Capsule does not block antibody binding to PspA, a surface virulence protein of Streptococcus pneumoniae

被引:26
作者
Daniels, Calvin C.
Briles, Travis C.
Mirza, Shaper
Hakansson, Anders P.
Briles, David E.
机构
[1] Childrens Hosp, Div Infect Dis, Boston, MA 02115 USA
[2] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL 35294 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
[4] Univ Alabama Birmingham, Dept Pediat, Birmingham, AL 35294 USA
关键词
Streptococcus pneumoniae; capsule; phosphocholine; pneumococcal surface protein A;
D O I
10.1016/j.micpath.2006.01.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Of the proteins on the surface of Streptococcus pneumoniae, one of those best able to elicit protection against pneumococcal infection is pneumococcal surface protein A (PspA). Although this protein is attached to the membrane molecule, lipoteichoic acid, which is well beneath the capsule, PspA's ability to inhibit complement deposition and killing by apolactoferrin, suggests that it must have surface exposure. This study provides quantitative data showing that the capsular polysaccharide on types 2 and 3 pneumococci provides little or no masking ability of antibodies to bind PspA. Capsule was even observed to enhance, rather than inhibit the binding of two protective monoclonal antibodies to their epitopes on cell surface PspA. These results with antibodies to PspA are in contrast to binding by antibodies to the phosphocholine (PC) epitope of the lipoteichoic and teichoic acids. The binding of antibody to PC was largely, but not completely, blocked by capsular polysaccharide. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:228 / 233
页数:6
相关论文
共 46 条
[1]   Genetic alteration of capsule type but not PspA type affects accessibility of surface-bound complement and surface antigens of Streptococcus pneumoniae [J].
Abeyta, M ;
Hardy, GG ;
Yother, J .
INFECTION AND IMMUNITY, 2003, 71 (01) :218-225
[2]   STUDIES ON THE CHEMICAL NATURE OF THE SUBSTANCE INDUCING TRANSFORMATION OF PNEUMOCOCCAL TYPES INDUCTION OF TRANSFORMATION BY A DESOXYRIBONUCLEIC ACID FRACTION ISOLATED FROM PNEUMOCOCCUS TYPE III [J].
Avery, Oswald T. ;
MacLeod, Colin M. ;
McCarty, Maclyn .
JOURNAL OF EXPERIMENTAL MEDICINE, 1944, 79 (02) :137-158
[3]   ANTIPNEUMOCOCCAL EFFECTS OF C-REACTIVE PROTEIN AND MONOCLONAL-ANTIBODIES TO PNEUMOCOCCAL CELL-WALL AND CAPSULAR ANTIGENS [J].
BRILES, DE ;
FORMAN, C ;
HOROWITZ, JC ;
VOLANAKIS, JE ;
BENJAMIN, WH ;
MCDANIEL, LS ;
ELDRIDGE, J ;
BROOKS, J .
INFECTION AND IMMUNITY, 1989, 57 (05) :1457-1464
[4]   Intranasal immunization of mice with a mixture of the pneumococcal proteins PsaA and PspA is highly protective against nasopharyngeal carriage of Streptococcus pneumoniae [J].
Briles, DE ;
Ades, E ;
Paton, JC ;
Sampson, JS ;
Carlone, GM ;
Huebner, RC ;
Virolainen, A ;
Swiatlo, E ;
Hollingshead, SK .
INFECTION AND IMMUNITY, 2000, 68 (02) :796-800
[5]   Immunizations with pneumococcal surface protein A and pneumolysin are protective against pneumonia in a murine model of pulmonary infection with Streptococcus pneumoniae [J].
Briles, DE ;
Hollingshead, SK ;
Paton, JC ;
Ades, EW ;
Novak, L ;
van Ginkel, FW ;
Benjamin, WH .
JOURNAL OF INFECTIOUS DISEASES, 2003, 188 (03) :339-348
[6]   MOUSE ANTIBODY TO PHOSPHOCHOLINE CAN PROTECT MICE FROM INFECTION WITH MOUSE-VIRULENT HUMAN ISOLATES OF STREPTOCOCCUS-PNEUMONIAE [J].
BRILES, DE ;
FORMAN, C ;
CRAIN, M .
INFECTION AND IMMUNITY, 1992, 60 (05) :1957-1962
[7]   ANTI-PHOSPHOCHOLINE ANTIBODIES FOUND IN NORMAL MOUSE SERUM ARE PROTECTIVE AGAINST INTRAVENOUS INFECTION WITH TYPE-3 STREPTOCOCCUS-PNEUMONIAE [J].
BRILES, DE ;
NAHM, M ;
SCHROER, K ;
DAVIE, J ;
BAKER, P ;
KEARNEY, J ;
BARLETTA, R .
JOURNAL OF EXPERIMENTAL MEDICINE, 1981, 153 (03) :694-705
[8]  
Briles DE, 2000, EFFECTS OF MICROBES ON THE IMMUNE SYSTEM, P263
[9]   Immunization of humans with recombinant pneumococcal surface protein A (rPspA) elicits antibodies that passively protect mice from fatal infection with Streptococcus pneumoniae bearing heterologous PspA [J].
Briles, DE ;
Hollingshead, SK ;
King, J ;
Swift, A ;
Braun, PA ;
Park, MK ;
Ferguson, LM ;
Nahm, MH ;
Nabors, GS .
JOURNAL OF INFECTIOUS DISEASES, 2000, 182 (06) :1694-1701
[10]  
BRILES DE, 2004, NEW GENERATION VACCI, P459