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Divergent Transcriptional Responses to Physiological and Xenobiotic Stress in Giardia duodenalis.
Ansell, Brendan R E; McConville, Malcolm J; Baker, Louise; Korhonen, Pasi K; Emery, Samantha J; Svärd, Staffan G; Gasser, Robin B; Jex, Aaron R.
Afiliação
  • Ansell BR; Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Melbourne, Victoria, Australia bransell@unimelb.edu.au.
  • McConville MJ; Bio21 Molecular Science and Biotechnology Institute, University of Melbourne, Melbourne, Victoria, Australia.
  • Baker L; Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Melbourne, Victoria, Australia Population Health and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
  • Korhonen PK; Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Melbourne, Victoria, Australia.
  • Emery SJ; Population Health and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
  • Svärd SG; Department of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.
  • Gasser RB; Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Melbourne, Victoria, Australia.
  • Jex AR; Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Melbourne, Victoria, Australia Population Health and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Antimicrob Agents Chemother ; 60(10): 6034-45, 2016 10.
Article em En | MEDLINE | ID: mdl-27458219
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transcrição Gênica / Giardia lamblia / Trofozoítos / Peróxido de Hidrogênio / Metronidazol / Antiprotozoários Tipo de estudo: Prognostic_studies Idioma: En Revista: Antimicrob Agents Chemother Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transcrição Gênica / Giardia lamblia / Trofozoítos / Peróxido de Hidrogênio / Metronidazol / Antiprotozoários Tipo de estudo: Prognostic_studies Idioma: En Revista: Antimicrob Agents Chemother Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Austrália