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传染性牛多瘤病毒的检测

Detection of infectious bovine polyomavirus.

作者信息

Nairn Carron, Lovatt Archie, Galbraith Daniel N

机构信息

Q-One Biotech Limited, Todd Campus, West of Scotland Science Park, Glasgow, G20 0XA, UK.

出版信息

Biologicals. 2003 Dec;31(4):303-6. doi: 10.1016/j.biologicals.2003.08.005.

DOI:10.1016/j.biologicals.2003.08.005
PMID:14624801
Abstract

Bovine polyomavirus (BPyV) is a member of the Polyomaviridae, a virus that was originally thought to be of simian origin but was later shown to be of bovine origin, the primate cultures having been contaminated through the use of foetal bovine serum. The significance of this agent to the biotechnology industry cannot be underestimated. The presence of BPyV in serum batches poses a serious risk for the contamination of human therapeutic products. The current PCR based assays provide a means of detecting virus sequences but give no indication as to the infectious nature of the virus. The communication reports the successful development of an assay to detect infectious BPyV using an in vitro amplification system followed by PCR. A lengthy culture period on bovine cells was required before replicating BPyV could be detected and distinguished from non-replicating virus in the cell culture supernatant. A mock-test assay using foetal bovine serum positive for BPyV showed that there was no evidence of replicating BPyV in the serum sample. The BPyV spiked serum control showed that replicating virus was present thus confirming that the serum itself did not inhibit replication of the virus. Cells harvested during the culture period were subjected to fixation, embedding and sectioning and examined by electron microscopy. Intact virus-like particles of approximately 40-50nm were observed in the nucleus of the bovine kidney cells, the site of polyomavirus replication.

摘要

牛多瘤病毒(BPyV)是多瘤病毒科的成员,该病毒最初被认为起源于猿猴,但后来证明起源于牛,灵长类细胞培养物因使用胎牛血清而受到污染。这种病原体对生物技术产业的重要性不可低估。血清批次中存在BPyV对人类治疗产品的污染构成严重风险。当前基于PCR的检测方法提供了一种检测病毒序列的手段,但无法表明病毒的感染性。该通讯报道了一种检测感染性BPyV的检测方法的成功开发,该方法使用体外扩增系统随后进行PCR。在能够检测到复制型BPyV并将其与细胞培养上清液中的非复制型病毒区分开来之前,需要在牛细胞上进行长时间培养。使用BPyV阳性的胎牛血清进行的模拟检测分析表明,血清样本中没有复制型BPyV的证据。添加BPyV的血清对照显示存在复制型病毒,从而证实血清本身不会抑制病毒的复制。在培养期间收获的细胞进行固定、包埋和切片,并通过电子显微镜检查。在牛肾细胞核(多瘤病毒复制的部位)中观察到了完整的约40 - 50nm的病毒样颗粒。

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