Ansell Brendan R E, McConville Malcolm J, Baker Louise, Korhonen Pasi K, Emery Samantha J, Svärd Staffan G, Gasser Robin B, Jex Aaron R
Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Melbourne, Victoria, Australia
Bio21 Molecular Science and Biotechnology Institute, University of Melbourne, Melbourne, Victoria, Australia.
Antimicrob Agents Chemother. 2016 Sep 23;60(10):6034-45. doi: 10.1128/AAC.00977-16. Print 2016 Oct.
Understanding how parasites respond to stress can help to identify essential biological processes. Giardia duodenalis is a parasitic protist that infects the human gastrointestinal tract and causes 200 to 300 million cases of diarrhea annually. Metronidazole, a major antigiardial drug, is thought to cause oxidative damage within the infective trophozoite form. However, treatment efficacy is suboptimal, due partly to metronidazole-resistant infections. To elucidate conserved and stress-specific responses, we calibrated sublethal metronidazole, hydrogen peroxide, and thermal stresses to exert approximately equal pressure on trophozoite growth and compared transcriptional responses after 24 h of exposure. We identified 252 genes that were differentially transcribed in response to all three stressors, including glycolytic and DNA repair enzymes, a mitogen-activated protein (MAP) kinase, high-cysteine membrane proteins, flavin adenine dinucleotide (FAD) synthetase, and histone modification enzymes. Transcriptional responses appeared to diverge according to physiological or xenobiotic stress. Downregulation of the antioxidant system and α-giardins was observed only under metronidazole-induced stress, whereas upregulation of GARP-like transcription factors and their subordinate genes was observed in response to hydrogen peroxide and thermal stressors. Limited evidence was found in support of stress-specific response elements upstream of differentially transcribed genes; however, antisense derepression and differential regulation of RNA interference machinery suggest multiple epigenetic mechanisms of transcriptional control.
了解寄生虫如何应对压力有助于识别重要的生物学过程。十二指肠贾第虫是一种寄生性原生生物,可感染人类胃肠道,每年导致2亿至3亿例腹泻病例。甲硝唑是一种主要的抗贾第虫药物,被认为会在感染性滋养体形式内造成氧化损伤。然而,治疗效果并不理想,部分原因是甲硝唑耐药感染。为了阐明保守的和应激特异性反应,我们校准了亚致死剂量的甲硝唑、过氧化氢和热应激,以便对滋养体生长施加大致相等的压力,并比较暴露24小时后的转录反应。我们鉴定出252个基因,它们在对所有三种应激源的反应中差异转录,包括糖酵解酶和DNA修复酶、丝裂原活化蛋白(MAP)激酶、高半胱氨酸膜蛋白、黄素腺嘌呤二核苷酸(FAD)合成酶和组蛋白修饰酶。转录反应似乎根据生理应激或异生物质应激而有所不同。仅在甲硝唑诱导的应激下观察到抗氧化系统和α-贾第蛋白的下调,而在过氧化氢和热应激源的反应中观察到GARP样转录因子及其下属基因的上调。在差异转录基因上游支持应激特异性反应元件的证据有限;然而,反义去抑制和RNA干扰机制的差异调节表明存在多种转录控制的表观遗传机制。