Bréard Emmanuel, Sailleau Corinne, Coupier Hervé, Mure-Ravaud Karine, Hammoumi Saliha, Gicquel Bernard, Hamblin Chris, Dubourget Philippe, Zientara Stéphan
UMR 1161 AFSSA-INRA-ENVA, Agence Française de Sécurité Sanitaire des Aliments - Alfort, 22 rue Pierre Curie, 94703 Maisons-Alfort, France.
Vet Res. 2003 Nov-Dec;34(6):777-89. doi: 10.1051/vetres:2003036.
Bluetongue (BT) virus serotype 2 (BTV 2) was first confirmed in Tunisia in February 2000 and has since spread northward and westward, infecting several other countries and islands, including Corsica, where clinical disease was reported in October 2000. BT was again reported on the Island in July 2001, some six months after a vaccination campaign against BTV 2. The molecular relationship between isolates of the BTV 2 Corsican wild-type viruses from 2000 and 2001, and the attenuated BTV 2 vaccine were determined by comparing corresponding sequences of genome segments 2, 7 and 10 with each other and with already published sequences available in the genome database. Complete genetic stability was observed between the isolates of the Corsican BTV 2. There was some divergence between the nucleotide sequences of segment 10 obtained from the wild-type and vaccine virus strains. Based on these differences, primers were selected that could be used in RT-PCR to differentiate between the wild-type and the vaccine viruses.
蓝舌病(BT)病毒血清型2(BTV 2)于2000年2月在突尼斯首次得到确认,此后向北和向西传播,感染了其他几个国家和岛屿,包括科西嘉岛,2000年10月在该岛报告了临床病例。2001年7月,在针对BTV 2开展疫苗接种运动约六个月后,该岛再次报告出现蓝舌病。通过将2000年和2001年科西嘉岛野生型BTV 2病毒分离株与减毒BTV 2疫苗的基因组片段2、7和10的相应序列相互比较,并与基因组数据库中已公布的序列进行比较,确定了它们之间的分子关系。在科西嘉岛BTV 2分离株之间观察到完全的遗传稳定性。从野生型和疫苗病毒株获得的片段10的核苷酸序列之间存在一些差异。基于这些差异,选择了可用于逆转录聚合酶链反应(RT-PCR)以区分野生型和疫苗病毒的引物。