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人鼻病毒1B感染人扁桃体上皮细胞和人肺支气管上皮细胞的比较代谢组学研究 被引量:1

Comparative Metabolomics Between Human Tonsillar Epithelial Cells and Human Lung Bronchial Epithelial Cells Infected with Human Rhinovirus 1B
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摘要 人鼻病毒(Human rhinovirus,HRV)是呼吸道感染的主要病原体之一,明确HRV的致病机制能为有效防控该病毒感染提供科学依据。为确定1B型HRV(human rhinovirus type 1B,HRV1B)感染致宿主细胞的代谢组改变及差异性,本文采用非靶向代谢组学技术研究HRV1B感染人扁桃体上皮细胞UT-SCC-60B和人肺支气管上皮细胞BEAS-2B后代谢组的改变情况。HRV1B感染UT-SCC-60B细胞6h和12h分别有21个差异显著代谢产物(differentially significant metabolites,DSMs)(上调13个、下调8个)和51个DSMs(上调42个、下调9个),HRV1B感染UT-SCC-60B和BEAS-2B细胞6h和12h后,比较分析发现分别有303个DSMs(上调69个,下调234个)和324个DSMs(上调88个,下调236个),未知DSMs占据比例较大。脂肪酸、脂质、氨基酸、核苷酸和糖类的比例随着感染时间的延长而增加,7-酮基脱氧胆酸、溶血磷脂酰胆碱、垂盆草甙、组氨酸-甘氨酸、腺苷酸等涉及到胆汁酸代谢、脂肪酸和脂质代谢、糖代谢、氨基酸代谢和核苷酸代谢。因此,细胞水平表明HRV1B感染改变了人上皮细胞的脂肪酸、脂质、氨基酸、核苷酸和糖类的代谢水平。 Human Rhinovirus 1B(HRV1B)as one major pathogens of respiratory infections,and illuminating pathogenesis mechanism of HRV1B will provide a better evidence for prevention and control for HRV1B.To research the metabolomic changes and differences in host cells infected with HRV1B,untargeted metabolomics was used to determine the metabolomics alterations between human tonsillar epithelial cells UT⁃SCC⁃60B and human lung bronchial epithelial cells BEAS⁃2B infected with HRV1B.A total of 21 differentially significant metabolites(DSMs)(13 DSMs were up⁃regulated and 8 DSMs were down⁃regulated)and 51 DSMs(42 DSMs were up⁃regulated and 9 DSMs were down⁃regulated)at post infection of HRV1B in UT⁃SCC⁃60B at 6h or 12h,respectively.A total of 303 DSMs(69 DSMs were up⁃regulated and 234 DSMs were down⁃regulated)and 324 DSMs(88 DSMs were up⁃regulated and 236 DSMs were down⁃regulated)at post infection of HRV1B in compared with BEAS⁃2B and UT⁃SCC⁃60B at 6h or 12h,respectively.Unknown metabolites took up most proportions.The trends of fatty acid,lipid,amino acid,nucleotide and carbohydrate were increased along with the prolonging of HRV1B infection.7⁃ketodeoxycholic acid,lysophosphatidylcholine,sarmentosin,histidylglycine and adenosine were referred to metabolomes of bile acid,fatty acid and lipid,carbohydrate,amino acid and nucleotide.In conclusion,metabolic levels of fatty acid,lipid,amino acid,nucleotide and carbohydrate were changed induced by HRV1B infection at the cellular level.
作者 苏萌 李丹 孙萍萍 王春阳 王蒋丽 王宏 章青 杜娈英 谢广成 SU Meng;LI Dan;SUN Pingping;WANG Chunyang;WANG Jiangli;WANG Hong;ZHANG Qing;DU Luanying;XIE Guangcheng(Department of Pathogenic Biology/Laboratory for Pathogens Prevention and Control,Chengde Medical University,Chengde 067000,China;Clinical Medical College,Xi’an Medical University,Xi’an 710021,China;Department of Microbiology Laboratory,Chengde Center for Disease Control and Prevention,Chengde 067000,China;National Institute for Viral Disease Control and Prevention,Chinese Center for Disease Control and Prevention,Beijing 102206,China)
出处 《病毒学报》 CAS CSCD 北大核心 2021年第4期845-852,共8页 Chinese Journal of Virology
基金 国家自然科学基金青年科学基金(项目号:81702008,81702010),题目:EV71衣壳蛋白经TLR2/TLR4异源二聚体活化细胞因子反应的研究,肠道病毒71型拮抗I型干扰素反应的机制研究 河北省自然科学基金青年科学基金(项目号:H2018406024),题目:TLR2募集TLR1和TLR6抗EV71感染的分子机制研究 承德医学院高层次人才科研启动基金(项目号:201702),题目:承德市婴幼儿群体中重要呼吸道感染病毒的流行特征研究 陕西省呼吸工程中心项目(项目号:2017GCKF04),题目:西安地区鼻病毒和肠道病毒D68在急性呼吸道感染患儿中的分子流行病学研究。
关键词 人鼻病毒1B 人扁桃体上皮细胞 人肺支气管上皮细胞 非靶向代谢组学 Human rhinovirus 1B(HRV1B) Human tonsillar epithelial cells Human lung bronchial epithelial cells Untargeted metabolomics
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  • 1Espinola EE, Russomando G, Aquino C, et al. Phylogeny-based classification of human rhinoviruses detected in hospitalized children with acute lower respiratory infection in Paraguay, 2010-2011. J Med Virol, 2013; 85, 1645-51.
  • 2Palmenberg AC, Rathe JA, Liggett SB. Analysis of the complete genome sequences of human rhinovirus. J Allergy Clin Immunol, 2010; 125, 1190-9.
  • 3Martinez J, Patkaniowska A, Urlaub H, et al. Single-stranded antisense siRNAs guide target RNA cleavage in RNAi. Cell, 2002; 110, 563-74.
  • 4Slater L, Bartlett NW, Haas JJ, et al. Co-ordinated role of TLR3, RIG-I and MDA5 in the innate response to rhinovirus in bronchial epithelium. PLoS Pathog, 2010; 6, e1001178.
  • 5Wanga QM, Chen SH. Human rhinovirus 3C protease as a potential target for the development of antiviral agents. Curr Protein Pept Sci, 2007; 8, 19-27.
  • 6Luan Y, Dai HL, Yang D, et al. Small interfering RNA against the 2C genomic region of coxsackievirus B3 exerts potential antiviral effects in permissive HeLa cells. Virus Res, 2012; 163, 183-9.
  • 7Yuan J, Cheung PK, Zhang HM, et al. Inhibition of coxsackievirus B3 replication by small interfering RNAs requires perfect sequence match in the central region of the viral positive strand. J Virol, 2005; 79, 2151-9.
  • 8Merl S, Wessely R. Anti-coxsackieviral efficacy of RNA interference is highly dependent on genomic target selection and emergence of escape mutants. Oligonucleotides, 2007; 17, 44-53.
  • 9Watts JK, Deleavey GF, Damha MJ. Chemically modified siRNA: tools and applications. Drug Discov Today, 2008; 13, 842-55.
  • 10Deng JX, Nie XJ, Lei YF, et al. The highly conserved 5' untranslated region as an effective target towards the inhibition of Enterovirus 71 replication by unmodified and appropriate 2'-modified siRNAs. J Biomed Sci, 2012; 19, 73.

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