Biological and molecular characterization of Tomato spotted wilt Virus in Israel     

Y. Antignus  M. Lapidot  N. Ganaim  J. Cohen  O. Lachman  M. Pearlsman  B. Raccah  A. Gera 《Phytoparasitica》1997,25(4):319-330

Received April 24, 1997; received in final form June 29, 1997. Symptoms resembling tomato spotted wilt virus (TSWV) infections were documented among ornamental and vegetable crops in commercial greenhouses and open fields in Israel. Plants exhibiting these symptoms were collected from January 1992 to December 1996. Among cultivated plants analyzed for TSWV by enzyme-linked immunosorbent assay (ELISA), 19 species representing five families were found to be infected; natural infection was also recorded in six plant species of weeds. Virus identity was characterized by host range, serology and electron microscopy. Serological reaction with the isolates, found in Israel, using antisera from different sources as well as the sequence analysis of the nucleocapsid gene, demonstrated that the Israeli isolates of TSWV are a member of tospovirus serogroup I, type I (BR-01 strain). No virus transmission was found in seeds collected from virus-infected vegetable and ornamental crops. A non-radioactive molecular probe derived from the cloned nucleocapsid isolate enables specific detection of the virus in crude sap from infected plants. The detection of TSWV in Israel constitutes a severe potential threat to the ornamental and vegetable industry.  相似文献   

动物组织中四环素类抗生素残留的ELISA检测研究——土霉素抗体的制备   总被引：3，自引：0，他引：3  

安清聪  张曦  陈克嶙 《畜牧与兽医》2004,36(9):8-10

四环素类抗生素属小分子半抗原物质 ,必须与大分子物质结合才能产生免疫原性。本试验采用重氮化法合成土霉素 牛血清白蛋白 (BSA OTC)及土霉素 鼠血清白蛋白 (RSA OTC)人工抗原 ,用紫外扫描对其进行鉴定。以BSA OTC免疫家兔制备抗血清 ,以RSA OTC为包被抗原 ,采用双向免疫扩散法和ELISA方法对抗血清进行鉴定。结果表明用重氮化法合成的人工抗原对四环素类药物有特异的抗原抗体反应 ,抗血清效价达 1 2 8× 1 0 5,完全能够满足四环素类药物残留的ELISA检测要求  相似文献   

PRRS ELISA试剂盒检测猪繁殖与呼吸综合征病毒抗体的应用   总被引：2，自引：0，他引：2  

吴延功王志亮  王君玮徐天刚张喜悦  宋翠平许立华 陈溥言 《中国动物检疫》2004,21(6):23-25

利用重组杆状病毒表达的PRRSV核衣壳蛋白作抗原制成ELISA诊断试剂盒，检测人工感染PRRSV猪血清、疫苗免疫抗体和田间血清，并与IDEXX公司生产的试剂盒进行比较。结果表明，该试剂盒在PRRSV感染后8天内就可检出感染性抗体，而用IDEXX公司生产的试剂盒在感染后的18天才检测到感染性抗体，对弱毒疫苗的免疫检测也基本能反映出疫苗的免疫应答状况。对华东地区PRRSV流行病学调查结果表明，PRRSV在国内普遍存在，同时也证明研制的试剂盒，是客观科学调查我国PRRS流行情较理想的检测工具。  相似文献   

禽流感病毒夹心ELISA快速检测方法的研究   总被引：21，自引：1，他引：21  

肖运才  李自力  胡思顺  石德时  许青荣  程峰  刘梅  毕丁仁  王桂枝 《畜牧兽医学报》2004,35(5):536-541

以禽流感病毒(AIV)湖北分离株(H9N2亚型)提纯物为免疫原，制备出鸡抗AIV和兔抗AIV抗体，经用琼脂扩散法测得效价分别为1:32和1:16。以纯化的鸡抗AIVIgG为包被抗体，兔抗AIVIgG为第二抗体，建立了检测AIV抗原的夹心ELISA法。结果表明，鸡抗AIVIgG的最佳包被浓度为1μg/mL，兔抗AIV IgG的最适工作浓度为5μg/mL；对已知的阳性样品，用夹心ELISA法测得的病毒滴度比血球凝集滴度高16倍以上，且能检出其它亚型的禽流感病毒；与新城疫病毒、传染性支气管炎病毒、减蛋综合征病毒、传染性喉气管炎病毒、传染性法氏囊病病毒、鸡痘病毒、马立克氏病病毒等无交叉反应，说明本方法有很高的特异性及敏感性。对14个鸡场送检的、患有呼吸道疾病或有腹膜炎、眼炎、产蛋下降、怀疑为禽流感感染的病鸡进行了检测，结果有7个鸡场为阳性。本方法的建立为禽流感病鸡群的临床检验提供了一种方便、敏感、快速的检测方法。  相似文献   

抗鸡传染性腺胃炎酶标抗体的制备和应用     

沈美艳  张广斌  李舫  牛钟相  朱瑞良 《中国家禽》2005,27(18):11-13

在前期从患病鸡腺胃内分离到呼肠孤病毒的基础上，以该病毒为免疫原对兔进行免疫制备高免血清，分离纯化IgG，进行辣根过氧化物酶（HRP）标记，并用ELISA双抗体夹心法对山东省青岛、枣庄、泰安等地区采集的传染性腺胃炎的腺胃样品进行检测，结果表明制备的抗鸡传染性腺胃炎呼肠孤病毒的酶标抗体检测传染性腺胃炎特异性强、灵敏度高、较简便。  相似文献   

BVDV in Australian alpacas: natural infection and clinical profiles following co‐mingling with a persistently infected heifer          下载免费PDF全文

CA Evans  E Erregger  F Hemmatzadeh  PD Cockcroft 《Australian veterinary journal》2018,96(7):262-268

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Seroprevalence of antibodies to Pestivirus infections in South Australian sheep flocks          下载免费PDF全文

CA Evans  SR Lanyon  RM O’Handley  MP Reichel  PD Cockcroft 《Australian veterinary journal》2018,96(8):312-314

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Evaluation of two commercial PRRSV antibody ELISA kits with samples of known status and singleton reactors     

Byoung-Joo SEO  Hyunil KIM  Ho-Seong CHO  Byoung-Yong PARK  Won-Il KIM 《The Journal of veterinary medical science / the Japanese Society of Veterinary Science》2016,78(1):133-138

Two commercial PRRSV ELISA kits (IDEXX and Bionote) were evaluated for their sensitivity and specificity using 476 PRRS-positive serum samples collected from 7 animal challenge experiments and 1,000 PRRS-negative sera. Both ELISA kits exhibited 100% sensitivity with sera collected 14 to 42 days post-infection, and the results from the kits were highly correlated (R²=0.9207). The specificity of IDEXX or Bionote kit was 99.9% or 99.7%, respectively. In addition, the Bionote ELISA kit was used to examine 100 sera that were determined to be falsely positive either by IDEXX 2XR or 3XR ELISA, and only 7 of these samples were found to be positive. These results indicate that both ELISA kits exhibited similar levels of sensitivity and specificity and would complement one another for the verification of false-positive samples.  相似文献   

检测马疱疹病毒4型抗体间接ELISA方法的建立及应用简     

田志革  郭巍  赵世华 《中国畜牧兽医》2014,41(1):11-14

In order to establish an indirect ELISA method for detection of equine herpesviruses type 4 （EHV4） antibody, the glycoprotein G （gG） protein with specific epitope worked as a detection antigen. After optimizing conditions, the indirect ELISA method was developed successfully，specificity and repeatability tests were determined. The result was that the EHV4 gG only reacted with antibodies against EHV4;but not with antibodies against EHV1; both the intro-batch and inter-batch variation coefficiencies were lower than 10%.Concordance of the indirect ELISA relative to commercial EHV1/4 antibody kit was above 90%.The results indicated that the indirect ELISA method could be used for the detection and epidemiological surveys of EHV4 infection.  相似文献   

Cell direct reprogramming：a new technique for treating diabetes     

REN Li-wei  YANG Xiao-fei  LI Fu-Rong 《园艺学报》2014,30(12):2284-2288

Diabetes is characterized by an absolute or relative deficiency in β-cell mass, which cannot be reversed with existing therapeutic strategies. The restoration of the endogenous islet β-cells can stabilize the level of blood glucose. The islet β-cells can be obtained from the directional differentiation of stem cells, but the process is complex and has the risk of teratomas generation. Cell direct reprogramming, one terminal differentiated cell can transdifferentiate into another kind of terminal differentiated cell, which is other than directional differentiation from stem cells. Direct reprogramming gives rise to the generation of islet β-cells from one terminal differentiated cell, may be preferable for diabetes therapy because of its unique advantage.  相似文献