Expression Analysis of Thirteen Genes in Response to Nifurtimox and Benznidazole in Mexican Isolates of Trypanosoma cruzi by Digital PCR
- 7 January 2025
- journal article
- research article
- Published by Springer Nature in Acta Parasitologica
- Vol. 70 (1) , 1-11
Abstract
Despite being the most relevant and critical option for managing Chagas disease, pharmacological therapy is currently limited by the availability of only two drugs, benznidazole and nifurtimox. Their effectiveness is further restricted in the chronic phase of the infection, as they induce severe side effects and require prolonged treatment. Additionally, the use of these drugs can lead to the emergence of substantial resistance problems, compounded by the potential natural resistance of some parasite isolates. This study analyzes the expression of 13 genes by digital PCR in four Mexican T. cruzi isolates treated with NFX and BZN. Each isolate exhibited a unique combination of enzyme expression in response to the oxidative stress induced by the antichagasic agents. Notably, we observed the overexpression of cruzipain (CZP), L-threonine dehydrogenase (TDH), and detoxification-related enzymes such as Glutathionyl spermidine synthetase (GST) and Superoxide dismutase-A (SOD). These findings highlight the need for further studies to elucidate the molecular mechanisms underlying this resistance, which pose both unexpected challenges for Chagas disease therapy and a biological barrier to the action of these drugs. These findings highlight the need for further studies to understand how these resistance mechanisms contribute to treatment failure and constitute a biological barrier to drug action.Keywords
Funding Information
- Conahcyt ((1138096))
- COVEYCIDET (11112017/2023.)
This publication has 50 references indexed in Scilit:
- Evaluation and Treatment of Chagas Disease in the United StatesJAMA, 2007
- Increased expression of iron-containing superoxide dismutase-A (TcFeSOD-A) enzyme in Trypanosoma cruzi population with in vitro-induced resistance to benznidazoleActa Tropica, 2006
- Trypanosoma cruzi: Analysis of the complete PUF RNA-binding protein familyExperimental Parasitology, 2006
- Deletion of copies of the gene encoding old yellow enzyme (TcOYE), a NAD(P)H flavin oxidoreductase, associates with in vitro-induced benznidazole resistance in Trypanosoma cruziMolecular and Biochemical Parasitology, 2006
- RNA-binding proteins and mRNA turnover in trypanosomesTrends in Parasitology, 2003
- A Key Role for Old Yellow Enzyme in the Metabolism of Drugs by Trypanosoma cruzi Journal of Experimental Medicine, 2002
- Sequence variation in the dihydrofolate reductase-thymidylate synthase (DHFR-TS) and trypanothione reductase (TR) genes of Trypanosoma cruziMolecular and Biochemical Parasitology, 2002
- Molecular characterization of susceptible and naturally resistant strains of Trypanosoma cruzi to benznidazole and nifurtimoxMolecular and Biochemical Parasitology, 1998
- A pteridine reductase gene ptr1 contiguous to a P-glycoprotein confers resistance to antifolates in Trypanosoma cruzi1Note: nucleotide sequence data reported in this paper have been submitted to the GenBankTM data base with the accession number U61221.1Molecular and Biochemical Parasitology, 1997
- Susceptibility and natural resistance of Trypanosoma cruzi strains to drugs used clinically in Chagas diseaseTransactions of the Royal Society of Tropical Medicine and Hygiene, 1987