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细胞壁黑色素通过螯合钙来阻碍多糖荚膜的生长。

Cell wall melanin impedes growth of the polysaccharide capsule by sequestering calcium.

作者信息

Baker Rosanna P, Liu Amy Z, Casadevall Arturo

出版信息

bioRxiv. 2024 Jun 20:2024.06.20.599928. doi: 10.1101/2024.06.20.599928.

Abstract

UNLABELLED

has emerged as a frontrunner among deadly fungal pathogens and is particularly life-threatening for many HIV-infected individuals with compromised immunity. Multiple virulence factors contribute to the growth and survival of within the human host, the two most prominent of which are the polysaccharide capsule and melanin. As both of these features are associated with the cell wall, we were interested to explore possible cooperative or competitive interactions between these two virulence factors. Whereas capsule thickness had no effect on the rate at which cells became melanized, build-up of the melanin pigment layer resulted in a concomitant loss of polysaccharide material, leaving melanized cells with significantly thinner capsules than their non-melanized counterparts. When melanin was provided exogenously to cells in a transwell culture system we observed a similar inhibition of capsule growth and maintenance. Our results show that melanin sequesters calcium thereby limiting its availability to form divalent bridges between polysaccharide subunits required for outer capsule assembly. The decreased ability of melanized cells to incorporate exported polysaccharide into the growing capsule correlated with the amount of shed polysaccharide, which could have profound negative impacts on the host immune response.

SIGNIFICANCE STATEMENT

is an opportunistic fungal pathogen that presents a significant health risk for immunocompromised individuals. We report an interaction between the two major cryptococcal virulence factors, the polysaccharide capsule and melanin. Melanin impacted the growth and maintenance of the polysaccharide capsule, resulting in loss of capsular material during melanization. Our results suggest that melanin can act as a sink for calcium, thereby limiting its availability to form ionic bridges between polysaccharide chains on the growing surface of the outer capsule. As polysaccharide is continuously exported to support capsule growth, failure of melanized cells to incorporate this material results in a higher concentration of shed polysaccharide in the extracellular milieu, which is expected to interfere with host immunity.

摘要

未标记

已成为致命真菌病原体中的佼佼者,对许多免疫功能受损的艾滋病毒感染者尤其具有生命威胁。多种毒力因子有助于其在人类宿主中的生长和存活,其中最突出的两个是多糖荚膜和黑色素。由于这两个特征都与细胞壁相关,我们有兴趣探索这两种毒力因子之间可能的协同或竞争相互作用。虽然荚膜厚度对细胞黑化的速率没有影响,但黑色素色素层的积累导致多糖物质同时损失,使黑化细胞的荚膜比未黑化细胞的荚膜明显更薄。当在跨孔培养系统中向外源提供黑色素时,我们观察到对荚膜生长和维持的类似抑制作用。我们的结果表明,黑色素螯合钙,从而限制其形成外荚膜组装所需多糖亚基之间二价桥的可用性。黑化细胞将输出的多糖整合到生长中的荚膜中的能力下降与脱落多糖的量相关,这可能对宿主免疫反应产生深远的负面影响。

意义声明

是一种机会性真菌病原体,对免疫功能低下的个体构成重大健康风险。我们报告了两种主要的新型隐球菌毒力因子,多糖荚膜和黑色素之间的相互作用。黑色素影响多糖荚膜的生长和维持,导致黑化过程中荚膜物质的损失。我们的结果表明,黑色素可以作为钙的汇,从而限制其在形成外荚膜生长表面多糖链之间离子桥的可用性。由于多糖不断输出以支持荚膜生长,黑化细胞无法整合这种物质导致细胞外环境中脱落多糖的浓度更高,这预计会干扰宿主免疫。

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