The findings, published in the March 21 online issue of Nature Chemical Biology, could lead to a potent TB therapy that would also prevent resistant TB strains from developing.
“This approach is totally different from the way any other anti-TB drug works,” says William R. Jacobs, Jr., Ph.D., the study’s senior author and professor of microbiology & immunology and of genetics at Einstein, as well as a Howard Hughes Medical Institute investigator. “In the past few years, extremely drug resistant strains of TB have arisen that can’t be eliminated by any drugs, so new strategies for attacking TB are urgently needed.”
Tuberculosis is caused by the bacterial species Mycobacterium tuberculosis. In searching for a new Achilles’ heel for M. tuberculosis, Dr. Jacobs and colleagues focused on an enzyme called GlgE. Previous research had suggested that GlgE might be essential for the growth of TB bacteria. GlgE would also be an excellent drug target because there are no enzymes similar to it in humans or in the bacteria of the human gut.
The GlgE research, done in collaboration with Dr. Stephen Bornemann at the John Innes Centre (UK), revealed a previously unknown enzymatic pathway by which TB bacteria convert the sugar trehalose (consisting of two glucose molecules) into longer sugar molecules known as alpha glucans – building blocks that are essential for maintaining bacterial structure and for making new microbes through cell division. GlgE was the third of four enzymes involved in this pathway leading to alpha glucans molecules.
Sure enough, when the researchers inhibited GlgE, the bacteria underwent “suicidal self-poisoning”: a sugar called maltose 1-phosphate accumulated to toxic levels that damaged bacterial DNA, causing the death of TB bacteria grown in Petri dishes as well as in infected mice.
“We were amazed when we knocked out GlgE that we saw this DNA damage response,” says Dr. Jacobs. “That’s usually a very effective way to kill bacteria, when you start damaging the DNA.”
“This approach is totally different from the way any other anti-TB drug works…We were amazed when we knocked out GlgE that we saw this DNA damage response.”
— William R. Jacobs, Jr., Ph.D.The researchers discovered a second way of killing TB after observing a crucial connection between their novel alpha glucan pathway and a second pathway that also synthesizes alpha glucans.
When the researchers knocked out one of the other enzymes in their novel pathway, the pathway’s shutdown didn’t kill the bacteria; similarly, inactivating an enzyme called Rv3032 in the second alpha glucan pathway failed to kill the microbes. But inactivating both of those enzymes caused what the researchers term synthetic lethality: two inactivations that separately were nonlethal but together cause bacterial death.
“The bacteria that cause TB need to synthesize alpha glucans,” notes Dr. Jacobs. “And from the bacterial point of view, you can’t knock out both of these alpha glucan pathways simultaneously or you’re dead. So if we were to make drugs against GlgE and Rv3032, the combination would be extremely potent. And since TB bacteria need both of those alpha glucan pathways to live, it’s very unlikely that this combination therapy would leave behind surviving bacteria that could develop into resistant strains.”
Dr. Jacobs adds that findings from this study could also enhance treatment of diseases caused by other species of mycobacteria. Leprosy, for example, which still occurs in the U.S. and other countries, is caused by a mycobacterium related to TB. Treating leprosy now involves using several different drugs, some of which are also used to treat tuberculosis.
The group’s paper, “Self-Poisoning of Mycobacterium tuberculosis by targeting GlgE in an a-glucan pathway,” appears in the March 21 online edition of Nature Chemical Biology. In addition to Dr. Jacobs, other Einstein researchers involved in the study were Rainer Kalscheuer, Ph.D., Brian Weinrick, Ph.D., and Karolin E. Biermann, M.S. Other researchers include Karl Syson and Stephen Bornemann, John Innes Centre; Zhen Liu and James C. Sacchettini, Texas A&M University; and Usha Veeraraghavan and Gurdyal Besra; University of Birmingham in the United Kingdom.
Albert Einstein College of Medicine has filed a patent application on behalf of Einstein and the John Innes Centre on the discoveries described in the paper.