p62 limits Salmonella Typhimurium in macrophages through its role in cell signalling

Full text loading... Abstract The intracellular autophagy receptor p62 (also known as Sqstm1) plays a dual role in autophagic flux and downstream Toll-like receptor (TLR) signalling and has been implicated in modulating immune responses. However, its specific function in controlling intracellular bacterial survival, particularly in macrophages, remains less well characterized. Salmonella enterica serovar Typhimurium (S. Tm) is a major global pathogen and a leading cause of gastroenteritis-associated morbidity. We have previously demonstrated that host restriction of S. Tm in macrophages involves the GTPase Rab32 and the BLOC-3 complex. In the present study, we identify a novel interaction between p62 and Rab32. Notably, p62 restricts Salmonella survival independently of the Rab32/BLOC-3 pathway. Indeed, p62-knockdown in macrophages resulted in a significantly increased intracellular bacterial survival, an effect that did not correlate with altered recruitment of canonical autophagy-related proteins, as assessed by fluorescence microscopy. Through RT-qPCR and infection assays, we further show that p62-depleted macrophages exhibit a dampened pro-inflammatory response, which corresponds with the increased bacterial burden. These findings provide new mechanistic insight into the role of p62 in modulating the macrophage inflammatory response during Salmonella infection, highlighting its contribution to host defence beyond its canonical functions in autophagy. - Received: - Version Posted: Funding - Biotechnology and Biological Sciences Research Council (Award BB/M010996/1) - Principal Award Recipient: Daniel Underwood - HORIZON EUROPE European Innovation Council (Award 2016-726152-TYPHI) - Principal Award Recipient: Not Applicable - Biotechnology and Biological Sciences Research Council (Award BB/N017854/1) - Principal Award Recipient: Not Applicable