Abstract

  Helicobacter pylori are gram negative spiral bacteria that colonize the human stomach. Infection with H. pylori is associated with chronic gastritis, peptic ulcer, gastric adenocarcinoma and gastric mucosa-associated lymphoid tissue (MALT)lymphoma. Antibiotic resistance is an ever increasing problem with the treatment of most microbial infections including H. pylori; and has become a growing problem worldwide with the eradication of this organism. In recent years, several treatment regimens have been proposed for H. pylori eradication. However, the only conditions for which such treatment is strongly recommended on the basis of unequivocal supporting evidence are peptic ulcer disease and low grade gastric MALT lymphoma. Success of antimicrobial regimens for H. pylori eradication depends on patient compliance and lack of antimicrobial resistance. Metronidazole (Mtz) containing regimens have been shown to limit effectiveness because of increasing prevalence of resistance to this drug.  A high prevalence (> 90%) of Mtz resistance in H. pylori has been reported especially in developing countries. Mtz resistance may be mediated through an inability of Mtz-resistant strains to remove oxygen from the site of Mtz reduction, thereby preventing Mtz activation.  This has been attributed to a mutation on the frxA and/or rdxA genes resulting in strains of the organism with defective nitro-reductases coded by these genes. Infection by Mtz or amoxicillin resistant strains is an important factor leading to treatment failure; subjecting all H. pylori clinical isolates to susceptibility testing most especially to Mtz is recommended. If not possible, a program to survey the prevalence of resistance should be implemented in a given area or population. This increasing emergence of antimicrobial resistance in H. pylori treatment posses serious public health problems and is therefore necessary that new drug regimens be examined.   Key words: Helicobacter pylori, drug resistance, metronidazole, gene mutations, public health.

Highlights

  • Helicobacter pylori are gram negative spiral bacteria that colonize the human stomach

  • Infection by Mtz sensitive (Mtzs) or amoxicillin resistant strains is an important factor leading to treatment failure; subjecting all H. pylori clinical isolates to susceptibility testing most especially to Mtz is recommended

  • Several studies have demonstrated that inactivation of rdxA or frxA led to increase in the minimum inhibitory concentration (MIC) for Mtz and simultaneous inactivation of both genes led to higher MIC than the inactivation of either gene (Kwon et al, 2000a), providing a possible explanation for the heterogeneity of resistance observed in the wide range of MIC for Mtz measured in H. pylori strains

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Summary

INTRODUCTION

Helicobacter pylori are gram negative spiral bacteria that colonize the human stomach. Infection with the organism is associated with chronic gastritis, peptic ulcer, gastric. Adenocarcinoma and gastric MALT lymphoma (Suerbaum and Michetti, 2002; Ndip et al, 2004, 2008). Breath and stool tests can determine if one is infected with H. pylori. The most accurate way to diagnose H. pylori, is through upper endoscopy of the oesophagus, stomach and duodenum (Ables et al, 2007). Eradication of the organism has been shown to result in ulcer healing, prevention of peptic ulcer recurrence and may reduce the prevalence of gastric cancer in high risk populations (Sepulvedo and Coelho, 2002; Tanih et al, 2009)

Antibiotic resistance is an ever increasing problem with
TRENDS IN METRONIDAZOLE RESISTANCE
THE ROLE OF RdxA NITROREDUCTASE IN METRONIDAZOLE RESISTANCE
THE ROLE OF FrxA NITROREDUCTASE IN METRONIDAZOLE RESISTANCE
Findings
CONCLUSION
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