Srikanta Deepa, Hole Camaron R, Williams Matthew, Khader Shabaana A, Doering Tamara L
Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri, USA.
Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri, USA
Infect Immun. 2017 Nov 17;85(12). doi: 10.1128/IAI.00195-17. Print 2017 Dec.
, the causative agent of cryptococcosis, is an opportunistic fungal pathogen that kills over 200,000 individuals annually. This yeast may grow freely in body fluids, but it also flourishes within host cells. Despite extensive research on cryptococcal pathogenesis, host genes involved in the initial engulfment of fungi and subsequent stages of infection are woefully understudied. To address this issue, we combined short interfering RNA silencing and a high-throughput imaging assay to identify host regulators that specifically influence cryptococcal uptake. Of 868 phosphatase and kinase genes assayed, we discovered 79 whose silencing significantly affected cryptococcal engulfment. For 25 of these, the effects were fungus specific, as opposed to general alterations in phagocytosis. Four members of this group significantly and specifically altered cryptococcal uptake; one of them encoded CaMK4, a calcium/calmodulin-dependent protein kinase. Pharmacological inhibition of CaMK4 recapitulated the observed defects in phagocytosis. Furthermore, mice deficient in CaMK4 showed increased survival compared to wild-type mice upon infection with This increase in survival correlated with decreased expression of pattern recognition receptors on host phagocytes known to recognize Altogether, we have identified a kinase that is involved in internalization by host cells and in host resistance to this deadly infection.
新型隐球菌病的病原体新型隐球菌是一种机会性真菌病原体,每年导致超过20万人死亡。这种酵母可以在体液中自由生长,但它也能在宿主细胞内大量繁殖。尽管对新型隐球菌发病机制进行了广泛研究,但参与真菌初始吞噬及后续感染阶段的宿主基因却鲜有研究。为解决这一问题,我们将短干扰RNA沉默与高通量成像分析相结合,以鉴定特异性影响新型隐球菌摄取的宿主调节因子。在检测的868个磷酸酶和激酶基因中,我们发现79个基因的沉默显著影响新型隐球菌的吞噬。其中25个基因的影响是真菌特异性的,而非吞噬作用的普遍改变。该组中的四个成员显著且特异性地改变了新型隐球菌的摄取;其中一个编码CaMK4,一种钙/钙调蛋白依赖性蛋白激酶。CaMK4的药理学抑制重现了观察到的吞噬缺陷。此外,与野生型小鼠相比,CaMK4缺陷小鼠在感染新型隐球菌后存活率增加。这种存活率的增加与宿主吞噬细胞上已知识别新型隐球菌的模式识别受体表达降低相关。总之,我们鉴定出一种激酶,它参与宿主细胞对新型隐球菌的内化以及宿主对这种致命感染的抗性。