Divergent Transcriptional Responses to Physiological and Xenobiotic Stress in Giardia duodenalis

Antimicrob Agents Chemother. 2016 Sep 23;60(10):6034-45. doi: 10.1128/AAC.00977-16. Print 2016 Oct.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiprotozoal Agents / pharmacology*
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism
  • DNA Repair Enzymes / genetics
  • DNA Repair Enzymes / metabolism
  • Epigenesis, Genetic
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Giardia lamblia / drug effects*
  • Giardia lamblia / genetics
  • Giardia lamblia / growth & development
  • Giardia lamblia / metabolism
  • Glycolysis / drug effects
  • Glycolysis / genetics
  • Histone Code / drug effects
  • Hot Temperature
  • Hydrogen Peroxide / pharmacology*
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Metronidazole / pharmacology*
  • Mitogen-Activated Protein Kinases / genetics
  • Mitogen-Activated Protein Kinases / metabolism
  • Models, Molecular
  • Nucleotidyltransferases / genetics
  • Nucleotidyltransferases / metabolism
  • Oxidation-Reduction
  • Oxidative Stress
  • Protozoan Proteins / genetics
  • Protozoan Proteins / metabolism
  • Transcription, Genetic*
  • Trophozoites / drug effects*
  • Trophozoites / growth & development
  • Trophozoites / metabolism

Substances

  • Antiprotozoal Agents
  • Cytoskeletal Proteins
  • GARP protein, Trypanosoma
  • Membrane Proteins
  • Protozoan Proteins
  • giardin protein, Giardia lamblia
  • Metronidazole
  • Hydrogen Peroxide
  • Mitogen-Activated Protein Kinases
  • Nucleotidyltransferases
  • FMN adenylyltransferase
  • DNA Repair Enzymes