Marschang Rachel E, Ihász Katalin, Kugler Renáta, Lengyel György, Fehér Enikő, Marton Szilvia, Bányai Krisztián, Aqrawi Tara, Farkas Szilvia L
LABOKLIN GmbH & Co. KG, Laboratory for Clinical Diagnostics, Bad Kissingen, Germany (Marschang)Centre for Agricultural Research, Institute for Veterinary Medical Research, Hungarian Academy of Sciences, Budapest, Hungary (Ihász, Kugler, Fehér, Marton, Bányai, Farkas)Medical Centre of Hungarian Defense Forces, Force Health Laboratory Institute, Budapest, Hungary (Lengyel)FG für Umweltund Tierhygiene, University of Hohenheim, Stuttgart, Germany (Aqrawi).
LABOKLIN GmbH & Co. KG, Laboratory for Clinical Diagnostics, Bad Kissingen, Germany (Marschang)Centre for Agricultural Research, Institute for Veterinary Medical Research, Hungarian Academy of Sciences, Budapest, Hungary (Ihász, Kugler, Fehér, Marton, Bányai, Farkas)Medical Centre of Hungarian Defense Forces, Force Health Laboratory Institute, Budapest, Hungary (Lengyel)FG für Umweltund Tierhygiene, University of Hohenheim, Stuttgart, Germany (Aqrawi)
J Vet Diagn Invest. 2016 May;28(3):309-14. doi: 10.1177/1040638716628584. Epub 2016 Mar 31.
Picornaviruses (PVs) of different terrestrial tortoise species, previously designated as Virus "X," have been frequently detected from various tissues by virus isolation in Terrapene heart cell culture as the preferred laboratory method for diagnosis. Here, we describe the development of 2 diagnostic reverse transcription (RT)-PCR-based assays for the identification and characterization of tortoise PVs belonging to the tentative genus Topivirus To test the novel diagnostic systems, PVs were isolated from swab and tissue samples collected in Germany, Italy, and Hungary between 2000 and 2013. All 25 tested isolates gave positive results with both novel consensus primer sets. Sequencing of the amplified products confirmed that all studied viruses were members of the new proposed genus Topivirus Phylogenetic analyses clearly distinguished 2 lineages within the genus. Based on sequence analysis, no association was observed between the geographic distribution and genetic relatedness. Furthermore, no strict host specificity was indicated. The PCR-based diagnosis may provide a time-saving and sensitive method to detect tortoise PVs, and evaluation of PV presence in these animals may help control virus spread.
以前被称为“X病毒”的不同陆龟物种的微小核糖核酸病毒(PVs),通过在木雕陆龟心脏细胞培养物中进行病毒分离,作为首选的实验室诊断方法,已频繁地从各种组织中检测到。在此,我们描述了两种基于逆转录(RT)-PCR的诊断方法的开发,用于鉴定和表征属于暂定的托皮病毒属的陆龟PVs。为了测试这种新型诊断系统,从2000年至2013年期间在德国、意大利和匈牙利采集的拭子和组织样本中分离出PVs。所有25个测试分离株对这两种新型共有引物组均给出阳性结果。扩增产物的测序证实,所有研究的病毒都是新提出的托皮病毒属的成员。系统发育分析清楚地区分了该属内的两个谱系。基于序列分析,未观察到地理分布与遗传相关性之间的关联。此外,未表明有严格的宿主特异性。基于PCR的诊断可能提供一种省时且灵敏的方法来检测陆龟PVs,并且评估这些动物中PV的存在情况可能有助于控制病毒传播。