{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["23(23)"],"submitter":["Silva-Gomes NLD"],"pubmed_abstract":["Ecto-nucleoside triphosphate diphosphohydrolases (NTPDases) are enzymes located on the surface of the T.&amp;nbsp;cruzi plasma membrane, which hydrolyze a wide range of tri-/-diphosphate nucleosides. In this work, we used previously developed genetically modified strains of Trypanosoma&amp;nbsp;cruzi (T. cruzi), hemi-knockout (KO +/-) and overexpressing (OE) the TcNTPDase-1 gene to evaluate the parasite infectivity profile in a mouse model of acute infection (n = 6 mice per group). Our results showed significantly higher parasitemia and mortality, and lower weight in animals infected with parasites OE TcNTPDase-1, as compared to the infection with the wild type (WT) parasites. On the other hand, animals infected with (KO +/-) parasites showed no mortality during the 30-day trial and mouse weight was more similar to the non-infected (NI) animals. In addition, they had low parasitemia (45.7 times lower) when compared with parasites overexpressing TcNTPDase-1 from the hemi-knockout (OE KO +/-) group. The hearts of animals infected with the OE KO +/- and OE parasites showed significantly larger regions of cardiac inflammation than those infected with the WT parasites (p &lt; 0.001). Only animals infected with KO +/- did not show individual electrocardiographic changes during the period of experimentation. Together, our results expand the knowledge on the role of NTPDases in T.&amp;nbsp;cruzi infectivity, reenforcing the potential of this enzyme as a chemotherapy target to treat Chagas disease (CD)."],"journal":["International journal of molecular sciences"],"pagination":["14661"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9736689"],"repository":["biostudies-literature"],"pubmed_title":["Overexpression of TcNTPDase-1 Gene Increases Infectivity in Mice Infected with Trypanosoma cruzi."],"pmcid":["PMC9736689"],"pubmed_authors":["Moreira C","Fragoso S","Ruivo LAS","Batista DDGJ","Oliveira GM","Soeiro MNC","Silva-Gomes NLD","Silva CFD","Meuser-Batista M","Moreira OC"],"additional_accession":[]},"is_claimable":false,"name":"Overexpression of TcNTPDase-1 Gene Increases Infectivity in Mice Infected with Trypanosoma cruzi.","description":"Ecto-nucleoside triphosphate diphosphohydrolases (NTPDases) are enzymes located on the surface of the T.&amp;nbsp;cruzi plasma membrane, which hydrolyze a wide range of tri-/-diphosphate nucleosides. In this work, we used previously developed genetically modified strains of Trypanosoma&amp;nbsp;cruzi (T. cruzi), hemi-knockout (KO +/-) and overexpressing (OE) the TcNTPDase-1 gene to evaluate the parasite infectivity profile in a mouse model of acute infection (n = 6 mice per group). Our results showed significantly higher parasitemia and mortality, and lower weight in animals infected with parasites OE TcNTPDase-1, as compared to the infection with the wild type (WT) parasites. On the other hand, animals infected with (KO +/-) parasites showed no mortality during the 30-day trial and mouse weight was more similar to the non-infected (NI) animals. In addition, they had low parasitemia (45.7 times lower) when compared with parasites overexpressing TcNTPDase-1 from the hemi-knockout (OE KO +/-) group. The hearts of animals infected with the OE KO +/- and OE parasites showed significantly larger regions of cardiac inflammation than those infected with the WT parasites (p &lt; 0.001). Only animals infected with KO +/- did not show individual electrocardiographic changes during the period of experimentation. Together, our results expand the knowledge on the role of NTPDases in T.&amp;nbsp;cruzi infectivity, reenforcing the potential of this enzyme as a chemotherapy target to treat Chagas disease (CD).","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Nov","modification":"2025-04-20T03:33:18.601Z","creation":"2025-04-20T03:33:18.601Z"},"accession":"S-EPMC9736689","cross_references":{"pubmed":["36498985"],"doi":["10.3390/ijms232314661"]}}