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针对鸟博德特氏菌外膜蛋白的单克隆抗体。

Monoclonal antibodies directed against the outer membrane protein of Bordetella avium.

作者信息

Liu Guanhua, Liang Manfei, Zuo Xuemei, Zhao Xue, Guo Fanxia, Yang Shifa, Zhu Ruiliang

机构信息

Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, College of Animal Science and Technology, Shandong Agricultural University, Shandong Taian, PR China.

出版信息

Monoclon Antib Immunodiagn Immunother. 2013 Aug;32(4):295-300. doi: 10.1089/mab.2012.0124.

Abstract

Bordetella avium is the etiologic agent of coryza and rhinotracheitis in poultry. This respiratory disease is responsible for substantial economic losses in the poultry industry. Monoclonal antibodies (MAbs) were produced against the outer membrane proteins (OMPs) of B. avium isolated from diseased chickens. BALB/c mice were immunized with the extracted B. avium OMPs. Then the splenocytes from immunized mice and SP2/0 myeloma cells were fused using PEG 4000. Three stable hybridoma clones (designated as 3G₁₀, 4A₃, and 4E₈) were produced via indirect ELISA and three rounds of subcloning. The MAbs were classified as IgG1, and can recognize the 58  kDa OMP band by Western blot assays. No MAb cross-reactivity with chicken Proteus mirabilis, Escherichia coli, and Salmonella was observed. A double antibody sandwich ELISA (DAS-ELISA) was developed using the rabbit polyclonal antibodies as the capture antibody and MAb 4A₃ as the detection antibody. Under the DAS-ELISA, the minimum detectable concentration of B. avium was 1 × 10(4) CFU/mL, and no cross-reactivity occurred with chicken Proteus mirabilis, Escherichia coli, and Salmonella. Results showed that the DAS-ELISA has good sensitivity and specificity. Clinical application showed the DAS-ELISA was more sensitive than the plate agglutination test. This study may be used to develop a quick and specific diagnostic kit, analyze epitopes, and establish systems for typing B. avium.

摘要

禽博德特氏菌是家禽鼻炎和鼻气管炎的病原体。这种呼吸道疾病给家禽业造成了巨大的经济损失。针对从患病鸡中分离出的禽博德特氏菌的外膜蛋白(OMPs)制备了单克隆抗体(MAbs)。用提取的禽博德特氏菌OMPs免疫BALB/c小鼠。然后使用聚乙二醇4000将免疫小鼠的脾细胞与SP2/0骨髓瘤细胞融合。通过间接ELISA和三轮亚克隆产生了三个稳定的杂交瘤克隆(命名为3G₁₀、4A₃和4E₈)。这些单克隆抗体被归类为IgG1,通过蛋白质印迹分析可识别58 kDa的OMP条带。未观察到单克隆抗体与鸡奇异变形杆菌、大肠杆菌和沙门氏菌有交叉反应。以兔多克隆抗体为捕获抗体,单克隆抗体4A₃为检测抗体,建立了双抗体夹心ELISA(DAS-ELISA)。在DAS-ELISA检测下,禽博德特氏菌的最低可检测浓度为1×10⁴CFU/mL,且与鸡奇异变形杆菌、大肠杆菌和沙门氏菌无交叉反应。结果表明,DAS-ELISA具有良好的敏感性和特异性。临床应用表明,DAS-ELISA比平板凝集试验更敏感。本研究可用于开发快速、特异的诊断试剂盒,分析表位,并建立禽博德特氏菌分型系统。

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