Laboratório de Hemoparasitas E Vetores, Centro de Ciências Agroveterinárias (CAV), Universidade Do Estado de Santa Catarina (UDESC), Av. Luiz de Camões, 2090, Conta Dinheiro, Lages, 88520-000, SC, Brazil.
Laboratório de Biologia Celular, EVAHPI-Extracellular Vesicles and Host-Parasite Interactions Research Group, Instituto Carlos Chagas-Fiocruz, Curitiba, 81310-020, Brazil.
Parasitol Res. 2024 Sep 3;123(9):314. doi: 10.1007/s00436-024-08330-x.
Trypanosoma evansi is a unicellular protozoan responsible for causing a disease known as "surra," which is found in different regions of the world and primarily affects horses and camels. Few information is known about virulence factors released from the parasite within the animals. The organism can secrete extracellular vesicles (EVs), which transport a variety of molecules, including proteins. Before being considered exclusively as a means for eliminating unwanted substances, extracellular vesicles (EVs) have emerged as key players in intercellular communication, facilitating interactions between cells, host cells, and parasites, and even between parasites themselves. Thus, they may be used as potential biomarkers. This study aimed to assess the induction of EVs production by Ca, conduct a proteomic analysis of the EVs released by T. evansi, and identify epitopes that could serve as biomarkers. The findings indicated that Ca is not an effective promoter of vesiculation in T. evansi. Furthermore, the proteomic analysis has identified multiple proteins that have been investigated as biomarkers or vaccine antigens, previously. A total of 442 proteins were identified, with 7 of them specifically recognizing 9 epitopes that are unique to T. evansi. At least one of these epitopes of TevSTIB805.9.11580 have been previously identified, which increases the possibility of further investigating its potential as a biomarker.
伊氏锥虫是一种单细胞原生动物,可引起“苏拉病”,这种疾病在世界不同地区都有发现,主要影响马和骆驼。关于寄生虫在动物体内释放的毒力因子,人们知之甚少。该生物可以分泌细胞外囊泡(EVs),这些囊泡可以携带多种分子,包括蛋白质。细胞外囊泡(EVs)曾经被认为只是一种消除有害物质的手段,而现在它们已成为细胞间通讯的关键参与者,促进了细胞、宿主细胞和寄生虫之间的相互作用,甚至是寄生虫之间的相互作用。因此,它们可以用作潜在的生物标志物。本研究旨在评估 Ca 诱导 EVs 产生的能力,对 T. evansi 释放的 EVs 进行蛋白质组学分析,并鉴定可能作为生物标志物的表位。研究结果表明,Ca 不是 T. evansi 囊泡化的有效促进剂。此外,蛋白质组学分析已经鉴定出多种先前被研究作为生物标志物或疫苗抗原的蛋白质。共鉴定出 442 种蛋白质,其中 7 种蛋白质特异性识别出 9 个特属于 T. evansi 的表位。其中至少有一个 TevSTIB805.9.11580 的表位以前已经被识别出来,这增加了进一步研究其作为生物标志物的可能性。