多巴胺能神经元调控决定了草履虫在产气克雷伯氏菌感染期间的先天免疫力。

IF 2.6 4区 医学 Q3 IMMUNOLOGY Microbes and Infection Pub Date : 2024-10-04 DOI:10.1016/j.micinf.2024.105430
Thirumugam Gowripriya, Radhakrishnan Yashwanth, Prabhanand Bhaskar James, Ramamurthi Suresh, Krishnaswamy Balamurugan
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引用次数: 0

摘要

先天性免疫信号是宿主抵御细菌病原体的前线。病原体引起的有害影响,如肠道神经元信号减少,会影响宿主的食物感知和居住行为。在这里,我们报告了多巴胺和 kpc-1 信号通过 p38/PMK-1 MAPK 信号通路控制秀丽隐杆线虫的肠道先天性免疫反应。草履虫感染产气荚膜杆菌会影响其觅食行为,而觅食行为依赖于多巴胺的调控。多巴胺受体(dop-1)和转运体(dat-1)的缺失会增加对病原体的吸引,而不是回避。产气荚膜杆菌感染通过呋喃样蛋白转化酶(kpc-1)影响龄-1的调节;kpc-1的缺失会影响依赖环境的呆小鸡的形成。相反,多巴-1突变拮抗性地调节肠道免疫调节,而kpc-1突变部分调节p38/PMK-1 MAPK通路。我们的研究结果表明,来自神经系统的多巴胺和kpc-1信号分别以拮抗和激动的方式控制肠道免疫。
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Dopaminergic neuronal regulation determines innate immunity of Caenorhabditis elegans during Klebsiella aerogenes infection.

The innate immune signals are the front line of host defense against bacterial pathogens. Pathogen-induced harmful effects, such as reduced neuronal signals to the intestine, affect the host's food sensing and dwelling behavior. Here, we report that dopamine and kpc-1 signals control the intestinal innate immune responses through the p38/PMK-1 MAPK signaling pathway in C. elegans. K. aerogenes infection in C. elegans affects the food-dwelling behavior, which depends on dopamine regulation. The absence of the dopamine receptor (dop-1) and transporter (dat-1) increases attraction to the pathogen instead of avoidance. The K. aerogenes infection affects age-1 regulation through the furin-like proprotein convertase (kpc-1); the absence of kpc-1 affects environment-dependent dauer formation. In contrast, the dop-1 mutation antagonistically regulates intestinal immune regulation, while the kpc-1 mutation partially regulates the p38/PMK-1 MAPK pathway. Our findings indicate that dopamine and kpc-1signaling from the nervous system control intestinal immunity in an antagonistic and agonistic manner, respectively.

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来源期刊
Microbes and Infection
Microbes and Infection 医学-病毒学
CiteScore
12.60
自引率
1.70%
发文量
90
审稿时长
40 days
期刊介绍: Microbes and Infection publishes 10 peer-reviewed issues per year in all fields of infection and immunity, covering the different levels of host-microbe interactions, and in particular: the molecular biology and cell biology of the crosstalk between hosts (human and model organisms) and microbes (viruses, bacteria, parasites and fungi), including molecular virulence and evasion mechanisms. the immune response to infection, including pathogenesis and host susceptibility. emerging human infectious diseases. systems immunology. molecular epidemiology/genetics of host pathogen interactions. microbiota and host "interactions". vaccine development, including novel strategies and adjuvants. Clinical studies, accounts of clinical trials and biomarker studies in infectious diseases are within the scope of the journal. Microbes and Infection publishes articles on human pathogens or pathogens of model systems. However, articles on other microbes can be published if they contribute to our understanding of basic mechanisms of host-pathogen interactions. Purely descriptive and preliminary studies are discouraged.
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