Li Tong, Raza Sayed Haidar Abbas, Yang Bintong, Sun Yufeng, Wang Guiqin, Sun Wuwen, Qian Aidong, Wang Chunfeng, Kang Yuanhuan, Shan Xiaofeng
College of Animal Science and Technology, Jilin Provincial Engineering Research Center of Animal Probiotics, Key Laboratory of Animal Production and Product Quality Safety of Ministry of Education, Jilin Agricultural University, Changchun, Jilin 130118, China.
College of Animal Science and Technology, Northwest A&F University, Yangling, Shanxi 712100, China.
Animals (Basel). 2020 Apr 2;10(4):608. doi: 10.3390/ani10040608.
is an important pathogen causing freshwater fish sepsis and ulcer syndrome. An increasing number of cases have demonstrated its significance as an aquatic zoonotic agent. The purpose of this study was to ensure the safety of freshwater products by evaluating the infection status of edible freshwater fish. In this experiment, we isolated from several species of apparently healthy freshwater fish, including , , , and . was identified through bacterial staining, culture characteristics, and 16S rDNA gene sequence. In addition, polymerase chain reaction (PCR) was used to investigate the distribution of seven major virulence genes, including aerolysin (: 88.51%), cytotoxic enterotoxin (: 71.26%), serine proteinase (: 54.02%), adhesin (: 40.23%), phospholipase (: 45.98%), nuclease (: 51.72%), and quorum sensing-controlled virulence factor (: 59.77%). In total, 496 strains of were isolated, including 87 strains of . The isolates of were Gram-negative, rod-shaped bacteria, and the colonies are yellow on Rimler-Shotts (RS) medium and showed greater than 99% homology with ATCC35624 according to analyses of the 16S rDNA sequence. Nearly 50% of the isolates carried at least four or more virulence genes, 25% of the isolates carried at least five types of virulence genes, and 59.77% isolates carried the gene, and the isolates carrying more virulence genes were found to be more virulent. These results are of great significance for further improving the food safety assessment of freshwater aquatic products.
是引起淡水鱼败血症和溃疡综合征的重要病原体。越来越多的病例表明其作为一种水生人畜共患病原体的重要性。本研究的目的是通过评估可食用淡水鱼的感染状况来确保淡水产品的安全性。在本实验中,我们从几种看似健康的淡水鱼中分离出了该病原体,包括[鱼的种类1]、[鱼的种类2]、[鱼的种类3]和[鱼的种类4]。通过细菌染色、培养特性和16S rDNA基因序列对其进行了鉴定。此外,还使用聚合酶链反应(PCR)来研究7种主要毒力基因的分布,包括气单胞菌溶素([基因名称1]:88.51%)、细胞毒性肠毒素([基因名称2]:71.26%)、丝氨酸蛋白酶([基因名称3]:54.02%)、黏附素([基因名称4]:40.23%)、磷脂酶([基因名称5]:45.98%)、核酸酶([基因名称6]:51.72%)和群体感应控制的毒力因子([基因名称7]:59.77%)。总共分离出496株该病原体菌株,其中包括87株[特定菌株类型]。该病原体的分离株为革兰氏阴性、杆状细菌,在Rimler-Shotts(RS)培养基上菌落呈黄色,根据对16S rDNA序列的分析,与[菌株名称]ATCC35624的同源性大于99%。近50%的该病原体分离株携带至少四个或更多毒力基因,25%的分离株携带至少五种类型的毒力基因,59.77%的分离株携带[基因名称7]基因,并且发现携带更多毒力基因的分离株毒性更强。这些结果对于进一步改进淡水水产品的食品安全评估具有重要意义。