Down regulation of NO signaling in Trypanosoma cruzi upon parasite-extracellular matrix interaction: changes in protein modification by nitrosylation and nitration
Adhesion of the Trypanosoma cruzi trypomastigotes, the causative agent of Chagas' disease in humans, to components of the extracellular matrix (ECM) is an important step in host cell invasion. The signaling events triggered in the parasite upon binding to ECM are less explored and, to our knowl...
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description | Adhesion of the Trypanosoma cruzi trypomastigotes, the causative agent of Chagas' disease in humans, to components of the extracellular matrix (ECM) is an important step in host cell invasion. The signaling events triggered in the parasite upon binding to ECM are less explored and, to our knowledge, there is no data available regarding •NO signaling.
Trypomastigotes were incubated with ECM for different periods of time. Nitrated and S-nitrosylated proteins were analyzed by Western blotting using anti-nitrotyrosine and S-nitrosyl cysteine antibodies. At 2 h incubation time, a decrease in NO synthase activity, •NO, citrulline, arginine and cGMP concentrations, as well as the protein modifications levels have been observed in the parasite. The modified proteins were enriched by immunoprecipitation with anti-nitrotyrosine antibodies (nitrated proteins) or by the biotin switch method (S-nitrosylated proteins) and identified by MS/MS. The presence of both modifications was confirmed in proteins of interest by immunoblotting or immunoprecipitation.
For the first time it was shown that T. cruzi proteins are amenable to modifications by S-nitrosylation and nitration. When T. cruzi trypomastigotes are incubated with the extracellular matrix there is a general down regulation of these reactions, including a decrease in both NOS activity and cGMP concentration. Notwithstanding, some specific proteins, such as enolase or histones had, at least, their nitration levels increased. This suggests that post-translational modifications of T. cruzi proteins are not only a reflex of NOS activity, implying other mechanisms that circumvent a relatively low synthesis of •NO. In conclusion, the extracellular matrix, a cell surrounding layer of macromolecules that have to be trespassed by the parasite in order to be internalized into host cells, contributes to the modification of •NO signaling in the parasite, probably an essential move for the ensuing invasion step. |
doi_str_mv | 10.1371/journal.pntd.0003683 |
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Trypomastigotes were incubated with ECM for different periods of time. Nitrated and S-nitrosylated proteins were analyzed by Western blotting using anti-nitrotyrosine and S-nitrosyl cysteine antibodies. At 2 h incubation time, a decrease in NO synthase activity, •NO, citrulline, arginine and cGMP concentrations, as well as the protein modifications levels have been observed in the parasite. The modified proteins were enriched by immunoprecipitation with anti-nitrotyrosine antibodies (nitrated proteins) or by the biotin switch method (S-nitrosylated proteins) and identified by MS/MS. The presence of both modifications was confirmed in proteins of interest by immunoblotting or immunoprecipitation.
For the first time it was shown that T. cruzi proteins are amenable to modifications by S-nitrosylation and nitration. When T. cruzi trypomastigotes are incubated with the extracellular matrix there is a general down regulation of these reactions, including a decrease in both NOS activity and cGMP concentration. Notwithstanding, some specific proteins, such as enolase or histones had, at least, their nitration levels increased. This suggests that post-translational modifications of T. cruzi proteins are not only a reflex of NOS activity, implying other mechanisms that circumvent a relatively low synthesis of •NO. In conclusion, the extracellular matrix, a cell surrounding layer of macromolecules that have to be trespassed by the parasite in order to be internalized into host cells, contributes to the modification of •NO signaling in the parasite, probably an essential move for the ensuing invasion step.</description><identifier>ISSN: 1935-2735</identifier><identifier>ISSN: 1935-2727</identifier><identifier>EISSN: 1935-2735</identifier><identifier>DOI: 10.1371/journal.pntd.0003683</identifier><identifier>PMID: 25856423</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Blotting, Western ; Cellular signal transduction ; Chagas Disease - metabolism ; Down-Regulation ; Extracellular matrix ; Extracellular Matrix - physiology ; Free radicals ; Genetic aspects ; Humans ; Immunoprecipitation ; Kinases ; Mammals ; Motility ; Nitric oxide ; Nitric Oxide - metabolism ; Parasites ; Properties ; Protein Processing, Post-Translational ; Proteins ; Protozoa ; Signal Transduction - physiology ; Tandem Mass Spectrometry ; Trypanosoma cruzi ; Trypanosoma cruzi - physiology ; Tyrosine - analogs & derivatives ; Virulence (Microbiology)</subject><ispartof>PLoS neglected tropical diseases, 2015-04, Vol.9 (4), p.e0003683-e0003683</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Pereira et al 2015 Pereira et al</rights><rights>2015 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: upon Parasite-Extracellular Matrix Interaction: Changes in Protein Modification by Nitrosylation and Nitration. PLoS Negl Trop Dis 9(4): e0003683. doi:10.1371/journal.pntd.0003683</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c590t-7d31490843051b656afc4b34c59bfdcd4821e8fe5a711e1cb37f0410c7cc5a4a3</citedby><cites>FETCH-LOGICAL-c590t-7d31490843051b656afc4b34c59bfdcd4821e8fe5a711e1cb37f0410c7cc5a4a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391712/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391712/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79569,79570</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25856423$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pereira, Milton</creatorcontrib><creatorcontrib>Soares, Chrislaine</creatorcontrib><creatorcontrib>Canuto, Gisele André Baptista</creatorcontrib><creatorcontrib>Tavares, Marina Franco Maggi</creatorcontrib><creatorcontrib>Colli, Walter</creatorcontrib><creatorcontrib>Alves, Maria Julia M</creatorcontrib><title>Down regulation of NO signaling in Trypanosoma cruzi upon parasite-extracellular matrix interaction: changes in protein modification by nitrosylation and nitration</title><title>PLoS neglected tropical diseases</title><addtitle>PLoS Negl Trop Dis</addtitle><description>Adhesion of the Trypanosoma cruzi trypomastigotes, the causative agent of Chagas' disease in humans, to components of the extracellular matrix (ECM) is an important step in host cell invasion. The signaling events triggered in the parasite upon binding to ECM are less explored and, to our knowledge, there is no data available regarding •NO signaling.
Trypomastigotes were incubated with ECM for different periods of time. Nitrated and S-nitrosylated proteins were analyzed by Western blotting using anti-nitrotyrosine and S-nitrosyl cysteine antibodies. At 2 h incubation time, a decrease in NO synthase activity, •NO, citrulline, arginine and cGMP concentrations, as well as the protein modifications levels have been observed in the parasite. The modified proteins were enriched by immunoprecipitation with anti-nitrotyrosine antibodies (nitrated proteins) or by the biotin switch method (S-nitrosylated proteins) and identified by MS/MS. The presence of both modifications was confirmed in proteins of interest by immunoblotting or immunoprecipitation.
For the first time it was shown that T. cruzi proteins are amenable to modifications by S-nitrosylation and nitration. When T. cruzi trypomastigotes are incubated with the extracellular matrix there is a general down regulation of these reactions, including a decrease in both NOS activity and cGMP concentration. Notwithstanding, some specific proteins, such as enolase or histones had, at least, their nitration levels increased. This suggests that post-translational modifications of T. cruzi proteins are not only a reflex of NOS activity, implying other mechanisms that circumvent a relatively low synthesis of •NO. 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Soares, Chrislaine ; Canuto, Gisele André Baptista ; Tavares, Marina Franco Maggi ; Colli, Walter ; Alves, Maria Julia M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c590t-7d31490843051b656afc4b34c59bfdcd4821e8fe5a711e1cb37f0410c7cc5a4a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Blotting, Western</topic><topic>Cellular signal transduction</topic><topic>Chagas Disease - metabolism</topic><topic>Down-Regulation</topic><topic>Extracellular matrix</topic><topic>Extracellular Matrix - physiology</topic><topic>Free radicals</topic><topic>Genetic aspects</topic><topic>Humans</topic><topic>Immunoprecipitation</topic><topic>Kinases</topic><topic>Mammals</topic><topic>Motility</topic><topic>Nitric oxide</topic><topic>Nitric Oxide - metabolism</topic><topic>Parasites</topic><topic>Properties</topic><topic>Protein Processing, Post-Translational</topic><topic>Proteins</topic><topic>Protozoa</topic><topic>Signal Transduction - physiology</topic><topic>Tandem Mass Spectrometry</topic><topic>Trypanosoma cruzi</topic><topic>Trypanosoma cruzi - physiology</topic><topic>Tyrosine - analogs & derivatives</topic><topic>Virulence (Microbiology)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pereira, Milton</creatorcontrib><creatorcontrib>Soares, Chrislaine</creatorcontrib><creatorcontrib>Canuto, Gisele André Baptista</creatorcontrib><creatorcontrib>Tavares, Marina Franco Maggi</creatorcontrib><creatorcontrib>Colli, Walter</creatorcontrib><creatorcontrib>Alves, Maria Julia M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS neglected tropical diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pereira, Milton</au><au>Soares, Chrislaine</au><au>Canuto, Gisele André Baptista</au><au>Tavares, Marina Franco Maggi</au><au>Colli, Walter</au><au>Alves, Maria Julia M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Down regulation of NO signaling in Trypanosoma cruzi upon parasite-extracellular matrix interaction: changes in protein modification by nitrosylation and nitration</atitle><jtitle>PLoS neglected tropical diseases</jtitle><addtitle>PLoS Negl Trop Dis</addtitle><date>2015-04-01</date><risdate>2015</risdate><volume>9</volume><issue>4</issue><spage>e0003683</spage><epage>e0003683</epage><pages>e0003683-e0003683</pages><issn>1935-2735</issn><issn>1935-2727</issn><eissn>1935-2735</eissn><abstract>Adhesion of the Trypanosoma cruzi trypomastigotes, the causative agent of Chagas' disease in humans, to components of the extracellular matrix (ECM) is an important step in host cell invasion. The signaling events triggered in the parasite upon binding to ECM are less explored and, to our knowledge, there is no data available regarding •NO signaling.
Trypomastigotes were incubated with ECM for different periods of time. Nitrated and S-nitrosylated proteins were analyzed by Western blotting using anti-nitrotyrosine and S-nitrosyl cysteine antibodies. At 2 h incubation time, a decrease in NO synthase activity, •NO, citrulline, arginine and cGMP concentrations, as well as the protein modifications levels have been observed in the parasite. The modified proteins were enriched by immunoprecipitation with anti-nitrotyrosine antibodies (nitrated proteins) or by the biotin switch method (S-nitrosylated proteins) and identified by MS/MS. The presence of both modifications was confirmed in proteins of interest by immunoblotting or immunoprecipitation.
For the first time it was shown that T. cruzi proteins are amenable to modifications by S-nitrosylation and nitration. When T. cruzi trypomastigotes are incubated with the extracellular matrix there is a general down regulation of these reactions, including a decrease in both NOS activity and cGMP concentration. Notwithstanding, some specific proteins, such as enolase or histones had, at least, their nitration levels increased. This suggests that post-translational modifications of T. cruzi proteins are not only a reflex of NOS activity, implying other mechanisms that circumvent a relatively low synthesis of •NO. In conclusion, the extracellular matrix, a cell surrounding layer of macromolecules that have to be trespassed by the parasite in order to be internalized into host cells, contributes to the modification of •NO signaling in the parasite, probably an essential move for the ensuing invasion step.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25856423</pmid><doi>10.1371/journal.pntd.0003683</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Blotting, Western Cellular signal transduction Chagas Disease - metabolism Down-Regulation Extracellular matrix Extracellular Matrix - physiology Free radicals Genetic aspects Humans Immunoprecipitation Kinases Mammals Motility Nitric oxide Nitric Oxide - metabolism Parasites Properties Protein Processing, Post-Translational Proteins Protozoa Signal Transduction - physiology Tandem Mass Spectrometry Trypanosoma cruzi Trypanosoma cruzi - physiology Tyrosine - analogs & derivatives Virulence (Microbiology) |
title | Down regulation of NO signaling in Trypanosoma cruzi upon parasite-extracellular matrix interaction: changes in protein modification by nitrosylation and nitration |
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