Chloramphenicol Is a Substrate for a Novel Nitroreductase Pathway in Haemophilus influenzae

Author:

Smith Arnold L.123,Erwin Alice L.1,Kline Toni4,Unrath William C. T.1,Nelson Kevin1,Weber Allan2,Howald William N.5

Affiliation:

1. Microbial Pathogens Program, Seattle Biomedical Research Institute, Seattle, Washington 98109

2. Department of Molecular Microbiology and Immunology, University of Missouri, Columbia, Missouri 65197

3. Departments of Pathobiology

4. Genome Sciences

5. Medicinal Chemistry, University of Washington, Seattle, Washington 98195

Abstract

ABSTRACT The p -nitroaromatic antibiotic chloramphenicol has been used extensively to treat life-threatening infections due to Haemophilus influenzae and Neisseria meningitidis ; its mechanism of action is the inhibition of protein synthesis. We found that during incubation with H. influenzae cells and lysates, chloramphenicol is converted to a 4-aminophenyl allylic alcohol that lacks antibacterial activity. The allylic alcohol moiety undergoes facile re-addition of water to restore the 1,3-diol, as well as further dehydration driven by the aromatic amine to form the iminoquinone. Several Neisseria species and most chloramphenicol-susceptible Haemophilus species, but not Escherichia coli or other gram-negative or gram-positive bacteria we examined, were also found to metabolize chloramphenicol. The products of chloramphenicol metabolism by species other than H. influenzae have not yet been characterized. The strains reducing the antibiotic were chloramphenicol susceptible, indicating that the pathway does not appear to mediate chloramphenicol resistance. The role of this novel nitroreductase pathway in the physiology of H. influenzae and Neisseria species is unknown. Further understanding of the H. influenzae chloramphenicol reduction pathway will contribute to our knowledge of the diversity of prokaryotic nitroreductase mechanisms.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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