Spa contributes to the virulence of type 18 group A streptococci

被引:21
作者
McLellan, DGJ
Chiang, EY
Courtney, HS
Hasty, DL
Wei, SC
Hu, MC
Walls, MA
Bloom, JJ
Dale, JB
机构
[1] Vet Adm Med Ctr, Memphis, TN 38104 USA
[2] Univ Tennessee, Dept Med, Memphis, TN 38104 USA
[3] Univ Tennessee, Dept Anat & Neurobiol, Memphis, TN 38104 USA
[4] ID Biomed Corp, Bothell, WA 98011 USA
关键词
D O I
10.1128/IAI.69.5.2943-2949.2001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Streptococcal protective antigen (Spa) is a newly described surface protein of group A streptococci that was recently shown to evoke protective antibodies (J. B. Dale, E. Y. Chiang, S. Liu, H. S. Courtney, and D. L. Hasty, J. Clin. Investig. 103:1261-1268, 1999). In this study, we have determined the complete sequence of the spa gene from type 18 streptococci, purified, recombinant Spa protein evoked antibodies that were bactericidal against type 18 streptococci, confirming the presence of protective epitopes, Sera from patients with acute rheumatic fever contained antibodies against recombinant Spa, indicating that the Spa protein is expressed in vivo and is immunogenic in humans. To determine the role of Spa in the virulence of group A streptococci, we created a series of insertional mutants that were (i) Spa negative and M18 positive, (ii) Spa positive and M18 negative, and (iii! Spa negative and M18 negative. The mutants and the parent M18 strain (18-282) were used in assays to determine resistance to phagocytosis, growth in human blood, and mouse virulence. The results show that Spa is a virulence determinant of group A streptococci and that expression of both Spa and M18 is required far optimal virulence of type 18 streptococci.
引用
收藏
页码:2943 / 2949
页数:7
相关论文
共 25 条
[1]  
BAIRD RW, 1991, J IMMUNOL, V146, P3132
[2]   PURIFICATION AND PROPERTIES OF M-PROTEIN EXTRACTED FROM GROUP-A STREPTOCOCCI WITH PEPSIN - COVALENT STRUCTURE OF AMINO TERMINAL REGION OF TYPE 24 M-ANTIGEN [J].
BEACHEY, EH ;
STOLLERMAN, GH ;
CHIANG, EY ;
CHIANG, TM ;
SEYER, JM ;
KANG, AH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1977, 145 (06) :1469-1483
[3]  
BRONZE MS, 1993, J IMMUNOL, V151, P2820
[5]  
CAPARON MG, 1991, METHOD ENZYMOL, V204, P556
[6]   STREPTOCOCCAL-C5A PEPTIDASE IS A HIGHLY SPECIFIC ENDOPEPTIDASE [J].
CLEARY, PP ;
PRAHBU, U ;
DALE, JB ;
WEXLER, DE ;
HANDLEY, J .
INFECTION AND IMMUNITY, 1992, 60 (12) :5219-5223
[7]   ANALYSIS OF THE ROLE OF M24 PROTEIN IN GROUP-A STREPTOCOCCAL ADHESION AND COLONIZATION BY USE OF OMEGA-INTERPOSON MUTAGENESIS [J].
COURTNEY, HS ;
BRONZE, MS ;
DALE, JB ;
HASTY, DL .
INFECTION AND IMMUNITY, 1994, 62 (11) :4868-4873
[8]   New protective antigen of group A streptococci [J].
Dale, JB ;
Chiang, EY ;
Liu, SY ;
Courtney, HS ;
Hasty, DL .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (09) :1261-1268
[9]   MULTIPLE, HEART CROSS-REACTIVE EPITOPES OF STREPTOCOCCAL M-PROTEINS [J].
DALE, JB ;
BEACHEY, EH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1985, 161 (01) :113-122
[10]   EPITOPES OF STREPTOCOCCAL M-PROTEINS SHARED WITH CARDIAC MYOSIN [J].
DALE, JB ;
BEACHEY, EH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1985, 162 (02) :583-591