Martinez Santiago José, Nardella Gonzalo Nicolás, Rodríguez Matías Exequiel, Rivero Cynthia Vanesa, Agüero Fernán, Romano Patricia Silvia
Laboratorio de Biología de Trypanosoma cruzi y la célula hospedadora. Instituto de Histología y Embriología, Universidad Nacional de Cuyo (IHEM-CONICET-UNCUYO), Mendoza, Argentina.
Facultad de Farmacia y Bioquímica. Universidad Juan A. Maza. Mendoza, Argentina.
Curr Res Microb Sci. 2022 Jun 30;3:100152. doi: 10.1016/j.crmicr.2022.100152. eCollection 2022.
, the etiologic agent of Chagas disease (CD) presents a wide genetic and phenotypic diversity that is classified into seven lineages or discrete typing units (DTU: TcI to TcVI and Tcbat). Although isolates and strains that belong to a particular group can share some attributes, such as geographic distribution, others like growth rate, cell tropism, and response to treatment can be highly variable. In addition, studies that test new trypanocidal drugs are frequently conducted on strains maintained for a long time in axenic culture, resulting in changes in parasite virulence and other important features. This work aimed to isolate and characterize a new strain from a chronic Chagas disease patient. The behavior of this isolate was studied by using standard assays and mice infection tests and compared with the Y strain (TcY), broadly used in research laboratories worldwide. Data showed that TcM behaves as a slow-growing strain that develops chronic infections in mice and displays high tropism to muscular tissues, in accordance with its clinical performance. In contrast, the Y strain behaved as an acute strain that can infect different types of cells and tissues. Interestingly, TcM, which belongs to DTU TcV, is more susceptible to benznidazole than TcY, a TcII strain considered moderately resistant to this drug. These differential properties contribute to the characterization of a TcV strain, one of the main lineages in the southern countries of South America, and open the possibility to introduce changes that improve the management of Chagas patients in the future.
恰加斯病(CD)的病原体呈现出广泛的遗传和表型多样性,可分为七个谱系或离散分型单元(DTU:TcI至TcVI和Tcbat)。尽管属于特定组的分离株和菌株可以共享一些属性,如地理分布,但其他属性,如生长速率、细胞嗜性和对治疗的反应可能高度可变。此外,测试新型杀锥虫药物的研究通常在无细胞培养中长期保存的菌株上进行,这会导致寄生虫毒力和其他重要特征发生变化。这项工作旨在从一名慢性恰加斯病患者中分离并鉴定一种新的菌株。通过使用标准测定法和小鼠感染试验研究了该分离株的行为,并与全球研究实验室广泛使用的Y菌株(TcY)进行了比较。数据显示,TcM表现为一种生长缓慢的菌株,可在小鼠中引发慢性感染,并对肌肉组织表现出高度嗜性,这与其临床表现一致。相比之下,Y菌株表现为一种急性菌株,可感染不同类型的细胞和组织。有趣的是,属于DTU TcV的TcM比TcY对苯并硝唑更敏感,TcY是一种被认为对该药物中度耐药的TcII菌株。这些差异特性有助于对TcV菌株进行表征,TcV菌株是南美洲南部国家的主要谱系之一,并为未来改善恰加斯病患者的管理引入变革开辟了可能性。