Walz P H, Bell T G, Grooms D L, Kaiser L, Maes R K, Baker J C
Department of Large Animal Clinical Sciences, College of Veterinary Medicine, Michigan State University, East Lansing 48824-1314, USA.
Can J Vet Res. 2001 Oct;65(4):241-7.
Altered platelet function has been reported in calves experimentally infected with type II bovine viral diarrhea virus (BVDV). The purpose of the present study was to further evaluate the ability of BVDV isolates to alter platelet function and to examine for the presence of a virus-platelet interaction during BVDV infection. Colostrum-deprived Holstein calves were obtained immediately after birth, housed in isolation, and assigned to 1 of 4 groups (1 control and 3 treatment groups). Control calves (n = 4) were sham inoculated, while calves in the infected groups (n = 4 for each group) were inoculated by intranasal instillation with 10(7) TCID50 of either BVDV 890 (type II), BVDV 7937 (type II), or BVDV TGAN (type I). Whole blood was collected prior to inoculation (day 0) and on days 4, 6, 8, 10, and 12 after inoculation for platelet function testing by optical aggregometry by using adenosine diphosphate and platelet activating factor. The maximum percentage aggregation and the slope of the aggregation curve decreased over time in BVDV-infected calves; however, statistically significant differences (Freidman repeated measures ANOVA on ranks, P < 0.05) were only observed in calves infected with the type II BVDV isolates. Bovine viral diarrhea virus was not isolated from control calves, but was isolated from all calves infected with both type II BVDV isolates from days 4 through 12 after inoculation. In calves infected with type I BVDV, virus was isolated from 1 of 4 calves on days 4 and 12 after inoculation and from all calves on days 6 and 8 after inoculation. Altered platelet function was observed in calves infected with both type II BVDV isolates, but was not observed in calves infected with type I BVDV. Altered platelet function may be important as a difference in virulence between type I and type II BVDV infection.
据报道,在实验感染II型牛病毒性腹泻病毒(BVDV)的犊牛中血小板功能发生了改变。本研究的目的是进一步评估BVDV分离株改变血小板功能的能力,并检查在BVDV感染期间是否存在病毒与血小板的相互作用。初乳剥夺的荷斯坦犊牛在出生后立即获得,单独饲养,并分为4组中的1组(1个对照组和3个处理组)。对照犊牛(n = 4)接受假接种,而感染组的犊牛(每组n = 4)通过鼻内滴注10(7) TCID50的BVDV 890(II型)、BVDV 7937(II型)或BVDV TGAN(I型)进行接种。在接种前(第0天)以及接种后第4、6、8、10和12天采集全血,通过使用二磷酸腺苷和血小板活化因子的光学聚集法进行血小板功能测试。在感染BVDV的犊牛中,最大聚集百分比和聚集曲线的斜率随时间下降;然而,仅在感染II型BVDV分离株的犊牛中观察到统计学上的显著差异(基于秩次的Friedman重复测量方差分析,P < 0.05)。未从对照犊牛中分离出牛病毒性腹泻病毒,但在接种后第4天至12天从所有感染II型BVDV分离株的犊牛中分离出该病毒。在感染I型BVDV的犊牛中,在接种后第4天和12天从4头犊牛中的1头分离出病毒,在接种后第6天和8天从所有犊牛中分离出病毒。在感染II型BVDV分离株的犊牛中观察到血小板功能改变,但在感染I型BVDV的犊牛中未观察到。血小板功能改变可能作为I型和II型BVDV感染之间毒力差异的一个因素而具有重要意义。