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本文引用的文献

1
Foot-and-mouth disease virus: a first inter-laboratory comparison trial to evaluate virus isolation and RT-PCR detection methods.口蹄疫病毒:一项评估病毒分离和逆转录-聚合酶链反应检测方法的首次实验室间比较试验
Vet Microbiol. 2006 Oct 31;117(2-4):130-40. doi: 10.1016/j.vetmic.2006.06.001. Epub 2006 Jul 17.
2
The alpha(v)beta6 integrin receptor for Foot-and-mouth disease virus is expressed constitutively on the epithelial cells targeted in cattle.口蹄疫病毒的α(v)β6整合素受体在牛的靶上皮细胞上持续表达。
J Gen Virol. 2005 Oct;86(Pt 10):2769-2780. doi: 10.1099/vir.0.81172-0.
3
Utility of recombinant integrin alpha v beta6 as a capture reagent in immunoassays for the diagnosis of foot-and-mouth disease.重组整联蛋白αvβ6作为捕获试剂在口蹄疫诊断免疫测定中的应用。
J Virol Methods. 2005 Jul;127(1):69-79. doi: 10.1016/j.jviromet.2005.02.014. Epub 2005 Apr 25.
4
Polyoma transformation of hamster cell clones--an investigation of genetic factors affecting cell competence.仓鼠细胞克隆的多瘤病毒转化——对影响细胞感受态的遗传因素的研究
Virology. 1962 Feb;16:147-51. doi: 10.1016/0042-6822(62)90290-8.
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Structure and receptor binding.结构与受体结合。
Virus Res. 2003 Jan;91(1):33-46. doi: 10.1016/s0168-1702(02)00258-7.
6
Sensitivity of primary cells immortalised by oncogene transfection for the detection and isolation of foot-and-mouth disease and swine vesicular disease viruses.
Vet Microbiol. 2002 Feb 4;84(4):307-16. doi: 10.1016/s0378-1135(01)00469-2.
7
Primary diagnosis of foot-and-mouth disease by reverse transcription polymerase chain reaction.通过逆转录聚合酶链反应进行口蹄疫的初步诊断。
J Virol Methods. 2000 Sep;89(1-2):167-76. doi: 10.1016/s0166-0934(00)00213-5.
8
The epithelial integrin alphavbeta6 is a receptor for foot-and-mouth disease virus.上皮整合素αvβ6是口蹄疫病毒的一种受体。
J Virol. 2000 Jun;74(11):4949-56. doi: 10.1128/jvi.74.11.4949-4956.2000.
9
Cell recognition by foot-and-mouth disease virus that lacks the RGD integrin-binding motif: flexibility in aphthovirus receptor usage.缺乏RGD整合素结合基序的口蹄疫病毒的细胞识别:口疮病毒受体使用的灵活性
J Virol. 2000 Feb;74(4):1641-7. doi: 10.1128/jvi.74.4.1641-1647.2000.
10
Diagnosis of foot-and-mouth disease by RT-PCR: evaluation of primers for serotypic characterisation of viral RNA in clinical samples.通过逆转录聚合酶链反应诊断口蹄疫:评估用于临床样本中病毒RNA血清型鉴定的引物
J Virol Methods. 1999 Dec;83(1-2):113-23. doi: 10.1016/s0166-0934(99)00113-5.

高敏感胎羊舌细胞系用于检测和分离口蹄疫病毒。

Highly sensitive fetal goat tongue cell line for detection and isolation of foot-and-mouth disease virus.

机构信息

Friedrich-Loeffler-Institute, Institute of Diagnostic Virology, Südufer 10, 17493 Greifswald-Insel Riems, Germany.

出版信息

J Clin Microbiol. 2009 Oct;47(10):3156-60. doi: 10.1128/JCM.00510-09. Epub 2009 Aug 5.

DOI:10.1128/JCM.00510-09
PMID:19656987
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2756941/
Abstract

A fetal goat cell line (ZZ-R 127) supplied by the Collection of Cell Lines in Veterinary Medicine of the Friedrich Loeffler Institute was examined for susceptibility to infection by foot-and-mouth disease (FMD) virus (FMDV) and by two other viruses causing clinically indistinguishable vesicular conditions, namely, the viruses of swine vesicular disease and vesicular stomatitis. Primary bovine thyroid (BTY) cells are generally the most sensitive cell culture system for FMDV detection but are problematic to produce, particularly for laboratories that infrequently perform FMD diagnostic tests and for those in countries where FMD is endemic that face problems in sourcing thyroid glands from FMD-negative calves. Strains representing all seven serotypes of FMDV could be isolated in ZZ-R 127 cells with a sensitivity that was considerably higher than that of established cell lines and within 0.5 log of that for BTY cells. The ZZ-R 127 cell line was found to be a sensitive, rapid, and convenient tool for the isolation of FMDV and a useful alternative to BTY cells for FMD diagnosis.

摘要

一个胎儿山羊细胞系(ZZ-R 127)由兽医医学细胞库提供,该细胞系被检查是否容易感染口蹄疫(FMD)病毒以及另外两种导致临床症状相似的水疱病的病毒,即猪水疱病病毒和水疱性口炎病毒。原发性牛甲状腺(BTY)细胞通常是最敏感的口蹄疫病毒检测细胞培养系统,但该系统的生产存在问题,特别是对于不经常进行口蹄疫诊断检测的实验室以及在口蹄疫流行的国家,这些实验室从非口蹄疫阴性小牛中获取甲状腺存在问题。在 ZZ-R 127 细胞中可以分离到代表所有七种血清型的 FMDV,其敏感性明显高于已建立的细胞系,与 BTY 细胞的敏感性相差 0.5 个对数。该 ZZ-R 127 细胞系是一种敏感、快速和方便的口蹄疫病毒分离工具,是 BTY 细胞的有用替代品,可用于口蹄疫诊断。