SPPV疫苗接种牛瘤状皮肤病病毒的分离

Lutfi Bakar, A. Hussein, S. Tamam, H. Madbouly
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引用次数: 1

摘要

2017年和2018年在贝尼-苏韦夫省观察到牛群中疑似LSDV的大规模暴发。采用绒毛膜-尿囊膜(CAM)途径,将以前接种过SPPV疫苗的病牛样本接种在胚鸡蛋(ECE)中。接种CAMs的组织病理学检查显示LSDV特征的嗜酸性大胞浆内包涵体。接种后的小鼠第1代出现血管充血出血,第2 ~ 4代后血管充血明显增多。第一次传代后观察到特征性的麻袋病变,第三次传代后清晰,接种后4天清晰。为了进行分子鉴定,从一组受感染的cam中提取DNA。使用了两对LSDV特异性引物,其中一对引物侧翼为G基因的554 bp产物,另一对引物侧翼为r030基因的172 bp产物。总之,已检测到LSDV感染,并通过PCR从2018年夏季接种SPPV疫苗的牛中分离和鉴定出该病毒。
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Isolation of Lumpy Skin Disease Virus Isolated from SPPV Vaccinated Cattle
Massive outbreaks of suspected LSDV in cattle population were observed during 2017 and 2018 at Beni-Suef governorate. Samples from diseased cattle, previously SPPV vaccinated with SPPV, were inoculated in embryonated chicken eggs (ECE) using chorio-allantoic membrane (CAM) route. Histopathological examination of the inoculated CAMs showed large eosinophilic intracytoplasmic inclusion bodies characteristic for LSDV. The inoculated CAMs were hemorrhagic with congestion blood vessels appeared by the 1st passage then become more pronounced after the second - fourth passages. Characteristic pock lesions were observed after the 1st passage and become clear after the third passage and become clearly observed 4 days post inoculation. For molecular identification, DNA was extracted from a pool of the infected CAMs. Two pairs of primers specific for LSDV including one flanking a 554 bp product of the G gene and second flanking 172 of the RP030 gene were used. In conclusion, LSDV infections have been detected and the virus has been isolated and identified by PCR from cattle previously vaccinated with SPPV vaccine during the summer of 2018.
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