Virology Department, Faculty of Veterinary Medicine, Benha University, Moshtahar, Toukh, Qalubiya, 13736, Egypt.
Department of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Virginia Tech, Blacksburg, VA, 24061, United States; Poultry Production Department, Faculty of Agriculture, Alexandria University, El-Shatby, Alexandria, 21545, Egypt.
Virus Res. 2019 Apr 2;263:47-54. doi: 10.1016/j.virusres.2019.01.005. Epub 2019 Jan 10.
Turkey adenovirus 3 (TAdV-3) belongs to the genus Siadenovirus, family Adenoviridae. Previously, nucleotide sequencing and annotation of the Virginia avirulent strain (VAS) of TAdV-3 genome, isolated in our laboratory, indicated the presence of a total of 23 genes and open reading frames (ORFs). The goals of this study were 1) to delineate the growth kinetics of the virus using a qPCR-based infectivity assay, and 2) to determine the virus gene expression profile during the early and late phases of infection in target B lymphocytes. The one-step growth curve experiment demonstrated 3 phases of virus replication cycle: a lag phase lasted for 12-18 h post-infection (h.p.i.), in which the virus titer declined; a log phase from 18 to 120 h.p.i., in which the number of infectious virus particles increased over 20,000 folds, and a brief decline phase thereafter. Southern blot analysis indicated that the synthesis of new viral DNA started by 8 h.p.i. Gene-specific RT-PCR analysis revealed the expression of mRNAs from the 23 TAdV-3 genes/ORFs. According to the temporal transcriptional profiling of TAdV-3 genome, genes could be divided into 3 groups based on the time of transcription initiation: group 1 showed detectable levels of transcription at 2 h.p.i and included 7 genes, i.e., hyd, III, pX, pVI, II, 100 K, and 33 K; group 2 included 12 genes whose mRNAs were detected for the first time at 4 h.p.i., i.e., ORF1, IVa2, pol, pTP, pIIIa, EP, DBP, E3, U exon, IV, ORF7, and ORF8; group 3 of transcripts were detectable starting 8 h.p.i. and included only 4 genes, i.e., 52 K, 22 K, pVII, and pVIII. Our data suggest that the transcriptional kinetics of genus Siadenovirus differ from that observed in other adenoviral genera; however, a few TAdV-3 genes showed similar expression patterns to their adenoviral homologs.
土耳其腺病毒 3(TAdV-3)属于腺病毒科的 Siadenovirus 属。先前,我们实验室分离的 TAdV-3 病毒弗吉尼亚无毒株(VAS)的核苷酸测序和注释表明,该病毒共包含 23 个基因和开放阅读框(ORF)。本研究的目的是 1)使用基于 qPCR 的感染性测定法描绘病毒的生长动力学,2)确定在靶 B 淋巴细胞感染的早期和晚期病毒基因表达谱。一步生长曲线实验表明病毒复制周期有 3 个阶段:感染后 12-18 小时的潜伏期,病毒滴度下降;18 至 120 小时的对数期,在此期间感染性病毒颗粒增加了 20000 多倍,此后出现短暂下降期。Southern 印迹分析表明,新病毒 DNA 的合成始于感染后 8 小时。基因特异性 RT-PCR 分析显示,23 个 TAdV-3 基因/ORF 的 mRNA 表达。根据 TAdV-3 基因组的时间转录谱分析,根据转录起始时间将基因分为 3 组:第 1 组在感染后 2 小时即可检测到转录水平,包括 7 个基因,即 hyd、III、pX、pVI、II、100K 和 33K;第 2 组包括 12 个基因,其 mRNA 首次在 4 小时时检测到,即 ORF1、IVa2、pol、pTP、pIIIa、EP、DBP、E3、U 外显子、IV、ORF7 和 ORF8;第 3 组转录本可在 8 小时后检测到,仅包括 4 个基因,即 52K、22K、pVII 和 pVIII。我们的数据表明,Siadenovirus 属的转录动力学与其他腺病毒属观察到的不同;然而,一些 TAdV-3 基因的表达模式与它们的腺病毒同源物相似。