Sugiyama M, Yuasa K, Bhuiyan M Z, Iwai Y, Masumi N, Ueda K
Institute of Pharmaceutical Sciences, Hiroshima University School of Medicine, Japan.
Appl Microbiol Biotechnol. 1996 Aug;46(1):61-6. doi: 10.1007/s002530050783.
A methicillin-resistant Staphylococcus aureus (MRSA) strain B-26, isolated clinically in Hiroshima University Hospital, is resistant to bleomycin together with kanamycin. In the present study, we analysed the nucleotide sequence of the 5.1-kb HindIII fragment containing the bleomycin- and kanamycin-resistance genes, which were previously cloned [Bhuiyan et al. (1995) Appl Microbiol Biotechnol 43: 65-69] from the chromosomal DNA of MRSA B-26. The present study found that the DNA sequence contains the duplicated target sequence (GATTAGAT) consisting of 8 bp for transposase and the entire nucleotide sequence of the plasmid pUB110, together with the sequence of inverted repeats (16 bp), designated IR-r and IR-1 in IS431 mec. The 8-bp duplication sequence, produced by the transposable element, was first found by us. We proposed that bleomycin resistance in MRSA B-26 is attributed to the IS431 mec-mediated integration of pUB110 into the chromosome.
从广岛大学医院临床分离出的一株耐甲氧西林金黄色葡萄球菌(MRSA)B - 26菌株,对博来霉素和卡那霉素均具有抗性。在本研究中,我们分析了包含博来霉素抗性基因和卡那霉素抗性基因的5.1 kb HindIII片段的核苷酸序列,该片段先前已从MRSA B - 26的染色体DNA中克隆出来[Bhuiyan等人(1995年),《应用微生物学与生物技术》43: 65 - 69]。本研究发现,该DNA序列包含由8个碱基对组成的转座酶重复靶序列(GATTAGAT)、质粒pUB110的完整核苷酸序列,以及在IS431 mec中称为IR - r和IR - 1的反向重复序列(16个碱基对)。我们首次发现了由转座元件产生的8个碱基对的重复序列。我们提出,MRSA B - 26对博来霉素的抗性归因于IS431 mec介导的pUB110整合到染色体中。