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除JNK/P38途径外,MAP3K15通过背侧-CC-CL-STAT轴促进甲壳类动物中多种病毒基因的表达。

MAP3K15 facilitates multiple viral genes expression in crustaceans via Dorsal-CC-CL-STAT axis besides the JNK/P38 pathway.

作者信息

Ran Xiao-Qin, Liu Chen-Chen, Xu Xue-Mei, Wu Xin-Meng, Kang Cui-Jie

机构信息

Shandong Provincial Key Laboratory of Animal Cells and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, Shandong, China.

出版信息

PLoS Pathog. 2025 Aug 1;21(8):e1013349. doi: 10.1371/journal.ppat.1013349. eCollection 2025 Aug.

Abstract

The mitogen-activated protein kinase (MAPK) pathway is a conserved signaling system that responds to extracellular signals and translates them into appropriate cellular responses. While multiple MAPK kinase kinases (MAP3Ks) play a crucial role in the step wise transmission of MAPK signals in response to the pathogen infection, little is known about the function of MAP3K15 (also known as apoptosis signal-regulated kinase 3, ASK3) in viral infection. Here, we provide evidence that shrimp MAP3K15 undergoes phosphorylation and activation during a DNA virus, white spot syndrome virus (WSSV) infection, the activated MAP3K15 interacted with the NF-кB homolog, Dorsal, to promote its nuclear translocation for expression of the coiled-coil-containing C-type lectin (CC-CL) and the viral immediate early (ie) genes. CC-CL then activates the JAK/STAT pathway as the ligand to its membrane receptor Domeless, driving the expression of more ie genes. In addition, the JNK/P38 signaling pathway is also activated to promote viral ie genes expression. Importantly, the viral amplification in a wide range of crustaceans were inhibited and the survival rates of host were improved effectively by suppressing MAP3K15 expression or utilizing SDK1, an inhibitor targeting the active form of MAP3K15, suggesting that the MAP3K15 has a critical and conserved function in viral infection. Taken together, this study elucidates a pivotal role and mechanism of MAP3K15 in DNA virus infection, providing novel insights and potential strategies for the control of WSSV infection in crustaceans aquaculture practice.

摘要

丝裂原活化蛋白激酶(MAPK)信号通路是一种保守的信号系统,可响应细胞外信号并将其转化为适当的细胞反应。虽然多种MAPK激酶激酶(MAP3Ks)在响应病原体感染时MAPK信号的逐步传递中起关键作用,但关于MAP3K15(也称为凋亡信号调节激酶3,ASK3)在病毒感染中的功能知之甚少。在这里,我们提供证据表明,对虾MAP3K15在DNA病毒白斑综合征病毒(WSSV)感染期间发生磷酸化并被激活,激活的MAP3K15与NF-κB同源物Dorsal相互作用,促进其核转位,以表达含卷曲螺旋的C型凝集素(CC-CL)和病毒立即早期(ie)基因。CC-CL然后作为其膜受体Domeless的配体激活JAK/STAT信号通路,驱动更多ie基因的表达。此外,JNK/P38信号通路也被激活以促进病毒ie基因的表达。重要的是,通过抑制MAP3K15的表达或使用靶向MAP3K15活性形式的抑制剂SDK1,可有效抑制多种甲壳类动物中的病毒扩增并提高宿主的存活率,这表明MAP3K15在病毒感染中具有关键且保守的功能。综上所述,本研究阐明了MAP3K15在DNA病毒感染中的关键作用和机制,为甲壳类水产养殖实践中控制WSSV感染提供了新的见解和潜在策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b07/12316391/1930a629c9f5/ppat.1013349.g001.jpg

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