Tsuboi T, Imada T
Tohoku Branch Laboratory, National Institute of Animal Health, 31, Uminai, Shichinohe, Kamikita, Japan.
Vet Microbiol. 1996 Mar;49(1-2):127-134. doi: 10.1016/0378-1135(95)00179-4.
Bovine oocytes enclosed within follicular epithelial (FE) cells were exposed to noncytopathogenic or cytopathogenic strains of bovine viral diarrhea-mucosal disease virus (BVD-MDV). After culture at 39 degrees C in humidified air with 5 percent CO2 for 24 h, the oocytes matured and then in vitro fertilization was performed. Some of the fertilized oocytes developed into blastocysts from day 8 to day 10 (day 1: date of insemination), and the rate of development to blastocysts was the same as for the unexposed control oocytes. In the developmental medium, each strain of BVD-MDV was present at 10(3) to 10(6) TCID (50)/0.25 ml from day 3 to day 10, respectively and the virus was isolated from the FE cells at high titers and from the embryos at low titers on day 10. BVD-MDV antigen was detected in the cytoplasm of the FE cells by indirect immunofluorescence. These findings indicate that BVD-MDV replicates well in FE cells. The results of this study suggest that BVD-MDV replication in cells around embryos has no effect on bovine embryo development.
将包裹在卵泡上皮(FE)细胞内的牛卵母细胞暴露于牛病毒性腹泻-黏膜病病毒(BVD-MDV)的非细胞致病性或细胞致病性毒株。在39℃、含5%二氧化碳的湿润空气中培养24小时后,卵母细胞成熟,然后进行体外受精。部分受精的卵母细胞在第8天至第10天(第1天:授精日期)发育成囊胚,发育成囊胚的比率与未暴露的对照卵母细胞相同。在发育培养基中,从第3天至第10天,每种BVD-MDV毒株分别以10(3)至10(6) 半数组织培养感染剂量(TCID)(50)/0.25 ml存在,并且在第10天从FE细胞中以高滴度分离到病毒,从胚胎中以低滴度分离到病毒。通过间接免疫荧光在FE细胞的细胞质中检测到BVD-MDV抗原。这些发现表明BVD-MDV在FE细胞中复制良好。本研究结果提示,BVD-MDV在胚胎周围细胞中的复制对牛胚胎发育无影响。