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兼职蛋白可诱导小鼠模型对念珠菌属产生保护作用。

Moonlighting proteins induce protection in a mouse model against Candida species.

机构信息

Departamento de Biología, División de Ciencias Naturales y Exactas, Campus Guanajuato, Universidad de Guanajuato, Noria Alta S/N, Col. Noria Alta, C.P. 36050, Guanajuato, Guanajuato, Mexico.

Departamento de Ingenierías Química, Electrónica y Biomédica, División de Ciencias e Ingenierías, Campus León, Universidad de Guanajuato, Guanajuato, Guanajuato, Mexico.

出版信息

Microb Pathog. 2018 Nov;124:21-29. doi: 10.1016/j.micpath.2018.08.024. Epub 2018 Aug 15.

Abstract

In recent years, C. albicans and C. glabrata have been identified as the main cause of candidemia and invasive candidiasis in hospitalized and immunocompromised patients. In order to colonize the human host, these fungi express several virulence factors such as the response to oxidative stress and the formation of biofilms. In the expression of these virulence factors, the cell wall of C. albicans and C. glabrata is of fundamental importance. As the outermost structure of the yeast, the cell wall is the first to come in contact with the reactive oxygen species (ROS) generated during the respiratory outbreak, and in the formation of biofilms, it is the first to adhere to organs or medical devices implanted in the human host. In both processes, several cell wall proteins (CWP) are required, since they promote attachment to human cells or abiotic surfaces, as well as to detoxify ROS. In our working group we have identified moonlighting CWP in response to oxidative stress as well as in the formation of biofilms. Having identified moonlighting CWP in Candida species in response to two virulence factors indicates that these proteins may possibly be immunodominant. The aim of the present work was to evaluate whether proteins of this type such as fructose-bisphosphate aldolase (Fba1), phosphoglycerate kinase (Pgk) and pyruvate kinase (Pk), could confer protection in a mouse model against C. albicans and C. glabrata. For this, recombinant proteins His-Fba1, His-Pgk and His-Pk were constructed and used to immunize several groups of mice. The immunized mice were infected with C. albicans or C. glabrata, and subsequently the liver, spleen and kidney were extracted and the number of CFU was determined. Our results showed that Pk confers immunity to mice against C. albicans, while Fba1 to C. glabrata. This data allows us to conclude that the moonlighting CWP, Fba1 and Pk confer in vivo protection in a specific way against each species of Candida. This makes them promising candidates for developing specific vaccines against these pathogens.

摘要

近年来,白念珠菌和光滑念珠菌已被确定为住院和免疫功能低下患者发生念珠菌血症和侵袭性念珠菌病的主要原因。为了定植于人体宿主,这些真菌表达了几种毒力因子,如对氧化应激的反应和生物膜的形成。在这些毒力因子的表达中,白念珠菌和光滑念珠菌的细胞壁至关重要。作为酵母的最外层结构,细胞壁首先接触到呼吸爆发过程中产生的活性氧(ROS),并且在生物膜的形成过程中,它首先附着在植入人体宿主的器官或医疗器械上。在这两个过程中,都需要几种细胞壁蛋白(CWP),因为它们促进与人体细胞或非生物表面的附着,以及对 ROS 的解毒。在我们的工作组中,我们已经鉴定出与氧化应激以及生物膜形成反应的兼职 CWP。已经鉴定出念珠菌属物种中响应两种毒力因子的兼职 CWP 表明,这些蛋白质可能是免疫显性的。本工作的目的是评估这类蛋白质(如果糖-1,6-二磷酸醛缩酶(Fba1)、磷酸甘油酸激酶(Pgk)和丙酮酸激酶(Pk))是否可以在小鼠模型中对白色念珠菌和光滑念珠菌提供保护。为此,构建了重组蛋白 His-Fba1、His-Pgk 和 His-Pk,并用于免疫几组小鼠。用免疫的小鼠感染白念珠菌或光滑念珠菌,然后提取肝脏、脾脏和肾脏,并确定 CFU 的数量。我们的结果表明,Pk 使小鼠对白色念珠菌具有免疫力,而 Fba1 对光滑念珠菌具有免疫力。这些数据使我们能够得出结论,兼职 CWP、Fba1 和 Pk 以特定方式赋予体内对每种念珠菌物种的保护。这使它们成为开发针对这些病原体的特异性疫苗的有前途的候选者。

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