Intestinal Microbiota Promote Enteric Virus Replication and Systemic Pathogenesis

被引:468
作者
Kuss, Sharon K. [1 ]
Best, Gavin T. [1 ]
Etheredge, Chris A. [1 ]
Pruijssers, Andrea J. [2 ,3 ]
Frierson, Johnna M. [3 ,4 ]
Hooper, Lora V. [1 ,5 ,6 ]
Dermody, Terence S. [2 ,3 ,4 ]
Pfeiffer, Julie K. [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Microbiol, Dallas, TX 75390 USA
[2] Vanderbilt Univ, Sch Med, Dept Pediat, Nashville, TN 37240 USA
[3] Vanderbilt Univ, Sch Med, Elizabeth B Lamb Ctr Pediat Res, Nashville, TN 37240 USA
[4] Vanderbilt Univ, Sch Med, Dept Pathol Microbiol & Immunol, Nashville, TN 37240 USA
[5] Univ Texas SW Med Ctr Dallas, Dept Immunol, Dallas, TX 75390 USA
[6] Howard Hughes Med Inst, Chevy Chase, MD USA
关键词
HUMAN POLIOVIRUS RECEPTOR; TRANSGENIC MICE;
D O I
10.1126/science.1211057
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Intestinal bacteria aid host health and limit bacterial pathogen colonization. However, the influence of bacteria on enteric viruses is largely unknown. We depleted the intestinal microbiota of mice with antibiotics before inoculation with poliovirus, an enteric virus. Antibiotic-treated mice were less susceptible to poliovirus disease and supported minimal viral replication in the intestine. Exposure to bacteria or their N-acetylglucosamine-containing surface polysaccharides, including lipopolysaccharide and peptidoglycan, enhanced poliovirus infectivity. We found that poliovirus binds lipopolysaccharide, and exposure of poliovirus to bacteria enhanced host cell association and infection. The pathogenesis of reovirus, an unrelated enteric virus, also was more severe in the presence of intestinal microbes. These results suggest that antibiotic-mediated microbiota depletion diminishes enteric virus infection and that enteric viruses exploit intestinal microbes for replication and transmission.
引用
收藏
页码:249 / 252
页数:4
相关论文
共 13 条
[1]  
ABRAMS GD, 1967, P SOC EXP BIOL MED, V126, P301
[2]   Utilization of sialic acid as a coreceptor is required for reovirus-induced biliary disease [J].
Barton, ES ;
Youree, BE ;
Ebert, DH ;
Forrest, JC ;
Connolly, JL ;
Valyi-Nagy, T ;
Washington, K ;
Wetzel, JD ;
Dermody, TS .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (12) :1823-1833
[3]   Homeostasis and Inflammation in the Intestine [J].
Garrett, Wendy S. ;
Gordon, Jeffrey I. ;
Glimcher, Laurie H. .
CELL, 2010, 140 (06) :859-870
[4]   Exploitation of the Intestinal Microflora by the Parasitic Nematode Trichuris muris [J].
Hayes, K. S. ;
Bancroft, A. J. ;
Goldrick, M. ;
Portsmouth, C. ;
Roberts, I. S. ;
Grencis, R. K. .
SCIENCE, 2010, 328 (5984) :1391-1394
[5]   The alpha/beta interferon response controls tissue tropism and pathogenicity of poliovirus [J].
Ida-Hosonuma, M ;
Iwasaki, T ;
Yoshikawa, T ;
Nagata, N ;
Sato, Y ;
Sata, T ;
Yoneyama, M ;
Fujita, T ;
Taya, C ;
Yonekawa, H ;
Koike, S .
JOURNAL OF VIROLOGY, 2005, 79 (07) :4460-4469
[6]   Host range of poliovirus is restricted to simians because of a rapid sequence change of the poliovirus receptor gene during evolution [J].
Ida-Hosonuma, M ;
Sasaki, Y ;
Toyoda, H ;
Nomoto, A ;
Gotoh, O ;
Yonekawa, H ;
Koike, S .
ARCHIVES OF VIROLOGY, 2003, 148 (01) :29-44
[7]   TRANSGENIC MICE SUSCEPTIBLE TO POLIOVIRUS [J].
KOIKE, S ;
TAYA, C ;
KURATA, T ;
ABE, S ;
ISE, I ;
YONEKAWA, H ;
NOMOTO, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (03) :951-955
[8]   Multiple host barriers restrict poliovirus trafficking in mice [J].
Kuss, Sharon K. ;
Etheredge, Chris A. ;
Pfeiffer, Julie K. .
PLOS PATHOGENS, 2008, 4 (06)
[9]   Establishment of a poliovirus oral infection system in human poliovirus receptor-expressing transgenic mice that are deficient in alpha/beta interferon receptor [J].
Ohka, Seii ;
Igarashi, Hiroko ;
Nagata, Noriyo ;
Sakai, Mai ;
Koike, Satoshi ;
Nochi, Tomonori ;
Kiyono, Hiroshi ;
Nomoto, Akio .
JOURNAL OF VIROLOGY, 2007, 81 (15) :7902-7912
[10]  
Pallansch MA., 2001, FIELDSVIROLOGY, V4th, P723