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抗胞内劳森菌多克隆抗体和单克隆抗体的制备与鉴定

Preparation and characterization of polyclonal and monoclonal antibodies against Lawsonia intracellularis.

作者信息

Guedes Roberto M C, Gebhart Connie J

机构信息

Department of Veterinary Pathobiology, University of Minnesota, Saint Paul, MN 55108, USA.

出版信息

J Vet Diagn Invest. 2003 Sep;15(5):438-46. doi: 10.1177/104063870301500506.

Abstract

Proliferative enteropathy is an intestinal infectious disease caused by the obligate intracellular bacterium Lawsonia intracellularis. Immunohistochemistry staining has superior sensitivity over hematoxylin and eosin and silver staining for detecting L. intracellularis in histological sections. A L. intracellularis-specific monoclonal antibody (MAb) produced in the UK (IG4 MAb) has been described in the literature. However, no monoclonal or polyclonal antibodies are commercially available. Therefore, the objective of this study was to produce and characterize new polyclonal and monoclonal antibodies against L. intracellularis that are suitable for diagnostic use. The new monoclonal (2001 MAb) and polyclonal antibodies (1999 PAb) were compared with the IG4 MAb using Western blot analysis of outer membrane proteins (OMPs) of 6 L. intracellularis isolates, Bilophila wadsworthia and Brachyspira hyodysenteriae and using immunohistochemistry of known positive and negative histologic samples and pure cultures of L. intracellularis, B. wadsworthia, B. hyodysenteriae, Salmonella choleraesuis, S. typhimurium, and Escherichia coli K88. Immunogold staining using 2001 MAb was performed to show the specificity of the antibody against an L. intracellularis surface protein. Western blot analysis showed that the 2001 MAb targeted an OMP of 77 kD, which made it different from the IG4 MAb that targeted an 18-kD OMP. The immunogold stain demonstrated the specificity of the 2001 MAb to a surface protein of L. intracellularis. The polyclonal antibody (1999 PAb) targeted 5 OMPs (77, 69, 54, 42, and 36 kD). Both the 2001 MAb and 1999 PAb stained known positive, but not negative, histologic samples. Both the 2001 MAb and 1999 PAb reacted with a pure culture of L. intracellularis but not with any other common enteric pathogens. These two new antibodies will be useful for immunodiagnosis of L. intracellularis.

摘要

增生性肠炎是一种由专性细胞内细菌胞内劳森菌引起的肠道传染病。在组织切片中检测胞内劳森菌时,免疫组织化学染色比苏木精-伊红染色和银染色具有更高的灵敏度。文献中已描述了一种在英国生产的胞内劳森菌特异性单克隆抗体(MAb)(IG4 MAb)。然而,尚无市售的单克隆或多克隆抗体。因此,本研究的目的是生产并鉴定适合诊断用途的针对胞内劳森菌的新型多克隆和单克隆抗体。使用6株胞内劳森菌分离株、沃兹沃思嗜胆菌和猪痢疾短螺旋体的外膜蛋白(OMPs)进行蛋白质印迹分析,并对已知阳性和阴性组织学样本以及胞内劳森菌、沃兹沃思嗜胆菌、猪痢疾短螺旋体、猪霍乱沙门氏菌、鼠伤寒沙门氏菌和大肠杆菌K88纯培养物进行免疫组织化学,将新的单克隆抗体(2001 MAb)和多克隆抗体(1999 PAb)与IG4 MAb进行比较。使用2001 MAb进行免疫金染色以显示该抗体对胞内劳森菌表面蛋白的特异性。蛋白质印迹分析表明,2001 MAb靶向一种77 kD的OMP,这使其与靶向18 kD OMP的IG4 MAb不同。免疫金染色证明了2001 MAb对胞内劳森菌表面蛋白的特异性。多克隆抗体(1999 PAb)靶向5种OMPs(77、69、54、42和36 kD)。2001 MAb和1999 PAb均对已知阳性组织学样本染色,但对阴性样本不染色。2001 MAb和1999 PAb均与胞内劳森菌纯培养物反应,但不与任何其他常见肠道病原体反应。这两种新抗体将有助于胞内劳森菌的免疫诊断。

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