Litwin C M, Martins T B, Hill H R
Department of Pathology, University of Utah, Salt Lake City, 84121, USA.
Am J Clin Pathol. 1997 Aug;108(2):202-9. doi: 10.1093/ajcp/108.2.202.
Bartonella henselae is now regarded as the etiologic agent of cat-scratch disease and a cause of bacillary angiomatosis. We examined the human immune response to Bartonella henselae infection using a newly developed enzyme immunoassay (EIA) and a Western blot procedure using outer-membrane proteins. The EIA showed 98.6% and 91.4% agreement with an indirect fluorescence method (IFA) for detection of IgM and IgG antibodies, respectively. By using Western blot analysis, reactivity to an 8-kd band showed significant correlation with positive results by the IgM IFA and EIA. In contrast, reactivity to 209-, 208.5-, 208-, 116-, and 80-kd bands was identified only in positive IgG IFA serum samples. The EIA and Western blot should be useful tests in determining the antibody response to B. henselae infection and may also be important in determining the critical epitopes in the host-parasite interaction of this organism.
亨氏巴尔通体现已被视为猫抓病的病原体以及杆菌性血管瘤病的病因。我们使用新开发的酶免疫测定法(EIA)和利用外膜蛋白的蛋白质印迹法,检测了人体对亨氏巴尔通体感染的免疫反应。EIA检测IgM和IgG抗体时,与间接荧光法(IFA)的一致性分别为98.6%和91.4%。通过蛋白质印迹分析,对一条8-kd条带的反应性与IgM IFA和EIA的阳性结果显示出显著相关性。相比之下,仅在IgG IFA血清阳性样本中鉴定出对209-kd、208.5-kd、208-kd、116-kd和80-kd条带的反应性。EIA和蛋白质印迹法在确定对亨氏巴尔通体感染的抗体反应方面应是有用的检测方法,在确定该生物体宿主-寄生虫相互作用中的关键表位方面可能也很重要。