Surface proteins of Streptococcus agalactiae and related proteins in other bacterial pathogens

被引:277
作者
Lindahl, G [1 ]
Stålhammar-Carlemalm, M [1 ]
Areschoug, T [1 ]
机构
[1] Lund Univ, Dept Med Microbiol Dermatol & Infect, SE-22362 Lund, Sweden
关键词
D O I
10.1128/CMR.18.1.102-127.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Streptococcus agalactiae (group B Streptococcus) is the major cause of invasive bacterial disease, including meningitis, in the neonatal period. Although prophylactic measures have contributed to a substantial reduction in the number of infections, development of a vaccine remains an important goal. While much work in this field has focused on the S. agalactiae polysaccharide capsule, which is an important virulence factor that elicits protective immunity, surface proteins have received increasing attention as potential virulence factors and vaccine components. Here, we summarize current knowledge about S. agalactiae surface proteins, with emphasis on proteins that have been characterized immunochemically and/or elicit protective immunity in animal models. These surface proteins have been implicated in interactions with human epithelial cells, binding to extracellular matrix components, and/or evasion of host immunity. Of note, several S. agalactiae surface proteins are related to surface proteins identified in other bacterial pathogens, emphasizing the general interest of the S. agalactiae proteins. Because some S. agalactiae surface proteins elicit protective immunity they hold promise as components in a vaccine based only on proteins or as carriers in polysaccharide conjugate vaccines.
引用
收藏
页码:102 / +
页数:27
相关论文
共 271 条
[71]   Equivalence of high-virulence clonotypes of serotype III group B Streptococcus agalactiae (GBS) [J].
Fleming, KE ;
Bohnsack, JF ;
Palacios, GC ;
Takahashi, S ;
Adderson, EE .
JOURNAL OF MEDICAL MICROBIOLOGY, 2004, 53 (06) :505-508
[72]   MOLECULAR-SPECIES OF R-PROTEIN ANTIGENS PRODUCED BY CLINICAL ISOLATES OF GROUP-B STREPTOCOCCI [J].
FLORES, AE ;
FERRIERI, P .
JOURNAL OF CLINICAL MICROBIOLOGY, 1989, 27 (05) :1050-1054
[73]   ANTIBODY PROFILES TO THE GROUP-B STREPTOCOCCAL BETA ANTIGEN IN MATERNAL AND INFANT PAIRED SERA [J].
FLORES, AE ;
NELSON, JA ;
WU, XY ;
FERRIERI, P .
APMIS, 1993, 101 (01) :41-49
[74]   Horizontal gene transfer and host specificity of beta-haemolytic streptococci:: the role of a putative composite transposon containing scpB and lmb [J].
Franken, C ;
Haase, G ;
Brandt, C ;
Weber-Heynemann, J ;
Martin, S ;
Lämmler, C ;
Podbielski, A ;
Lütticken, R ;
Spellerberg, B .
MOLECULAR MICROBIOLOGY, 2001, 41 (04) :925-935
[75]   Comparison of bipA Alleles within and across Bordetella species [J].
Fuchslocher, B ;
Millar, LL ;
Cotter, PA .
INFECTION AND IMMUNITY, 2003, 71 (06) :3043-3052
[76]   'Avirulence genes' in animal pathogens? [J].
Galán, JE .
TRENDS IN MICROBIOLOGY, 1998, 6 (01) :3-6
[77]   GROUP-B STREPTOCOCCI INVADE ENDOTHELIAL-CELLS - TYPE-III CAPSULAR POLYSACCHARIDE ATTENUATES INVASION [J].
GIBSON, RL ;
LEE, MK ;
SODERLAND, C ;
CHI, EY ;
RUBENS, CE .
INFECTION AND IMMUNITY, 1993, 61 (02) :478-485
[78]  
Glaser P, 2001, SCIENCE, V294, P849
[79]   The nature of an ideal therapeutic human antibody [J].
Glassy, MC ;
Koda, K .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2002, 2 (01) :1-2
[80]   Mutually exclusive distribution of IS1548 and GBSi1, an active group II intron identified in human isolates of group B streptococci [J].
Granlund, M ;
Michel, F ;
Norgren, M .
JOURNAL OF BACTERIOLOGY, 2001, 183 (08) :2560-2569