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Disarming Fungal Pathogens: Bacillus safensis Inhibits Virulence Factor Production and Biofilm Formation by Cryptococcus neoformans and Candida albicans

机译:解除真菌病原体:枯草芽孢杆菌通过新隐球菌白色念珠菌抑制毒力因子的产生和生物膜的形成

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ABSTRACT Bacteria interact with each other in nature and often compete for limited nutrient and space resources. However, it is largely unknown whether and how bacteria also interact with human fungal pathogens naturally found in the environment. Here, we identified a soil bacterium, Bacillus safensis , which potently blocked several key Cryptococcus neoformans virulence factors, including formation of the antioxidant pigment melanin and production of the antiphagocytic polysaccharide capsule. The bacterium also inhibited de novo cryptococcal biofilm formation but had only modest inhibitory effects on already formed biofilms or planktonic cell growth. The inhibition of fungal melanization was dependent on direct cell contact and live bacteria. B.?safensis also had anti-virulence factor activity against another major human-associated fungal pathogen, Candida albicans . Specifically, dual-species interaction studies revealed that the bacterium strongly inhibited C.?albicans filamentation and biofilm formation. In particular, B.?safensis physically attached to and degraded candidal filaments. Through genetic and phenotypic analyses, we demonstrated that bacterial chitinase activity against fungal cell wall chitin is a factor contributing to the antipathogen effect of B.?safensis . IMPORTANCE Pathogenic fungi are estimated to contribute to as many human deaths as tuberculosis or malaria. Two of the most common fungal pathogens, Cryptococcus neoformans and Candida albicans , account for up to 1.4 million infections per year with very high mortality rates. Few antifungal drugs are available for treatment, and development of novel therapies is complicated by the need for pathogen-specific targets. Therefore, there is an urgent need to identify novel drug targets and new drugs. Pathogens use virulence factors during infection, and it has recently been proposed that targeting these factors instead of the pathogen itself may represent a new approach to develop antimicrobials. Here, we identified a soil bacterium that specifically blocked virulence factor production and biofilm formation by C.?neoformans and C.?albicans . We demonstrate that the bacterial antipathogen mechanism is based in part on targeting the fungal cell wall, a structure not found in human cells.
机译:摘要细菌在自然界中相互影响,经常争夺有限的营养和空间资源。然而,很大程度上未知细菌是否以及如何与环境中自然存在的人类真菌病原体相互作用。在这里,我们确定了一种土壤细菌,即安全芽孢杆菌,该细菌有效地阻断了几个关键的新型隐球菌毒力因子,包括抗氧化剂色素黑色素的形成和抗吞噬多糖胶囊的生产。该细菌还抑制了新生球菌生物膜的形成,但对已经形成的生物膜或浮游细胞的生长只有中等程度的抑制作用。真菌黑色素的抑制取决于直接的细胞接触和活细菌。沙门氏菌也对另一种主要的人类相关真菌病原体白色念珠菌具有抗毒力。具体而言,双物种相互作用研究表明该细菌强烈抑制白色念珠菌丝化和生物膜形成。尤其是,非洲黑麦芽孢杆菌物理上附着并降解了念珠丝。通过遗传和表型分析,我们证明了针对真菌细胞壁几丁质的细菌几丁质酶活性是促成枯草芽孢杆菌抗病原作用的一个因素。重要信息据估计,致病真菌导致的死亡人数与结核病或疟疾一样多。两种最常见的真菌病原体,新隐球菌和白色念珠菌,每年导致多达140万例感染,死亡率很高。很少有抗真菌药物可用于治疗,并且由于需要病原体特异性靶标,新疗法的开发变得复杂。因此,迫切需要鉴定新药物靶标和新药物。病原体在感染过程中使用毒力因子,最近有人提出,针对这些因子而不是病原体本身可能是开发抗菌素的新方法。在这里,我们确定了一种土壤细菌,该细菌特异性地阻止了新孢梭菌和白色念珠菌的致病因子产生和生物膜形成。我们证明了细菌抗病原体机制部分基于靶向真菌细胞壁,这种细胞在人类细胞中未发现。

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