Sibille P, Avraméas A, Moraillon A, Richardson J, Sonigo P, Pancino G, Strosberg A D
Institut Cochin de Génétique Moléculaire, Unité d'Immunopharmacologie moléculaire et génétique des virus, CNRS UPR 415, Paris, France.
Vet Microbiol. 1995 Jul;45(2-3):259-67. doi: 10.1016/0378-1135(94)00128-j.
A new enzyme-linked-immunosorbent assay (ELISA) for the detection of antibodies to feline immunodeficiency virus was compared with previously described ELISAs. Serum samples from 184 infected or uninfected cats were tested using a whole virus lysate kit and ELISAs based on recognition of one of two synthetic peptides (P237 and P253) localized in the transmembrane domain of the viral envelope. The whole virus lysate commercial kit led to the detection of 6% false positive and 4.3% false negative sera. The ELISA based on peptide P253 gave no false positive result and failed to detect only one serum that was subsequently shown to be positive by radio-immunoprecipitation assay. A sandwich-ELISA test using Galanthus nivalis agglutinin, a lectin that specifically binds terminal mannose groups of the envelope proteins was used as a confirmatory test for equivocal results with peptide ELISA and gave similar results. This study indicates that recognition of P253 could serve as a sensitive and specific test for the diagnosis of seropositivity to feline immunodeficiency virus, and moreover that the Galanthus nivalis ELISA could be useful in equivocal cases as a confirmatory test.
一种用于检测猫免疫缺陷病毒抗体的新型酶联免疫吸附测定(ELISA)方法与先前描述的ELISA方法进行了比较。使用全病毒裂解物试剂盒以及基于识别位于病毒包膜跨膜结构域的两种合成肽(P237和P253)之一的ELISA,对184只感染或未感染的猫的血清样本进行了检测。全病毒裂解物商业试剂盒检测出6%的假阳性血清和4.3%的假阴性血清。基于肽P253的ELISA未出现假阳性结果,仅未能检测出一份随后经放射免疫沉淀测定显示为阳性的血清。使用雪花莲凝集素(一种特异性结合包膜蛋白末端甘露糖基团的凝集素)的夹心ELISA试验,作为肽ELISA结果不明确时的确认试验,得到了相似的结果。这项研究表明,识别P253可作为诊断猫免疫缺陷病毒血清阳性的灵敏且特异的检测方法,此外,雪花莲ELISA在结果不明确的情况下作为确认试验可能会有用。