Competence-programmed predation of noncompletent cells in the human pathogen Streptococcus pneumoniae:: Genetic requirements

被引:227
作者
Guiral, S
Mitchell, TJ
Martin, B
Claverys, JP
机构
[1] Univ Toulouse 3, CNRS, UMR 5100, Lab Microbiol & Genet Mol, F-31062 Toulouse, France
[2] Univ Glasgow, Div Infect & Immun, Inst Biomed Life Sci, Glasgow G12, Lanark, Scotland
关键词
allolysis bacteriocin; competence; predation; virulence;
D O I
10.1073/pnas.0500879102
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
Natural competence for genetic transformation is the best-characterized feature of the major human pathogen Streptococcus pneumoniae. Recent studies have shown the virulence of competence-deficient mutants to be attenuated, but the nature of the connection between competence and virulence remained unknown. Here we document the release, triggered by competent cells, of virulence factors (e.g., the cytolytic toxin pneumolysin) from noncompetent cells. This phenomenon, which we name allolysis, involves a previously undescribed bacteriocin system consisting of a two-peptide bacteriocin, CibAB, and its immunity factor, CibC; the major autolysin, LytA, and lysozyme, LytC; and a proposed new amidase, CbpD. We show that CibAB are absolutely required for allolysis, whereas LytA and LytC can be supplied either by the competent cells or by the targeted cells. We propose that allolysis constitutes a competence-programmed mechanism of predation of noncompetent cells, which benefits to the competent cells and contributes to virulence by coordinating the release of virulence factors.
引用
收藏
页码:8710 / 8715
页数:6
相关论文
共 54 条
[1]   Development of competence in Streptococcus pneumoniae:: pheromone autoinduction and control of quorum sensing by the oligopeptide permease [J].
Alloing, G ;
Martin, B ;
Granadel, C ;
Claverys, JP .
MOLECULAR MICROBIOLOGY, 1998, 29 (01) :75-83
[2]   Differential fluorescence induction reveals Streptococcus pneumoniae loci regulated by competence stimulatory peptide [J].
Bartilson, M ;
Marra, A ;
Christine, J ;
Asundi, JS ;
Schneider, WP ;
Hromockyj, AE .
MOLECULAR MICROBIOLOGY, 2001, 39 (01) :126-135
[3]   PNEUMOLYSIN-NEGATIVE MUTANT OF STREPTOCOCCUS-PNEUMONIAE CAUSES CHRONIC BACTEREMIA RATHER THAN ACUTE SEPSIS IN MICE [J].
BENTON, KA ;
EVERSON, MP ;
BRILES, DE .
INFECTION AND IMMUNITY, 1995, 63 (02) :448-455
[4]   Glyceraldehyde-3-phosphate dehydrogenase of Streptococcus pneumoniae is a surface-displayed plasminogen-binding protein [J].
Bergmann, S ;
Rohde, M ;
Hammerschmidt, S .
INFECTION AND IMMUNITY, 2004, 72 (04) :2416-2419
[5]   α-Enolase of Streptococcus pneumoniae is a plasmin(ogen)-binding protein displayed on the bacterial cell surface [J].
Bergmann, S ;
Rohde, M ;
Chhatwal, GS ;
Hammerschmidt, S .
MOLECULAR MICROBIOLOGY, 2001, 40 (06) :1273-1287
[6]   REDUCED VIRULENCE OF A DEFINED PNEUMOLYSIN-NEGATIVE MUTANT OF STREPTOCOCCUS-PNEUMONIAE [J].
BERRY, AM ;
YOTHER, J ;
BRILES, DE ;
HANSMAN, D ;
PATON, JC .
INFECTION AND IMMUNITY, 1989, 57 (07) :2037-2042
[7]   A competence regulon in Streptococcus pneumoniae revealed by genomic analysis [J].
Campbell, EA ;
Choi, SY ;
Masure, HR .
MOLECULAR MICROBIOLOGY, 1998, 27 (05) :929-939
[8]  
Chatellier S, 2000, EUR J IMMUNOL, V30, P993, DOI 10.1002/(SICI)1521-4141(200004)30:4<993::AID-IMMU993>3.0.CO
[9]  
2-I
[10]   Adaptation to the environment:: Streptococcus pneumoniae, a paradigm for recombination-mediated genetic plasticity? [J].
Claverys, JP ;
Prudhomme, M ;
Mortier-Barrière, I ;
Martin, B .
MOLECULAR MICROBIOLOGY, 2000, 35 (02) :251-259