TLR9 Negatively Regulates Intracellular Bacterial Killing by Pyroptosis in Burkholderia pseudomallei - Infected Mouse Macrophage Cell Line (Raw264.7)

• Published in: Microbiology spectrum Vol. 10; no. 5; p. e0348822
• Main Authors: Pudla, Matsayapan, Sanongkiet, Sucharat, Ekchariyawat, Peeraya, Luangjindarat, Chularat, Ponpuak, Marisa, Utaisincharoen, Pongsak
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 26.10.2022
• Subjects: Animals; Burkholderia pseudomallei; Burkholderia pseudomallei - metabolism; caspase-11; Caspases - metabolism; Cell Line; Cytokines - metabolism; Lactate Dehydrogenases - metabolism; macrophage defense; Macrophages; Melioidosis - metabolism; Melioidosis - microbiology; Mice; Pathogenesis and Host Response; Pyroptosis; Research Article; TLR9; Toll-Like Receptor 2 - metabolism; Toll-Like Receptor 4 - metabolism; Toll-Like Receptor 5 - metabolism; Toll-Like Receptor 9 - metabolism; Toll-Like Receptors - genetics; Toll-Like Receptors - metabolism; TLR9; pyroptosis; Burkholderia pseudomallei; caspase-11; macrophage defense
• ISSN: 2165-0497; 2165-0497
• DOI: 10.1128/spectrum.03488-22

Melioidosis is a serious infectious disease caused by Burkholderia pseudomallei. This bacterium is able to survive and multiply inside the immune cells such as macrophages. It is well established that Toll-like receptors (TLRs), particularly surface TLRs such as TLR2, TLR4, and TLR5, play an essential role in defending against this bacterial infection. However, the involvement of endosomal TLRs in the infection has not been elucidated. In this study, we demonstrated that the number of intracellular bacteria is reduced in TLR9-depleted RAW264.7 cells infected with B. pseudomallei, suggesting that TLR9 is involved in intracellular bacterial killing in macrophages. As several reports have previously demonstrated that pyroptosis is essential for restricting intracellular bacterial killing, particularly in B. pseudomallei infection, we also observed an increased release of cytosolic enzyme lactate dehydrogenase (LDH) in TLR9-depleted cells infected with B. pseudomallei, suggesting TLR9 involvement in pyroptosis in this context. Consistently, the increases in caspase-11 and gasdermind D (GSDMD) activations, which are responsible for the LDH release, were also detected. Moreover, we demonstrated that the increases in pyroptosis and bacterial killing in B. pseudomallei infected TLR9-depleted cells were due to the augmentation of the IFN-β, one of the key cytokines known to regulate caspase-11. Altogether, this finding showed that TLR9 suppresses macrophage killing of B. pseudomallei by regulating pyroptosis. This information provides a novel mechanism of TLR9 in the regulation of intracellular bacterial killing by macrophages, which could potentially be leveraged for therapeutic intervention. Surface TLRs have been well established to play an essential role in Burkholderia pseudomallei infection. However, the role of endosomal TLRs has not been elucidated. In the present study, we demonstrated that TLR9 plays a crucial role by negatively regulating cytokine production, particularly IFN-β, a vital cytokine to control pyroptosis via caspase-11 activation. By depletion of TLR9, the percentage of pyroptosis was significantly increased, leading to suppression of intracellular survival in B. pseudomallei-infected macrophages. These findings provide a new role of TLR9 in macrophages.