Department of Animal Medicine, Production and Health (MAPS), Padua University,35020 Legnaro, Italy.
Vitalant Research Institute, San Francisco, CA 94118, USA.
Viruses. 2020 Feb 28;12(3):265. doi: 10.3390/v12030265.
The discovery of a globally distributed porcine circovirus (; PCV-3) has led to intense research activity and the production of a large amount of molecular data. Different research groups have proposed several, not always concordant, genotypes for this virus. While such categories could aid an easier interpretation of PCV-3 molecular epidemiology, any classification, to be useful in practical settings, must be univocal and of help in the understanding of underlying biological features and epidemiology. Based on these premises, the possibility of defining PCV-3 genotypes was evaluated on the broadest available dataset of PCV-3 complete genome ( = 357) and open reading frame 2 (ORF2, = 653) sequences. Genetic distance and phylogenetic clustering were selected as the main objective criteria. Additional factors, including the number of within-cluster sequences, host and geographic clustering, concordance between different genomic regions, and analysis method were also taken in account to generate a classification that could be effectively applied in research and diagnostic settings. A maximum within-genotype genetic distance of 3% at the complete genome and 6% at the ORF2 levels, bootstrap support higher than 90%, and concordance between analysis methods allowed us to clearly define two clades which could be potentially defined as genotypes. Further subdivision was not suggested due to the absence of a meaningful association between PCV-3 and its biological/epidemiological features. Nevertheless, since one of the clades included two strains only, thus far we formally propose the definition of only one PCV-3 genotype (PCV-3a). The established criteria will allow us to automatically recognize other genotypes when more strain sequences are characterized.
猪圆环病毒 3 型(PCV-3)的发现引发了大量的研究活动,并产生了大量的分子数据。不同的研究小组提出了几种不同的基因型,这些基因型并不总是一致的。虽然这些类别可以帮助更容易地解释 PCV-3 的分子流行病学,但任何分类,如果要在实际应用中有用,就必须是明确的,并有助于理解潜在的生物学特征和流行病学。基于这些前提,在最广泛的可用 PCV-3 全基因组(=357)和开放阅读框 2(ORF2,=653)序列数据集上评估了 PCV-3 基因型定义的可能性。遗传距离和系统发育聚类被选为主要的目标标准。还考虑了其他因素,包括聚类内序列的数量、宿主和地理聚类、不同基因组区域之间的一致性以及分析方法,以生成一种可在研究和诊断环境中有效应用的分类。全基因组水平的基因型内最大遗传距离为 3%,ORF2 水平的最大遗传距离为 6%,支持率高于 90%,不同分析方法之间的一致性允许我们清楚地定义两个可以被定义为基因型的分支。由于 PCV-3 与其生物学/流行病学特征之间没有有意义的关联,因此没有进一步细分。然而,由于其中一个分支只包含两个菌株,因此迄今为止,我们正式提出只定义一种 PCV-3 基因型(PCV-3a)。所建立的标准将允许我们在更多的菌株序列被表征时自动识别其他基因型。