Khalid Shahin, Mostafa Abdel-Glil, Izzet Burçin Saticıoğlu, Muhammed Duman, Soner Altun, Silvia Colussi, Giuseppe Esposito, Pier Luigi Acutis, Prearo Marino, Brandon Spondler, Ilhan Altinok, Charalampos Kotzamanidis, Ana Isabel Vela, Esteban Soto, Carlos Augusto Gomes Leal, Nihed Ajmi, Sergio Aoki
{"title":"Diving Into the Depths: Unveiling the Main Etiologies of Piscine Lactococcosis With a Novel Multiplex qPCR Assay.","authors":"Khalid Shahin, Mostafa Abdel-Glil, Izzet Burçin Saticıoğlu, Muhammed Duman, Soner Altun, Silvia Colussi, Giuseppe Esposito, Pier Luigi Acutis, Prearo Marino, Brandon Spondler, Ilhan Altinok, Charalampos Kotzamanidis, Ana Isabel Vela, Esteban Soto, Carlos Augusto Gomes Leal, Nihed Ajmi, Sergio Aoki","doi":"10.1111/jfd.14147","DOIUrl":null,"url":null,"abstract":"<p><p>Piscine lactococcosis poses a significant threat to a wide range of cultured and wild fish populations worldwide, typically presenting as acute haemorrhagic septicemia with high morbidity and mortality. Although Lactococcus garvieae was historically considered the sole causative agent of piscine lactococcosis, recent studies have identified L. petauri and L. formosensis as additional, highly pathogenic species. In this study, we developed a novel TaqMan-based multiplex qPCR assay for the simultaneous detection and differentiation of L. garvieae, L. petauri and L. formosensis, following a pangenome analysis of the publicly available genomes of these bacterial species. The assay demonstrated high sensitivity and specificity across 156 bacterial isolates obtained from various cultured fish species and geographical locations between 2008 and 2024, as well as against a panel of non-target bacteria. It also successfully detected target pathogens in 146 field tissue samples, including tissues preserved in 70% ethanol, formalin-fixed paraffin-embedded (FFPE) tissues and tissues fixed on FTA cards. Compared to classical bacteriology, the multiplex qPCR assay yielded higher detection rates and enabled precise identification of the causative species of piscine lactococcosis. Overall, the multiplex qPCR assay developed in this study provides a reliable, rapid, highly sensitive and species-specific molecular approach for diagnosing piscine lactococcosis, contributing to better surveillance and management of the disease in aquaculture.</p>","PeriodicalId":15849,"journal":{"name":"Journal of fish diseases","volume":" ","pages":"e14147"},"PeriodicalIF":2.2000,"publicationDate":"2025-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of fish diseases","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1111/jfd.14147","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"FISHERIES","Score":null,"Total":0}
引用次数: 0
Abstract
Piscine lactococcosis poses a significant threat to a wide range of cultured and wild fish populations worldwide, typically presenting as acute haemorrhagic septicemia with high morbidity and mortality. Although Lactococcus garvieae was historically considered the sole causative agent of piscine lactococcosis, recent studies have identified L. petauri and L. formosensis as additional, highly pathogenic species. In this study, we developed a novel TaqMan-based multiplex qPCR assay for the simultaneous detection and differentiation of L. garvieae, L. petauri and L. formosensis, following a pangenome analysis of the publicly available genomes of these bacterial species. The assay demonstrated high sensitivity and specificity across 156 bacterial isolates obtained from various cultured fish species and geographical locations between 2008 and 2024, as well as against a panel of non-target bacteria. It also successfully detected target pathogens in 146 field tissue samples, including tissues preserved in 70% ethanol, formalin-fixed paraffin-embedded (FFPE) tissues and tissues fixed on FTA cards. Compared to classical bacteriology, the multiplex qPCR assay yielded higher detection rates and enabled precise identification of the causative species of piscine lactococcosis. Overall, the multiplex qPCR assay developed in this study provides a reliable, rapid, highly sensitive and species-specific molecular approach for diagnosing piscine lactococcosis, contributing to better surveillance and management of the disease in aquaculture.
鱼类乳球菌病对世界范围内广泛的养殖和野生鱼类种群构成重大威胁,通常表现为急性出血性败血症,发病率和死亡率高。虽然garviee乳球菌历来被认为是鱼类乳球菌病的唯一病原体,但最近的研究发现,petauri乳球菌和台湾乳球菌是另外的高致病性物种。在这项研究中,我们开发了一种新的基于taqman的多重qPCR方法,用于同时检测和区分L. garvieae, L. petauri和L. formosensis,并对这些细菌物种的公开基因组进行了泛基因组分析。该分析对2008年至2024年间从各种养殖鱼类和地理位置获得的156种细菌分离株以及一组非目标细菌显示出高灵敏度和特异性。该方法还成功检测了146份野外组织样品的目标病原体,包括70%乙醇保存的组织、福尔马林固定石蜡包埋(FFPE)组织和FTA卡固定的组织。与传统细菌学相比,多重qPCR检测具有更高的检出率,并且能够精确鉴定鱼乳球菌病的致病物种。总之,本研究建立的多重qPCR检测方法为诊断鱼乳球菌病提供了一种可靠、快速、高灵敏度和物种特异性的分子方法,有助于更好地监测和管理水产养殖疾病。
期刊介绍:
Journal of Fish Diseases enjoys an international reputation as the medium for the exchange of information on original research into all aspects of disease in both wild and cultured fish and shellfish. Areas of interest regularly covered by the journal include:
-host-pathogen relationships-
studies of fish pathogens-
pathophysiology-
diagnostic methods-
therapy-
epidemiology-
descriptions of new diseases