Progress toward characterization of the group a Streptococcus metagenome:: Complete genome sequence of a macrolide-resistant serotype M6 strain

被引:134
作者
Banks, DJ
Porcella, SF
Barbian, KD
Beres, SB
Philips, LE
Voyich, JM
DeLeo, FR
Martin, JM
Somerville, GA
Musser, JM
机构
[1] Baylor Coll Med, Dept Pathol, Ctr Human Bacterial Pathogenesis Res, Houston, TX 77030 USA
[2] NIAID, Lab Human Bacterial Pathogenesis, Rocky Mt Labs, NIH, Hamilton, MT USA
[3] Univ Pittsburgh, Childrens Hosp Pittsburgh, Sch Med, Dept Pediat,Div Allergy Immunol & Infect Dis, Pittsburgh, PA USA
关键词
D O I
10.1086/422697
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We describe the genome sequence of a macrolide-resistant strain (MGAS10394) of serotype M6 group A Streptococcus (GAS). The genome is 1,900,156 bp in length, and 8 prophage-like elements or remnants compose 12.4% of the chromosome. A 8.3-kb prophage remnant encodes the SpeA4 variant of streptococcal pyrogenic exotoxin A. The genome of strain MGAS10394 contains a chimeric genetic element composed of prophage genes and a transposon encoding the mefA gene conferring macrolide resistance. This chimeric element also has a gene encoding a novel surface-exposed protein (designated "R6 protein"), with an LPKTG cell-anchor motif located at the carboxyterminus. Surface expression of this protein was confirmed by flow cytometry. Humans with GAS pharyngitis caused by serotype M6 strains had antibody against the R6 protein present in convalescent, but not acute, serum samples. Our studies add to the theme that GAS prophage-encoded extracellular proteins contribute to host-pathogen interactions in a strain-specific fashion.
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收藏
页码:727 / 738
页数:12
相关论文
共 39 条
  • [1] Yersinia pestis, the cause of plague, is a recently emerged clone of Yersinia pseudotuberculosis
    Achtman, M
    Zurth, K
    Morelli, C
    Torrea, G
    Guiyoule, A
    Carniel, E
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (24) : 14043 - 14048
  • [2] Structure and distribution of an unusual chimeric genetic element encoding macrolide resistance in phylogenetically diverse clones of group A Streptococcus
    Banks, DJ
    Porcella, SF
    Barbian, KD
    Martin, JM
    Musser, JM
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2003, 188 (12) : 1898 - 1908
  • [3] The fundamental contribution of phages to GAS evolution, genome diversification and strain emergence
    Banks, DJ
    Beres, SB
    Musser, JM
    [J]. TRENDS IN MICROBIOLOGY, 2002, 10 (11) : 515 - 521
  • [4] BANKS DJ, 2004, BACTERIOPHAGES BACTE
  • [5] Genome sequence of a serotype M3 strain of group A Streptococcus:: Phage-encoded toxins, the high-virulence phenotype, and clone emergence
    Beres, SB
    Sylva, GL
    Barbian, KD
    Lei, BF
    Hoff, JS
    Mammarella, ND
    Liu, MY
    Smoot, JC
    Porcella, SF
    Parkins, LD
    Campbell, DS
    Smith, TM
    McCormick, JK
    Leung, DYM
    Schlievert, PM
    Musser, JM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (15) : 10078 - 10083
  • [6] Genetic linkage of exotoxin alleles and emm gene markers for tissue tropism in group A Streptococci
    Bessen, DE
    Izzo, MW
    Fiorentino, TR
    Caringal, RM
    Hollingshead, SK
    Beall, B
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1999, 179 (03) : 627 - 636
  • [7] ENVIRONMENTAL-REGULATION OF VIRULENCE IN GROUP A STREPTOCOCCI - TRANSCRIPTION OF THE GENE ENCODING M PROTEIN IS STIMULATED BY CARBON-DIOXIDE
    CAPARON, MG
    GEIST, RT
    PEREZCASAL, J
    SCOTT, JR
    [J]. JOURNAL OF BACTERIOLOGY, 1992, 174 (17) : 5693 - 5701
  • [8] COLON AE, 1972, J VIROL, V9, P551
  • [9] COLON AE, 1971, J VIROL, V8, P103
  • [10] Pathogenesis of group A streptococcal infections
    Cunningham, MW
    [J]. CLINICAL MICROBIOLOGY REVIEWS, 2000, 13 (03) : 470 - +