Divergent Transcriptional Responses to Physiological and Xenobiotic Stress in Giardia duodenalis

被引:14
作者
Ansell, Brendan R. E. [1 ]
McConville, Malcolm J. [2 ]
Baker, Louise [1 ,3 ]
Korhonen, Pasi K. [1 ]
Emery, Samantha J. [3 ]
Svard, Staffan G. [4 ]
Gasser, Robin B. [1 ]
Jex, Aaron R. [1 ,3 ]
机构
[1] Univ Melbourne, Fac Vet & Agr Sci, Melbourne, Vic, Australia
[2] Univ Melbourne, Bio21 Mol Sci & Biotechnol Inst, Melbourne, Vic, Australia
[3] Walter & Eliza Hall Inst Med Res, Populat Hlth & Immun, Melbourne, Vic, Australia
[4] Uppsala Univ, Dept Cell & Mol Biol, Uppsala, Sweden
基金
澳大利亚研究理事会;
关键词
ENTAMOEBA-HISTOLYTICA; NITROIMIDAZOLE DRUGS; RESISTANCE MECHANISMS; ANTIGENIC VARIATION; GENE-EXPRESSION; REACTIVE OXYGEN; CELL-CYCLE; LAMBLIA; METRONIDAZOLE; PROTEIN;
D O I
10.1128/AAC.00977-16
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 alpha-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.
引用
收藏
页码:6034 / 6045
页数:12
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