Pees Michael, Neul Annkatrin, Müller Kristin, Schmidt Volker, Truyen Uwe, Leinecker Nadja, Marschang Rachel E
Clinic for Birds and Reptiles, University of Leipzig, An den Tierkliniken 17, 04103 Leipzig, Germany.
Institute of Pathology, University of Leipzig, An den Tierkliniken 33, 04103 Leipzig, Germany.
Vet Microbiol. 2016 Jan 15;182:213-22. doi: 10.1016/j.vetmic.2015.11.024. Epub 2015 Nov 22.
Ferlaviruses are important pathogens of snakes. However, factors influencing the pathogenicity of individual isolates as well as optimal protocols for virus detection in tissues of infected snakes have been insufficiently studied. The objectives of this study were to compare virus detection using previously described PCR and cell culture protocols following infection with three genetically distinct ferlaviruses in corn snakes (Pantherophis guttatus) as a model species. Groups of 12 corn snakes were each inoculated intratracheally with a genogroup A, B, or C ferlavirus. Tracheal washes and cloacal swabs were tested for virus shedding on days 16 and 28. Three animals were each euthanized on days 4, 16, 28, and 49. Beside immunohistochemistry of lung tissue, several organs (lung, intestine, pancreas, kidney, brain) were tested for the presence of ferlavirus. Distinct differences were noted in the pathogenicity of the three viruses, with a genotype B isolate causing the greatest pathology. PCR was more sensitive in comparison to cell culture, but results varied depending on the tissues. Ferlaviruses spread rapidly into the tissues, including the brain. Overall average detection rate was 72%, and was highest on day 16. There were differences between the groups, with the most virulent strain causing 100% positive samples at the end of the study. Some snakes were able to clear the infection. Shedding via cloaca was seen only on day 28. For ante-mortem sampling, a tracheal wash sample is recommended, for post mortem diagnosis, a pooled organ sample should be tested.
费拉病毒是蛇类的重要病原体。然而,影响单个分离株致病性的因素以及在感染蛇组织中进行病毒检测的最佳方案尚未得到充分研究。本研究的目的是比较在作为模式物种的玉米蛇(Pantherophis guttatus)中感染三种基因不同的费拉病毒后,使用先前描述的PCR和细胞培养方案进行病毒检测的情况。将12只玉米蛇分为几组,每组通过气管内接种A、B或C基因群的费拉病毒。在第16天和第28天对气管冲洗液和泄殖腔拭子进行病毒脱落检测。在第4天、16天、28天和49天分别对三只动物实施安乐死。除了对肺组织进行免疫组织化学检测外,还对几个器官(肺、肠、胰腺、肾、脑)进行了费拉病毒检测。三种病毒的致病性存在明显差异,其中B基因型分离株引起的病理变化最大。与细胞培养相比,PCR更敏感,但结果因组织而异。费拉病毒迅速扩散到包括脑在内的组织中。总体平均检测率为72%,在第16天最高。各组之间存在差异,最具毒力的毒株在研究结束时导致100%的样本呈阳性。一些蛇能够清除感染。仅在第28天观察到通过泄殖腔排出病毒。对于生前采样,建议采集气管冲洗液样本;对于死后诊断,应检测混合器官样本。