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March 2, 2009
Volume 87, Number 09
p. 12


Drug Combo Kills Resistant TB

Inhibitor and antibiotic work together against tuberculosis

Celia Henry Arnaud

A COMBINATION of two commercially available drugs is effective against extensively drug-resistant (XDR) Mycobacterium tuberculosis, lab tests show (Science 2009, 323, 1215). XDR strains are resistant to all the drugs typically used to treat TB.

Meropenem (gray) binds in the active site of the TB β-lactamase BlaC. © 2009 Science
Meropenem (gray) binds in the active site of the TB β-lactamase BlaC.

Biochemist John S. Blanchard of Albert Einstein College of Medicine at Yeshiva University, in New York City, and coworkers tested the drugs meropenem, a β-lactam antibiotic, and clavulanate, a β-lactamase inhibitor. β-Lactam antibiotics have not found use as TB drugs because mycobacterial β-lactamase enzymes normally hydrolyze them before they can reach their target.

Blanchard's lab had previously shown that clavulanate is an irreversible inhibitor of the β-lactamase produced by M. tuberculosis, an enzyme called BlaC. The researchers combined meropenem with clavulanate because BlaC hydrolyzes meropenem very slowly.

The combination inhibited 13 XDR TB strains, as well as organisms in a nonreplicative "persistent" state. This state is usually not susceptible to antibiotics and represents the largest reservoir of the mycobacterium in humans.

Blanchard speculates that the clavulanate-meropenem pair is so effective because meropenem itself also inhibits BlaC. "Meropenem, by being able to bind to and inhibit the β-lactamase, commits suicide so the rest of the meropenem molecules can go find their targets," he says.

The observed effect "may stimulate further drug development research into capturing the β-lactam class of antibiotics for use as anti-TB agents," says William Bishai, codirector of the Center for Tuberculosis Research at Johns Hopkins School of Medicine.

One of the stumbling blocks in developing the drug combination for use in patients is figuring out the pharmacokinetics, says Clifton E. Barry III, head of the TB research section at the National Institutes of Health and Blanchard's collaborator. "You want to be able to give the β-lactamase inhibitor and the β-lactam in a way that maximizes the lifetime of the β-lactam," he says.

Blanchard and his team hope their results will overturn long-held beliefs about β-lactams. "I've been told that β-lactams are not effective against TB, and we're wasting our time trying them," Blanchard says. "When you run up to paradigms and suggest that the paradigms may not exactly be true, you run into a lot of skepticism."

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Chemical & Engineering News
ISSN 0009-2347
Copyright © 2009 American Chemical Society


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