Department of Internal Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Int J Parasitol. 2012 Oct;42(11):1007-15. doi: 10.1016/j.ijpara.2012.08.006. Epub 2012 Sep 23.
The protozoan parasite, Entamoeba histolytica, invades the host colon causing significant tissue destruction and inflammation. Upon host infection, the parasite is confronted with reactive oxygen and nitrogen species (ROS/RNS) that cause large-scale changes in gene expression profiles, which likely support the parasite's adaptation to the host environment. We have previously identified oxidative and nitrosative stress responsive genes using whole-genome expression profiling. Functional studies on two such genes are now reported and demonstrate that they have roles in parasite virulence. EHI_056680 encodes a small hypothetical protein named E. histolytica stress-induced adhesion factor (EhSIAF); EHI_188210 encodes a putative phospholipid transporting P-type ATPase/flippase (EhPTPA). Over-expression of each protein in E. histolytica trophozoites enhanced parasite survival in response to oxidative stress. Exposure to oxidative and nitrosative stress did not affect the localization of EhSIAF or EhPTPA but markedly increased EhPTPA protein levels. Interestingly, over-expression of each gene resulted in parasites with increased adherence to healthy mammalian cells, but increased adherence to apoptotic cells was noted only in EhSIAF over-expressing parasites. However, despite having increased adherence to both healthy and apoptotic host cells, EhSIAF-over-expressing parasites were reduced in their ability to destroy mammalian cell monolayers, raising the intriguing possibility that EhSIAF over-expression caused signaling defects or resulted in a dominant negative phenotype. Over-expression of EhSIAF and EhPTPA also resulted in decreased motility in a transwell motility assay. Thus, we have confirmed that two genes that are upregulated by ROS confer increased resistance to oxidative stress and have identified an unexpected role of EhSIAF and EhPTPA in host cell adherence and a role of EhSIAF in parasite virulence. Our data imply that stress response genes may play multi-factorial roles in amoebic pathogenesis.
原生动物寄生虫溶组织内阿米巴会侵袭宿主的结肠,导致严重的组织破坏和炎症。在宿主感染后,寄生虫会面临活性氧和氮物种(ROS/RNS)的攻击,这些物质会导致基因表达谱的大规模变化,这可能支持寄生虫适应宿主环境。我们之前使用全基因组表达谱分析鉴定了氧化应激和硝化应激反应基因。现在报告了对其中两个基因的功能研究,结果表明它们在寄生虫的毒力中发挥作用。EHI_056680 编码一种名为溶组织内阿米巴应激诱导黏附因子(EhSIAF)的小假设蛋白;EHI_188210 编码一种假定的磷脂转运 P 型 ATP 酶/翻转酶(EhPTPA)。在溶组织内阿米巴滋养体中过表达这两种蛋白都增强了寄生虫对氧化应激的存活能力。氧化应激和硝化应激的暴露并不影响 EhSIAF 或 EhPTPA 的定位,但显著增加了 EhPTPA 蛋白水平。有趣的是,两种基因的过表达都导致寄生虫对健康哺乳动物细胞的黏附增加,但只有在 EhSIAF 过表达的寄生虫中才观察到对凋亡细胞的黏附增加。然而,尽管 EhSIAF 过表达的寄生虫对健康和凋亡宿主细胞的黏附增加,但它们破坏哺乳动物细胞单层的能力降低,这提出了一个有趣的可能性,即 EhSIAF 过表达导致信号缺陷或导致显性负表型。EhSIAF 和 EhPTPA 的过表达也导致在 Transwell 迁移试验中迁移能力降低。因此,我们已经证实,两个由 ROS 上调的基因赋予了对氧化应激的更高抗性,并发现 EhSIAF 和 EhPTPA 在宿主细胞黏附中的意想不到的作用,以及 EhSIAF 在寄生虫毒力中的作用。我们的数据表明,应激反应基因可能在阿米巴病发病机制中发挥多方面的作用。