Researchers at the Indian Institute of Science (IISc) have uncovered an important mechanism that allows the tuberculosis (TB) bacterium to persist in the human host for decades. The team, including researchers from the National Centre for Biological Sciences (NCBS) and Institute For Stem Cell Science and Regenerative Medicine (InStem), Bengaluru, found that a single gene involved in the production of iron-sulphur clusters could be crucial for the persistence of the TB bacterium.
TB is caused by Mycobacterium tuberculosis (Mtb), which can be present in the human body for decades without any symptoms.
"Mtb needs humans to survive. In many cases of Mtb infection, the immune system can detect the bug and clear it out," said Mayashree Das, a PhD student at IISc, and first author of the study published in the journal Science Advances.
However, in several asymptomatic individuals, Mtb hides within deep oxygen-limiting pockets of the lung and enters a state of dormancy in which it does not divide and is metabolically inactive, successfully evading the immune system and TB drugs.
"Due to persistence, there is a bacterial reservoir in a subset of the human population at any point which can reactivate and cause infection. Unless we understand persistence, we will not be able to eradicate TB," said Amit Singh, Associate Professor at IISc and corresponding author of the study.
Singh's team grew Mtb in liquid cultures containing special supplements needed for its growth.
Several proteins in Mtb depend on iron-sulphur clusters for functioning. These clusters consist of iron and sulphur atoms organised in various configurations like chains or cuboids.
The iron atoms in the cluster can pass on electrons from one site of a protein complex to another in cellular reactions such as respiration and carbon metabolism.
"The iron-sulphur cluster-containing proteins are important for essential processes such as energy production by respiration, enabling the bacteria to survive harsh conditions of the lungs and causing infection. So, we wanted to study the mechanisms that Mtb uses to build these iron-sulphur clusters," said Singh.
These clusters are mainly produced by Mtb's SUF operon, a set of genes that get switched on together, the researchers said.
However, there is another single gene called IscS that can also produce the clusters, they said.
To solve this mystery of why the bacterium needs both, the researchers generated a mutant version of Mtb that lacked the IscS gene.
They found that under normal and oxygen-limiting conditions, iron-sulphur clusters are produced mainly by the action of the IscS gene.
However, when the bacterium faces a lot of oxidative stress, the iron atoms of the clusters become oxidised and released, damaging the clusters. Therefore, there is an increased demand for producing more clusters, which switches on the SUF operon.
The researchers then sought to find out how the IscS gene contributes to disease progression. They infected mice models with the mutant version of Mtb lacking the IscS gene.
The absence of the IscS gene led to severe disease in the infected mice rather than a persistent, chronic infection typically seen in TB patients.
This is because, in the absence of the IscS gene, the SUF operon is highly activated - but in an unregulated fashion - leading to hypervirulence, the researchers said.
Depleting both IscS and the SUF system dramatically reduced the persistence of Mtb in mice, they said.
