来自Cromileptes altivelis的CC25-like (CaCC25-like)通过趋化和直接抑菌活性促进抗微生物免疫防御。

IF 3.9 2区 农林科学 Q1 FISHERIES
Fish & shellfish immunology Pub Date : 2025-10-01 Epub Date: 2025-07-19 DOI:10.1016/j.fsi.2025.110575
Hehe Du, Yajing Xiang, Jingwen Zheng, Guisen Chen, Panpan Zhang, Jingqun Ao, Yongcan Zhou, Yun Sun
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引用次数: 0

摘要

座头石斑鱼(Cromileptes altivelis)是一种高价值的海洋物种,由于疾病频繁爆发和死亡率升高,在水产养殖中面临重大挑战。趋化因子作为先天免疫和适应性免疫的关键介质,在协调白细胞迁移和病原体清除中发挥重要作用。然而,与哺乳动物相比,它们的功能角色仍然缺乏特征。在本研究中,我们在C. altivelis中鉴定了一个cc25样基因(CaCC25-like),并研究了其免疫相关功能。cacc25 -样蛋白编码一个96个氨基酸的蛋白,包含一个保守的SCY结构域和NCCL基元,与硬骨鱼CC25同源物具有高度的同源性(42.45%-97.92%),但与哺乳动物CC25的相似性较低(
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CC25-like from Cromileptes altivelis (CaCC25-like) promotes antimicrobial immunity defense through chemotactic and direct antibacterial activity.

The humpback grouper (Cromileptes altivelis), a high-value marine species, encounters substantial challenges in aquaculture due to frequent disease outbreaks and elevated mortality rates. Chemokines, which serve as pivotal mediators of both innate and adaptive immunity, play an essential role in orchestrating leukocyte migration and pathogen clearance. However, their functional roles remain poorly characterized compared to those in mammals. In this study, we identified a CC25-like gene in C. altivelis (CaCC25-like) and investigated its immune-related functions. The CaCC25-like encodes a 96-amino-acid protein that contains a conserved SCY domain and NCCL motif, showing high homology to teleost CC25 orthologs (42.45 %-97.92 %) but low similarity to mammalian CC25 (<25 %). Under normal physiological conditions, CaCC25-like was ubiquitously expressed, with the highest expression levels in the liver. Following challenge with Vibrio harveyi, its expression was significantly upregulated in both the spleen and head kidney. Recombinant CaCC25-like protein (rCaCC25-like) induced dose-dependent chemotactic activity and proliferation of head kidney lymphocytes. Furthermore, rCaCC25-like exhibited direct antibacterial activity against V. harveyi, Streptococcus agalactiae, and Escherichia coli, reducing their survival rates by 19.83 %-79.57 %. Overexpression of CaCC25-like in vivo decreased bacterial colonization in immune tissues by 16.07 %-78.11 %, whereas siRNA-mediated knockdown of CaCC25-like increased pathogen loads by up to 6.59-fold. These findings demonstrate CaCC25-like as a multifunctional immune effector that enhances leukocyte recruitment, proliferation, and microbial clearance in humpback grouper. This study not only deepens the understanding of teleost chemokine biology, but also provides a solid foundation for developing immunomodulatory strategies aimed at improving disease resistance in aquaculture.

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来源期刊
Fish & shellfish immunology
Fish & shellfish immunology 农林科学-海洋与淡水生物学
CiteScore
7.50
自引率
19.10%
发文量
750
审稿时长
68 days
期刊介绍: Fish and Shellfish Immunology rapidly publishes high-quality, peer-refereed contributions in the expanding fields of fish and shellfish immunology. It presents studies on the basic mechanisms of both the specific and non-specific defense systems, the cells, tissues, and humoral factors involved, their dependence on environmental and intrinsic factors, response to pathogens, response to vaccination, and applied studies on the development of specific vaccines for use in the aquaculture industry.
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