Revealing parasite influence in metabolic pathways in Apicomplexa infected patients |
title_sort | revealing parasite influence in metabolic pathways in apicomplexa infected patients |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3024860/ https://www.ncbi.nlm.nih.gov/pubmed/21172048 http://dx.doi.org/10.1186/1471-2105-11-S11-S13 |
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