Istituto Zooprofilattico Sperimentale dell'Umbria e delle Marche "Togo Rosati", 06126 Perugia, Italy.
TranslaTUM Center for Translational Cancer Research, Technical University of Munich, 81675 Munich, Germany.
Viruses. 2022 Mar 25;14(4):686. doi: 10.3390/v14040686.
Small ruminant lentiviruses (SRLVs) represent a very heterogeneous group of ss-RNA viruses that infect sheep and goats worldwide. They cause important, deleterious effects on animal production and limit the animal trade. SRLVs show a high genetic variability due to high mutation rate and frequent recombination events. Indeed, five genotypes (A-E) and several subtypes have been detected. The aim of this work was to genetically characterize SRLVs circulating in central Italy. On this basis, a phylogenetic study on the genetic region of 133 sheep, collected from 19 naturally infected flocks, was conducted. In addition, to evaluate the frequency of mutation and the selective pressure on this region, a WebLogo 3 analysis was performed, and the dN/dS ratio was computed. The results showed that 26 samples out of 133 were clustered in genotype A and 106 samples belonged to genotype B, as follows: A9 ( = 8), A11 ( = 10), A24 ( = 7), B1 ( = 2), B2 ( = 59), and B3 ( = 45). No recombination events were found. Mutations were localized mainly in the VR-2 region, and the dN/dS ratio of 0.028 indicated the existence of purifying selection. Since the genetic diversity of SRLVs could make serological identification difficult, it is important to perform molecular characterization to ensure a more reliable diagnosis, to maintain flock health status, and for the application of local and national control programs.
小反刍兽疫病毒(SRLV)是一组非常异质的 ss-RNA 病毒,可感染全球的绵羊和山羊。它们对动物生产造成了重要的有害影响,并限制了动物贸易。由于高突变率和频繁的重组事件,SRLV 表现出很高的遗传变异性。实际上,已经检测到五种基因型(A-E)和几种亚型。本研究的目的是对意大利中部流行的 SRLV 进行遗传特征分析。在此基础上,对 133 只绵羊的遗传区进行了基因分析,这些绵羊是从 19 个自然感染的羊群中采集的。此外,为了评估该区域的突变频率和选择压力,进行了 WebLogo 3 分析,并计算了 dN/dS 比值。结果表明,在 133 个样本中,有 26 个样本聚类为基因型 A,106 个样本属于基因型 B,具体为:A9(8 个)、A11(10 个)、A24(7 个)、B1(2 个)、B2(59 个)和 B3(45 个)。未发现重组事件。突变主要定位于 VR-2 区,dN/dS 比值为 0.028,表明存在纯化选择。由于 SRLV 的遗传多样性可能使血清学鉴定变得困难,因此进行分子特征分析对于确保更可靠的诊断、维持羊群健康状况以及应用当地和国家控制计划非常重要。