Rojas José M, Rodríguez-Martín Daniel, Martín Verónica, Sevilla Noemí
Centro de Investigación en Sanidad Animal (CISA-INIA), Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria, Valdeolmos, Madrid, Spain,
Vet Med (Auckl). 2019 Feb 14;10:17-27. doi: 10.2147/VMRR.S163804. eCollection 2019.
This review provides an overview of current and potential new diagnostic techniques against bluetongue virus (BTV), an transmitted by arthropods that affects ruminants. Bluetongue is a disease currently notifiable to the World Organization for Animal Health (OIE), causing great economic losses due to decreased trade associated with bluetongue outbreaks and high mortality and morbidity. BTV cross-reacts with many antigenically related viruses including viruses that causes African Horse sickness and epizootic haemorrhagic disease of deer. Therefore, reliable diagnostic approaches to detect BTV among these other antigenically related viruses are used or being developed. The antigenic determinant for differentiation of virus species/serogroups among orbiviruses is the VP7 protein, meanwhile VP2 is serotype specific. Serologically, assays are established in many laboratories, based mainly on competitive ELISA or serum neutralization assay (virus neutralization assay [VNT]) although new techniques are being developed. Virus isolation from blood or semen is, additionally, another means of BTV diagnosis. Nevertheless, most of these techniques for viral isolation are time-consuming and expensive. Currently, reverse-transcription polymerase chain reaction (RT-PCR) panels or real-time RT-PCR are widely used methods although next-generation sequencing remains of interest for future virus diagnosis.
本综述概述了针对蓝舌病病毒(BTV)的现有及潜在新型诊断技术,BTV由节肢动物传播,可感染反刍动物。蓝舌病是一种目前须向世界动物卫生组织(OIE)通报的疾病,因蓝舌病疫情导致贸易减少以及高死亡率和发病率,造成了巨大经济损失。BTV与许多抗原相关病毒发生交叉反应,包括导致非洲马瘟和鹿流行性出血病的病毒。因此,正在使用或开发可靠的诊断方法,以便在这些其他抗原相关病毒中检测出BTV。环状病毒属病毒种/血清群分化的抗原决定簇是VP7蛋白,同时VP2具有血清型特异性。在血清学方面,许多实验室已建立检测方法,主要基于竞争ELISA或血清中和试验(病毒中和试验[VNT]),不过新技术也在不断研发。此外,从血液或精液中分离病毒是诊断BTV的另一种方法。然而,大多数这些病毒分离技术既耗时又昂贵。目前,逆转录聚合酶链反应(RT-PCR)检测板或实时RT-PCR是广泛使用的方法,尽管下一代测序对于未来的病毒诊断仍具有吸引力。