Beier D, Riebe R, Blankenstein P, Starick E, Bondzio A, Marquardt O
Federal Research Centre for Virus Diseases of Animals, Seestrabetasse 55, D-16868 Wusterhausen, Germany.
J Virol Methods. 2004 Nov;121(2):239-46. doi: 10.1016/j.jviromet.2004.06.017.
Due to the prevalence of different bovine leukosis virus (BLV) species in the cattle population in Europe, problems may arise in the serological diagnosis of BLV infections. In addition, earlier investigations demonstrated that contamination of the BLV antigen-producing cell culture systems by bovine viral diarrhea virus (BVDV) may give rise to misinterpretation of serological test results after BVDV vaccination of cattle. By co-cultivation of peripheral leukocytes of a BLV-infected cow with a permanent sheep kidney cell line, a new BLV-producing cell line named PO714 was established. This line carries a BLV provirus of the Belgian species and has been tested to be free of a variety of possibly contaminating viruses and mycoplasms. Investigations of a panel of well-characterised sera by agar gel immunodiffusion (AGID) and capture ELISA (cELISA) tests using antigen prepared from this new cell line in comparison with antigen of the well-known cell line FLK/BLV yielded comparable results. False positive results caused by BVDV cross-reactions could be eliminated when tests were carried out with antigen derived from the new cell line.
由于欧洲牛群中不同牛白血病病毒(BLV)毒株的广泛存在,BLV感染的血清学诊断可能会出现问题。此外,早期研究表明,牛病毒性腹泻病毒(BVDV)污染产生BLV抗原的细胞培养系统可能会导致牛接种BVDV疫苗后血清学检测结果出现误判。通过将感染BLV的奶牛外周血白细胞与永久性绵羊肾细胞系共同培养,建立了一种新的产生BLV的细胞系,命名为PO714。该细胞系携带比利时毒株的BLV前病毒,并且已经检测证明不含多种可能污染的病毒和支原体。使用从该新细胞系制备的抗原,通过琼脂凝胶免疫扩散(AGID)和捕获ELISA(cELISA)试验,对一组特征明确的血清进行检测,并与著名的FLK/BLV细胞系抗原进行比较,结果相当。当使用来自新细胞系的抗原进行检测时,可以消除由BVDV交叉反应引起的假阳性结果。