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Establishment of a Bovine Viral Diarrhea Virus Type 2 Intranasal Challenge Model for Assessing Vaccine Efficacy

机译:牛病毒性腹泻病毒2型鼻内攻击模型评估疫苗效力的建立。

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摘要

The objective of this study was to develop a bovine viral diarrhea virus type 2 (BVDV-2) challenge model suitable for evaluation of efficacy of BVDV vaccines; a model that mimics natural infection and induces clear leukopenia and viremia. Clinical, hematological and virological parameters were evaluated after infection of two age groups of calves (3 and 9 months) with two BVDV-2 strains (1362727 and 502643). Calves became pyrexic between 8 and 9 days post inoculation and exhibited symptoms, such as nasal discharge, mild depression, cough, and inappetence. Leukopenia with associated lymphopenia and neutropenia was evident in all groups with lowest leukocyte and lymphocyte counts reached 8 dpi and granulocyte counts between 11 and 16 dpi, dependent on the strain and age of the calves. A more severe thrombocytopenia was seen in those animals inoculated with strain 1362727. Leukocyte and nasal swab samples were positive by virus isolation, as early as 3 dpi and 2 dpi respectively, independent of the inocula used. All calves seroconverted with high levels of BVDV-2 neutralizing antibodies. BVDV RNA was evident as late as 90 dpi and provides the first evidence of the presence of replicating virus long after recovery from BVDV-2 experimental infection. In summary, moderate disease can be induced after experimental infection of calves with a low titer of virulent BVDV-2, with leukopenia, thrombocytopenia, viremia, and virus shedding. These strains represent an attractive model to assess the protective efficacy of existing and new vaccines against BVDV-2.
机译:这项研究的目的是开发一种适合评估BVDV疫苗功效的2型牛病毒性腹泻病毒(BVDV-2)攻击模型。模仿自然感染并诱发明显的白细胞减少症和病毒血症的模型。在两个年龄组的犊牛(3和9个月)感染了两种BVDV-2菌株(1362727和502643)后,评估了临床,血液学和病毒学参数。犊牛在接种后8至9天开始出现高热,并表现出一些症状,例如流鼻涕,轻度抑郁,咳嗽和食欲不振。在所有组中,白细胞减少症伴有淋巴细胞减少和中性粒细胞减少,在所有组中均明显,白细胞和淋巴细胞计数最低,达到8 dpi,粒细胞计数在11至16 dpi之间,具体取决于小牛的株和年龄。在接种了1362727菌株的那些动物中观察到了更严重的血小板减少症。通过病毒分离,白细胞和鼻拭子样本呈阳性,分别早于3 dpi和2 dpi,与所使用的接种物无关。所有犊牛均通过高水平的BVDV-2中和抗体进行血清转化。从BVDV-2实验性感染中恢复很久以后,BVDV RNA才出现,直到90 dpi才出现,并提供了复制病毒存在的第一个证据。总之,在实验性感染具有低滴度的强毒BVDV-2的小牛后,可诱发中度疾病,并伴有白细胞减少症,血小板减少症,病毒血症和病毒脱落。这些菌株代表了一个有吸引力的模型,可以评估现有和新疫苗针对BVDV-2的保护功效。

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