Extensive genetic diversity among clinical isolates of Streptococcus pyogenes serotype M5

被引:14
作者
Desai, M
Tanna, A
Efstratiou, A
George, R
Clewley, J
Stanley, J
机构
[1] Cent Publ Hlth Lab, Div Virus Reference, Mol Biol Unit, London NW9 5HT, England
[2] Cent Publ Hlth Lab, Resp & Syst Infect Lab, Diphtheria Reference Unit, London NW9 5HT, England
来源
MICROBIOLOGY-UK | 1998年 / 144卷
关键词
group A Streptococcus; emm gene; polymorphism;
D O I
10.1099/00221287-144-3-629
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The genetic diversity of clinical isolates of Streptococcus pyogenes serotype M5 has been characterized. Strain genotypes were defined by macrorestriction profile, 165 ribotype, emm gene subtype, insertion element IS1239 profile, and exotoxin gene determinant. By these criteria, clinical isolates of M5 constituted a multiplicity of strain clusters rather than a homogeneous population as found for certain serotypes. Distance matrices and an unrooted tree were constructed from macrorestriction data with three rarely cutting endonucleases, determined by PFGE. A single IS1239 profile was common to 85% of isolates but there was great diversity of both ribotype and macrorestriction profile, and 18 different emm gene subtypes were detected by PCR-RFLP. DNA sequence analysis of the antigen-coding 5' (hypervariable) region of emm gene amplicons (about 240 bp) showed that 14/18 exhibited up to 6% divergence. Four amplicons had highly divergent sequences - corresponding to those previously determined for emm 6, emm 11, emm 18 and emm 77. Further serological and hybridization studies were used to analyse the discrepancy between the Lancefield serotype of these strains (Ms) and their emm genotype, Overall, this study shows a high degree of genetic diversity in serotype M5, with implications for the Lancefield scheme itself, for the epidemiology of group A streptococci, and for recombinant DNA strategies for M protein-based vaccine development.
引用
收藏
页码:629 / 637
页数:9
相关论文
共 21 条
  • [1] Survey of emm gene sequences and T-antigen types from systemic Streptococcus pyogenes infection isolates collected in San Francisco, California; Atlanta, Georgia; and Connecticut in 1994 and 1995
    Beall, B
    Facklam, R
    Hoenes, T
    Schwartz, B
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (05) : 1231 - 1235
  • [2] Sequencing emm-specific PCR products for routine and accurate typing of group a streptococci
    Beall, B
    Facklam, R
    Thompson, T
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (04) : 953 - 958
  • [3] CLONAL BASIS FOR RESURGENCE OF SERIOUS STREPTOCOCCUS-PYOGENES DISEASE IN THE 1980S
    CLEARY, PP
    KAPLAN, EL
    HANDLEY, JP
    WLAZLO, A
    KIM, MH
    HAUSER, AR
    SCHLIEVERT, PM
    [J]. LANCET, 1992, 339 (8792) : 518 - 521
  • [4] A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY
    FEINBERG, AP
    VOGELSTEIN, B
    [J]. ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) : 6 - 13
  • [5] FELSENSTEIN J, 1988, PHYLIP PHYLOGENETIC
  • [6] STREPTOCOCCAL M-PROTEIN - MOLECULAR DESIGN AND BIOLOGICAL BEHAVIOR
    FISCHETTI, VA
    [J]. CLINICAL MICROBIOLOGY REVIEWS, 1989, 2 (03) : 285 - 314
  • [7] Johnson DR., 1996, LAB DIAGNOSIS GROUP
  • [8] CHARACTERIZATION AND DISTRIBUTION OF INSERTION-SEQUENCE IS1239 IN STREPTOCOCCUS-PYOGENES
    KAPUR, V
    REDA, KB
    LI, LL
    HO, LJ
    RICH, RR
    MUSSER, JM
    [J]. GENE, 1994, 150 (01) : 135 - 140
  • [9] LANCEFIELD RC, 1962, J IMMUNOL, V89, P307
  • [10] GEOGRAPHIC AND TEMPORAL DISTRIBUTION AND MOLECULAR CHARACTERIZATION OF 2 HIGHLY PATHOGENIC CLONES OF STREPTOCOCCUS-PYOGENES EXPRESSING ALLELIC VARIANTS OF PYROGENIC EXOTOXIN-A (SCARLET FEVER TOXIN)
    MUSSER, JM
    KAPUR, V
    KANJILAL, S
    SHAH, U
    MUSHER, DM
    BARG, NL
    JOHNSTON, KH
    SCHLIEVERT, PM
    HENRICHSEN, J
    GERLACH, D
    RAKITA, RM
    TANNA, A
    COOKSON, BD
    HUANG, JC
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1993, 167 (02) : 337 - 346