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Characterization of two novel variants of staphylococcal cassette chromosome mec elements in oxacillin-resistant Staphylococcus lugdunensis.
Chang, Shih-Cheng; Lee, Ming-Hsun; Yeh, Chun-Fu; Liu, Tsui-Ping; Lin, Jung-Fu; Ho, Cheng-Mao; Lu, Jang-Jih.
Afiliación
  • Chang SC; Department of Laboratory Medicine, Linkou Chang Gung Memorial Hospital, Taoyuan, Taiwan.
  • Lee MH; Department of Medical Biotechnology and Laboratory Science, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Yeh CF; Division of Infectious Diseases, Department of Internal Medicine, Linkou Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Taoyuan, Taiwan.
  • Liu TP; Division of Infectious Diseases, Department of Internal Medicine, Linkou Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Taoyuan, Taiwan.
  • Lin JF; Department of Laboratory Medicine, Linkou Chang Gung Memorial Hospital, Taoyuan, Taiwan.
  • Ho CM; Division of Infectious Diseases, Department of Internal Medicine, Linkou Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Taoyuan, Taiwan.
  • Lu JJ; Department of Laboratory Medicine, China Medical University Hospital, Taichung, Taiwan.
J Antimicrob Chemother ; 72(12): 3258-3262, 2017 Dec 01.
Article en En | MEDLINE | ID: mdl-28962025
ABSTRACT

OBJECTIVES:

Staphylococcus lugdunensis, a species of CoNS, has become an important hospital pathogen because of increasing resistance to ß-lactam antibiotics such as methicillin and oxacillin. Methicillin resistance is mainly due to the acquisition of the staphylococcal cassette chromosome (SCC) mec (SCCmec). Little is known about the structure of SCCmec in methicillin- or oxacillin-resistant CoNS.

METHODS:

WGS was performed to determine the structure of SCCmec elements of two clinical S. lugdunensis isolates CMUH-22 and CMUH-25.

RESULTS:

These elements were found to be flanked by DRs and IRs with unique mosaic structures and a common integration site in the 3' end of the rlmH gene. The sequences of the regions located between rlmH and the ISSau4-like transposase genes of both elements were similar to those of SCCmec Vt of Staphylococcus aureus PM1. The SCCmec (type V, 5C2&4) of CMUH-25 harboured a novel ccrC complex and a C2-like mec complex in opposite orientations, similar to the type V SCCmec of S. aureus WIS. The sequences of the ccrA4B4 genes and J1 and J2 regions of CMUH-25 were similar to those of the SCC element of Staphylococcus haemolyticus NCTC 11042. In contrast, portions of the sequence of the J1 region of type Vt (5C2) SCCmec in strain CMUH-22 were highly similar to portions of those of Staphylococcus epidermidis RP62A and the composite SCCmec type V of S. aureus WAMRSA40.

CONCLUSIONS:

These observations suggest that the SCCmec elements of CMUH-25 and CMUH-22 evolved separately and assembled through different recombination events.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Oxacilina / Cromosomas Bacterianos / Resistencia betalactámica / Orden Génico / Staphylococcus lugdunensis / Antibacterianos Límite: Humans Idioma: En Revista: J Antimicrob Chemother Año: 2017 Tipo del documento: Article País de afiliación: Taiwán

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Oxacilina / Cromosomas Bacterianos / Resistencia betalactámica / Orden Génico / Staphylococcus lugdunensis / Antibacterianos Límite: Humans Idioma: En Revista: J Antimicrob Chemother Año: 2017 Tipo del documento: Article País de afiliación: Taiwán