Sithigorngul Paisarn, Rukpratanporn Sombat, Pecharaburanin Nilawan, Suksawat Pornthip, Longyant Siwaporn, Chaivisuthangkura Parin, Sithigorngul Weerawan
Department of Biology, Faculty of Science, Srinakharinwirot University, Bangkok 10110, Thailand.
J Microbiol Methods. 2007 Dec;71(3):256-64. doi: 10.1016/j.mimet.2007.09.012. Epub 2007 Oct 24.
Mouse monoclonal antibodies (MAbs) and rabbit polyclonal antibody (PAb) against Vibrio harveyi were generated from immunization of mice and rabbits with highly virulent isolate of V. harveyi. Two MAbs specific to virulent isolates of V. harveyi were obtained and one of them (VH4) was selected to conjugate with colloidal gold as the detector antibody was laid on a sample pad. Rabbit polyclonal antibody was used as the capture antibody at the test line (T) and goat anti-mouse IgG antibody (GAM) was used as the capture antibody at the control line (C) of nitrocellulose strip. The ready-to-use strip was held in a plastic case and then stored in a desiccated plastic bag. A sample volume of 100 microl of bacterial suspension from various sources mixed with application buffer was applied to the sample chamber at one end of the strip and allowed to flow by chromatography through the nitrocellulose membrane to the other end. In test samples containing virulent isolates of V. harveyi, the bacteria would bind to the monoclonal antibody conjugated with colloidal gold and the resulting complex would be captured by the antibodies at the test line to give a reddish-purple band. Any unbound monoclonal antibody conjugated with colloidal gold moved across the test line would be captured by the GAM and form a band at the control line (C). In sample without V. harveyi or with V. harveyi below the limit (<10(6) CFU/ml) of detection for the kit, only the control line band was observed. If the test sample was pre-enriched in tryptic soy broth (TSB) for 6 h before application to the strip, the sensitivity would increase to 1-10 CFU/ml which is comparable to that of PCR. This method could be used to detect pathogenic isolates of V. harveyi in pond water or infected shrimp in order to monitor and to reduce the risk of V. harveyi outbreak in the shrimp culture. The beneficial features of this kit are that simple, convenient and quick results (within 15 min) can be obtained without the requirement of sophisticated tools or special equipments and skills.
用哈维氏弧菌的高毒力分离株免疫小鼠和兔子,制备了抗哈维氏弧菌的小鼠单克隆抗体(MAbs)和兔多克隆抗体(PAb)。获得了两种针对哈维氏弧菌毒力分离株的单克隆抗体,其中一种(VH4)被选择与胶体金偶联作为检测抗体放置在样品垫上。兔多克隆抗体用作硝酸纤维素膜测试线(T)的捕获抗体,山羊抗小鼠IgG抗体(GAM)用作对照线(C)的捕获抗体。即用型试纸条装在塑料盒中,然后保存在干燥的塑料袋中。将100微升来自各种来源的细菌悬液与应用缓冲液混合后的样品体积加到试纸条一端的样品室中,使其通过色谱法流经硝酸纤维素膜到达另一端。在含有哈维氏弧菌毒力分离株的测试样品中,细菌会与胶体金偶联的单克隆抗体结合,产生的复合物会被测试线的抗体捕获,出现红紫色条带。任何未结合的与胶体金偶联的单克隆抗体穿过测试线后会被GAM捕获,在对照线(C)形成条带。在不含哈维氏弧菌或哈维氏弧菌含量低于试剂盒检测限(<10⁶ CFU/ml)的样品中,仅观察到对照线条带。如果测试样品在应用于试纸条之前在胰蛋白胨大豆肉汤(TSB)中预富集6小时,灵敏度将提高到1 - 10 CFU/ml,这与PCR相当。该方法可用于检测池塘水中或受感染虾中的哈维氏弧菌致病分离株,以监测并降低对虾养殖中哈维氏弧菌爆发的风险。该试剂盒的优点是无需复杂工具、特殊设备和技能,即可简单、方便且快速(15分钟内)获得结果。