
A novel type‐III staphylococcal cassette chromosome mec (SCC mec ) variant among Indian isolates of methicillin‐resistant Staphylococcus aureus
Author(s) -
Arakere Gayathri,
Nadig Savitha,
Ito Teruyo,
Ma Xiao Xue,
Hiramatsu Keiichi
Publication year - 2009
Publication title -
fems microbiology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.899
H-Index - 151
eISSN - 1574-6968
pISSN - 0378-1097
DOI - 10.1111/j.1574-6968.2008.01482.x
Subject(s) - sccmec , staphylococcus aureus , biology , operon , microbiology and biotechnology , plasmid , genotype , multiplex polymerase chain reaction , clone (java method) , insertion sequence , methicillin resistant staphylococcus aureus , genetics , chromosome , gene , polymerase chain reaction , transposable element , bacteria , genome , escherichia coli
We identified a novel type‐III staphylococcal cassette chromosome mec (SCC mec ) element carried by eight methicillin‐resistant Staphylococcus aureus (MRSA) strains from different wards and patients in an Indian hospital. Although the pulsed‐field gel electrophoresis pattern and spa types of eight strains were identical and clonally related to other nosocomial Indian isolates that belonged to sequence type (ST) 239 and spa type t037, the minimum inhibitory concentration (MIC) of these eight variants was noticeably low compared with the typical type‐III isolates from the same hospital, and we were unable to identify ccrC and hsdR by multiplex PCR, although mer operon and transposases A, B, and C of Tn 554 were amplified. By amplifying the entire SCC mec region by long‐range PCR and determining parts of the nucleotide sequences of one isolate (V14), we found that the strain carried a novel SCC mec element containing a 422 bp sequence, which is highly homologous to that identified in strain CCR1‐9583, mer operon and plasmid pT181 integrated in tandem via IS 431 in the J3 region. It also carried a cassette chromosome, previously reported to be an SCC‐like element, downstream of type‐III SCC mec . Because PCR amplification of representative genes showed that these eight strains carried the same genetic elements, they belong to a novel MRSA clone that differs from most nosocomial clones carrying type‐III SCC mec and SCC mercury , despite belonging to the ST239 genotype.