College of Veterinary Medicine, Shandong Agricultural University, 61 Daizong Road, 271018, Tai'an, Shandong, China.
Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, 61 Daizong Road, 271018, Tai'an, Shandong, China.
Emerg Microbes Infect. 2018 Jun 26;7(1):117. doi: 10.1038/s41426-018-0111-4.
The avian leukosis virus subgroup K (ALV-K), a novel subgroup in Chinese indigenous chicken breeds, has been difficult to isolate in the past due to its poor replication ability. However, according to the latest monitoring data, the replication ability and isolation rate of ALV-K have clearly increased, and new strains with mutations in the pol gene have also been found. To determine the effects of such mutations on the biological characteristics of ALV-K, a pair of infectious clones were constructed and rescued. The first virus was an ALV-K Chinese isolate with mutations in its pol gene, named rSDAUAK-11. The second virus was a recuperative rSDAUAK-11 from which mutations in the pol gene were recovered according to the corresponding region of the ALV-K prototype virus JS11C1, named rRSDAUAK-11. In addition, two quantitative real-time polymerase chain reaction assays were developed to specifically detect these virus strains. Using such methods, we observed a marked improvement of the reverse transcriptase activity, replication ability and vertical transmission ability of rSDAUAK-11, which also revealed a formidable competitive advantage in mixed infection with rRSDAUAK-11 and corresponded to the differences between the wild strains SDAUAK-11 and JS11C1. Accordingly, our findings not only show that mutations in the pol gene are an important molecular mechanism contributing to corresponding changes in the biological characteristics of the newest ALV-K but also emphasize the potential future eradication of ALV.
禽白血病病毒 K 亚群(ALV-K)是中国本土鸡种中的一个新亚群,由于其复制能力较差,过去一直难以分离。然而,根据最新的监测数据,ALV-K 的复制能力和分离率明显增加,并且发现了具有 pol 基因突变的新毒株。为了确定这些突变对 ALV-K 生物学特性的影响,构建并拯救了一对感染性克隆。第一个病毒是一种具有 pol 基因突变的 ALV-K 中国分离株,命名为 rSDAUAK-11。第二个病毒是根据 ALV-K 原型病毒 JS11C1 的相应区域恢复 pol 基因突变的可恢复性 rSDAUAK-11,命名为 rRSDAUAK-11。此外,还开发了两种定量实时聚合酶链反应检测方法,专门用于检测这些病毒株。使用这些方法,我们观察到 rSDAUAK-11 的逆转录酶活性、复制能力和垂直传播能力显著提高,并且在与 rRSDAUAK-11 混合感染时表现出强大的竞争优势,这与野生株 SDAUAK-11 和 JS11C1 之间的差异相对应。因此,我们的研究结果不仅表明 pol 基因的突变是导致最新 ALV-K 生物学特性相应变化的重要分子机制,还强调了未来根除 ALV 的潜力。