Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Epidemiology, Seestrasse 55, D-16868 Wusterhausen, Germany.
Vet Parasitol. 2010 Jul 15;171(1-2):32-40. doi: 10.1016/j.vetpar.2010.03.017. Epub 2010 Mar 17.
Besnoitia besnoiti, an apicomplexan parasite causes economically important disease in cattle in many countries of Africa and Asia is re-emerging in Europe. Serological identification of infected cattle is important because introduction of these animals into naive herds seems to play a major role in the transmission of the parasite. We report new, simplified immunoblot-based serological tests for the detection of B. besnoiti-specific antibodies. Antigens were used under non-reducing conditions in the immunoblots, because reduction of the antigen with beta-mercaptoethanol diminished the antigenicity in both, tachyzoites and bradyzoites. Ten B. besnoiti tachyzoite and ten bradyzoite antigens of 15-45 kDa molecular weight were recognized by B. besnoiti infected cattle, but not or only weakly detected by cattle infected with related protozoan parasites, Neospora caninum, Toxoplasma gondii, Sarcocystis cruzi, Sarcocystis hominis, or Sarcocystis hirsuta. The sensitivity and specificity of B. besnoiti immunoblots were determined with sera from 62 German cattle with clinically confirmed besnoitiosis and 404 sera from unexposed German cattle including 214 sera from animals with a N. caninum-specific antibody response. Using a new scoring system, the highest specificity (100%) and sensitivity (90%) of the immunoblots were observed when reactivity to at least four of the ten selected tachyzoite or bradyzoite antigens was considered as positive. When a cut-off based on this scoring system was applied to both the tachyzoite- and the bradyzoite-based immunoblots, there was an almost perfect agreement with the indirect fluorescent antibody test with a titre of 200 as the positive cut-off. We identified and partially characterized 10 tachyzoite and 10 bradyzoite B. besnoiti antigens which may help to develop new specific and sensitive serological tests based on individual antigens and in the identification of possible vaccine candidates.
贝氏贝蛔虫,一种顶复门寄生虫,在非洲和亚洲的许多国家引起了对牛具有重要经济意义的疾病,目前正在欧洲重新出现。对感染牛的血清学鉴定很重要,因为这些动物的引入似乎在寄生虫的传播中起着主要作用。我们报告了新的、简化的免疫印迹血清学检测方法,用于检测 B. besnoiti 特异性抗体。在免疫印迹中使用非还原条件下的抗原,因为用β-巯基乙醇还原抗原会降低速殖子和缓殖子的抗原性。10 种贝氏贝蛔虫速殖子和 10 种缓殖子抗原的分子量为 15-45 kDa,被感染的牛识别,但未被感染相关原生动物寄生虫的牛识别,如 Neospora caninum、Toxoplasma gondii、Sarcocystis cruzi、Sarcocystis hominis 或 Sarcocystis hirsuta。用来自 62 头德国临床确诊贝蛔虫病牛的血清和 404 头德国未暴露牛的血清(包括 214 头对 N. caninum 特异性抗体有反应的血清)来确定 B. besnoiti 免疫印迹的敏感性和特异性。使用新的评分系统,当至少有四种选择的速殖子或缓殖子抗原的反应被认为是阳性时,免疫印迹的特异性(100%)和敏感性(90%)最高。当基于该评分系统的截止值应用于速殖子和缓殖子免疫印迹时,与间接荧光抗体试验的一致性几乎完美,以 200 的滴度作为阳性截止值。我们鉴定并部分描述了 10 种贝氏贝蛔虫速殖子和 10 种缓殖子抗原,这可能有助于开发基于单个抗原的新的特异性和敏感性血清学检测方法,并鉴定可能的疫苗候选物。