One of the world's most deadly diseases, tuberculosis - primarily a lung disease - infects more than eight million people and is responsible for 1.5 million deaths each year, researchers said.
According to the Centres for Disease Control and Prevention, approximately one-third of the world's population is infected with tuberculosis.
The bacterium that causes tuberculosis, Mycobacterium tuberculosis, or Mtb, previously was thought to infect the body only through inhalation and subsequent infection of cells in the lungs, researchers said.
They found that microfold cell (M-cell) translocation is a new and previously unknown mechanism by which Mtb enters the body.
M-cells are specialised epithelial cells that transport particles from the airway or mucosal surface to the compartment below the cell, researchers said.
"The current model of disease is that when Mtb bacteria are inhaled, they reach the end of the lung - the alveolus - and then are ingested by a macrophage, a type of white blood cell that swallows and kills invading bacteria," said Michael Shiloh from UT Southwestern.
"This is a key finding that suggests disease onset outside of alveolar macrophages is not only possible, but also important in the pathogenesis of tuberculosis infection," he added.
This mechanism of M-cell mediated movement of Mtb may help explain an ancient disease called scrofula. In this disease, tuberculosis infection rarely appears in the lung but instead causes disease in the lymph nodes of the neck.
Preventing Mtb from attaching to receptors on the M-cell surface - such as by vaccinating against a bacterial protein - could block the bacteria's entry, infection and spread to other organs, said Shiloh.
"We are taking several experimental approaches to identify the Mtb genes and proteins that are involved in this process," said Vidhya Nair from UT Southwestern.
The findings were published in the journal Cell Reports.
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