Targeting genes within this cluster represents a good strategy for preventing tuberculosis and other mycobacterial infections, said Rajesh S. Gokhale, an HHMI international research scholar at the National Institute of Immunology in
The tuberculosis bacterium, which infects more than one-third of the worlds inhabitants, is a leading cause of death and disease worldwide.
Gokhale and colleagues report their findings in early online publication
When M. tuberculosis infects humans, it takes up residence in immune cells called macrophages. To survive in this harsh environment, mycobacteria, like many other types of bacteria, need iron to carry out life-sustaining functions, such as creating proteins and synthesizing nucleotides to form DNA. However, free iron is not easily found in an intracellular environment. To obtain this rare element, most bacteria manufacture and secrete chemical compounds called siderophores that scavenge iron from the environment.
Researchers discovered siderophoreschemical compounds used by bacteria to scavenge iron from their cellular environmentwell over 50 years ago, but the genes involved in adding the long-chain lipid anchor that enables M. tuberculosis to do so more efficiently, remained a mystery until now.
Mycobacteria have evolved siderophores with lipid-chain tails that enable them to exploit the macrophages lipid-trafficking system to capture iron more efficiently. Instead of using siderophores that diffuse freely, mycobacteria anchor their siderophores to lipid membranes by means of a long fatty acid tail. After these siderophores bind to iron within the macrophage, the lipid tail makes the iron sticky enough to permit delivery to the very compartment in macrophages where the mycobacteria are lurking.
Using microarray data, the available literature, and intuition, Gokhales group identified the location of the four genes that produce the lipid tail after observing that the expression of the genes significantly increased in response to low iron concentrations. The gene required for the synthesis of the siderophore core, called mbt-1, functions the same way, so Gokhales team named the new locus mbt-2 and the new genes mbtK, mbtL, mbtM, and mbtN.
Now that the major siderophore genes and their functions have been defined, understanding the biosynthetic pathway provides an opportunity to develop small-molecule inhibitors with the potential for developing anti-tuberculosis drugs, said Gokhale. His team has already determined that some of genes from the mbt-2 cluster is conserved across several other bacterial species that cause various pulmonary, skin, and organ diseases. Since the mbt-1 genes are also conserved across many bacterial families, the mbt genes appear to be ideal antibacterial targets for treating tuberculosis and other bacterial infections, he said.
Source: Howard Hughes Medical Institute