An immunohistochemical method of detecting Mycoplasma species antigens by use of monoclonal antibodies on paraffin sections of pneumonic bovine and caprine lungs.

F Rodriguez, S Kennedy, T D Bryson, A Fernandez, J L Rodriguez, H J Ball
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引用次数: 25

Abstract

Lung samples from pneumonic lesions in cattle and goats, naturally or experimentally infected with strains of the Mycoplasma mycoides cluster, were fixed in formalin and embedded in paraffin. An immunohistochemical technique using monoclonal or polyclonal antibodies was performed on tissue sections in order to detect Mycoplasma antigens. Four monoclonal antibodies (MAbs), one (2A3) raised against M. mycoides ssp. mycoides small colony (SC) and large colony (LC), two (1D3 and 5E5) against M. mycoides ssp. capri, and one (5A10) against M. bovis, were used. A range of polyclonal antibodies, raised to the individual subspecies of the M. mycoides cluster, and one to Pasteurella haemolytica, was also used. The MAb 2A3 showed positive immunostaining in lung sections from cattle and goats naturally and experimentally infected with M. mycoides ssp. mycoides SC and LC, but not with pneumonic lesions of cattle and goats due to other members of the M. mycoides cluster, M. bovis or Pasteurella spp. The MAb 1D3 showed immunostaining in lung sections from goats naturally and experimentally infected with M. mycoides ssp. capri, but again not with pneumonic lesions caused by other members of the M. mycoides cluster, M. bovis or Pasteurella spp. The MAb 5E5 immunoreacted in sections from pneumonic lesions from all animals infected with one of the three M. mycoides cluster subspecies used in the study, but not with M. bovis or Pasteurella infected tissue. Immunoreaction was mainly found in the cell debris around necrotic areas, as well as in macrophages, neutrophils and epithelial cells. The localization of antigens of the M. mycoides cluster using polyclonal antisera followed basically the same pattern as that obtained with the monoclonals. However, a wide cross reactivity was found between different antisera and relatively high background immunostaining was also seen, especially in necrotic areas. The results suggest that immunohistochemical methods using monoclonal antibodies are useful tools for the diagnosis and study of the pathogenesis of pneumonia caused by the Mycoplasmas of the M. mycoides cluster.

利用单克隆抗体在肺炎牛和羊肺石蜡切片上检测支原体抗原的免疫组织化学方法。
从自然或实验感染了支原体群集菌株的牛和山羊的肺炎病变中提取肺样本,用福尔马林固定并包埋在石蜡中。使用单克隆或多克隆抗体对组织切片进行免疫组织化学技术以检测支原体抗原。4个单克隆抗体(MAbs), 1个(2A3)被制备。小菌落(SC)和大菌落(LC), 2个(1D3和5E5)对M. mycoides ssp。卡普里和一种(5A10)抗牛分枝杆菌。还使用了一系列针对真菌支原体单个亚种的多克隆抗体和一种针对溶血巴斯德氏杆菌的多克隆抗体。在自然感染和实验感染真菌支原体的牛和山羊肺切片中,MAb 2A3免疫染色呈阳性。在牛和山羊的肺切片中,单抗1D3在自然感染和实验感染M. mycoides ssp的山羊的肺切片中显示出免疫染色,但在牛和山羊的肺切片中没有发现由M. mycoides集群的其他成员、牛分枝杆菌或巴氏杆菌引起的肺病变。MAb 5E5在所有感染了本研究中使用的三种mycoides集群亚种之一的动物的肺炎病变切片中都有免疫反应,但对牛分枝杆菌或巴斯德氏杆菌感染的组织没有免疫反应。免疫反应主要见于坏死区周围的细胞碎片,以及巨噬细胞、中性粒细胞和上皮细胞。多克隆抗体与单克隆抗体的定位模式基本一致。然而,在不同的抗血清之间发现了广泛的交叉反应性,也看到了相对较高的背景免疫染色,特别是在坏死区域。结果提示,单克隆抗体免疫组化方法是诊断和研究支原体肺炎发病机制的有效工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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