Origins and evolution of methicillin-resistant Staphylococcus aureus clonal lineages

被引:63
作者
Gomes, A. R.
Westh, H.
de Lencastre, H.
机构
[1] Rockefeller Univ, Microbiol Lab, New York, NY 10021 USA
[2] Univ Nova Lisboa, Mol Genet Lab, Inst Tecnol Quim & Biol, Oeiras, Portugal
[3] Hvidovre Univ Hosp, Dept Clin Microbiol, Copenhagen, Denmark
[4] State Serum Inst, Staphylococcus Lab, Copenhagen, Denmark
[5] Rockefeller Univ, Microbiol Lab, New York, NY 10021 USA
关键词
D O I
10.1128/AAC.00521-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Most methicillin-resistant Staphylococcus aureus (MRSA) isolates identified among blood isolates collected in Denmark between 1957 and 1970 belonged to either phage group III or the closely related 83A complex and had a PSTM antibiotype (resistance to penicillin [P], streptomycin [S], tetracycline [T], and methicillin [M]). Recently, some of these isolates were shown to have the same genetic backgrounds as contemporary epidemic MRSA isolates, and Danish methicillin-susceptible S. aureus (MSSA) isolates from the 1960s with a PST antibiotype were proposed to have been the recipients of the mecA gene in those lineages. In this study, we investigated the genetic backgrounds of isolates from the 83A complex that were fully susceptible or resistant to penicillin only in order to try to trace the evolutionary trajectory of contemporary MRSA lineages. We also studied MSSA and MRSA isolates from other phage groups in order to investigate if they had the potential to develop into contemporary MRSA clones. Most susceptible or penicillin-resistant isolates from phage group III or the 83A complex belonged to sequence type 8 (ST8) or ST5, while four isolates were ST254. STs 30, 45 and 25 were represented by MSSA isolates from other phage groups, which also included several singletons. Representatives of most of the current major epidemic MRSA lineages were identified among fully susceptible isolates collected in the 1960s, suggesting that these were MSSA lineages which carried genetic traits important for superior epidemicity before the acquisition of methicillin resistance.
引用
收藏
页码:3237 / 3244
页数:8
相关论文
共 52 条
[31]   Interactions among strategies associated with bacterial infection:: Pathogenicity, epidemicity, and antibiotic resistance [J].
Martínez, JL ;
Baquero, F .
CLINICAL MICROBIOLOGY REVIEWS, 2002, 15 (04) :647-+
[32]   Pulsed-field gel electrophoresis typing of oxacillin-resistant Staphylococcus aureus isolates from the United States:: Establishing a national database [J].
McDougal, LK ;
Steward, CD ;
Killgore, GE ;
Chaitram, JM ;
McAllister, SK ;
Tenover, FC .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (11) :5113-5120
[33]   Natural population dynamics and expansion of pathogenic clones of Staphylococcus aureus [J].
Melles, DC ;
Gorkink, RFJ ;
Boelens, HAM ;
Snijders, SV ;
Peeters, JK ;
Moorhouse, MJ ;
van der Spek, PJ ;
van Leeuwen, WB ;
Simons, G ;
Verbrugh, HA ;
van Belkum, A .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (12) :1732-1740
[34]   Molecular characterisation of the dominant UK methicillin-resistant Staphylococcus aureus strains, EMRSA-15 and EMRSA-16 [J].
Moore, PCL ;
Lindsay, JA .
JOURNAL OF MEDICAL MICROBIOLOGY, 2002, 51 (06) :516-521
[35]   Identification and characterization of phage variants of a strain of epidemic methicillin-resistant Staphylococcus aureus (EMRSA-15) [J].
O'Neill, GL ;
Murchan, S ;
Gil-Setas, A ;
Aucken, HM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (04) :1540-1548
[36]   Secrets of success of a human pathogen:: molecular evolution of pandemic clones of meticillin-resistant Staphylocloccus aureus [J].
Oliveira, DC ;
Tomasz, A ;
de Lencastre, H .
LANCET INFECTIOUS DISEASES, 2002, 2 (03) :180-189
[37]   Multiplex PCR strategy for rapid identification of structural types and variants of the mec element in methicillin-resistant Staphylococcus aureus [J].
Oliveira, DC ;
de Lencastre, H .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (07) :2155-2161
[38]   The evolution of pandemic clones of methicillin-resistant Staphylococcus aureus:: Identification of two ancestral genetic backgrounds and the associated mec elements [J].
Oliveira, DC ;
Tomasz, A ;
de Lencastre, H .
MICROBIAL DRUG RESISTANCE-MECHANISMS EPIDEMIOLOGY AND DISEASE, 2001, 7 (04) :349-361
[39]   CHARACTERIZATION OF A STRAIN OF METHICILLIN-RESISTANT STAPHYLOCOCCUS-AUREUS (EMRSA-15) BY CONVENTIONAL AND MOLECULAR METHODS [J].
RICHARDSON, JF ;
REITH, S .
JOURNAL OF HOSPITAL INFECTION, 1993, 25 (01) :45-52
[40]   Molecular epidemiology of methicillin-resistant Staphylococcus aureus in 12 New York hospitals [J].
Roberts, RB ;
de Lencastre, A ;
Eisner, W ;
Severina, EP ;
Shopsin, B ;
Kreiswirth, BN ;
Tomasz, A .
JOURNAL OF INFECTIOUS DISEASES, 1998, 178 (01) :164-171