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大黄鱼内脏白点病病原变形假单胞菌的抗生素敏感性分析

Antibiotic susceptibility profile of Pseudomonas plecoglossicida, the pathogen of visceral white-spot disease in large yellow croaker (Larimichthys crocea)

  • 摘要: 大黄鱼(Larimichthys crocea)是我国最重要的海水养殖鱼类之一,其中福建省宁德市产量占全国养殖总量的80%以上。近年来,由变形假单胞菌(Pseudomonas plecoglossicida)引起的大黄鱼内脏白点病严重影响了大黄鱼养殖产业的发展。本研究分析了2013—2023年分离的19株变形假单胞菌的抗生素敏感性和耐药基因。采用Kirby-Bauer纸片法对19个菌株进行了31种抗生素药物的敏感试验。结果显示,不同年份的变形假单胞菌对氨基糖苷类、喹诺酮类、四环素类、碳青霉烯类的抗生素敏感性较强,对其他类型抗生素敏感性较弱,2023年分离的变形假单胞菌对恩诺沙星、多西环素等抗生素出现不敏感。耐药基因检测结果显示:耐药基因aph(3ʹ)-IaqnrSfloRSul1携带率为100%,tetA为95%,其他耐药基因携带率低于90%,耐药表型与耐药基因检出率不完全对应,表明耐药性的形成可能涉及多个基因的复杂相互作用或存在其他未揭示的耐药机制。同时本研究发现外膜蛋白OprM缺失突变株(ΔoprM)、转录调控因子DeoR缺失突变株(ΔdeoR)、T3SS效应分子ExoU缺失突变株(ΔexoU)、转录调控蛋白ExsA缺失突变株(ΔexsA)、易位蛋白PopB-PopD缺失突变株(ΔpopBD)、针状结构蛋白PscC-PscF缺失突变株(ΔpscC-F)对恩诺沙星、氟苯尼考等抗生素的敏感性增强,提示外膜蛋白OprM、T3SS和调控蛋白DeoR在影响变形假单胞菌对抗生素敏感性方面具有重要作用。研究结果对大黄鱼内脏白点病的防控具有指导意义。

     

    Abstract: The large yellow croaker (Larimichthys crocea)is one of the most important marine aquaculture fish species in China, with over 80% of production in Ningde City, Fujian Province. In recent years, visceral white-spot disease caused by Pseudomonas plecoglossicida has seriously affected the development of large yellow croaker aquaculture industry. In this study, antibiotic susceptibility and resistance genes of 19 strains of P. plecoglossicida isolated from 2013 to 2023 were analyzed. The 19 strains were tested for susceptibility to 31 antibiotic drugs using the Kirby-Bauer paper slide method. The results showed that P. plecoglossicida isolated from different years exhibited high susceptibility to to aminoglycosides, quinolones, tetracyclines, carbapenems, but low susceptibility to other classes of antibiotics. P. plecoglossicida strains isolated in 2023 appeared to be insensitive to antibiotics of enrofloxacin and doxycycline. The results of resistance gene detection showed that carriage rates of the resistance genes aph(3ʹ)-Ia, qnrS, floR, Sul1 were 100%, while that of tetA was 95%. The carriage rates of other resistance genes were below 90%, and the resistance phenotypes did not correspond exactly to the rate of detection of resistance genes, indicating that the formation of resistance may involve the complexity of multiple gene, suggesting that the formation of drug resistance may involve the complex interaction of multiple genes or the existence of other unrevealed drug resistance mechanisms. Furthermore, we found that the outer membrane protein OprM deletion mutant (ΔoprM), the transcriptional regulator DeoR deletion mutant (ΔdeoR), and T3SS effector molecule ExoU deletion mutant (ΔexoU), the transcriptional regulator protein ExsA deletion mutant (ΔexsA), the translocator proteins PopB-PopD deletion mutant (ΔpopBD), and the acinar structural protein PscC-PscB, were found in the same strain, and the resistance phenotype corresponded exactly to the detection rate of resistance genes, suggesting that resistance may involve complex interactions among multiple genes or other unknown mechanisms. (ΔpscC-F), a mutant with deletion of the structural proteins PscC-PscF (ΔpscC-F), showed enhanced sensitivity to antibiotics such as enrofloxacin and florfenicol, suggesting that the outer membrane proteins OprM, T3SS, and the regulator protein DeoR play important roles in influencing the susceptibility of P. plecoglossicida to antibiotics. These findings provide valuable insights for the prevention and control of visceral white-spot disease in large yellow croaker.

     

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