High genetic variability of the agr locus in Staphylococcus species

被引:152
作者
Dufour, P
Jarraud, S
Vandenesch, F
Greenland, T
Novick, RP
Bes, M
Etienne, J
Lina, G
机构
[1] Fac Med Laennec, Ctr Natl Toxemies Staphylococques, EA 1655, F-69372 Lyon 08, France
[2] Hop Louis Pradel, Lab Immunol & Biol Pulm IMR375, Bron, France
[3] NYU, Sch Med, Dept Microbiol, New York, NY 10016 USA
[4] NYU, Sch Med, Skirball Inst, Program Mol Pathogenesis, New York, NY 10016 USA
关键词
D O I
10.1128/jb.184.4.1180-1186.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The agr quorum-sensing and signal transduction system was initially described in Staphylococcus aureus, where four distinct allelic variants have been sequenced. Western blotting suggests the presence of homologous loci in many other staphylococci, and this has been confirmed for S. epidermidis and S. lugdunensis. In this study we isolated agr-like loci from a range of staphylococci by using PCR amplification from primers common to the six published agr sequences and bracketing the most variable region, associated with quorum-sensing specificity. Positive amplifications were obtained from 14 of 34 staphylococcal species or subspecies tested. Sequences of the amplicons identified 24 distinct variants which exhibited extensive sequence divergence with only 10% of the nucleotides absolutely conserved on multiple alignment. This variability involved all three open reading frames involved in quorum sensing and signal transduction. However, these variants retained several protein signatures, including the conserved cysteine residue of the autoinducing peptide, with the exception of S. intermedius of pigeon origin, which contained a serine in place of cysteine at this position. We discuss hypotheses on the mode of action and the molecular evolution of the agr locus based on comparisons between the newly determined sequences.
引用
收藏
页码:1180 / 1186
页数:7
相关论文
共 35 条
[1]  
Aiyar A, 2000, Methods Mol Biol, V132, P221
[2]  
[Anonymous], 2000, SCIENCE, DOI DOI 10.1126/SCIENCE.287.5452.391A
[3]   Probing the structure of RNAIII, the Staphylococcus aureus agr regulatory RNA, and identification of the RNA domain involved in repression of protein A expression [J].
Benito, Y ;
Kolb, FA ;
Romby, P ;
Lina, G ;
Etienne, J ;
Vandenesch, F .
RNA, 2000, 6 (05) :668-679
[4]   Distribution of the synergistic haemolysin genes hld and slush with respect to agr in human Staphylococci [J].
Donvito, B ;
Etienne, J ;
Greenland, T ;
Mouren, C ;
Delorme, V ;
Vandenesch, F .
FEMS MICROBIOLOGY LETTERS, 1997, 151 (02) :139-144
[5]   Signal transduction in bacteria: molecular mechanisms of stimulus-response coupling [J].
Goudreau, PN ;
Stock, AM .
CURRENT OPINION IN MICROBIOLOGY, 1998, 1 (02) :160-169
[6]   The PROSITE database, its status in 1999 [J].
Hofmann, K ;
Bucher, P ;
Falquet, L ;
Bairoch, A .
NUCLEIC ACIDS RESEARCH, 1999, 27 (01) :215-219
[7]   THE ROLE OF THE DELTA-LYSIN GENE (HLD) IN THE REGULATION OF VIRULENCE GENES BY THE ACCESSORY GENE REGULATOR (AGR) IN STAPHYLOCOCCUS-AUREUS [J].
JANZON, L ;
ARVIDSON, S .
EMBO JOURNAL, 1990, 9 (05) :1391-1399
[8]   Exfoliatin-producing strains define a fourth agr specificity group in Staphylococcus aureus [J].
Jarraud, S ;
Lyon, GJ ;
Figueiredo, AMS ;
Gérard, L ;
Vandenesch, F ;
Etienne, J ;
Muir, TW ;
Novick, RP .
JOURNAL OF BACTERIOLOGY, 2000, 182 (22) :6517-6522
[9]   Cell density control of staphylococcal virulence mediated by an octapeptide pheromone [J].
Ji, GY ;
Beavis, RC ;
Novick, RP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (26) :12055-12059
[10]   Bacterial interference caused by autoinducing peptide variants [J].
Ji, GY ;
Beavis, R ;
Novick, RP .
SCIENCE, 1997, 276 (5321) :2027-2030