Porta Natalia Gabriela, Alvarez Irene, Suarez Archilla Guillermo, Ruiz Vanesa, Abdala Alejandro, Trono Karina
Instituto Nacional de Tecnología Agropecuaria (INTA) - Instituto de Virología, Centro de Investigaciones en Ciencias Veterinarias y Agronómicas, Nicolas Repetto y de los Reseros s/n (1686), Hurlingham, Buenos Aires, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas, CONICET, Godoy Cruz 2290 (C1425FQB), CABA, Argentina.
Instituto Nacional de Tecnología Agropecuaria (INTA) - Instituto de Virología, Centro de Investigaciones en Ciencias Veterinarias y Agronómicas, Nicolas Repetto y de los Reseros s/n (1686), Hurlingham, Buenos Aires, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas, CONICET, Godoy Cruz 2290 (C1425FQB), CABA, Argentina.
Rev Argent Microbiol. 2019 Oct-Dec;51(4):316-323. doi: 10.1016/j.ram.2019.01.004. Epub 2019 Apr 22.
Bovine leukemia virus (BLV) is an important cattle pathogen that causes major economic losses worldwide, especially in dairy farms. The use of animal models provides valuable insight into the pathogenesis of viral infections. Experimental infections of sheep have been conducted using blood from BLV-infected cattle, infectious BLV molecular clones or tumor-derived cells. The Fetal Lamb Kidney cell line, persistently infected with BLV (FLK-BLV), is one of the most commonly used long-term culture available for the permanent production of virus. FLK-BLV cells or the viral particles obtained from the cell-free culture supernatant could be used as a source of provirus or virus to experimentally infect sheep. In this report, we aimed to determine the minimum amount of FLK-BLV cells or cell-free supernatant containing BLV needed to produce infection in sheep. We also evaluated the amount of antibodies obtained from a naturally-infected cow required to neutralize this infection. We observed that both sheep experimentally inoculated with 5000 FLK-BLV cells became infected, as well as one of the sheep receiving 500 FLK-BLV cells. None of the animals inoculated with 50 FLK-BLV cells showed evidence of infection. The cell-free FLK-BLV supernatant proved to be infective in sheep up to a 1:1000 dilution. Specific BLV antibodies showed neutralizing activity as none of the sheep became infected. Conversely, the animals receiving a BLV-negative serum showed signs of BLV infection. These results contribute to the optimization of a sheep bioassay which could be useful to further characterize BLV infection.
牛白血病病毒(BLV)是一种重要的牛病原体,在全球范围内造成重大经济损失,尤其是在奶牛场。动物模型的使用为深入了解病毒感染的发病机制提供了有价值的见解。已使用来自感染BLV的牛的血液、感染性BLV分子克隆或肿瘤衍生细胞对绵羊进行了实验性感染。持续感染BLV的胎羊肾细胞系(FLK-BLV)是最常用的可长期培养以持续产生病毒的细胞系之一。FLK-BLV细胞或从无细胞培养上清液中获得的病毒颗粒可用作原病毒或病毒来源,用于实验性感染绵羊。在本报告中,我们旨在确定在绵羊中产生感染所需的最低数量的FLK-BLV细胞或含有BLV的无细胞上清液。我们还评估了从自然感染的奶牛获得的中和这种感染所需的抗体量。我们观察到,实验接种5000个FLK-BLV细胞的两只绵羊均被感染,接种500个FLK-BLV细胞的绵羊中有一只也被感染。接种50个FLK-BLV细胞的动物均未显示感染迹象。无细胞的FLK-BLV上清液在绵羊中稀释至1:1000仍具有感染性。特异性BLV抗体显示出中和活性,因为没有一只绵羊被感染。相反,接受BLV阴性血清的动物出现了BLV感染迹象。这些结果有助于优化绵羊生物测定法,这可能有助于进一步表征BLV感染。