紫海胆地中海弧菌病病原鉴定及致病机理研究

    Study on pathogen identification and pathogenic mechanism of Vibrio mediterranean disease in Heliocidaris crassispina

    • 摘要:
      目的 本研究旨在明确2024年5月福建东山养殖场紫海胆(Heliocidaris crassispina)大面积发病的病原,为其病害防控提供依据。
      方法 从东山县某养殖场催肥暂养的患病海胆病灶处取样,将样品接种至硫代硫酸盐柠檬酸盐胆盐蔗糖(TCBS)琼脂培养基和2216E培养基上,置于培养箱培养24~48 h后,从培养基上挑取单菌落,经多次分离纯化,获得优势菌,编号为HD4。通过观察菌株形态特征、生理生化特征及分子生物学鉴定,开展人工回归感染试验、基因组测序和药物敏感性试验,对致病菌进行鉴定和描述。
      结果 从体表病灶部位分离得到1株优势菌株HD4,基于形态观察、Biolog自动微生物鉴定、序列分析及生理生化鉴定分析结果,鉴定该株菌为地中海弧菌(Vibrio mediterranei)。人工回归感染试验结果显示,从病原菌HD4感染的紫海胆中分离得到一株优势菌,编号为HD-3,经鉴定其与HD4为同一株菌,且紫海胆出现死亡现象,表明菌株HD4对紫海胆有明显的致病性。基因组测序结果显示,菌株HD4携带49种毒力基因,包括SRH裂解酶基因luxS、脂蛋白基因llpA、趋化性蛋白基因cheWcheY、GDP-甘露糖-6-磷酸异构酶基因gmhA/lpcA、脂多糖相关酶基因kdsA、鞭毛蛋白基因fliM、酪氨酸激酶基因tapT等,可促进细菌入侵并导致海胆组织损伤。药物敏感性试验结果表明,该菌株对恩诺沙星、甲砜霉素、氟甲喹、磺胺间甲嘧啶钠、磺胺甲噁唑+甲氧苄啶、氟苯尼考6种水产用抗菌药物均表现出较高的敏感性。
      结论 本研究明确了地中海弧菌HD4为此次发病的病原菌,其携带的多种致病因子在致病中起重要作用。本研究结果为紫海胆病害防控提供科学参考。

       

      Abstract:
      Objective This study aims to identify the pathogen of a widespread disease outbreak among Heliocidaris crassispina farms in Dongshan, Fujian, in May 2024, providing a basis for disease control and prevention.
      Method Samples were collected from diseased H. crassispina in a farm in Dongshan County, and then inoculated onto thiosulfate citrate bile salts sucrose (TCBS) agar medium and 2216E medium. After 24-48 h of culture in an incubator, single colonies were picked from the culture medium and purified repeatedly to obtain a dominant strain with the number HD4. The pathogenic strain HD4 was identified and described through the observation of the morphological characteristics, physiological and biochemical characteristics, and molecular biology identification, artificial regression infection test, and then the whole-genome sequencing and drug susceptibility test were carried out.
      Results Strain HD4 was isolated as the dominant bacterium from the surface lesions. Combined with morphological characteristics, Biolog identification, sequence analysis, and physiological/biochemical profiles, the strain was confirmed as Vibrio mediterranei. A dominant strain (HD-3) isolated from the infected H. crassispina was verified as identical to pathogenic strain HD4. The artificial regression infection test resulted in H. crassispina mortality, demonstrating the significant pathogenicity of V. mediterranei HD4 to H. crassispina. Genome sequencing revealed that pathogenic strain HD4 harbored 49 virulence genes, including luxS-SRH lyase, llpA lipoprotein, chemotaxis proteins cheW and cheY, gmhA/lpcA (GDP-mannose-6-phosphate isomerase), kdsA (lipopolysaccharide-related enzyme), flagellin fliM, and tapT (tyrosine kinase), etc., which are involved in promoting bacterial invasion and inducing tissue damage in H. crassispina. Drug susceptibility testing showed that the pathogenic strain HD4 was highly sensitive to six aquatic antibacterial agents, including enrofloxacin, thiamphenicol, flumequine, sulfamonomethoxine sodium, sulfamethoxazole+trimethoprim, and florfenicol.
      Conclusion V. mediterraneus HD4 is identified as the pathogen of the disease outbreak, and the multiple pathogenic factors it carried played an important role in the pathogenesis. The study provides a scientific reference for the control and prevention of abalone diseases.

       

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