Maarif Athok Shofiudin, Nishikawa Yukari, Takata Miyako, Kanai Kyosuke, Riyandani Edo, Mukuda Kengo, Mimura Momone, Yamaguchi Kosuke, Kato Hiroyuki, Okamoto Ryo, Okada Kensaku, Kitaura Tsuyoshi, Nakamoto Masaki, Yamasaki Akira, Kageyama Seiji, Chikumi Hiroki
Division of Infectious Diseases, Graduate School of Medicine, Faculty of Medicine, Tottori University, Nishi-cho 86, Yonago 683-8503, Tottori, Japan.
Division of School of Health Science, Department of Pathobiological Science and Technology, Faculty of Medicine, Tottori University, Yonago Nishi-cho 86, Yonago 683-8503, Tottori, Japan.
Int J Mol Sci. 2025 Jun 27;26(13):6221. doi: 10.3390/ijms26136221.
Persistent SARS-CoV-2 infections involve prolonged viral replication and immune system interactions, potentially driving viral evolution and immune escape. This study examines viral characteristics and host gene expression changes in persistent infections. The nasopharyngeal samples from four patients with persistent SARS-CoV-2 infections at Tottori University Hospital, Japan, were analyzed. Viral isolates were cultured, and infectivity was assessed using TCID assays. To investigate host responses, RNA sequencing (RNA-seq) was performed to identify differentially expressed genes (DEGs), and Gene Ontology (GO) enrichment analysis mapped affected biological pathways. Viral genome sequencing detected mutations associated with prolonged infection. The results showed significant infectivity differences between early- and late-phase infection. Gene expression analysis revealed a strong early phase of pro-inflammatory response (IL6, TNF, IL1B, CXCL10) followed by immune suppression. GO enrichment analysis highlighted inflammation and cytokine-mediated immune pathways. Genomic sequencing identified mutations in ORF1ab and the spike (S) protein, potentially aiding immune escape. The findings underscore that SARS-CoV-2 adapts during persistent infections, altering infectivity and immune responses. These highlight the need for continued monitoring of prolonged infections to mitigate immune escape and viral evolution.
持续性严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染涉及病毒的长期复制以及与免疫系统的相互作用,这可能会推动病毒进化和免疫逃逸。本研究调查了持续性感染中的病毒特征和宿主基因表达变化。对日本鸟取大学医院4例持续性SARS-CoV-2感染患者的鼻咽样本进行了分析。培养病毒分离株,并使用半数组织培养感染剂量(TCID)试验评估其感染性。为了研究宿主反应,进行了RNA测序(RNA-seq)以鉴定差异表达基因(DEG),并通过基因本体(GO)富集分析来确定受影响的生物学途径。病毒基因组测序检测到与长期感染相关的突变。结果显示早期和晚期感染之间存在显著的感染性差异。基因表达分析显示,早期存在强烈的促炎反应(IL6、TNF、IL1B、CXCL10),随后是免疫抑制。GO富集分析突出了炎症和细胞因子介导的免疫途径。基因组测序在开放阅读框1ab(ORF1ab)和刺突(S)蛋白中发现了突变,这可能有助于免疫逃逸。这些发现强调,SARS-CoV-2在持续性感染过程中会发生适应性变化,从而改变感染性和免疫反应。这些结果凸显了持续监测长期感染以减轻免疫逃逸和病毒进化的必要性。