The impairment of methylmenaquinol:fumarate reductase affects hydrogen peroxide susceptibility and accumulation in

Issmat I Kassem1, Mahesh Khatri, Yasser M Sanad

  • 1Food Animal Health Research Program, Ohio Agricultural Research and Development Center, Department of Veterinary Preventive Medicine, The Ohio State University, Wooster, Ohio.

Microbiologyopen
|February 12, 2014
PubMed

Insights

The methylmenaquinol:fumarate reductase (Mfr) in Campylobacter jejuni plays a role in managing oxidative stress. Deleting Mfr increases susceptibility to hydrogen peroxide and affects iron homeostasis, impacting bacterial persistence.

Area of Science:

  • Microbiology
  • Biochemistry
  • Cell Biology

Background:

  • Methylmenaquinol:fumarate reductase (Mfr) is a Campylobacter jejuni protein involved in fumarate metabolism.
  • Oxidative stress can be generated by redox enzymes, impacting bacterial survival.

Purpose of the Study:

  • To investigate the role of Mfr in Campylobacter jejuni's response to hydrogen peroxide (H2O2) exposure.
  • To understand Mfr's contribution to oxidative stress, iron homeostasis, and host-pathogen interactions.

Main Methods:

  • Comparison of wild-type (WT) and Mfr mutant (∆mfrA) Campylobacter jejuni strains under H2O2 stress.
  • Measurement of H2O2 susceptibility, catalase activity, katA expression, and intracellular iron levels.
  • Assessment of bacterial persistence in RAW macrophages and morphological changes using scanning electron microscopy.

Main Results:

  • The ∆mfrA strain exhibited increased susceptibility to H2O2 and higher H2O2 concentrations in cultures compared to WT.
  • Catalase activity and katA expression were reduced in the ∆mfrA strain under H2O2 stress.
  • Intracellular iron decreased in the ∆mfrA strain, and iron supplementation reduced H2O2 susceptibility; the mutant showed enhanced macrophage persistence.

Conclusions:

  • Mfr is implicated in maintaining iron homeostasis in H2O2-stressed Campylobacter jejuni.
  • Mfr influences bacterial susceptibility to oxidative stress and intracellular iron levels.
  • The Mfr mutant displays altered interactions with host macrophages, suggesting a role in virulence.

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