Sharma R, Woldehiwet Z
University of Liverpool, Department of Veterinary Pathology, Neston, Wirral, UK.
Epidemiol Infect. 1992 Feb;108(1):135-45. doi: 10.1017/s095026880004958x.
Enzyme-linked immunoabsorbent assay (ELISA) was used to titrate virus-specific IgG, IgM and IgA levels in nasal secretions, lung lavage fluids and serum samples sequentially obtained from lambs experimentally infected with bovine respiratory syncytial virus (RSV). Virus-specific IgG and IgM responses were measured by the indirect double antibody sandwich ELISA using anti-bovine RSV monoclonal antibody, as capture antibody, and peroxidase-conjugated anti-sheep IgG and anti-sheep IgM. Virus-specific IgA antibodies were measured by antibody capture assay using anti-sheep IgA (alpha-chain specific) and anti-bovine RSV monoclonal antibodies. Bovine RSV-specific IgM and IgA antibodies were detected in the serum samples within 6 days post-inoculation (p.i.). Virus-specific IgC antibodies appeared in serum samples 4 days later. In nasal secretions, IgA antibodies appeared 7 days p.i. but IgM antibodies were not detected until 12-16 days p.i. In serum samples, IgM titres were predominant for the first 2 weeks p.i. IgC titres becoming predominant thereafter. In nasal secretions and lung lavage fluids, IgA titres were significantly higher than IgM or IgG titres up to 21 days p.i. (0.01).
采用酶联免疫吸附测定法(ELISA)对从实验感染牛呼吸道合胞病毒(RSV)的羔羊身上依次采集的鼻分泌物、肺灌洗液和血清样本中的病毒特异性IgG、IgM和IgA水平进行滴定。使用抗牛RSV单克隆抗体作为捕获抗体,以及过氧化物酶标记的抗绵羊IgG和抗绵羊IgM,通过间接双抗体夹心ELISA法测定病毒特异性IgG和IgM反应。使用抗绵羊IgA(α链特异性)和抗牛RSV单克隆抗体,通过抗体捕获测定法测量病毒特异性IgA抗体。在接种后(p.i.)6天内,在血清样本中检测到牛RSV特异性IgM和IgA抗体。4天后,病毒特异性IgG抗体出现在血清样本中。在鼻分泌物中,IgA抗体在接种后7天出现,但直到接种后12 - 16天才检测到IgM抗体。在血清样本中,接种后前2周IgM滴度占主导,此后IgG滴度占主导。在鼻分泌物和肺灌洗液中,直到接种后21天,IgA滴度显著高于IgM或IgG滴度(P<0.01)。