Center for Artificial Intelligence Research, Wake Forest University School of Medicine, Winston-Salem, NC 27101, USA.
Department of Biology, George Mason University, Fairfax, VA 22030, USA.
Int J Mol Sci. 2024 Oct 17;25(20):11142. doi: 10.3390/ijms252011142.
Mpox, caused by the Mpox virus (MPXV), emerged globally in 2022 with the Clade IIb strain, presenting a critical public health challenge. While MPXV is primarily characterized by fever and rash, gastrointestinal (GI) complications, such as diarrhea and proctitis, have also been observed. This study is a reanalysis of GSE219036 without own data and focuses on the impact of MPXV infection on the colon, using human-induced pluripotent stem cell-derived colon organoids as a model. We applied a tailored statistical framework for RNA-seq data, Generalized Linear Models with Quasi-Likelihood F-tests and Relaxed Magnitude-Altitude Scoring (GLMQL-RMAS), to identify differentially expressed genes (DEGs) across MPXV clades: MPXV I (Zr-599 Congo Basin), MPXV IIa (Liberia), and MPXV IIb (2022 MPXV). Through a novel methodology called Cross-RMAS, we ranked genes by integrating statistical significance and biological relevance across all clades. Machine learning analysis using the genes identified by Cross-RMAS, demonstrated 100% accuracy in differentiating between the different MPXV strains and mock samples. Furthermore, our findings reveal that MPXV Clade I induces the most extensive alterations in gene expression, with significant upregulation of stress response genes, such as and , and downregulation of genes involved in cytoskeletal organization and vesicular trafficking, such as and . In contrast, Clade IIb shows the least impact on gene expression. Through Gene Ontology (GO) analysis, we identified pathways involved in protein folding, immune response, and epithelial integrity that are disrupted in infected cells, suggesting mechanisms by which MPXV may contribute to GI symptoms.
猴痘,由猴痘病毒(MPXV)引起,于 2022 年在全球出现,其毒株为 Clade IIb,对公共卫生构成了重大挑战。虽然 MPXV 的主要特征是发热和皮疹,但也观察到了胃肠道(GI)并发症,如腹泻和直肠炎。本研究是对 GSE219036 的重新分析,没有自己的数据,重点关注 MPXV 感染对结肠的影响,使用人诱导多能干细胞衍生的结肠类器官作为模型。我们应用了一种针对 RNA-seq 数据的定制统计框架,广义线性模型与拟似然 F 检验和 Relaxed Magnitude-Altitude Scoring(GLMQL-RMAS),以识别不同 MPXV 亚群之间的差异表达基因(DEGs):MPXV I(Zr-599 刚果盆地)、MPXV IIa(利比里亚)和 MPXV IIb(2022 年 MPXV)。通过一种称为 Cross-RMAS 的新方法,我们通过整合所有亚群的统计显著性和生物学相关性对基因进行排名。使用 Cross-RMAS 鉴定的基因进行机器学习分析,可在区分不同的 MPXV 株和模拟样本方面达到 100%的准确率。此外,我们的研究结果表明,MPXV I 亚群诱导基因表达的改变最为广泛,应激反应基因如 和 显著上调,而参与细胞骨架组织和囊泡运输的基因如 和 下调。相比之下,Clade IIb 对基因表达的影响最小。通过基因本体论(GO)分析,我们确定了参与蛋白质折叠、免疫反应和上皮完整性的途径在感染细胞中被破坏,这表明 MPXV 可能导致 GI 症状的机制。