Lee A, Wylie M, Smyth V J, Skibinska A, Patterson I A, Forster F, Welsh M D, Todd D
a School of Biological Sciences, Medical Biology Centre , Queen's University of Belfast , Belfast , UK.
Avian Pathol. 2013;42(5):434-42. doi: 10.1080/03079457.2013.822467.
Chicken astroviruses (CAstVs) have been characterized recently. Due to their relatively poor growth in cell culture, virus-specific antigens are not readily available for the development of diagnostic reagents and vaccines. For this purpose two capsid protein antigens, specified by the 11672 isolate of CAstV, were produced in insect cells following infection with recombinant baculoviruses. The GST-11672 capsid protein, a fusion protein comprising the capsid protein and glutathione-S-transferase (GST) as an N-terminal affinity tag, and the 11672 capsid protein alone were detected by western blotting as proteins of ~100 and 70 kDa, respectively. Immunization with the affinity-purified GST-11672 capsid protein produced a polyclonal rabbit antiserum, which reacted by indirect immunofluorescence with Group B CAstVs but which showed no reactivity with the Group A CAstV isolate, 612. When used as part of an immunoperoxidase-based immunohistochemical procedure, this rabbit antiserum facilitated the detection of CAstV antigen in formalin-fixed, paraffin-embedded kidney tissue at the sites of histopathology characteristic of nephritis. Although further evaluation with sera from commercial chickens is required, a prototype indirect antibody-detecting enzyme-linked immunosorbent assay (ELISA) based on affinity-purified GST-11672 capsid protein as coating antigen demonstrated considerable potential with low ELISA absorbance values being generated with sera from specific pathogen free (SPF) chickens, and high absorbance values being generated with serum samples from experimentally infected chickens. Immunization experiments of SPF chickens showed that, when administered as mixtures with oil adjuvant, crude cell lysates containing the GST-11672 capsid protein or the 11672 capsid protein elicited virus-specific antibody responses that were detectable by indirect immunofluorescence and by virus neutralization assays.
鸡星状病毒(CAstVs)最近已得到鉴定。由于它们在细胞培养中的生长相对较差,病毒特异性抗原不易用于诊断试剂和疫苗的开发。为此,在用重组杆状病毒感染后,在昆虫细胞中产生了由CAstV的11672分离株指定的两种衣壳蛋白抗原。GST-11672衣壳蛋白是一种融合蛋白,由衣壳蛋白和作为N端亲和标签的谷胱甘肽-S-转移酶(GST)组成,单独的11672衣壳蛋白通过蛋白质印迹法分别检测为约100 kDa和70 kDa的蛋白质。用亲和纯化的GST-11672衣壳蛋白免疫产生了多克隆兔抗血清,该抗血清通过间接免疫荧光与B组CAstVs反应,但与A组CAstV分离株612无反应性。当用作基于免疫过氧化物酶的免疫组织化学程序的一部分时,这种兔抗血清有助于在福尔马林固定、石蜡包埋的肾脏组织中肾炎特征性组织病理学部位检测CAstV抗原。尽管需要用商业鸡的血清进行进一步评估,但基于亲和纯化的GST-11672衣壳蛋白作为包被抗原的间接抗体检测酶联免疫吸附测定(ELISA)原型显示出相当大的潜力,来自无特定病原体(SPF)鸡的血清产生的ELISA吸光度值较低,而来自实验感染鸡的血清样本产生的吸光度值较高。SPF鸡的免疫实验表明,当与油佐剂混合给药时,含有GST-11672衣壳蛋白或11672衣壳蛋白的粗细胞裂解物引发了病毒特异性抗体反应,可通过间接免疫荧光和病毒中和试验检测到。