Evolutionary models of the emergence of methicillin-resistant Staphylococcus aureus

被引:336
作者
Robinson, DA [1 ]
Enright, MC [1 ]
机构
[1] Univ Bath, Dept Biol & Biochem, Bath BA2 7AY, Avon, England
基金
英国惠康基金;
关键词
D O I
10.1128/AAC.47.12.3926-3934.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Five major lineages of methicillin-resistant Staphylococcus aureus (MRSA) have evolved since the introduction of methicillin for the treatment of infections caused by penicillin-resistant S. aureus in 1959. The clones of these lineages are responsible for the vast majority of hospital-acquired MRSA disease globally. We have constructed high-resolution evolutionary models for each lineage using a parsimony approach with 15 partial gene sequences from 147 geographically diverse isolates. On the basis of these models, we infer that MRSA has emerged at least 20 times upon acquisition of the methicillin resistance determinant, which is carried on a mobile genetic element called the staphylococcal cassette chromosome mec (SCCmec). The acquisition of SCCmec by sensitive clones was four times more common than the replacement of one SCCmec with another. Notably, SCCmec type IV was found in twice as many clones as any other SCCmec type, and it is this SCCmec type which is commonly found in clones from patients with community-acquired MRSA disease. Our findings suggest that most clones of MRSA arise by the acquisition of SCCmec type IV by methicillin-sensitive isolates.
引用
收藏
页码:3926 / 3934
页数:9
相关论文
共 34 条
  • [1] Genome and virulence determinants of high virulence community-acquired MRSA
    Baba, T
    Takeuchi, F
    Kuroda, M
    Yuzawa, H
    Aoki, K
    Oguchi, A
    Nagai, Y
    Iwama, N
    Asano, K
    Naimi, T
    Kuroda, H
    Cui, L
    Yamamoto, K
    Hiramatsu, K
    [J]. LANCET, 2002, 359 (9320) : 1819 - 1827
  • [2] BARBER M, 1948, LANCET, V2, P641
  • [3] The changing epidemiology of Staphylococcus aureus?
    Chambers, HF
    [J]. EMERGING INFECTIOUS DISEASES, 2001, 7 (02) : 178 - 182
  • [4] Infection with vancomycin-resistant Staphylococcus aureus containing the vanA resistance gene
    Chang, S
    Sievert, DM
    Hageman, JC
    Boulton, ML
    Tenover, FC
    Downes, FP
    Shah, S
    Rudrik, JT
    Pupp, GR
    Brown, WJ
    Cardo, D
    Fridkin, SK
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (14) : 1342 - 1347
  • [5] The evolution of methicillin resistance in Staphylococcus aureus:: Similarity of genetic backgrounds in historically early methicillin-susceptible and -resistant isolates and contemporary epidemic clones
    Crisóstomo, MI
    Westh, H
    Tomasz, A
    Chung, M
    Oliveira, DC
    de Lencastre, H
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (17) : 9865 - 9870
  • [6] de Sousa MA, 2003, J CLIN MICROBIOL, V41, P159, DOI [10.1128/JCM.41.1.159-163.2003, 10.1128/JCM.41.1.159-163.2002]
  • [7] Intercontinental spread of a multidrug-resistant methicillin-resistant Staphylococcus aureus clone
    de Sousa, MA
    Sanches, IS
    Ferro, ML
    Vaz, MJ
    Saraiva, Z
    Tendeiro, T
    Serra, J
    de Lencastre, H
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (09) : 2590 - 2596
  • [8] Multilocus sequence typing for characterization of methicillin-resistant and methicillin-susceptible clones of Staphylococcus aureus
    Enright, MC
    Day, NPJ
    Davies, CE
    Peacock, SJ
    Spratt, BG
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (03) : 1008 - 1015
  • [9] The evolutionary history of methicillin-resistant Staphylococcus aureus (MRSA)
    Enright, MC
    Robinson, DA
    Randle, G
    Feil, EJ
    Grundmann, H
    Spratt, BG
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (11) : 7687 - 7692
  • [10] How clonal is Staphylococcus aureus?
    Feil, EJ
    Cooper, JE
    Grundmann, H
    Robinson, DA
    Enright, MC
    Berendt, T
    Peacock, SJ
    Smith, JM
    Murphy, M
    Spratt, BG
    Moore, CE
    Day, NPJ
    [J]. JOURNAL OF BACTERIOLOGY, 2003, 185 (11) : 3307 - 3316