Khadija Akter, Young June Hong, Ihn Han, Eun Ha Choi
{"title":"非热等离子体射流通过靶向NF-κB和MAPK途径减轻人冠状病毒229e感染的肺细胞的病毒复制和炎症。","authors":"Khadija Akter, Young June Hong, Ihn Han, Eun Ha Choi","doi":"10.1016/j.micpath.2025.107838","DOIUrl":null,"url":null,"abstract":"<p><p>SARS-CoV-2 is a pressing global health issue, largely driven by uncontrolled viral replication and severe proinflammatory responses. Despite significant technological progress made by humanity, medical science has frequently found itself incapable of effectively addressing pathogenic outbreaks. Nonthermal plasma is a promising technology for combating pathogenic microorganisms. Considering the pressing demand for new treatment options, we have investigated the prospects of plasma-treated medium (PTM) enriched with reactive oxygen and nitrogen species (ROS/RNS) as a promising approach to combat human corona virus (HCoV-229E). The PTM was prepared using nonthermal plasma jet (NTPJ) with air as a flowing gas. NTPJ treatment effectively reduced the viral infection in MRC-5 lung cells, as evidenced through the assessment of the cytopathogenic effects. The mRNA expression of the viral gene ACE-2, Spike (S) gene, Rd/Rp Helicase gene and the generation of inflammation markers, IL-6, TNF-α, IL-1β, IFN-γ,COX-2,NF-κB, CXCL-10, and CCl-5 were significantly reduced with NTPJ. Moreover, confocal microscopy analysis revealed a significant reduction in spike glycoprotein and nucleocapsid protein levels in the cytoplasm. This finding was further supported by flow cytometry analysis, which confirmed a significant decrease in spike glycoprotein levels. Furthermore, mechanism studies indicated that NTPJ may influence cellular processes in HCoV-229E infected lung cells by disrupting the NF-κB and MAPK pathways, particularly evidenced by changes in phosphorylation levels. The pretreatment of the virus with SP600125 inhibitor and NTPJ resulted in a significant reduction in the expression ratio of viral genes ACE-2, S gene and RdRP/Helicase. Therefore, these results suggest that NTPJ enhances both anti-viral and anti-inflammatory responses, making it a promising candidate for prevention and treatment of corona virus infections.</p>","PeriodicalId":18599,"journal":{"name":"Microbial pathogenesis","volume":" ","pages":"107838"},"PeriodicalIF":3.3000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nonthermal plasma jet mitigates viral replication and inflammation in human coronavirus 229E-infected lung cells by targeting the NF-κB and MAPK pathways.\",\"authors\":\"Khadija Akter, Young June Hong, Ihn Han, Eun Ha Choi\",\"doi\":\"10.1016/j.micpath.2025.107838\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>SARS-CoV-2 is a pressing global health issue, largely driven by uncontrolled viral replication and severe proinflammatory responses. Despite significant technological progress made by humanity, medical science has frequently found itself incapable of effectively addressing pathogenic outbreaks. Nonthermal plasma is a promising technology for combating pathogenic microorganisms. Considering the pressing demand for new treatment options, we have investigated the prospects of plasma-treated medium (PTM) enriched with reactive oxygen and nitrogen species (ROS/RNS) as a promising approach to combat human corona virus (HCoV-229E). The PTM was prepared using nonthermal plasma jet (NTPJ) with air as a flowing gas. NTPJ treatment effectively reduced the viral infection in MRC-5 lung cells, as evidenced through the assessment of the cytopathogenic effects. The mRNA expression of the viral gene ACE-2, Spike (S) gene, Rd/Rp Helicase gene and the generation of inflammation markers, IL-6, TNF-α, IL-1β, IFN-γ,COX-2,NF-κB, CXCL-10, and CCl-5 were significantly reduced with NTPJ. Moreover, confocal microscopy analysis revealed a significant reduction in spike glycoprotein and nucleocapsid protein levels in the cytoplasm. This finding was further supported by flow cytometry analysis, which confirmed a significant decrease in spike glycoprotein levels. Furthermore, mechanism studies indicated that NTPJ may influence cellular processes in HCoV-229E infected lung cells by disrupting the NF-κB and MAPK pathways, particularly evidenced by changes in phosphorylation levels. The pretreatment of the virus with SP600125 inhibitor and NTPJ resulted in a significant reduction in the expression ratio of viral genes ACE-2, S gene and RdRP/Helicase. Therefore, these results suggest that NTPJ enhances both anti-viral and anti-inflammatory responses, making it a promising candidate for prevention and treatment of corona virus infections.</p>\",\"PeriodicalId\":18599,\"journal\":{\"name\":\"Microbial pathogenesis\",\"volume\":\" \",\"pages\":\"107838\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Microbial pathogenesis\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.micpath.2025.107838\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/6/25 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbial pathogenesis","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.micpath.2025.107838","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/25 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
Nonthermal plasma jet mitigates viral replication and inflammation in human coronavirus 229E-infected lung cells by targeting the NF-κB and MAPK pathways.
SARS-CoV-2 is a pressing global health issue, largely driven by uncontrolled viral replication and severe proinflammatory responses. Despite significant technological progress made by humanity, medical science has frequently found itself incapable of effectively addressing pathogenic outbreaks. Nonthermal plasma is a promising technology for combating pathogenic microorganisms. Considering the pressing demand for new treatment options, we have investigated the prospects of plasma-treated medium (PTM) enriched with reactive oxygen and nitrogen species (ROS/RNS) as a promising approach to combat human corona virus (HCoV-229E). The PTM was prepared using nonthermal plasma jet (NTPJ) with air as a flowing gas. NTPJ treatment effectively reduced the viral infection in MRC-5 lung cells, as evidenced through the assessment of the cytopathogenic effects. The mRNA expression of the viral gene ACE-2, Spike (S) gene, Rd/Rp Helicase gene and the generation of inflammation markers, IL-6, TNF-α, IL-1β, IFN-γ,COX-2,NF-κB, CXCL-10, and CCl-5 were significantly reduced with NTPJ. Moreover, confocal microscopy analysis revealed a significant reduction in spike glycoprotein and nucleocapsid protein levels in the cytoplasm. This finding was further supported by flow cytometry analysis, which confirmed a significant decrease in spike glycoprotein levels. Furthermore, mechanism studies indicated that NTPJ may influence cellular processes in HCoV-229E infected lung cells by disrupting the NF-κB and MAPK pathways, particularly evidenced by changes in phosphorylation levels. The pretreatment of the virus with SP600125 inhibitor and NTPJ resulted in a significant reduction in the expression ratio of viral genes ACE-2, S gene and RdRP/Helicase. Therefore, these results suggest that NTPJ enhances both anti-viral and anti-inflammatory responses, making it a promising candidate for prevention and treatment of corona virus infections.
期刊介绍:
Microbial Pathogenesis publishes original contributions and reviews about the molecular and cellular mechanisms of infectious diseases. It covers microbiology, host-pathogen interaction and immunology related to infectious agents, including bacteria, fungi, viruses and protozoa. It also accepts papers in the field of clinical microbiology, with the exception of case reports.
Research Areas Include:
-Pathogenesis
-Virulence factors
-Host susceptibility or resistance
-Immune mechanisms
-Identification, cloning and sequencing of relevant genes
-Genetic studies
-Viruses, prokaryotic organisms and protozoa
-Microbiota
-Systems biology related to infectious diseases
-Targets for vaccine design (pre-clinical studies)