猪肺炎支原体232株诱导肺泡巨噬细胞差异基因表达谱的综合分析。

G Wang, J Li, Y Liu
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引用次数: 0

摘要

猪肺泡巨噬细胞(pam)可通过吞噬作用抵抗肺炎支原体(Mycoplasma hypopneumoniae, Mhp)感染。然而,目前尚不清楚Mhp刺激后PAM中发生了哪些基因表达变化。因此,采用差异基因表达(DGE)分析技术对感染Mhp菌株232的PAMs进行差异表达基因分析。在感染后12小时(hpi)和24小时(hpi), pam中分别鉴定出86个和889个差异表达(DE)基因。利用基因本体(Gene Ontology, GO)分析,DE基因参与了54个(12 hpi)和128个(24 hpi) GO富集项。利用京都基因与基因组百科全书(KEGG)分析,DE基因涉及101个(12 hpi)和250个(24 hpi) KEGG富集项。利用匠心通路分析(Ingenuity Pathway Analysis, IPA),将DE基因连接起来,形成25个内部相互作用的子网络。STRING分析显示131个DE基因编码的蛋白参与网络相互作用。五个新基因与肺炎支原体的临床症状和病理变化密切相关。这是首次使用DGE分析技术研究PAM对Mhp感染的转录反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrated analysis of differential gene expression profiles in porcine alveolar macrophages induced by Mycoplasma hyopneumoniae strain 232.

Porcine alveolar macrophages (PAMs) can resist infection caused by Mycoplasma hyopneumoniae (Mhp) through phagocytosis. However, it is unknown what gene expression changes occur in PAM after Mhp stimulation. Therefore, the differential gene expression (DGE) profiling technique was employed to analyze differentially expressed genes in PAMs infected with Mhp strain 232. Eighty-six and 889 differentially expressed (DE) genes were identified in PAMs at 12 hours post-infection (hpi) and 24 hpi. Using Gene Ontology (GO) analysis, DE genes were involved in 54 (12 hpi) and 128 (24 hpi) GO enrichment items. Using Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis, DE genes were involved in 101 (12 hpi) and 250 (24 hpi) KEGG enrichment items. Using Ingenuity Pathway Analysis (IPA), DE genes were connected, forming 25 internally interacting subnetworks. STRING analysis revealed 131 proteins encoded by DE genes involved in network interactions. Five novel genes were closely related to clinical symptoms and pathological changes of Mycoplasma hyopneumoniae. This is the first study to investigate PAM transcriptional responses to Mhp infection using the DGE profiling technique.

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