Literature DB >> 3921658

Metronidazole inhibition of hydrogen production in vivo in drug-sensitive and resistant strains of Trichomonas vaginalis.

D Lloyd, B Kristensen.   

Abstract

H2 production by the human protozoan parasite Trichomonas vaginalis was monitored continuously under a mobile gas phase using a membrane-inlet mass spectrometer. Simultaneous and continuous measurement of dissolved H2, O2 and CO2 indicated that H2 evolution was inhibited at levels of O2 (less than 0.25 microM) undetectable by the technique, whereas CO2 production was stimulated. Respiration was not stimulated by admitting H2 to the gas phase. Metronidazole inhibited both H2 and CO2 production. Values of K1 for inhibition of H2 formation in strain ATCC 30001 (metronidazole sensitive) of 0.16 mM and in strain 85 (metronidazole resistant) of 1.0 mM were obtained. These data suggest that metronidazole not only competes with protons as electron acceptor but that the drug itself or a product of reduction actively inhibits some hydrogenosomal enzyme or electron carrier involved in H2 production. Under these conditions metronidazole inhibition leads to irreversible loss of cell motility.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 3921658     DOI: 10.1099/00221287-131-4-849

Source DB:  PubMed          Journal:  J Gen Microbiol        ISSN: 0022-1287


  8 in total

Review 1.  Current therapeutics, their problems, and sulfur-containing-amino-acid metabolism as a novel target against infections by "amitochondriate" protozoan parasites.

Authors:  Vahab Ali; Tomoyoshi Nozaki
Journal:  Clin Microbiol Rev       Date:  2007-01       Impact factor: 26.132

2.  A systematic review of the literature on mechanisms of 5-nitroimidazole resistance in Trichomonas vaginalis.

Authors:  Keonte J Graves; Jan Novak; W Evan Secor; Patricia J Kissinger; Jane R Schwebke; Christina A Muzny
Journal:  Parasitology       Date:  2020-07-30       Impact factor: 3.234

Review 3.  Treatment of infections caused by metronidazole-resistant Trichomonas vaginalis.

Authors:  Sarah L Cudmore; Kiera L Delgaty; Shannon F Hayward-McClelland; Dino P Petrin; Gary E Garber
Journal:  Clin Microbiol Rev       Date:  2004-10       Impact factor: 26.132

4.  Hydrogenosome metabolism is the key target for antiparasitic activity of resveratrol against Trichomonas vaginalis.

Authors:  Natalia Mallo; Jesús Lamas; José M Leiro
Journal:  Antimicrob Agents Chemother       Date:  2013-03-11       Impact factor: 5.191

5.  Flavodiiron protein from Trichomonas vaginalis hydrogenosomes: the terminal oxygen reductase.

Authors:  Tamara Smutná; Vera L Gonçalves; Lígia M Saraiva; Jan Tachezy; Miguel Teixeira; Ivan Hrdy
Journal:  Eukaryot Cell       Date:  2008-11-14

6.  Novel functions of an iron-sulfur flavoprotein from Trichomonas vaginalis hydrogenosomes.

Authors:  Tamara Smutná; Katerina Pilarová; Ján Tarábek; Jan Tachezy; Ivan Hrdý
Journal:  Antimicrob Agents Chemother       Date:  2014-03-24       Impact factor: 5.191

7.  Metabolism in anoxic permeable sediments is dominated by eukaryotic dark fermentation.

Authors:  Michael F Bourke; Philip J Marriott; Ronnie N Glud; Harald Hasler-Sheetal; Manoj Kamalanathan; John Beardall; Chris Greening; Perran L M Cook
Journal:  Nat Geosci       Date:  2016-11-28       Impact factor: 16.908

8.  Identification of the NADH-oxidase gene in Trichomonas vaginalis.

Authors:  Aline Lamien-Meda; David Leitsch
Journal:  Parasitol Res       Date:  2019-12-18       Impact factor: 2.289

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.