Dong Xuan, Meng Fanfeng, Hu Tao, Ju Sidi, Li Yang, Sun Peng, Wang Yixin, Chen Wenqing, Zhang Fushou, Su Hongqin, Li Sifei, Cui He, Chen Junxia, Xu Shuzhen, Fang Lichun, Luan Huaibiao, Zhang Zhenjie, Chang Shuang, Li Jianliang, Wang Lei, Zhao Peng, Shi Weifeng, Cui Zhizhong
College of Veterinary Medicine, Shandong Agricultural UniversityTaian, China.
Institute of Pathogen Biology, Taishan Medical CollegeTaian, China.
Front Microbiol. 2017 Jun 26;8:1168. doi: 10.3389/fmicb.2017.01168. eCollection 2017.
Subgroup J avian leukosis virus (ALV-J), a typical retrovirus, is characterized of existence of a cloud of diverse variants and considerable genetic diversity. Previous studies describing the evolutionary dynamics of ALV-J genetic variants mainly focused on the early infection period or few randomly selected clones. Here, we inoculated 30 specific-pathogen-free chickens with the same founder ALV-J stock of known genetic background. Six (three antibody positive and three antibody negative) chickens were selected among 15 chickens with viremia. Viruses were serially isolated in 36 weeks and then sequenced using MiSeq high-throughput sequencing platform. This produced the largest ALV-J dataset to date, composed of more than three million clean reads. Our results showed that host humoral immunity could greatly enhance the genetic diversity of ALV-J genetic variants. In particular, selection pressures promoted a dynamic proportional changes in ALV-J genetic variants frequency. Cross-neutralization experiment showed that along with the change of the dominant variant, the antibody titers specific to infectious clones corresponding to the most dominant variants in weeks 12 and 28 have also changed significantly in sera collected in weeks 16 and 32. In contrast, no shift of dominant variant was observed in antibody-negative chickens. Moreover, we identified a novel hypervariable region in the gp85 gene. Our study reveals the interaction between ALV-J and the host, which could facilitate the development of vaccines and antiviral drugs.
J亚群禽白血病病毒(ALV-J)是一种典型的逆转录病毒,其特征是存在大量不同的变异体且具有相当大的遗传多样性。先前描述ALV-J遗传变异体进化动态的研究主要集中在早期感染阶段或少数随机选择的克隆。在此,我们用已知遗传背景的同一始祖ALV-J毒株接种了30只无特定病原体的鸡。在15只出现病毒血症的鸡中挑选了6只(3只抗体阳性和3只抗体阴性)。病毒在36周内连续分离,然后使用MiSeq高通量测序平台进行测序。这产生了迄今为止最大的ALV-J数据集,由超过三百万条干净 reads 组成。我们的结果表明,宿主体液免疫可极大地增强ALV-J遗传变异体的遗传多样性。特别是,选择压力促进了ALV-J遗传变异体频率的动态比例变化。交叉中和实验表明,随着优势变异体的变化,在第16周和第32周采集的血清中,针对第12周和第28周最优势变异体对应的感染性克隆的抗体滴度也发生了显著变化。相比之下,在抗体阴性的鸡中未观察到优势变异体的转移。此外,我们在gp85基因中鉴定出一个新的高变区。我们的研究揭示了ALV-J与宿主之间的相互作用,这有助于疫苗和抗病毒药物的开发。