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小型反刍动物慢病毒长末端重复序列R区域的缺失与肺部病变减轻有关。

A deletion in the R region of long terminal repeats in small ruminant lentiviruses is associated with decreased pathology in the lung.

作者信息

Angelopoulou K, Poutahidis T, Brellou G D, Greenland T, Vlemmas I

机构信息

Laboratory of Biochemistry and Toxicology, School of Veterinary Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.

出版信息

Vet J. 2008 Mar;175(3):346-55. doi: 10.1016/j.tvjl.2007.01.025. Epub 2007 May 10.

Abstract

A particular variant of the maedi visna virus (MVV) that although present in blood causes no clinical signs in infected sheep has been described. This variant carries a 13-14 nucleotide deletion in the R region of the proviral long terminal repeats. The hypothesis that this specific deletion may be associated with low pathogenicity has been investigated by comparing the distribution of proviral sequences, the histopathological lesions and the expression of viral proteins in the brain, lungs and udders of sheep naturally infected with viral strains carrying the deletion. Provirus could be demonstrated in most of the tissues examined from sheep infected with either type of virus, and the tissue-derived virus carried the typical deletion in the study flock animals. Histopathological analysis revealed that the lungs were significantly less affected in the animals infected with virus carrying the deletion. Concomitantly, viral expression was significantly reduced in the lungs of these animals. The findings suggest that the reduced pathogenicity of MVV with the specific deletion in the R region is not due to a restriction in the availability of specific tissues to infection, but is associated with a reduced capacity for viral expression in the lungs.

摘要

已经描述了梅迪 - 维斯纳病毒(MVV)的一种特殊变体,该变体虽然存在于血液中,但在感染的绵羊中不会引起临床症状。这种变体在前病毒长末端重复序列的R区域存在13 - 14个核苷酸的缺失。通过比较携带该缺失的病毒株自然感染的绵羊的脑、肺和乳房中前病毒序列的分布、组织病理学病变以及病毒蛋白的表达,对这种特定缺失可能与低致病性相关的假说进行了研究。在感染任何一种病毒的绵羊的大多数检测组织中都能检测到前病毒,并且在研究群体动物中,组织衍生病毒携带典型的缺失。组织病理学分析表明,感染携带缺失的病毒的动物肺部受影响明显较小。与此同时,这些动物肺部的病毒表达显著降低。研究结果表明,R区域具有特定缺失的MVV致病性降低并非由于特定组织对感染的易感性受限,而是与肺部病毒表达能力降低有关。

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