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用于 PRRSV 研究的猪肺泡巨噬细胞(PAMs)RT-qPCR 归一化的参考基因的选择和验证。

Selection and validation of reference genes for RT-qPCR normalization of porcine alveolar macrophages (PAMs) for PRRSV studies.

机构信息

Laboratory of Virology, Department of Translational Physiology, Infectiology and Public Health, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.

Laboratory of Veterinary Morphology, Department of Morphology, Imaging, Orthopedics, Rehabilitation and Nutrition, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.

出版信息

Sci Rep. 2023 May 31;13(1):8840. doi: 10.1038/s41598-023-35873-3.

Abstract

Porcine alveolar macrophages (PAMs) are widely used for in vitro studies of porcine respiratory viruses. Gene expression in these cells is altered by viral infection and cellular immune response. Real-time reverse transcription polymerase chain reaction (RT-qPCR) is a powerful technique for analyzing these changes. In order to obtain reliable quantitative RT-qPCR data and come to sound conclusions, stable reference genes are needed for normalization of target gene expression. In the present study, we evaluated the expression stability of nine reference genes in PAMs during cultivation and upon porcine reproductive and respiratory syndrome virus (PRRSV) inoculation. Using geNorm and NormFinder algorithms, we identified PSAP and GAPDH as the most stable reference genes under all experimental conditions. The selected reference genes were used for the normalization of CD163 expression under different conditions. This study demonstrates that selection of appropriate reference genes is essential for normalization and validation of RT-qPCR data across all experimental conditions. This study provides a new set of stable reference genes for future studies with porcine respiratory viruses in PAMs.

摘要

猪肺泡巨噬细胞(PAMs)广泛用于猪呼吸道病毒的体外研究。病毒感染和细胞免疫反应会改变这些细胞中的基因表达。实时逆转录聚合酶链反应(RT-qPCR)是分析这些变化的强大技术。为了获得可靠的定量 RT-qPCR 数据并得出合理的结论,需要稳定的参考基因来标准化靶基因表达。在本研究中,我们评估了 9 个参考基因在 PAMs 培养过程中和接种猪繁殖与呼吸综合征病毒(PRRSV)时的表达稳定性。使用 geNorm 和 NormFinder 算法,我们确定 PSAP 和 GAPDH 是所有实验条件下最稳定的参考基因。选择的参考基因用于在不同条件下对 CD163 表达进行归一化。本研究表明,选择合适的参考基因对于所有实验条件下的 RT-qPCR 数据的归一化和验证至关重要。本研究为未来在 PAMs 中研究猪呼吸道病毒提供了一组新的稳定参考基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1010/10232543/c50bc79ab2d0/41598_2023_35873_Fig1_HTML.jpg

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