Departamento de Análises Clínicas e Toxicológicas, Faculdade de Ciências Farmacêuticas, Universidade de São Paulo, Brazil, Avenida Professor Lineu Prestes, 580, São Paulo, 05508-000, Brazil.
J Med Microbiol. 2019 Jan;68(1):87-94. doi: 10.1099/jmm.0.000876. Epub 2018 Nov 19.
Sporothrix brasiliensis, a member of the Sporothrix schenckii complex, is a major cause of epidemic outbreaks of sporotrichosis due to its greater virulence and ability to evade the immune system. The absence of studies about this species led to this study, with the aim to evaluate the importance of Toll-like receptor-2 (TLR-2) during S. brasiliensis infection.
In vitro assays were performed using bone marrow-derived macrophages from both wild-type (C57BL/6) and TLR-2 knockout () mice. In vivo assays were also performed, on which the mice (C57BL/6 and TLR-2) were intraperitoneally infected with S. brasiliensis yeast American Type Culture Collection MYA-4831 and euthanized on days 7, 14 and 28 post infection. The following parameters were then evaluated: fungal burden in spleen, liver, kidney and brain; the production of cytokines TNF-α, IFN-γ, IL-4, IL-2, IL-6 and IL-10.
The in vitro results showed that the absence of TLR-2 resulted in impaired phagocytosis, microbicide mechanisms utilizing the production of nitric oxide, and the cytokine production (TNF-α, IL-6 and IL-10). The in vivo results demonstrated that the absence of TLR-2 during experimental S. brasiliensis infection promoted increased dissemination after 14 and 28 days and suggests a polarized Th17 response in an attempt to control the infection.
TLR-2 signalling appears to be important in the innate immune response against S. brasiliensis.
巴西利蒙球孢子菌(Sporothrix brasiliensis)是申克孢子丝菌复合体的一个成员,由于其较强的毒力和逃避免疫系统的能力,是导致孢子丝菌病爆发流行的主要原因。由于缺乏对该物种的研究,因此进行了这项研究,旨在评估 Toll 样受体 2(TLR-2)在巴西利蒙球孢子菌感染中的重要性。
使用来自野生型(C57BL/6)和 TLR-2 敲除()小鼠的骨髓来源的巨噬细胞进行体外测定。还进行了体内测定,将小鼠(C57BL/6 和 TLR-2)经腹腔感染巴西利蒙球孢子菌酵母美国典型培养物保藏中心 MYA-4831,并在感染后第 7、14 和 28 天处死。然后评估以下参数:脾、肝、肾和脑中的真菌负荷;细胞因子 TNF-α、IFN-γ、IL-4、IL-2、IL-6 和 IL-10 的产生。
体外结果表明,TLR-2 的缺失导致吞噬作用受损、利用一氧化氮产生的杀菌机制以及细胞因子(TNF-α、IL-6 和 IL-10)的产生受损。体内结果表明,在实验性巴西利蒙球孢子菌感染期间 TLR-2 的缺失促进了 14 和 28 天后的传播增加,并提示试图控制感染的 Th17 反应的极化。
TLR-2 信号似乎在巴西利蒙球孢子菌的固有免疫反应中很重要。