Hanna S A, Monteiro da Silva J L, Giannini M J
Departamento de Análises Clínicas, Faculdade de Ciências Farmacêuticas UNESP, Rua Expedicionários do Brasil, Araraquara.
Microbes Infect. 2000 Jul;2(8):877-84. doi: 10.1016/s1286-4579(00)00390-7.
Paracoccidioides brasiliensis is a dimorphic fungus known to produce invasive systemic disease in humans. The 43-kDa glycoprotein of P. brasiliensis is the major diagnostic antigen of paracoccidioidomycosis and may act as a virulence factor, since it is a receptor for laminin.Very little is known about early interactions between this fungus and the host cells, so we developed in vitro a model system employing cultured mammalian cells (Vero cells), in order to investigate the factors and virulence mechanisms of P.brasiliensis related to the adhesion and invasion process. We found that there is a permanent interaction after 30 min of contact between the fungus and the cells. The yeasts multiply in the cells for between 5 and 24 h. Different strains of P. brasiliensis were compared, and strain 18 (high virulence) was the most strongly adherent, followed by strain 113 (virulent), 265 (considered of low virulence) and 113M (mutant obtained by ultraviolet radiation, deficient in gp43). P. brasiliensis adhered to the epithelial cells by a narrow tube, while depressions were noticed in the cell surface, suggesting an active cavitation process. An inhibition assay was performed and it was verified that anti-gp43 serum and a pool of sera from individuals with paracoccidioidomycosis were able to inhibit the adhesion of P. brasiliensis to the Vero cells. Glycoprotein 43 (gp43) antiserum abolished 85% of the binding activity of P. brasiliensis. This fungus can also invade the Vero cells, and intraepithelial parasitism could be an escape mechanism in paracoccidioidomycosis.
巴西副球孢子菌是一种已知可在人类中引起侵袭性全身疾病的双相真菌。巴西副球孢子菌的43 kDa糖蛋白是副球孢子菌病的主要诊断抗原,并且可能作为一种毒力因子,因为它是层粘连蛋白的受体。关于这种真菌与宿主细胞之间的早期相互作用知之甚少,因此我们在体外建立了一个使用培养的哺乳动物细胞(Vero细胞)的模型系统,以研究与巴西副球孢子菌黏附及侵袭过程相关的因素和毒力机制。我们发现真菌与细胞接触30分钟后存在持续的相互作用。酵母在细胞内繁殖5至24小时。对不同菌株的巴西副球孢子菌进行了比较,菌株18(高毒力)黏附力最强,其次是菌株113(有毒力)、265(被认为毒力低)和113M(通过紫外线辐射获得的突变体,缺乏gp43)。巴西副球孢子菌通过一根细管黏附在上皮细胞上,同时在细胞表面发现凹陷,提示存在活跃的空泡化过程。进行了抑制试验,证实抗gp43血清和来自副球孢子菌病患者的血清池能够抑制巴西副球孢子菌对Vero细胞的黏附。糖蛋白43(gp43)抗血清消除了巴西副球孢子菌85%的结合活性。这种真菌也能侵袭Vero细胞,上皮内寄生可能是副球孢子菌病中的一种逃逸机制。