Ma'ayeh Showgy Y, Knörr Livia, Svärd Staffan G
Department of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.
Department of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.
Int J Parasitol. 2015 Dec;45(14):925-38. doi: 10.1016/j.ijpara.2015.07.005. Epub 2015 Sep 1.
Giardia intestinalis is a microaerophilic parasite that infects the human upper small intestine, an environment that is fairly aerobic with reactive oxygen species being produced to fight off the parasite. It is quite perplexing how Giardia, lacking conventional eukaryotic antioxidant machinery (e.g. catalase, superoxide dismutase and glutathione peroxidase), can cope with the oxidative stress in this environment. We used transcriptomics (RNA sequencing and quantitative PCR) to study giardial gene expression changes in response to oxygen (O2; 1h) and hydrogen peroxide (H2O2; 150 μM, 500 μM and 1mM for 1h). The results showed phenotypic and transcriptional differences between Giardia isolates of different genotypes (WB, assemblage A and GS, assemblage B), with GS being more tolerant to H2O2 and exhibiting higher basic transcript levels of antioxidant genes (e.g. NADH oxidase lateral transfer candidate, peroxiredoxin 1 (Prx1) and thioredoxin (Trx)-like proteins). Cysteine is a major antioxidant in Giardia and its role in oxidative defense could be highlighted here by the up-regulation of gene transcripts encoding the cysteine-rich variable surface proteins (VSPs) and high cysteine membrane proteins (HCMPs). Genes in the thioredoxin system (Prx1, Trx and Trx reductase) occupied a central role in the gene expression response to oxidative stress, together with genes encoding metabolic (NADPH-producing enzymes, glutathione and glycerol biosynthetic enzymes) and O2-consuming nitric oxide detoxification enzymes (e.g. nitroreductase, flavohemoprotein and a flavodiiron protein). This study reveals the intricate network of genes associated with the oxidative stress response in Giardia, and provides a stepping-stone towards future studies at the protein level.
肠贾第虫是一种微需氧寄生虫,可感染人类上小肠,而上小肠环境相当需氧,会产生活性氧以抵御该寄生虫。令人十分困惑的是,肠贾第虫缺乏传统的真核生物抗氧化机制(如过氧化氢酶、超氧化物歧化酶和谷胱甘肽过氧化物酶),却能在这种环境中应对氧化应激。我们利用转录组学(RNA测序和定量PCR)研究了肠贾第虫在氧气(O₂;1小时)和过氧化氢(H₂O₂;150μM、500μM和1mM,处理1小时)作用下的基因表达变化。结果显示,不同基因型(WB,A群;GS,B群)的肠贾第虫分离株在表型和转录方面存在差异,GS对H₂O₂的耐受性更强,且抗氧化基因(如NADH氧化酶侧向转移候选基因、过氧化物还原酶1(Prx1)和硫氧还蛋白(Trx)样蛋白)的基础转录水平更高。半胱氨酸是肠贾第虫中的主要抗氧化剂,编码富含半胱氨酸的可变表面蛋白(VSP)和高半胱氨酸膜蛋白(HCMP)的基因转录本上调,可凸显其在氧化防御中的作用。硫氧还蛋白系统中的基因(Prx1、Trx和Trx还原酶)在对氧化应激的基因表达反应中占据核心地位,同时还有编码代谢(产生NADPH的酶、谷胱甘肽和甘油生物合成酶)和消耗O₂的一氧化氮解毒酶(如硝基还原酶、黄素血红蛋白和黄素二铁蛋白)的基因。本研究揭示了肠贾第虫中与氧化应激反应相关的复杂基因网络,并为未来在蛋白质水平的研究奠定了基础。