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Development of the first oligonucleotide microarray for global gene expression profiling in guinea pigs: defining the transcription signature of infectious diseases

机译:第一个用于豚鼠全局基因表达谱分析的寡核苷酸微阵列的开发:确定传染病的转录特征

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Background The Guinea pig (Cavia porcellus) is one of the most extensively used animal models to study infectious diseases. However, despite its tremendous contribution towards understanding the establishment, progression and control of a number of diseases in general and tuberculosis in particular, the lack of fully annotated guinea pig genome sequence as well as appropriate molecular reagents has severely hampered detailed genetic and immunological analysis in this animal model. Results By employing the cross-species hybridization technique, we have developed an oligonucleotide microarray with 44,000 features assembled from different mammalian species, which to the best of our knowledge is the first attempt to employ microarray to study the global gene expression profile in guinea pigs. To validate and demonstrate the merit of this microarray, we have studied, as an example, the expression profile of guinea pig lungs during the advanced phase of M. tuberculosis infection. A significant upregulation of 1344 genes and a marked down regulation of 1856 genes in the lungs identified a disease signature of pulmonary tuberculosis infection. Conclusion We report the development of first comprehensive microarray for studying the global gene expression profile in guinea pigs and validation of its usefulness with tuberculosis as a case study. An important gap in the area of infectious diseases has been addressed and a valuable molecular tool is provided to optimally harness the potential of guinea pig model to develop better vaccines and therapies against human diseases.
机译:背景豚鼠(Cavia porcellus)是研究传染病最广泛使用的动物模型之一。然而,尽管它为理解许多疾病,特别是结核病的建立,发展和控制做出了巨大贡献,但是缺乏完整注释的豚鼠基因组序列以及适当的分子试剂,严重地阻碍了详细的遗传和免疫学分析。这个动物模型。结果通过使用跨物种杂交技术,我们开发了具有从不同哺乳动物物种组装的44,000个特征的寡核苷酸微阵列,据我们所知,这是首次尝试使用微阵列研究豚鼠的整体基因表达谱。为了验证和证明该微阵列的优点,我们以结核分枝杆菌感染晚期阶段的豚鼠肺的表达谱为例进行了研究。肺中1344个基因的显着上调和1856个基因的显着下调确定了肺结核感染的疾病特征。结论我们报道了第一个综合性芯片的开发,该芯片用于研究豚鼠的全球基因表达谱,并以结核病为例进行了验证。解决了传染病领域的一个重要空白,并提供了一种有价值的分子工具,可以最佳地利用豚鼠模型的潜力来开发更好的针对人类疾病的疫苗和疗法。

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