Department of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, Kentucky, United States of America.
Center for Microbiomics, Inflammation and Pathogenicity, Louisville, Kentucky, United States of America.
PLoS Pathog. 2024 Oct 18;20(10):e1012651. doi: 10.1371/journal.ppat.1012651. eCollection 2024 Oct.
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.
白三烯 B4(LTB4)是一种炎症脂质,在病原体反应中产生,对于启动控制感染所需的炎症级联反应至关重要。然而,在鼠疫中,鼠疫耶尔森菌抑制 LTB4 的及时合成以及随后的炎症反应。我们之前使用细菌突变体确定,鼠疫耶尔森菌通过直接通过 III 型分泌系统(T3SS)分泌到宿主细胞中的 Yop 效应蛋白来抑制 LTB4 的合成。在这里,我们表明 T3SS 是产生 LTB4 所需的主要病原体相关分子模式(PAMP),这对于响应耶尔森菌和沙门氏菌都是如此。然而,我们也出乎意料地发现,中性粒细胞和巨噬细胞中 T3SS 介导的 LTB4 合成需要两种截然不同的宿主信号通路的激活。我们发现吞噬作用和 NLRP3/CASP1 炎性小体显著影响巨噬细胞中 LTB4 的合成,但不影响中性粒细胞。相反,SKAP2/PLC 信号通路是中性粒细胞中 T3SS 介导的 LTB4 产生所必需的。最后,虽然识别 T3SS 是产生 LTB4 所必需的,但我们还发现第二个不相关的 PAMP 介导的信号激活了合成所需的 MAP 激酶途径。总之,这些数据表明巨噬细胞和中性粒细胞需要不同的宿主因子和信号通路来快速产生 LTB4 以响应细菌。此外,尽管巨噬细胞和中性粒细胞可能依赖于不同的信号通路来进行 T3SS 依赖性 LTB4 合成,但鼠疫耶尔森菌已经进化出了毒力机制来对抗这种反应,即白细胞抑制 LTB4 合成并在宿主中定植。