Walsh Scott R, Linnerth-Petrik Nicolle M, Yu Darrick L, Foster Robert A, Menzies Paula I, Diaz-Méndez Andrés, Chalmers Heather J, Wootton Sarah K
Vet Res. 2013 Jul 30;44(1):66. doi: 10.1186/1297-9716-44-66.
Enzootic nasal adenocarcinoma (ENA) is a contagious neoplasm of the secretory epithelial cells of the nasal mucosa of sheep and goats. It is associated with the betaretrovirus, enzootic nasal tumor virus (ENTV), but a causative relationship has yet to be demonstrated. In this study, 14-day-old lambs were experimentally infected via nebulization with cell-free tumor filtrates derived from naturally occurring cases of ENA. At 12 weeks post-infection (wpi), one of the five infected lambs developed clinical signs, including continuous nasal discharge and open mouth breathing, and was euthanized. Necropsy revealed the presence of a large bilateral tumor occupying the nasal cavity. At 45 wpi, when the study was terminated, none of the remaining infected sheep showed evidence of tumors either by computed tomography or post-mortem examination. ENTV-1 proviral DNA was detected in the nose, lung, spleen, liver and kidney of the animal with experimentally induced ENA, however there was no evidence of viral protein expression in tissues other than the nose. Density gradient analysis of virus particles purified from the experimentally induced nasal tumor revealed a peak reverse transcriptase (RT) activity at a buoyant density of 1.22 g/mL which was higher than the 1.18 g/mL density of peak RT activity of virus purified from naturally induced ENA. While the 1.22 g/mL fraction contained primarily immature unprocessed virus particles, mature virus particles with a similar morphology to naturally occurring ENA could be identified by electron microscopy. Full-length sequence analysis of the ENTV-1 genome from the experimentally induced tumor revealed very few nucleotide changes relative to the original inoculum with only one conservative amino acid change. Taken together, these results demonstrate that ENTV-1 is associated with transmissible ENA in sheep and that under experimental conditions, lethal tumors are capable of developing in as little as 12 wpi demonstrating the acutely oncogenic nature of this ovine betaretrovirus.
绵羊和山羊的地方性鼻腺癌(ENA)是一种由鼻腔黏膜分泌上皮细胞引起的传染性肿瘤。它与β逆转录病毒——地方性鼻肿瘤病毒(ENTV)有关,但因果关系尚未得到证实。在本研究中,14日龄的羔羊通过雾化接种来自自然发生的ENA病例的无细胞肿瘤滤液进行实验性感染。感染后12周(wpi),五只感染羔羊中的一只出现了临床症状,包括持续的鼻分泌物和张口呼吸,随后实施安乐死。尸检发现双侧鼻腔有一个大肿瘤。在45 wpi研究结束时,其余感染绵羊通过计算机断层扫描或死后检查均未显示肿瘤迹象。在实验性诱导的ENA动物的鼻、肺、脾、肝和肾中检测到ENTV-1前病毒DNA,但除鼻组织外,其他组织均未发现病毒蛋白表达的证据。对从实验性诱导的鼻肿瘤中纯化的病毒颗粒进行密度梯度分析,结果显示,在浮力密度为1.22 g/mL时逆转录酶(RT)活性达到峰值,高于从自然诱导的ENA中纯化的病毒RT活性峰值密度1.18 g/mL。虽然1.22 g/mL组分主要包含未成熟的未加工病毒颗粒,但通过电子显微镜可以鉴定出形态与自然发生的ENA相似的成熟病毒颗粒。对实验性诱导肿瘤中的ENTV-1基因组进行全长序列分析发现,与原始接种物相比,核苷酸变化极少,只有一个保守氨基酸变化。综上所述,这些结果表明ENTV-1与绵羊的可传播ENA有关,并且在实验条件下,致死性肿瘤在短短12 wpi时就能够形成,证明了这种绵羊β逆转录病毒具有急性致癌性。