Veterinary Medical Research Institute, Eötvös Loránd Research Network, 1581 Budapest, P.O. box 18, Hungary.
Chemical and Veterinary Investigation Office Westphalia, Zur Taubeneiche 10-12, 59821 Arnsberg, Germany.
Infect Genet Evol. 2022 Sep;103:105326. doi: 10.1016/j.meegid.2022.105326. Epub 2022 Jun 30.
In both a Eurasian blue tit (Cyanistes caeruleus) and a great tit (Parus major), found dead in North Rhine-Westphalia, Germany, intranuclear inclusion bodies were observed in the kidneys during the histologic examination. Siadenoviruses were detected in both samples, and the nucleotide sequence of the partial DNA polymerase, obtained from the blue tit, was almost identical with that of great tit adenovirus type 1, reported from Hungary previously. The sequence, derived from the German great tit sample was more similar to great tit adenovirus 2, yet divergent enough to forecast the possible establishment of a novel viral type and species. Therefore, the complete genome was subjected to next generation sequencing. The annotation revealed a typical siadenoviral genome layout, and phylogenetic analyses proved the distinctness of the novel virus type: great tit adenovirus 3. We propose the establishment of a new species (Siadenovirus carbocapituli) within the genus Siadenovirus to contain great tit adenovirus types 2 and 3. As both of the newly-detected viruses originated from histologically confirmed cases, and several siadenoviruses have been associated with avian nephritis earlier, we assume that the renal pathology might have been also of adenoviral origin. Additionally, we performed structural studies on two virus-coded proteins. The viral sialidase and the fiber knob were modeled using the AlphaFold2 program. According to the results of the sialic acid docking studies, the fiber trimer of the new great tit adenovirus 3 binds this acid with good affinity. As sialic acid is expressed in the kidney, it can be hypothesized that it is used during the receptor binding and entry of the virus. Strong binding of sialic acid was also predictable for the viral sialidase albeit its enzymatic activity remains disputable since, within its catalytic site, an asparagine residue was revealed instead of the conserved aspartic acid.
在德国北莱茵-威斯特法伦州死亡的欧亚鸲(Cyanistes caeruleus)和大山雀(Parus major)的肾脏组织切片检查中均观察到了核内包涵体。在这两个样本中均检测到了腺病毒,并且从蓝鸲中获得的部分 DNA 聚合酶的核苷酸序列与先前从匈牙利报道的大山雀腺病毒 1 几乎相同。从德国大山雀样本中获得的序列与大山雀腺病毒 2 更为相似,但差异足够大,可以预测可能建立新的病毒类型和物种。因此,对整个基因组进行了下一代测序。注释揭示了典型的腺病毒基因组结构,系统发育分析证明了新型病毒的独特性:大山雀腺病毒 3。我们建议在腺病毒属内建立一个新的物种(Siadenovirus carbocapituli),包含大山雀腺病毒 2 和 3。由于这两种新发现的病毒均源自组织学确诊病例,并且先前已有几种腺病毒与禽肾炎有关,因此我们假设肾脏病理学也可能是腺病毒引起的。此外,我们还对两种病毒编码蛋白进行了结构研究。使用 AlphaFold2 程序对病毒的唾液酸酶和纤维头进行了建模。根据唾液酸对接研究的结果,新型大山雀腺病毒 3 的病毒三聚体与该酸具有良好的亲和力。由于唾液酸在肾脏中表达,因此可以假设它在病毒的受体结合和进入过程中被使用。尽管该病毒的唾液酸酶的酶活性仍存在争议,但也可以预测它对唾液酸具有很强的结合能力,因为在其催化位点中发现了天冬酰胺残基而不是保守的天冬氨酸。