弧菌

臭氧化海水对于弧菌DNA的损伤作用

Damage of ozone-produced oxidant to Vibrio DNA

食品中副溶血弧菌荧光定量PCR方法快速检测

Rapid detection of Vibrio parahaemolyticus in food by fluorescence quantitative PCR

实时荧光PCR检测水产品中副溶血性弧菌

Real-time fluorescence PCR detection of Vibrio parahaemolyticus in aquatic products

副溶血性弧菌ELISA快速检测试剂盒的研制

Initial development of ELISA kit for rapid detection for Vibrio Parahaemolyticus

F群弧菌引起腹泻的流行病学调查分析

Epidemiological survey of Diarrhea Induced by Group F vibrio

与哈威弧菌结合之多胜肽；适合体之筛选II。

I.Screening of Vibrio harveyi-Binding Peptide Aptamers II .

实时荧光定量PCR法与常规PCR法及细菌培养法检测副溶血弧菌的比较

Comparison among real-time PCR , PCR and bacterium culture in detection of Vibrio parahaemolyticus

海产品中副溶血弧菌PCR检测方法的建立与评价

Development and Evaluation of PCR Method for the Detection of Vibrio parahaemolyticus in Seafoods

添加有扩增内标的副溶血弧菌PCR检测方法的研究

Study on the detection of Vibrio parahaemolyticus using PCR method with an internal amplification control

ColiK（12）细胞约释放2个蛭弧菌No.1细胞。

Coli K_ ( 12 ) is about 2 .

大黄鱼溶藻弧菌LPS的间接ELISA检测

Detection of the Vibrio alginolyticus LPS of Pseudosciaena crocea by indirect ELISA

利用LAMP法检测哈维氏弧菌在国内尚属首次报道。

Using LAMP amplication to detect Vibrio harveyi is the first report in China .

溶藻弧菌溶血素基因反向PCR克隆及其原核表达

Cloning haemolysin gene of Vibrio alginolyticus through reverse PCR and expression of the gene in prokaryotic cell

用PCR方法对分离自浙江省部分地区的副溶血弧菌临床和海产品分离株的3种溶血素基因进行检测。

PCR method was used to examine three different hemolysin genes in isolates from clinical and seafood samples in Zhejiang province .

在扇贝的消化盲囊和性腺内也分离到异养菌和弧菌，分别为103～105个g和103～105个／g。

The bacterial numbers of the digestive diverticula and gonads of scallops were also calculated , fluctuating from 103 to 106 cells per gram .

其中弧菌属（Vibrio）的细菌种有37种以上。

And there are more than 37 species belong to Vibrio .

结果表明鳗弧菌m3的细胞胞外产物苗有显著的免疫保护作用。

Results revealed that the protection of CEV against Vibrio anguillarum m3 was conspicuous .

PCR检测和测序结果表明已成功地构建了鳗弧菌金属蛋白酶基因突变株。

In conclusion , the construction of metalloprotease gene mutant will surely be beneficial to further study of the pathogenesis of Vibrio anguillarum .

用副溶血弧菌人工感染对虾的死亡率C组为58.3%，与对照组（33.3%）存在显著差异（P<0.05）。

At same time , mortality ( 58.3 % ) due to Vibrio parahaemolyticus infection in Group C was significantly higher than that in Control Group ( 33.3 % ) .

副溶血性弧菌tdh基因的分子信标PCR技术检测

Detection of thermostable direct hemolysin gene in Vibrio parahaemolyticus by molecular beacon PCR

本文建立了网箱养殖大黄鱼病原菌&副溶血弧菌酶联免疫吸附法，也即间接ELISA快速检测方法。

Presented in this paper is a method of indirect Enzyme Linked Immunosorbent Assay ( ELISA ) for rapid diagnosis of pathogenic V. parahaemolyticus .

在红霉素诱导下，共得到3个差异表达的蛋白溶藻弧菌全菌蛋白，分别是磷酸烯醇丙酮酸羧激酶、外膜蛋白N和磷酸丙糖异构酶。

There were 3 spots differentially expressed of V. alginolyticus induced by erythromycin . The 3 protein pots are triosephosphate isomerase and outer membrane pro - tein N and phosphoenolpyruvate carboxykinase .

从电镀厂的含铬淤泥中分离获得一株抗铬的脱硫弧菌（SRI）。

Chromate resistance of Desulfovibrio sp . SRI was isolated from chromium - contaminated sludge in electroplating plants .

副溶血性弧菌对痢特灵（FR）的耐药率为66.3%，其次是氨苄西林（AMP），为61%。

Drug resistance of V.parahaemolyticus to FR and AMP were 66.3 % , 61 % respectively .

副溶血弧菌感染12h和24h杂色鲍肝脏全长cDNA文库的构建

Construction of liver full-length cDNA libraries of abalone Haliotis diversicolor infected with Vibrio parahaemolyticus for 12 h and 24 h

在鲍苗大规模死亡前后分离的细菌经过鉴定为塔式弧菌及Vibriosp。

The bacteria separated before and after the extensive death of juvenile abalone were Vibrio tubiashii and Vibrio sp.

用常规生理生化方法将细菌鉴定到属，其中3株为弧菌属细菌（Vibriospp.）

By the traditional physical and chemical methods , 3 of these strains were identified as Vibrio spp .

1995年7&9月，以养殖中国对虾为材料，实验室用弧菌菌悬液注射感染对虾，血清中测得一定量的酚氧化酶（PO）。

From July to September 1995 , phenoloxidase ( PO ) activity was measured after cultured shrimps were challenged by Vibrio SPP .

副溶血弧菌（Vibrioparahaemolyticus，VP）是一种海水中常见的条件致病菌，可引起海水养殖鱼类疾病。

Vibrio parahaemolyticus is a familiar conditional pathogen bacterium in marine ; it can induce the disease of fish .

采用MPN法进行副溶血性弧菌定量检测；

The Vibrio parahaemolyticus was determined qualitatively by MPN method .