Identification of a type I nitroreductase gene in non-virulent Trypanosoma rangeli
Trypanosomatid type I nitroreductases (NTRs), i.e., mitochondrial enzymes that metabolise nitroaromatic pro-drugs, are essential for parasite growth, infection, and survival. Here, a type I NTR of non-virulent protozoan Trypanosoma rangeli is described and compared to those of other trypanosomatids....
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description | Trypanosomatid type I nitroreductases (NTRs), i.e., mitochondrial enzymes that metabolise nitroaromatic pro-drugs, are essential for parasite growth, infection, and survival. Here, a type I NTR of non-virulent protozoan Trypanosoma rangeli is described and compared to those of other trypanosomatids. The NTR gene was isolated from KP1(+) and KP1(-) strains, and its corresponding transcript and 5' untranslated region (5'UTR) were determined. Bioinformatics analyses and nitro-drug activation assays were also performed. The results indicated that the type I NTR gene is present in both KP1(-) and KP1(+) strains, with 98% identity. However, the predicted subcellular localisation of the protein differed among the strains (predicted as mitochondrial in the KP1(+) strain). Comparisons of the domains and 3D structures of the NTRs with those of orthologs demonstrated that the nitroreductase domain of T. rangeli NTR is conserved across all the strains, including the residues involved in the interaction with the FMN cofactor and in the tertiary structure characteristics of this oxidoreductase protein family. mRNA processing and expression were also observed. In addition, T. rangeli was shown to be sensitive to benznidazole and nifurtimox in a concentration-dependent manner. In summary, T. rangeli appears to have a newly discovered functional type I NTR. |
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Here, a type I NTR of non-virulent protozoan Trypanosoma rangeli is described and compared to those of other trypanosomatids. The NTR gene was isolated from KP1(+) and KP1(-) strains, and its corresponding transcript and 5' untranslated region (5'UTR) were determined. Bioinformatics analyses and nitro-drug activation assays were also performed. The results indicated that the type I NTR gene is present in both KP1(-) and KP1(+) strains, with 98% identity. However, the predicted subcellular localisation of the protein differed among the strains (predicted as mitochondrial in the KP1(+) strain). Comparisons of the domains and 3D structures of the NTRs with those of orthologs demonstrated that the nitroreductase domain of T. rangeli NTR is conserved across all the strains, including the residues involved in the interaction with the FMN cofactor and in the tertiary structure characteristics of this oxidoreductase protein family. mRNA processing and expression were also observed. In addition, T. rangeli was shown to be sensitive to benznidazole and nifurtimox in a concentration-dependent manner. In summary, T. rangeli appears to have a newly discovered functional type I NTR.</description><identifier>ISSN: 0074-0276</identifier><identifier>ISSN: 1678-8060</identifier><identifier>EISSN: 1678-8060</identifier><identifier>EISSN: 0074-0276</identifier><identifier>DOI: 10.1590/0074-02760160532</identifier><identifier>PMID: 28591312</identifier><language>eng</language><publisher>Brazil: Instituto Oswaldo Cruz, Ministério da Saúde</publisher><subject>Base Sequence ; DNA, Protozoan - genetics ; Genetic Variation - genetics ; Humans ; Nitroreductases - genetics ; PARASITOLOGY ; Sequence Analysis, DNA ; Short Communication ; TROPICAL MEDICINE ; Trypanosoma cruzi ; Trypanosoma rangeli ; Trypanosoma rangeli - enzymology ; Trypanosoma rangeli - genetics ; type I nitroreductase</subject><ispartof>Memórias do Instituto Oswaldo Cruz, 2017-07, Vol.112 (7), p.504-509</ispartof><rights>This work is licensed under a Creative Commons Attribution 4.0 International License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c501t-5afdf802fd8feb5d7769d04a8af130099523a2b0c6d03f375c481ffaedf34a2c3</citedby><cites>FETCH-LOGICAL-c501t-5afdf802fd8feb5d7769d04a8af130099523a2b0c6d03f375c481ffaedf34a2c3</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/PMC5452488/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452488/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28591312$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Montenegro, Marjorie</creatorcontrib><creatorcontrib>Cuervo, Claudia</creatorcontrib><creatorcontrib>Cardenas, Constanza</creatorcontrib><creatorcontrib>Duarte, Silvia</creatorcontrib><creatorcontrib>Díaz, Jenny R</creatorcontrib><creatorcontrib>Thomas, M Carmen</creatorcontrib><creatorcontrib>Lopez, Manuel C</creatorcontrib><creatorcontrib>Puerta, Concepcion J</creatorcontrib><title>Identification of a type I nitroreductase gene in non-virulent Trypanosoma rangeli</title><title>Memórias do Instituto Oswaldo Cruz</title><addtitle>Mem Inst Oswaldo Cruz</addtitle><description>Trypanosomatid type I nitroreductases (NTRs), i.e., mitochondrial enzymes that metabolise nitroaromatic pro-drugs, are essential for parasite growth, infection, and survival. Here, a type I NTR of non-virulent protozoan Trypanosoma rangeli is described and compared to those of other trypanosomatids. The NTR gene was isolated from KP1(+) and KP1(-) strains, and its corresponding transcript and 5' untranslated region (5'UTR) were determined. Bioinformatics analyses and nitro-drug activation assays were also performed. The results indicated that the type I NTR gene is present in both KP1(-) and KP1(+) strains, with 98% identity. However, the predicted subcellular localisation of the protein differed among the strains (predicted as mitochondrial in the KP1(+) strain). Comparisons of the domains and 3D structures of the NTRs with those of orthologs demonstrated that the nitroreductase domain of T. rangeli NTR is conserved across all the strains, including the residues involved in the interaction with the FMN cofactor and in the tertiary structure characteristics of this oxidoreductase protein family. mRNA processing and expression were also observed. In addition, T. rangeli was shown to be sensitive to benznidazole and nifurtimox in a concentration-dependent manner. In summary, T. rangeli appears to have a newly discovered functional type I NTR.</description><subject>Base Sequence</subject><subject>DNA, Protozoan - genetics</subject><subject>Genetic Variation - genetics</subject><subject>Humans</subject><subject>Nitroreductases - genetics</subject><subject>PARASITOLOGY</subject><subject>Sequence Analysis, DNA</subject><subject>Short Communication</subject><subject>TROPICAL MEDICINE</subject><subject>Trypanosoma cruzi</subject><subject>Trypanosoma rangeli</subject><subject>Trypanosoma rangeli - enzymology</subject><subject>Trypanosoma rangeli - genetics</subject><subject>type I nitroreductase</subject><issn>0074-0276</issn><issn>1678-8060</issn><issn>1678-8060</issn><issn>0074-0276</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>DOA</sourceid><recordid>eNpVkkmPEzEQhS0EYobAnRPykUsP5a2XCxIaDRBpJCQYzla1l-CoYwe7e6T8exwSIubkpfw-P70qQt4yuGFqgA8AnWyAdy2wFpTgz8g1a7u-6aGF5-T6Ur4ir0rZQt2KVr4kV7xXAxOMX5Pva-viHHwwOIcUafIU6XzYO7qmMcw5ZWcXM2NxdOOioyHSmGLzGPIyVSF9yIc9xlTSDmnGuHFTeE1eeJyKe3NeV-Tn57uH26_N_bcv69tP941RwOZGobe-B-5t792obNe1gwWJPXomAIZBcYF8BNNaEF50ysieeY_OeiGRG7Ei6xPXJtzqfQ47zAedMOi_FylvNOY5mMlpNirZDrKTYFDyYURhpXXt6IexcwP6yro5sYoJbkp6m5Ycq3n945ihPmbIgXVQTwAKZBV8PAn2y7hz1tQsMk5PXDytxPBLb9KjVlJx2fcV8P4MyOn34sqsd6EYN00YXVqKZgN0gktRW7YicHpqciolO3_5hoE-zoG-mDzPQZW8-9_eRfCv8eIPY7Wsrw</recordid><startdate>201707</startdate><enddate>201707</enddate><creator>Montenegro, Marjorie</creator><creator>Cuervo, Claudia</creator><creator>Cardenas, Constanza</creator><creator>Duarte, Silvia</creator><creator>Díaz, Jenny R</creator><creator>Thomas, M Carmen</creator><creator>Lopez, Manuel C</creator><creator>Puerta, Concepcion J</creator><general>Instituto Oswaldo Cruz, Ministério da Saúde</general><general>Fundação Oswaldo Cruz (FIOCRUZ)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>GPN</scope><scope>DOA</scope></search><sort><creationdate>201707</creationdate><title>Identification of a type I nitroreductase gene in non-virulent Trypanosoma rangeli</title><author>Montenegro, Marjorie ; Cuervo, Claudia ; Cardenas, Constanza ; Duarte, Silvia ; Díaz, Jenny R ; Thomas, M Carmen ; Lopez, Manuel C ; Puerta, Concepcion J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c501t-5afdf802fd8feb5d7769d04a8af130099523a2b0c6d03f375c481ffaedf34a2c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Base Sequence</topic><topic>DNA, Protozoan - genetics</topic><topic>Genetic Variation - genetics</topic><topic>Humans</topic><topic>Nitroreductases - genetics</topic><topic>PARASITOLOGY</topic><topic>Sequence Analysis, DNA</topic><topic>Short Communication</topic><topic>TROPICAL MEDICINE</topic><topic>Trypanosoma cruzi</topic><topic>Trypanosoma rangeli</topic><topic>Trypanosoma rangeli - enzymology</topic><topic>Trypanosoma rangeli - genetics</topic><topic>type I nitroreductase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Montenegro, Marjorie</creatorcontrib><creatorcontrib>Cuervo, Claudia</creatorcontrib><creatorcontrib>Cardenas, Constanza</creatorcontrib><creatorcontrib>Duarte, Silvia</creatorcontrib><creatorcontrib>Díaz, Jenny R</creatorcontrib><creatorcontrib>Thomas, M Carmen</creatorcontrib><creatorcontrib>Lopez, Manuel C</creatorcontrib><creatorcontrib>Puerta, Concepcion J</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>PubMed Central (Full Participant titles)</collection><collection>SciELO</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Memórias do Instituto Oswaldo Cruz</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Montenegro, Marjorie</au><au>Cuervo, Claudia</au><au>Cardenas, Constanza</au><au>Duarte, Silvia</au><au>Díaz, Jenny R</au><au>Thomas, M Carmen</au><au>Lopez, Manuel C</au><au>Puerta, Concepcion J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of a type I nitroreductase gene in non-virulent Trypanosoma rangeli</atitle><jtitle>Memórias do Instituto Oswaldo Cruz</jtitle><addtitle>Mem Inst Oswaldo Cruz</addtitle><date>2017-07</date><risdate>2017</risdate><volume>112</volume><issue>7</issue><spage>504</spage><epage>509</epage><pages>504-509</pages><issn>0074-0276</issn><issn>1678-8060</issn><eissn>1678-8060</eissn><eissn>0074-0276</eissn><abstract>Trypanosomatid type I nitroreductases (NTRs), i.e., mitochondrial enzymes that metabolise nitroaromatic pro-drugs, are essential for parasite growth, infection, and survival. Here, a type I NTR of non-virulent protozoan Trypanosoma rangeli is described and compared to those of other trypanosomatids. The NTR gene was isolated from KP1(+) and KP1(-) strains, and its corresponding transcript and 5' untranslated region (5'UTR) were determined. Bioinformatics analyses and nitro-drug activation assays were also performed. The results indicated that the type I NTR gene is present in both KP1(-) and KP1(+) strains, with 98% identity. However, the predicted subcellular localisation of the protein differed among the strains (predicted as mitochondrial in the KP1(+) strain). Comparisons of the domains and 3D structures of the NTRs with those of orthologs demonstrated that the nitroreductase domain of T. rangeli NTR is conserved across all the strains, including the residues involved in the interaction with the FMN cofactor and in the tertiary structure characteristics of this oxidoreductase protein family. mRNA processing and expression were also observed. In addition, T. rangeli was shown to be sensitive to benznidazole and nifurtimox in a concentration-dependent manner. In summary, T. rangeli appears to have a newly discovered functional type I NTR.</abstract><cop>Brazil</cop><pub>Instituto Oswaldo Cruz, Ministério da Saúde</pub><pmid>28591312</pmid><doi>10.1590/0074-02760160532</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Base Sequence DNA, Protozoan - genetics Genetic Variation - genetics Humans Nitroreductases - genetics PARASITOLOGY Sequence Analysis, DNA Short Communication TROPICAL MEDICINE Trypanosoma cruzi Trypanosoma rangeli Trypanosoma rangeli - enzymology Trypanosoma rangeli - genetics type I nitroreductase |
title | Identification of a type I nitroreductase gene in non-virulent Trypanosoma rangeli |
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