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Teixeira, T. L.

Publications and source records attributed to Teixeira, T. L..

2 recordsLinked to original sources

A comparative analysis of BrdU and EdU genotoxicity shows that trypanosomatids exhibit unique responses to the presence of these thymidine analogs in their DNA

The thymidine analogs 5-bromo-2'-deoxyuridine (BrdU) and 5-ethynyl-2'-deoxyuridine (EdU) are widely used to monitor DNA synthesis. Although studies have reported EdU toxicity in certain cell types, no reports to date describe genotoxic effects associated with BrdU/EdU use in trypanosomatids, etiological agents of neglected tropical diseases. This lack of studies raises two possibilities: either these nucleotides are not toxic to these parasites, or the observed genotoxicity was not relevant under the experimental conditions used. Here, we assessed the potential toxicity of BrdU and EdU across three pathogenic trypanosomatids: Trypanosoma cruzi, Trypanosoma brucei, and Leishmania major. Our findings show that EdU has greater genotoxic potential than BrdU. Nevertheless, trypanosomatids respond markedly differently to DNA alterations caused by this analog: T. cruzi cells stop replicating and accumulate in S phase, T. brucei tolerates the DNA lesions generated, while part of the L. major population appears to display an altruistic behavior that benefits the survivors. Furthermore, in silico assays suggest that, once incorporated into DNA, the ethynyl group increases the EdU's polarity, thereby altering DNA structure more strongly than BrdU does after the first round of DNA replication. Together, our findings suggest that using thymidine analogs in trypanosomatids should be preceded by rigorous preliminary analysis, especially when using EdU. Otherwise, the data may be biased by a BrdU/EdU-triggered DNA damage response. We believe this study may serve as an atlas to guide the initial selection of thymidine analog concentrations and exposure periods.

molecular biology↗

Reduced levels of inositol hexakisphosphate kinase (IP6K) impair life-cycle transitions and the intracellular development of Trypanosoma cruzi within human cardiomyocytes

Trypanosoma cruzi is the etiological agent of Chagas disease. During its life cycle, T. cruzi undergoes several key differentiation processes that are essential for its survival. The precise mechanisms that regulate these processes remain elusive, and any interference in this cycle would represent a breakthrough in the development of effective therapy against Chagas disease. Here, after depleting a single IP6K allele of T. cruzi, we observed that key differentiation processes (metacyclogenesis, amastigogenesis and trypomastigogenesis) were profoundly impaired. Epimastigote forms of IP6K-deficient T. cruzi exhibited morphological alterations and reduced metacyclogenesis. IP6K-deficient metacyclic forms had reduced infective potential in human cardiomyocytes. IP6K-deficient amastigote forms showed impaired ability to transform into trypomastigotes, with most of the population egressing from human cardiomyocytes without completing trypomastigogenesis. Together, our results suggest that IP6K is critical to sustain the T. cruzi life cycle. Since disruption of both IP6K alleles was lethal and the primary structure of IP6K shares only [~]25% similarity with its human homolog, this kinase emerges as a promising target for drug development against Chagas disease. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=153 HEIGHT=200 SRC="FIGDIR/small/700787v2_ufig1.gif" ALT="Figure 1"> View larger version (44K): org.highwire.dtl.DTLVardef@1cb37f0org.highwire.dtl.DTLVardef@c59fb8org.highwire.dtl.DTLVardef@791cb7org.highwire.dtl.DTLVardef@14c68fd_HPS_FORMAT_FIGEXP M_FIG C_FIG

microbiology↗