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Drug resistance in Giardia duodenalis

Ansell, Brendan R. E. (author)
Univ Melbourne, Fac Vet & Agr Sci, Parkville, Vic 3010, Australia.
McConville, Malcolm J. (author)
Univ Melbourne, Inst Bio21, Parkville, Vic 3010, Australia.
Ma'ayeh, Showgy Y. (author)
Uppsala universitet,Mikrobiologi
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Dagley, Michael J. (author)
Univ Melbourne, Inst Bio21, Parkville, Vic 3010, Australia.
Gasser, Robin B. (author)
Univ Melbourne, Fac Vet & Agr Sci, Parkville, Vic 3010, Australia.
Svärd, Staffan G. (author)
Uppsala universitet,Mikrobiologi
Jex, Aaron R. (author)
Univ Melbourne, Fac Vet & Agr Sci, Parkville, Vic 3010, Australia.
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Univ Melbourne, Fac Vet & Agr Sci, Parkville, Vic 3010, Australia Univ Melbourne, Inst Bio21, Parkville, Vic 3010, Australia. (creator_code:org_t)
Elsevier BV, 2015
2015
English.
In: Biotechnology Advances. - : Elsevier BV. - 0734-9750 .- 1873-1899. ; 33:6, s. 888-901
  • Research review (peer-reviewed)
Abstract Subject headings
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  • Giardia duodenalis is a microaerophilic parasite of the human gastrointestinal tract and a major contributor to diarrheal and post-infectious chronic gastrointestinal disease world-wide. Treatment of G. duodenalis infection currently relies on a small number of drug classes. Nitroheterocyclics, in particular metronidazole, have represented the front line treatment for the last 40 years. Nitroheterocyclic-resistant G. duodenalis have been isolated from patients and created in vitro, prompting considerable research into the biomolecular mechanisms of resistance. These compounds are redox-active and are believed to damage proteins and DNA after being activated by oxidoreductase enzymes in metabolically active cells. In this review, we explore the molecular phenotypes of nitroheterocyclic-resistant G. duodenalis described to date in the context of the protisfs unusual glycolytic and antioxidant systems. We propose that resistance mechanisms are likely to extend well beyond currently described resistance-associated enzymes (i.e., pyruvate ferredoxin oxidoreductases and nitroreductases), to include NAD(P)H- and flavin-generating pathways, and possibly redox-sensitive epigenetic regulation. Mechanisms that allow G. duodenalis to tolerate oxidative stress may lead to resistance against both oxygen and nitroheterocyclics, with implications for clinical control. The present review highlights the potential for systems biology tools and advanced bioinformatics to further investigate the multifaceted mechanisms of nitroheterocyclic resistance in this important pathogen.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology (hsv//eng)

Keyword

Giardia
Nitroheterocyclic
Drug resistance
Metronidazole
Nitazoxanide
Furazolidone
NAD(P)H oxidoreductase
Sir2 NAD-dependent histone deacetylase
Treatment failure

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