Department of Microbiology and Immunology, McGill University, Montréal, QC, Canada.
Infectious Diseases and Immunity in Global Health Program, The Research Institute of the McGill University Health Centre, Montréal, QC, Canada.
Front Cell Infect Microbiol. 2022 Feb 3;11:709258. doi: 10.3389/fcimb.2021.709258. eCollection 2021.
Protozoan parasites of the genus Leishmania are transmitted by the bite of infected sand flies leading to a wide range of diseases called leishmaniasis. Recently, we demonstrated that spp.derived exosomes/extracellular vesicles (EVs/LeishEXO) were released in the lumen of the sand fly midgut and to be co-egested with the parasite during the blood meal and that LeishEXO were found to stimulate an inflammatory response conducting to an exacerbated cutaneous leishmaniasis, also it was shown that these vesicles cargo important virulence factors like GP63. Thus, this study aimed to confirm through morphological and proteomic analysis a novel model specificity utilizing another set of GP63-altered parasite strains. Consequently, we proposed to further study the impact of different GP63 vesicle expression levels on their ability to modulate innate inflammatory cell responses, and finally to determine the importance of GP63 vesicle content on the exacerbation of the cutaneous spp. pathology after their host co-inoculation. Our results revealed that the protein composition of extracted extracellular vesicles were similar to each other and that GP63 was the sole virulence factor changed in the exosomes composition confirming the specificity of the chosen novel model. We further demonstrated that vesicles with different GP63 EVs cargo displayed distinctive macrophage immunomodulatory capabilities at both gene and protein expression . Finally, we showed their diverse impact on the spp. cutaneous pathology in an setting and confirmed GP63 as a primordial component of the ability of these EVs in augmenting the inflammatory cutaneous response in spp. infection. Our findings provide new insight on the immune response happening in cutaneous leishmaniasis, shade light on the mechanism behind the host-pathogen interaction occurring in the initial moments of infection, thus creating the opportunity of using them as the target of new pharmacological treatments and vaccinations.
原生动物利什曼原虫属的寄生虫通过受感染的沙蝇叮咬传播,导致一系列被称为利什曼病的疾病。最近,我们证明了 spp.衍生的外泌体/细胞外囊泡 (EV/LeishEXO) 在沙蝇中肠的腔中释放,并在吸血时与寄生虫一起被共同摄取,并且 LeishEXO 被发现刺激炎症反应,导致皮肤利什曼病加剧,还表明这些囊泡携带重要的毒力因子,如 GP63。因此,本研究旨在通过形态和蛋白质组学分析,利用另一组改变的 GP63 的寄生虫菌株来证实一种新的模型特异性。因此,我们建议进一步研究不同 GP63 囊泡表达水平对其调节固有炎症细胞反应能力的影响,最后确定 GP63 囊泡内容物在其宿主共同接种后加剧皮肤 spp.病理的重要性。我们的结果表明,提取的细胞外囊泡的蛋白质组成彼此相似,并且 GP63 是外泌体组成中唯一改变的毒力因子,证实了所选新型模型的特异性。我们进一步证明,具有不同 GP63 EV 货物的囊泡在基因和蛋白质表达水平上显示出独特的巨噬细胞免疫调节能力 。最后,我们在 背景下展示了它们对皮肤利什曼病的不同影响,并证实了 GP63 是这些 EV 增强皮肤利什曼病感染中炎症反应能力的原始组成部分。我们的研究结果为皮肤利什曼病中的免疫反应提供了新的见解,揭示了宿主-病原体相互作用发生在感染初始时刻背后的机制,从而为利用它们作为新的药物治疗和疫苗接种的靶点提供了机会。