草鱼宿主-微生物-寄生虫相互作用:来自多filiis感染的见解。

IF 4.1 2区 生物学 Q2 MICROBIOLOGY
Fangxiang Li, Dongdong Jiang, Qing Wang, Ouqin Chang, Jiyuan Yin, Meiling Yu, Houjun Pan
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引用次数: 0

摘要

纤毛虫多filiphothirius对草鱼养殖业构成重大威胁。然而,对宿主微生物群转移和免疫反应的有限了解阻碍了有效的控制策略。本研究综合分析了多毛螺旋体感染后宿主病理指标、免疫反应和皮肤/鳃/肠道微生物群的变化。组织病理学检查发现鳃和鳍组织内嵌有多棘棘鱼,伴有上皮坏死和炎症细胞浸润。生化分析显示,天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)、尿素(urea)和肌酐(CREA)水平明显升高,表明肝肾功能受损。定量RT-PCR分析显示,粘膜免疫基因IgT和促炎细胞因子TNF-α上调,全身免疫基因IgM有升高趋势。16S rRNA测序显示皮肤微生物群多样性显著减少。在属水平上,条件致病菌气单胞菌和弧菌在肠道中增殖,而黄杆菌和巨假杆菌在皮肤和鳃中增加。相关分析发现气单胞菌/弧菌丰度与宿主表型呈正相关,而鞘膜单胞菌、不动杆菌和莱氏菌呈负相关。这些发现表明,多毛线虫感染可引起宿主微生物群失调和潜在的机会性细菌感染。这项研究促进了我们对宿主-微生物-寄生虫三方相互作用的理解,并支持了鱼类养殖中微生物社区寄生虫病的控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Host-Microbiota-Parasite Interactions in Grass Carp: Insights from Ichthyophthirius multifiliis Infection.

The ciliate parasite Ichthyophthirius multifiliis poses significant threats to grass carp (Ctenopharyngodon idellus) aquaculture. However, the limited understanding of host microbiota shifts and immune responses hinders effective control strategies. This study integrated analyses of host pathological indices, immune response and skin/gill/gut microbiota shifts after I. multifiliis infection. A histopathological examination identified gill and fin tissues embedded with I. multifiliis, accompanied by epithelial necrosis, and inflammatory cell infiltration. Biochemical profiling revealed marked elevations in aspartate aminotransferase (AST), alanine aminotransferase (ALT), urea (UREA), and creatinine (CREA) levels, indicating impaired hepatic and renal function. Quantitative RT-PCR analyses demonstrated the up-regulation of mucosal immune gene IgT and pro-inflammatory cytokine TNF-α while increasing the trend of systemic immune gene IgM. 16S rRNA sequencing revealed significant reductions in skin microbiota diversity. At the genus level, opportunistic pathogens Aeromonas and Vibrio proliferated in the intestine, whereas Flavobacterium and Candidatus Megaira increased in the skin and gills. Correlation analyses identified positive associations between Aeromonas/Vibrio abundance and host phenotype, contrasting with negative correlations observed for Sphingomonas, Acinetobacter, and Leifsonia. These findings demonstrate that I. multifiliis infection induces host microbiome dysbiosis and potentially opportunistic bacterial infections. This investigation advances our understanding of tripartite host-microbiota-parasite interactions and supports microbial community-based parasitosis control in fish culture.

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来源期刊
Microorganisms
Microorganisms Medicine-Microbiology (medical)
CiteScore
7.40
自引率
6.70%
发文量
2168
审稿时长
20.03 days
期刊介绍: Microorganisms (ISSN 2076-2607) is an international, peer-reviewed open access journal which provides an advanced forum for studies related to prokaryotic and eukaryotic microorganisms, viruses and prions. It publishes reviews, research papers and communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Electronic files and software regarding the full details of the calculation or experimental procedure, if unable to be published in a normal way, can be deposited as supplementary electronic material.
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