Department of Genetics, The University of Texas MD Anderson Cancer Center, Houston, United States.
Department of Microbiology and Molecular Genetics, McGovern Medical School at UTHealth, Houston, United States.
Elife. 2024 Mar 6;12:RP90051. doi: 10.7554/eLife.90051.
The survival of hosts during infections relies on their ability to mount effective molecular and behavioral immune responses. Despite extensive research on these defense strategies in various species, including the model organism , the neural mechanisms underlying their interaction remain poorly understood. Previous studies have highlighted the role of neural G-protein-coupled receptors (GPCRs) in regulating both immunity and pathogen avoidance, which is particularly dependent on aerotaxis. To address this knowledge gap, we conducted a screen of mutants in neuropeptide receptor family genes. We found that loss-of-function mutations in activated immunity while suppressing pathogen avoidance behavior. Through further analysis, NPR-15 was found to regulate immunity by modulating the activity of key transcription factors, namely GATA/ELT-2 and TFEB/HLH-30. Surprisingly, the lack of pathogen avoidance of mutant animals was not influenced by oxygen levels. Moreover, our studies revealed that the amphid sensory neuron ASJ is involved in mediating the immune and behavioral responses orchestrated by NPR-15. Additionally, NPR-15 was found to regulate avoidance behavior via the TRPM (transient receptor potential melastatin) gene, GON-2, which may sense the intestinal distension caused by bacterial colonization to elicit pathogen avoidance. Our study contributes to a broader understanding of host defense strategies and mechanisms underlining the interaction between molecular and behavioral immune responses.
宿主在感染过程中的存活依赖于其产生有效分子和行为免疫反应的能力。尽管在包括模式生物在内的各种物种中对这些防御策略进行了广泛的研究,但它们相互作用的神经机制仍知之甚少。先前的研究强调了神经 G 蛋白偶联受体(GPCR)在调节免疫和病原体回避中的作用,而这特别依赖于趋化作用。为了解决这一知识空白,我们对神经肽受体家族基因的突变体进行了筛选。我们发现, 失活突变激活了免疫,同时抑制了病原体回避行为。通过进一步分析,发现 NPR-15 通过调节关键转录因子 GATA/ELT-2 和 TFEB/HLH-30 的活性来调节免疫。令人惊讶的是, NPR-15 突变体动物缺乏病原体回避行为不受氧气水平的影响。此外,我们的研究表明,嗅鞘感觉神经元 ASJ 参与了 NPR-15 介导的免疫和行为反应的调节。此外,还发现 NPR-15 通过 TRPM(瞬时受体电位 melastatin)基因 GON-2 调节回避行为,该基因可能感知细菌定植引起的肠道扩张,从而引发病原体回避。我们的研究有助于更全面地了解宿主防御策略和机制,强调了分子和行为免疫反应之间的相互作用。