Overexpression of TcNTPDase-1 Gene Increases Infectivity in Mice Infected with Trypanosoma cruzi .
Natália Lins da Silva-GomesLeonardo Alexandre de Souza RuivoClaudia MoreiraMarcelo Meuser BatistaCristiane França da SilvaDenise da Gama Jaen BatistaStênio FragosoGabriel Melo de OliveiraMaria de Nazaré Correia SoeiroOtacílio da Cruz MoreiraPublished in: International journal of molecular sciences (2022)
Ecto-nucleoside triphosphate diphosphohydrolases (NTPDases) are enzymes located on the surface of the T.&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&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 < 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.&nbsp;cruzi infectivity, reenforcing the potential of this enzyme as a chemotherapy target to treat Chagas disease (CD).
Keyphrases
- plasmodium falciparum
- wild type
- mouse model
- body mass index
- physical activity
- trypanosoma cruzi
- cell proliferation
- left ventricular
- escherichia coli
- oxidative stress
- clinical trial
- cardiovascular events
- heart failure
- randomized controlled trial
- squamous cell carcinoma
- hepatitis b virus
- weight gain
- study protocol
- coronary artery disease
- intensive care unit
- metabolic syndrome
- high fat diet induced
- adipose tissue
- atrial fibrillation
- locally advanced
- risk assessment
- skeletal muscle
- drug induced
- mechanical ventilation
- open label
- rectal cancer
- toxoplasma gondii
- transition metal