Distinct mechanisms of type 3 secretion system recognition control LTB4 synthesis in neutrophils and macrophages
Open Access
- 18 October 2024
- journal article
- research article
- Published by Public Library of Science (PLoS) in PLOS Pathogens
- Vol. 20 (10) , e1012651
Abstract
Leukotriene B4 (LTB4) is an inflammatory lipid produced in response to pathogens that is critical for initiating the inflammatory cascade needed to control infection. However, during plague, Yersinia pestis inhibits the timely synthesis of LTB4 and subsequent inflammation. Using bacterial mutants, we previously determined that Y. pestis inhibits LTB4 synthesis via the action of the Yop effector proteins that are directly secreted into host cells through a type 3 secretion system (T3SS). Here, we show that the T3SS is the primary pathogen associated molecular pattern (PAMP) required for production of LTB4 in response to both Yersinia and Salmonella. However, we also unexpectantly discovered that T3SS-mediated LTB4 synthesis by neutrophils and macrophages require the activation of two distinctly different host signaling pathways. We identified that phagocytosis and the NLRP3/CASP1 inflammasome significantly impact LTB4 synthesis by macrophages but not neutrophils. Instead, the SKAP2/PLC signaling pathway is required for T3SS-mediated LTB4 production by neutrophils. Finally, while recognition of the T3SS is required for LTB4 production, we also discovered that a second unrelated PAMP-mediated signal activates the MAP kinase pathway needed for synthesis. Together, these data demonstrate significant differences in the host factors and signaling pathways required by macrophages and neutrophils to quickly produce LTB4 in response to bacteria. Moreover, while macrophages and neutrophils might rely on different signaling pathways for T3SS-dependent LTB4 synthesis, Y. pestis has evolved virulence mechanisms to counteract this response by either leukocyte to inhibit LTB4 synthesis and colonize the host.Keywords
Funding Information
- National Institute of Allergy and Infectious Diseases (T32AI132146)
- National Institute of Allergy and Infectious Diseases (R01AI148241)
- National Institute of Allergy and Infectious Diseases (R01AI178106)
- National Institute of General Medical Sciences (P20GM125504)
- Jewish Heritage Foundation
This publication has 97 references indexed in Scilit:
- Phospholipase C2019
- Ca2+ homeostasis and endoplasmic reticulum (ER) stress: An integrated view of calcium signalingBiochemical and Biophysical Research Communications, 2015
- The Yersinia pestis type III secretion system: expression, assembly and role in the evasion of host defensesImmunologic Research, 2013
- Identifying Yersinia YopH-Targeted Signal Transduction Pathways that Impair Neutrophil Responses during In Vivo Murine InfectionCell Host & Microbe, 2013
- LTB4 Is a Signal-Relay Molecule during Neutrophil ChemotaxisDevelopmental Cell, 2012
- Phospholipase C signaling and calcium influxAdvances in Biological Regulation, 2012
- NLRP3 inflammasome–mediated neutrophil recruitment and hypernociception depend on leukotriene B4in a murine model of goutArthritis & Rheumatism, 2011
- A Yersinia Effector Protein Promotes Virulence by Preventing Inflammasome Recognition of the Type III Secretion SystemCell Host & Microbe, 2010
- Biophysical characterization of the EF-hand and SAM domain containing Ca2+ sensory region of STIM1 and STIM2Biochemical and Biophysical Research Communications, 2008
- Inhibition of K+ efflux prevents mitochondrial dysfunction, and suppresses caspase-3-, apoptosis-inducing factor-, and endonuclease G-mediated constitutive apoptosis in human neutrophilsCellular Signalling, 2006