{"title":"草鱼宿主-微生物-寄生虫相互作用:来自多filiis感染的见解。","authors":"Fangxiang Li, Dongdong Jiang, Qing Wang, Ouqin Chang, Jiyuan Yin, Meiling Yu, Houjun Pan","doi":"10.3390/microorganisms13040872","DOIUrl":null,"url":null,"abstract":"<p><p>The ciliate parasite <i>Ichthyophthirius multifiliis</i> poses significant threats to grass carp (<i>Ctenopharyngodon idellus</i>) 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>I. multifiliis</i> infection. A histopathological examination identified gill and fin tissues embedded with <i>I. multifiliis</i>, 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 <i>IgT</i> and pro-inflammatory cytokine <i>TNF-α</i> while increasing the trend of systemic immune gene <i>IgM.</i> 16S rRNA sequencing revealed significant reductions in skin microbiota diversity. At the genus level, opportunistic pathogens <i>Aeromonas</i> and <i>Vibrio</i> proliferated in the intestine, whereas <i>Flavobacterium</i> and <i>Candidatus</i> Megaira increased in the skin and gills. Correlation analyses identified positive associations between <i>Aeromonas/Vibrio</i> abundance and host phenotype, contrasting with negative correlations observed for <i>Sphingomonas</i>, <i>Acinetobacter</i>, and <i>Leifsonia</i>. These findings demonstrate that <i>I. multifiliis</i> 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.</p>","PeriodicalId":18667,"journal":{"name":"Microorganisms","volume":"13 4","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2025-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12029742/pdf/","citationCount":"0","resultStr":"{\"title\":\"Host-Microbiota-Parasite Interactions in Grass Carp: Insights from <i>Ichthyophthirius multifiliis</i> Infection.\",\"authors\":\"Fangxiang Li, Dongdong Jiang, Qing Wang, Ouqin Chang, Jiyuan Yin, Meiling Yu, Houjun Pan\",\"doi\":\"10.3390/microorganisms13040872\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The ciliate parasite <i>Ichthyophthirius multifiliis</i> poses significant threats to grass carp (<i>Ctenopharyngodon idellus</i>) 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>I. multifiliis</i> infection. A histopathological examination identified gill and fin tissues embedded with <i>I. multifiliis</i>, 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 <i>IgT</i> and pro-inflammatory cytokine <i>TNF-α</i> while increasing the trend of systemic immune gene <i>IgM.</i> 16S rRNA sequencing revealed significant reductions in skin microbiota diversity. At the genus level, opportunistic pathogens <i>Aeromonas</i> and <i>Vibrio</i> proliferated in the intestine, whereas <i>Flavobacterium</i> and <i>Candidatus</i> Megaira increased in the skin and gills. Correlation analyses identified positive associations between <i>Aeromonas/Vibrio</i> abundance and host phenotype, contrasting with negative correlations observed for <i>Sphingomonas</i>, <i>Acinetobacter</i>, and <i>Leifsonia</i>. These findings demonstrate that <i>I. multifiliis</i> 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.</p>\",\"PeriodicalId\":18667,\"journal\":{\"name\":\"Microorganisms\",\"volume\":\"13 4\",\"pages\":\"\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-04-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12029742/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Microorganisms\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.3390/microorganisms13040872\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microorganisms","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3390/microorganisms13040872","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
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.
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.