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渔业研究 ›› 2020, Vol. 42 ›› Issue (6): 598-607.DOI: 10.14012/j.cnki.fjsc.2020. 06.007

• 论文与报告 • 上一篇    下一篇

凡纳滨对虾急性肝胰腺坏死病病原分离鉴定及耐药性分析

林楠   

  1. 福建省水产技术推广总站
  • 收稿日期:2020-10-13 修回日期:2020-10-29 出版日期:2020-12-25 发布日期:2021-01-07
  • 通讯作者: 林楠
  • 基金资助:
    福建省渔业结构调整专项资金

Isolation,identification and drug resistance analysis of bacterial pathogen associated with acute hepatopancreas necrosis disease from Litopenaeus vannamei

  • Received:2020-10-13 Revised:2020-10-29 Online:2020-12-25 Published:2021-01-07

摘要: 本研究从疑似患急性肝胰腺坏死病(Acute hepatopancreas necrosis disease, AHPND) 的凡纳滨对坏(Litopenaeus vannamei)肝胰腺组织中分离到一株优势菌株,采用16S rRNA分析,结合生理生化和质谱特征,鉴定该株优势菌为副溶血狐菌(Vibrio parahemolyticus)。毒力基因分析结果显示,菌株携带毒力蛋白PirA&BVP相关毒力基因PirVPA和PirVPB,但不携 带副溶血弧菌主要致病因子耐热直接溶血毒素基因Tdh和相对耐热溶血毒素基因Trh。对健康对虾进行回归感染,72 h全部死亡,临床症状符合典型AHPND症状。药物敏感性分析结 果显示,该菌株对甲砜霉素、氟苯尼考等6种药物敏感,对氨苄西林钠、盐酸土霉素等4种药物耐药,对硫酸新霉素、恩诺沙星等2种药物表现为中介。这可为对虾急性肝胰腺坏死病的流行病学研究和防控技术开发提供基础资料。

Abstract: In the present study,a bacterial strain was isolated from the hepatopancreas tissue of Litopenaeus vannamei in Fujian Province with suspected acute hepatopancreas necrosis disease. The 16S rRNA gene sequence,physiological and biochemical characteristics,mass - spectrometer characteristic analysis results showed that it was Vibrio parahemolyticus. Virulence gene detection showed that the strain could be positively amplified with the virulence genes including Pirvp? and PirvpB. However it showed negative amplification results for the thermostable direct hemolyticus gene (Tdh) and tdh - related hemolysin gene (Trh) . All of the health shrimps died at 72 hours after infected with the isolated strain,and infected shrimps presented with symptoms similar to the natural incidence. Drug resistance analysis showed that the isolate was sensitive to thiamphenicol, florfenicol and other 4 drugs. However it was resistant to ampicillin sodium,oxycycline,ciprofloxacin,doxycycline,and was intermediate to neomycin sulfate and enrofloxacin. The results provided basic data for epidemiological research and disease prevention of AHPND.