Ochoa-Martínez Paulina, López-Monteon Aracely, López-Domínguez Jaime, Manning-Cela Rebeca Georgina, Ramos-Ligonio Angel
Doctorado en Ciencias Biomédicas, Centro de Investigaciones Biomédicas, Universidad Veracruzana, Xalapa, Veracruz, Mexico.
Edificio D, Facultad de Ciencias Químicas, LADISER Inmunología y Biología Molecular, Universidad Veracruzana, Orizaba, Veracruz, México.
Acta Parasitol. 2025 Jan 7;70(1):15. doi: 10.1007/s11686-024-00986-w.
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.
尽管药物治疗是管理恰加斯病最相关且关键的选择,但目前仅受两种药物——苯并硝唑和硝呋替莫的可用性限制。在感染的慢性阶段,它们的有效性进一步受限,因为它们会引发严重的副作用且需要长期治疗。此外,这些药物的使用会导致大量耐药问题的出现,一些寄生虫分离株的潜在天然耐药性更是雪上加霜。本研究通过数字PCR分析了用硝呋替莫(NFX)和苯并硝唑(BZN)处理的四个墨西哥克氏锥虫分离株中13个基因的表达。每个分离株在响应抗恰加斯病药物诱导的氧化应激时都表现出独特的酶表达组合。值得注意的是,我们观察到克氏锥虫蛋白酶(CZP)、L-苏氨酸脱氢酶(TDH)以及解毒相关酶如谷胱甘肽亚精胺合成酶(GST)和超氧化物歧化酶-A(SOD)的过表达。这些发现凸显了进一步研究以阐明这种耐药性背后分子机制的必要性,这给恰加斯病治疗带来了意想不到的挑战,也构成了这些药物作用的生物屏障。这些发现凸显了进一步研究以了解这些耐药机制如何导致治疗失败并构成药物作用生物屏障的必要性。