Short hairpin RNA-expressing bacteria elicit RNA interference in mammals

被引:194
作者
Xiang, Shuanglin [1 ]
Fruehauf, Johannes [1 ]
Li, Chiang J. [1 ]
机构
[1] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Div Gastroenterol, Boston, MA 02215 USA
关键词
D O I
10.1038/nbt1211
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
RNA-interference (RNAi) is a potent mechanism, conserved from plants to humans for specific silencing of genes, which holds promise for functional genomics and gene-targeted therapies. Here we show that bacteria engineered to produce a short hairpin RNA (shRNA) targeting a mammalian gene induce trans-kingdom RNAi in vitro and in vivo. Nonpathogenic Escherichia coli were engineered to transcribe shRNAs from a plasmid containing the invasin gene Inv and the listeriolysin O gene HlyA, which encode two bacterial factors needed for successful transfer of the shRNAs into mammalian cells. Upon oral or intravenous administration, E. coli encoding shRNA against CTNNB1 (catenin beta-1) induce significant gene silencing in the intestinal epithelium and in human colon cancer xenografts in mice. These results provide an example of trans-kingdom RNAi in higher organisms and suggest the potential of bacteria-mediated RNAi for functional genomics, therapeutic target validation and development of clinically compatible RNAi-based therapies.
引用
收藏
页码:697 / 702
页数:6
相关论文
共 27 条
[1]   Genome-wide RNAi analysis of Caenorhabditis elegans fat regulatory genes [J].
Ashrafi, K ;
Chang, FY ;
Watts, JL ;
Fraser, AG ;
Kamath, RS ;
Ahringer, J ;
Ruvkun, G .
NATURE, 2003, 421 (6920) :268-272
[2]   Increased expression of periplasmic Cu,Zn superoxide dismutase enhances survival of Escherichia coli invasive strains within nonphagocytic cells [J].
Battistoni, A ;
Pacello, F ;
Folcarelli, S ;
Ajello, M ;
Donnarumma, G ;
Greco, R ;
Ammendolia, MG ;
Touati, D ;
Rotilio, G ;
Valenti, P .
INFECTION AND IMMUNITY, 2000, 68 (01) :30-37
[3]   Inhibition of respiratory viruses by nasally administered siRNA [J].
Bitko, V ;
Musiyenko, A ;
Shulyayeva, O ;
Barik, S .
NATURE MEDICINE, 2005, 11 (01) :50-55
[4]   Induction of an interferon response by RNAi vectors in mammalian cells [J].
Bridge, AJ ;
Pebernard, S ;
Ducraux, A ;
Nicoulaz, AL ;
Iggo, R .
NATURE GENETICS, 2003, 34 (03) :263-264
[5]   Oral somatic transgene vaccination using attenuated S-typhimurium [J].
Darji, A ;
Guzman, CA ;
Gerstel, B ;
Wachholz, P ;
Timmis, KN ;
Wehland, J ;
Chakraborty, T ;
Weiss, S .
CELL, 1997, 91 (06) :765-775
[6]   Transport of dsRNA into cells by the transmembrane protein SID-1 [J].
Feinberg, EH ;
Hunter, CP .
SCIENCE, 2003, 301 (5639) :1545-1547
[7]   Functional genomic analysis of C-elegans chromosome I by systematic RNA interference [J].
Fraser, AG ;
Kamath, RS ;
Zipperlen, P ;
Martinez-Campos, M ;
Sohrmann, M ;
Ahringer, J .
NATURE, 2000, 408 (6810) :325-330
[8]   Functional gene transfer from intracellular bacteria to mammalian cells [J].
Grillot-Courvalin, C ;
Goussard, S ;
Huetz, F ;
Ojcius, DM ;
Courvalin, P .
NATURE BIOTECHNOLOGY, 1998, 16 (09) :862-866
[9]   Sequence-specific potent induction of IFN-α by short interfering RNA in plasmacytoid dendritic cells through TLR7 [J].
Hornung, V ;
Guenthner-Biller, M ;
Bourquin, C ;
Ablasser, A ;
Schlee, M ;
Uematsu, S ;
Noronha, A ;
Manoharan, M ;
Akira, S ;
de Fougerolles, A ;
Endres, S ;
Hartmann, G .
NATURE MEDICINE, 2005, 11 (03) :263-270
[10]   IDENTIFICATION OF INVASIN - A PROTEIN THAT ALLOWS ENTERIC BACTERIA TO PENETRATE CULTURED-MAMMALIAN-CELLS [J].
ISBERG, RR ;
VOORHIS, DL ;
FALKOW, S .
CELL, 1987, 50 (05) :769-778