Novel fusion antigen displayed-bacterial ghosts vaccine candidate against infection of Escherichia coli O157:H7

被引:20
作者
Cai, Kun [2 ]
Tu, Wei [2 ]
Liu, Yuenan [2 ]
Li, Tao [2 ]
Wang, Hui [1 ,2 ]
机构
[1] Anhui Med Univ, Dept Microbiol, Hefei 230032, Peoples R China
[2] Beijing Inst Microbiol & Epidemiol, State Key Lab Pathogens & Biosecur, Beijing 100071, Peoples R China
基金
中国国家自然科学基金;
关键词
MEMBRANE PROTEIN OMPA; SHIGA-TOXIN; OUTER-MEMBRANE; IMMUNE-RESPONSES; O157-H7; MICE; EXPRESSION; SURFACE; IMMUNOGENICITY; IMMUNIZATION;
D O I
10.1038/srep17479
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
Infection with Escherichia coli O157:H7 may develop into hemorrhagic colitis, or hemolytic uremic syndrome (HUS), which usually causes kidney failure or even death. The adhesion and toxins are the important virulent factors. In this study, a novel vaccine candidate rSOBGs was constructed based on the bacterial ghost (BG). rSOBGs maintained the integrity of cellular morphology and displayed the linear Stx2Am-Stx1B antigen on the surface of outer membrane. rSOBGs induced Stxs-specific IgA/IgG antibodies and stronger intimin-specific IgA/IgG antibodies effectively in sera in this study. In vivo, the rSOBGs provided the higher protection rate (52%) than native bacterial ghost-OBGs (12%) when challenged intragastricly with high dose (500 LD50) viable E. coli O157: H7. Meanwhile, the rSOBGs provided higher protection rate (73.33%) than OBGs when challenged with 2 LD50 even to 5 LD50 lysed E. coli O157: H7. In vitro, the rSOBGs-immunized sera possessed neutralizing activity to lysed pathogenic bacteria. Furthermore, the results of histopathology also displayed that the administration of rSOBGs have the ability to reduce or inhibit the adhesion lesions and toxins damages of organs. The novel vaccine candidate rSOBGs induced both anti-toxin and antiadhesion immune protection, suggesting the possibility to prevent the infectious diseases caused by Escherichia coli O157: H7.
引用
收藏
页数:10
相关论文
共 42 条
[1]   EXPRESSION AND PURIFICATION OF SHIGA-LIKE TOXIN-II B-SUBUNITS [J].
ACHESON, DWK ;
DEBREUCKER, SA ;
JACEWICZ, M ;
LINCICOME, LL ;
DONOHUEROLFE, A ;
KANE, AV ;
KEUSCH, GT .
INFECTION AND IMMUNITY, 1995, 63 (01) :301-308
[2]  
[Anonymous], 1994, MMWR Recomm Rep, V43, P1
[3]   Associations between virulence factors of Shiga toxin-producing Escherichia coli and disease in humans [J].
Boerlin, P ;
McEwen, SA ;
Boerlin-Petzold, F ;
Wilson, JB ;
Johnson, RP ;
Gyles, CL .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (03) :497-503
[4]   THE NUCLEOTIDE-SEQUENCE CODING FOR MAJOR OUTER-MEMBRANE PROTEIN OMPA OF SHIGELLA-DYSENTERIAE [J].
BRAUN, G ;
COLE, ST .
NUCLEIC ACIDS RESEARCH, 1982, 10 (07) :2367-2378
[5]   Enhanced immunogenicity of a novel Stx2Am-Stx1B fusion protein in a mice model of enterohemorrhagic Escherichia coli O157:H7 infection [J].
Cai, Kun ;
Gao, Xiang ;
Li, Tao ;
Wang, Qin ;
Hou, Xiaojun ;
Tu, Wei ;
Xiao, Le ;
Tian, Maoren ;
Liu, Yuenan ;
Wang, Hui .
VACCINE, 2011, 29 (05) :946-952
[6]  
Cai K, 2010, CAN J MICROBIOL, V56, P389, DOI [10.1139/W10-025, 10.1139/w10-025]
[7]   Parenteral immunization with a glycoconjugate vaccine containing the O157 antigen of Escherichia coli O157:H7 elicits a systemic humoral immune response in mice, but fails to prevent colonization by the pathogen [J].
Conlan, JW ;
Cox, AD ;
KuoLee, R ;
Webb, A ;
Perry, MB .
CANADIAN JOURNAL OF MICROBIOLOGY, 1999, 45 (04) :279-286
[8]  
DORNMAIR K, 1990, J BIOL CHEM, V265, P18907
[9]   Evaluation of the protective efficacy of Vibrio cholerae ghost (VCG) candidate vaccines in rabbits [J].
Eko, FO ;
Schukovskaya, T ;
Lotzmanova, EY ;
Firstova, VV ;
Emalyanova, NV ;
Klueva, SN ;
Kravtzov, AL ;
Livanova, LF ;
Kutyrev, VV ;
Igietseme, JU ;
Lubitz, W .
VACCINE, 2003, 21 (25-26) :3663-3674
[10]   CRYSTAL-STRUCTURE OF THE HOLOTOXIN FROM SHIGELLA-DYSENTERIAE AT 2.5-ANGSTROM RESOLUTION [J].
FRASER, ME ;
CHERNAIA, MM ;
KOZLOV, YV ;
JAMES, MNG .
NATURE STRUCTURAL BIOLOGY, 1994, 1 (01) :59-64