The Role of BRCT Domain from LmjPES in Pathogenesis.

Leishmaniasis is caused by protozoan parasites from the genus and remains one of the major threats to global health, impacting millions of people worldwide as well as animals including dogs. Several treatments have been used for managing leishmaniasis; nevertheless, drug resistance has emerged as an important obstacle to disease control. Therefore, there is an urgent need to discover new therapeutic targets. The aim of this work was to study the role played by the breast cancer associated 1 C-terminal (BRCT) domain from LmjPES protein (Pescadillo ribosomal biogenesis factor) in 's pathogenesis through the construction of novel genomic tools. For this purpose, integrative plasmids that were able to express the domain from and a hypothetical defective lacking this domain were constructed. It was observed that the overexpression of the aforementioned domain in . dysregulated the mRNA expression of 152 genes (95 up-regulated and 57 down-regulated) in respect to control parasites. Furthermore, clustering studies of these altered genes revealed an enrichment in genes related to metabolic processes, transporter activity, response to stimuli, and protein folding, which are categories described to be associated with the metacyclogenesis process and parasite survival. Interestingly, these genes reached normal levels of expression in parasites transfected with a defective (a mutated gene lacking the coding sequence of the domain). In addition, it was found that the footpad of mice inoculated with overexpressing parasites had significantly greater inflammation compared to the size of the footpad of animals infected with the control parasites. Based on all these results, it was suggested that the BRCT domain from LmjPES might play a role in . 's infection process and pathogenesis.