Inhibition of respiratory viruses by nasally administered siRNA

被引:555
作者
Bitko, V [1 ]
Musiyenko, A [1 ]
Shulyayeva, O [1 ]
Barik, S [1 ]
机构
[1] Univ S Alabama, Coll Med, Dept Biochem & Mol Biol, Mobile, AL 36688 USA
关键词
D O I
10.1038/nm1164
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Respiratory syncytial virus (RSV) and parainfluenza virus (PIV) are two respiratory pathogens of paramount medical significance that exert high mortality. At present, there is no reliable vaccine or antiviral drug against either virus. Using an RNA interference (RNAi) approach, we show that individual as well as joint infection by RSV and PIV can be specifically prevented and inhibited by short interfering RNAs (siRNAs), instilled intranasally in the mouse, with or without transfection reagents. The degree of protection matched the antiviral activity of the siRNA in cell culture, allowing an avenue for quick screening of an efficacious siRNA. When targeting both viruses in a joint infection, excess of one siRNA moderated the inhibitory effect of the other, suggesting competition for the RNAi machinery. Our results suggest that, if properly designed, low dosages of inhaled siRNA might offer a fast, potent and easily administrable antiviral regimen against respiratory viral diseases in humans.
引用
收藏
页码:50 / 55
页数:6
相关论文
共 45 条
  • [21] Functional siRNAs and miRNAs exhibit strand bias (vol 115, pg 209, 2003)
    Khvorova, A
    Reynolds, A
    Jayasena, SD
    [J]. CELL, 2003, 115 (04) : 505 - 505
  • [22] Interferon induction by siRNAs and ssRNAs synthesized by phage polymerase
    Kim, DH
    Longo, M
    Han, Y
    Lundberg, P
    Cantin, E
    Rossi, JJ
    [J]. NATURE BIOTECHNOLOGY, 2004, 22 (03) : 321 - 325
  • [23] New drugs and treatment for respiratory syncytial virus
    Maggon, K
    Barik, S
    [J]. REVIEWS IN MEDICAL VIROLOGY, 2004, 14 (03) : 149 - 168
  • [24] Inhibition of hepatitis B virus in mice by RNA interference
    McCaffrey, AP
    Nakai, H
    Pandey, K
    Huang, Z
    Salazar, FH
    Xu, H
    Wieland, SF
    Marion, PL
    Kay, MA
    [J]. NATURE BIOTECHNOLOGY, 2003, 21 (06) : 639 - 644
  • [25] Structural characterization of respiratory syncytial virus fusion inhibitor escape mutants: homology model of the F protein and a syncytium formation assay
    Morton, CJ
    Cameron, R
    Lawrence, LJ
    Lin, B
    Lowe, M
    Luttick, A
    Mason, A
    McKimm-Breschkin, J
    Parker, MW
    Ryan, J
    Smout, M
    Sullivan, J
    Tucker, SP
    Young, PR
    [J]. VIROLOGY, 2003, 311 (02) : 275 - 288
  • [26] The RNAi revolution
    Novina, CD
    Sharp, PA
    [J]. NATURE, 2004, 430 (6996) : 161 - 164
  • [27] Potential therapeutic implications of new insights into respiratory syncytial virus disease
    Openshaw, PJM
    [J]. RESPIRATORY RESEARCH, 2002, 3 (Suppl 1)
  • [28] The complex relationship between respiratory syncytial virus and allergy in lung disease
    Peebles, RS
    Hashimoto, K
    Graham, BS
    [J]. VIRAL IMMUNOLOGY, 2003, 16 (01) : 25 - 34
  • [29] Nonspecific, concentration-dependent stimulation and repression of mammalian gene expression by small interfering RNAs (siRNAs)
    Persengiev, SP
    Zhu, XC
    Green, MR
    [J]. RNA, 2004, 10 (01) : 12 - 18
  • [30] A role for immune complexes in enhanced respiratory syncytial virus disease
    Polack, FP
    Teng, MN
    Collins, PL
    Prince, GA
    Exner, M
    Regele, H
    Lirman, DD
    Rabold, R
    Hoffman, SJ
    Karp, CL
    Kleeberger, SR
    Wills-Karp, M
    Karron, RA
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (06) : 859 - 865