Granulocytes act as a niche for Mycobacterium tuberculosis growth

Granulocyte recruitment to the pulmonary compartment is a hallmark of progressive tuberculosis (TB). This process is well-documented to promote immunopathology, but can also enhance the replication of the pathogen. Both the specific granulocytes responsible for increasing mycobacterial burden and the underlying mechanisms remain obscure. We report that the known immunomodulatory effects of these cells, such as suppression of protective T-cell responses, play a limited role in altering host control of mycobacterial replication in susceptible mice. Instead, we find that the adaptive immune response preferentially restricts the burden of bacteria within monocytes and macrophages compared to granulocytes. Specifically, mycobacteria within inflammatory lesions are preferentially found within long-lived granulocytes that express intermediate levels of the Ly6G marker and low levels of antimicrobial genes. These cells progressively accumulate in the lung and correlate with bacterial load and disease severity, and the ablation of Ly6G-expressing cells lowers mycobacterial burden. These observations suggest a model in which dysregulated granulocytic influx promotes disease by creating a permissive intracellular niche for mycobacterial growth and persistence.

Automated summary

The recruitment of granulocytes to the pulmonary compartment is a hallmark of progressive tuberculosis. However, the adaptive immune response plays a crucial role in restricting bacterial burden, with long-lived granulocytes expressing intermediate levels of the Ly6G marker and low levels of antimicrobial genes correlating with disease severity. Ablation of these cells lowers mycobacterial burden, indicating a dysregulated granulocytic influx may create an intracellular niche for mycobacterial growth and persistence.