Vanroose G, Nauwynck H, Van Soom A, Vanopdenbosch E, de Kruif A
Department of Reproduction, Obstetrics and Herd Health, Faculty of Veterinary Medicine, University of Ghent, Merelbeke, Belgium.
Biol Reprod. 1998 Mar;58(3):857-66. doi: 10.1095/biolreprod58.3.857.
The aim of the present study was to determine whether or not cytopathic (CP) and noncytopathic (NCP) bovine viral diarrhea virus (BVDV) are able to replicate within in vitro-produced embryos and to investigate whether inoculation of embryos with BVDV affects their normal development. Zona pellucida (ZP)-free oocytes, zygotes, 8-cell-stage embryos, morulae, and hatched blastocysts (HB) were incubated for 1 h in 1 ml of Minimal Essential Medium containing 10(6.00) tissue culture infectious dose (TCID)50/ml NCP BVDV isolate 22,146 or 10(6.25) TCID50/ml CP BVDV strain Oregon C24V. At 0, 12, 24, 36, 48, 60, and 72 h postinoculation (hpi), groups of embryos were collected for virus titration. A small amount of newly produced virus was detected in 8-cell embryos at 60 hpi (10(1.8) TCID50/100 cells), but only for CP BVDV. For ZP-free morulae and HB, maximal intracellular virus titers were, respectively, 10(1.47) and 10(2.33) TCID50/100 cells at 48 hpi for the CP biotype and 10(0.64) and 10(0.84) TCID50/100 cells at 72 hpi for the NCP biotype. Only an infection with CP BVDV had a significant inhibitory effect on further development of ZP-free morulae. It can be concluded that ZP-free in vitro-produced embryos are permissive to an infection with BVDV, with increasing susceptibility of the embryos in accordance with their developmental stage. In contrast to observations in ZP-free in vitro-produced embryos, no virus replication or signs of embryonic degeneration were detected in ZP-intact in vitro-derived embryos.
本研究的目的是确定致细胞病变(CP)和非致细胞病变(NCP)的牛病毒性腹泻病毒(BVDV)是否能够在体外生产的胚胎内复制,并研究用BVDV接种胚胎是否会影响其正常发育。将无透明带(ZP)的卵母细胞、受精卵、8细胞期胚胎、桑椹胚和孵化囊胚(HB)在含有10(6.00)组织培养感染剂量(TCID)50/ml NCP BVDV分离株22,146或10(6.25) TCID50/ml CP BVDV毒株俄勒冈C24V的1 ml最低必需培养基中孵育1小时。在接种后0、12、24、36、48、60和72小时(hpi),收集胚胎组进行病毒滴定。在接种后60小时,在8细胞胚胎中检测到少量新产生的病毒(10(1.8) TCID50/100个细胞),但仅针对CP BVDV。对于无ZP的桑椹胚和HB,CP生物型在接种后48小时的最大细胞内病毒滴度分别为10(1.47)和10(2.33) TCID50/100个细胞,NCP生物型在接种后72小时的最大细胞内病毒滴度分别为10(0.64)和10(0.84) TCID50/100个细胞。仅CP BVDV感染对无ZP桑椹胚的进一步发育有显著抑制作用。可以得出结论,无ZP的体外生产胚胎对BVDV感染敏感,胚胎的易感性随其发育阶段增加。与在无ZP的体外生产胚胎中的观察结果相反,在完整ZP的体外衍生胚胎中未检测到病毒复制或胚胎退化迹象。