Bhetariya P J, Kriesel J D, Fischer K F
Department of Internal Medicine, Division of Infectious Diseases, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Department of Pathology, University of Utah School of Medicine, Salt Lake City, Utah, USA.
J Emerg Dis Virol. 2017 Aug;3(2). doi: 10.16966/2473-1846.133. Epub 2017 Jul 24.
It has been suggested that Human endogenous retroviruses (HERVs) are associated with multiple sclerosis (MS) pathogenesis. The objective of this study was to broadly evaluate the expression of HERV core (GAG) and envelope (ENV) genes in diseased brain white matter samples from MS patients compared to normal controls.
Twenty-eight HERV GAG and 88 ENV gene sequences were retrieved, classified by phylogeny, and grouped into clades. Consensus qPCR primers were designed for each clade, and quantitative PCR was performed on 33 MS and 9 normal control frozen brain samples. MS samples included chronic progressive (n=5), primary progressive (n=4), secondary progressive (n=14), relapsing remitting (n=3) and unclassified confirmed MS cases (n=7). The levels of GAG and ENV RNA within each of the samples were quantitated and normalized using the neuronal reference gene RPL19. Expression differences were analyzed for MS control.
Expression of GAG clades 1A, 3B, and 3C mapping to HERV-E and HERV-K were significantly increased compared to controls, while GAG clade 3A expression was decreased. Expression of HERV ENV clades 2, 3A, 3B, mapping to RTVL, HERV-E and HERV-K and MSRV (HERV-W), were significantly increased in the MS group. However, the relative expression differences between the MS and control groups were small, differing less than 1.5-fold.
Expression of GAG and ENV mapping to HERV-E, RTVL and HERV-K10 families were significantly increased in the MS group. However, the relative expression differences between the MS and control groups were small, differing less than 1.5-fold. These results indicate that the expression of HERV GAG and ENV regions do not differ greatly between MS and controls in these frozen brain samples.
有人提出人类内源性逆转录病毒(HERV)与多发性硬化症(MS)的发病机制有关。本研究的目的是广泛评估与正常对照相比,MS患者患病脑白质样本中HERV核心(GAG)和包膜(ENV)基因的表达情况。
检索了28个HERV GAG和88个ENV基因序列,按系统发育分类,并分组为进化枝。为每个进化枝设计了共识qPCR引物,并对33个MS和9个正常对照的冷冻脑样本进行了定量PCR。MS样本包括慢性进展型(n = 5)、原发进展型(n = 4)、继发进展型(n = 14)、复发缓解型(n = 3)和未分类确诊的MS病例(n = 7)。使用神经元参考基因RPL19对每个样本中的GAG和ENV RNA水平进行定量和标准化。分析MS与对照之间的表达差异。
与对照相比,映射到HERV-E和HERV-K的GAG进化枝1A、3B和3C的表达显著增加,而GAG进化枝3A的表达降低。映射到RTVL、HERV-E、HERV-K和MSRV(HERV-W)的HERV ENV进化枝2、3A、3B在MS组中的表达显著增加。然而,MS组与对照组之间的相对表达差异较小,相差不到1.5倍。
映射到HERV-E、RTVL和HERV-K10家族的GAG和ENV在MS组中的表达显著增加。然而,MS组与对照组之间的相对表达差异较小,相差不到1.5倍。这些结果表明,在这些冷冻脑样本中,MS与对照之间HERV GAG和ENV区域的表达差异不大。