Poor growth of human adenovirus-12 compared to adenovirus-2 correlates with a failure to impair PKR activation during the late phase of infection

被引:3
作者
Wu, Chengjun [1 ]
Bai, Lufeng [1 ]
Li, Zhiqun [2 ]
Samuel, Charles E. [2 ]
Akusjarvi, Goran [1 ]
Svensson, Catharina [1 ]
机构
[1] Uppsala Univ, Dept Med Biochem & Microbiol, S-75123 Uppsala, Sweden
[2] Univ Calif Santa Barbara, Dept Mol Cellular & Dev Biol, Santa Barbara, CA 93106 USA
基金
瑞典研究理事会;
关键词
Adenovirus; VA RNA; IFN; PKR; eIF2; alpha; INTERFERON REGULATORY FACTOR-3; VIRUS-ASSOCIATED RNA; PROTEIN-KINASE PKR; VAI RNA; GENE-EXPRESSION; MESSENGER-RNA; E1A PROTEINS; I INTERFERON; TRANSLATION; INDUCTION;
D O I
10.1016/j.virol.2014.11.012
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human adenovirus type 12 (HAdV-12) displays a relatively low virulence and slow replication in cultured human cells, which is manifested by premature death of HAdV-12-infected cells. Whereas HAdV-2 induction of IFN-beta expression was transient, HAdV-12-infected cells maintained high levels of IFN-beta expression, protein kinase R (PKR) activation and eIF-2 alpha phosphorylation throughout the infectious cycle. The importance of the IFN-inducible PKR kinase in restriction of HAdV-12 was supported by the enhanced growth of the virus following PKR knockdown in HeLa cells. Ectopic expression of HAdV-2 VA RNAI increased HAdV-12 hexon protein expression, suggesting that insufficient VA RNA expression contributes to the restricted growth of HAdV-12. Although some adenovirus species are known to persist in human lymphoid tissues, HAdV12 has so far not been found. Thus, it is possible that the inability of HAdV12 to evade the INF response may have implications for the virus to establish long-lasting or persistent infections. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:120 / 128
页数:9
相关论文
共 40 条
  • [1] INHIBITION OF THE CELLULAR-RESPONSE TO INTERFERONS BY PRODUCTS OF THE ADENOVIRUS TYPE-5 E1A ONCOGENE
    ACKRILL, AM
    FOSTER, GR
    LAXTON, CD
    FLAVELL, DM
    STARK, GR
    KERR, IM
    [J]. NUCLEIC ACIDS RESEARCH, 1991, 19 (16) : 4387 - 4393
  • [2] Suppression of RNA interference by adenovirus virus-associated RNA
    Andersson, MG
    Haasnoot, PCJ
    Xu, N
    Berenjian, S
    Berkhout, B
    Akusjärvi, G
    [J]. JOURNAL OF VIROLOGY, 2005, 79 (15) : 9556 - 9565
  • [3] Comprehensive sequence analysis of the E1A proteins of human and simian adenoviruses
    Avvakumov, N
    Kajon, AE
    Hoeben, RC
    Mymryk, JS
    [J]. VIROLOGY, 2004, 329 (02) : 477 - 492
  • [4] Identification of specific cellular genes up-regulated late in adenovirus type 12 infection
    Dorn, A
    Zhao, HX
    Granberg, F
    Hösel, M
    Webb, D
    Svensson, C
    Pettersson, U
    Doerfler, W
    [J]. JOURNAL OF VIROLOGY, 2005, 79 (04) : 2404 - 2412
  • [5] PHOSPHORYLATION OF INITIATION-FACTOR ELF-2 AND CONTROL OF RETICULOCYTE PROTEIN-SYNTHESIS
    FARRELL, PJ
    BALKOW, K
    HUNT, T
    JACKSON, RJ
    TRACHSEL, H
    [J]. CELL, 1977, 11 (01) : 187 - 200
  • [6] Key Role of Splenic Myeloid DCs in the IFN-αβ Response to Adenoviruses In Vivo
    Fejer, Gyoergy
    Drechsel, Lisa
    Liese, Jan
    Schleicher, Ulrike
    Ruzsics, Zsolt
    Imelli, Nicola
    Greber, Urs F.
    Keck, Simone
    Hildenbrand, Bernd
    Krug, Anne
    Bogdan, Christian
    Freudenberg, Marina A.
    [J]. PLOS PATHOGENS, 2008, 4 (11)
  • [7] Fields BN, 2013, FIELDS VIROLOGY
  • [8] An overview of real-time quantitative PCR: Applications to quantify cytokine gene expression
    Giulietti, A
    Overbergh, L
    Valckx, D
    Decallonne, B
    Bouillon, R
    Mathieu, C
    [J]. METHODS, 2001, 25 (04) : 386 - 401
  • [9] Triggering the innate antiviral response through IRF-3 activation
    Hiscott, John
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (21) : 15325 - 15329
  • [10] INHIBITION OF INTERFERON-INDUCIBLE GENE-EXPRESSION BY ADENOVIRUS E1A PROTEINS - BLOCK IN TRANSCRIPTIONAL COMPLEX-FORMATION
    KALVAKOLANU, DVR
    BANDYOPADHYAY, SK
    HARTER, ML
    SEN, GC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (17) : 7459 - 7463