| Autor: |
Blanco, Carolina Moreira, de Souza, Hugo Amorim dos Santos, Martins, Priscilla da Costa, Fabbri, Camila, Souza, Fernanda Souza de, Lima-Junior, Josué da Costa, Lopes, Stefanie Costa Pinto, Pratt-Riccio, Lilian Rose, Daniel-Ribeiro, Cláudio Tadeu, Totino, Paulo Renato Rivas |
| Zdroj: |
Molecular Biology Reports; 4/29/2024, Vol. 51 Issue 1, p1-5, 5p |
| Abstrakt: |
Background: Metacaspases comprise a family of cysteine proteases implicated in both cell death and cell differentiation of protists that has been considered a potential drug target for protozoan parasites. However, the biology of metacaspases in Plasmodium vivax − the second most prevalent and most widespread human malaria parasite worldwide, whose occurrence of chemoresistance has been reported in many endemic countries, remains largely unexplored. Therefore, the present study aimed to address, for the first time, the expression pattern of metacaspases in P. vivax parasites. Methods and results: P. vivax blood-stage parasites were obtained from malaria patients in the Brazilian Amazon and the expression of the three putative P. vivax metacaspases (PvMCA1-3) was detected in all isolates by quantitative PCR assay. Of note, the expression levels of each PvMCA varied noticeably across isolates, which presented different frequencies of parasite forms, supporting that PvMCAs may be expressed in a stage-specific manner as previously shown in P. falciparum. Conclusion: The detection of metacaspases in P. vivax blood-stage parasites reported herein, allows the inclusion of these proteases as a potential candidate drug target for vivax malaria, while further investigations are still required to evaluate the activity, role and essentiality of metacaspases in P. vivax biology. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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