Arakere Gayathri, Nadig Savitha, Ito Teruyo, Ma Xiao Xue, Hiramatsu Keiichi
Sir Dorabji Tata Centre for Research in Tropical Diseases, Innovation Centre, Indian Institute of Science Campus, Bangalore, India.
FEMS Microbiol Lett. 2009 Mar;292(1):141-8. doi: 10.1111/j.1574-6968.2008.01482.x. Epub 2009 Jan 29.
We identified a novel type-III staphylococcal cassette chromosome mec (SCCmec) 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 Tn554 were amplified. By amplifying the entire SCCmec region by long-range PCR and determining parts of the nucleotide sequences of one isolate (V14), we found that the strain carried a novel SCCmec 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 IS431 in the J3 region. It also carried a cassette chromosome, previously reported to be an SCC-like element, downstream of type-III SCCmec. 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 SCCmec and SCCmercury, despite belonging to the ST239 genotype.
我们在一家印度医院中,从不同病房和患者身上分离出的8株耐甲氧西林金黄色葡萄球菌(MRSA)菌株中,鉴定出了一种新型的III型葡萄球菌盒式染色体mec(SCCmec)元件。尽管这8株菌株的脉冲场凝胶电泳图谱和spa型相同,并且与其他属于序列型(ST)239和spa型t037的印度医院分离株具有克隆相关性,但与同一医院的典型III型分离株相比,这8个变体的最低抑菌浓度(MIC)明显较低。尽管Tn554的mer操纵子以及转座酶A、B和C能够被扩增,但通过多重PCR我们无法鉴定出ccrC和hsdR。通过长距离PCR扩增整个SCCmec区域,并测定其中一个分离株(V14)的部分核苷酸序列,我们发现该菌株携带一种新型SCCmec元件,其中包含一段422 bp的序列,该序列与CCR1 - 9583菌株中鉴定出的序列高度同源,mer操纵子和质粒pT181通过IS431在J3区域串联整合。它还在III型SCCmec的下游携带了一个盒式染色体,此前曾报道该染色体是一种类似SCC的元件。由于对代表性基因的PCR扩增表明这8株菌株携带相同的遗传元件,所以它们属于一个新型的MRSA克隆,尽管属于ST239基因型,但与大多数携带III型SCCmec和SCCmercury的医院克隆不同。