This work was funded by the American Lung Association and the Pittsfield Anti-Tuberculosis Association. If it is essential for the pathogen to grow, and if we are able to deplete it in the pathogen, we will be able to interfere in the infection process." "We'd like to confirm its function in the pathogen and its impact on the pathogen's growth. "We know it's involved, but not exactly what it's doing," she says. Rahlwes also plans to further investigate the protein's role in the enzymatic pathway and which parts it is interacting with. Next steps include trying to duplicate the mutant of this gene in the pathogenic form of mycobacteria, to demonstrate that the gene is indeed essential as predicted for infection to take place, the microbiologists say. "The mutated gene caused the production of different glycolipids in the mutant of the mutant." "This led us to the discovery of a new gene in the biosynthesis of this glycolipid, which we termed lipomannan elongation factor or LmeA," Rahlwes says.
YASU MORITA UMASS PLUS
It turns out that the "mutant mutant" has an initial growth defect plus another mutation in the same glycolipid biosynthesis pathway and the second mutation allows these bacteria to enjoy more normal growth. Why did one defect make them grow slowly and poorly, but two defects made them run normally again?" It didn't make sense, and we became curious about what was going on. Then we isolated a mutant of the mutant, and these suddenly began growing well again. Morita explains, "We were growing some of the mutant Mycobacterium in a Petri dish, and they grew very poorly the mutant colonies had a growth disadvantage. It had been identified earlier in the Morita lab and was known to have some unusual properties. Understanding how the bacteria make these glycolipids might provide us a way to interfere with them and stop them from being able to infect us."įor this work, Rahlwes used genetic screening methods to explore the mutant of Mycobacterium that contains the protein known as PimE. TB has many, many tricks and this is one of them. He explains, "The protein that Kathryn characterized is part of the process by which these molecules trick the human immune system so that it doesn't attack the bacteria as hard as it should, so they survive in the body.
Morita sees the biosynthesis pathways that cells use to form these envelope layers as a promising path in the search for new drug targets in TB, a disease that has seen increasing multi-drug resistance. The Morita lab is expert in investigating the multi-layered cell envelope components that surround mycobacteria, including several glycolipids known or predicted to be essential for the overall viability of disease-causing Mycobacterium tuberculosis (Mtb), which have impermeable cell walls that block antibiotics.
We investigated a protein that had not been characterized before, nobody knew its role." Details appear in the Journal of Biological Chemistry. If they don't have it, the enzymatic machinery they use to biosynthesize the glycolipid won't work, and they cannot become infectious. Doctoral candidate and first author Kathryn Rahlwes, working with a non-pathogenic form of the bacterium in Morita's lab, says, "We found mutant bacteria that were unable to express this protein.
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