School of Molecular Bioscience, The University of Sydney, Sydney, Australia.
Microb Drug Resist. 2012 Aug;18(4):364-71. doi: 10.1089/mdr.2012.0008. Epub 2012 Mar 14.
Commensal Escherichia coli from healthy adult humans were screened for antibiotic resistance genes. Two unrelated strains contained the sul2 sulphonamide resistance gene and strAB streptomyicn resistance genes with the dfrA14 trimethoprim resistance gene cassette in the strA gene and conferred resistance to trimethoprim and sulphamethoxazole. A 6.8 kb plasmid, pCERC1, that contains these resistance genes was recovered and sequenced. Deletions were constructed, and the pCERC1 replication region was confined to a 1 kb segment carrying genes for RNAs that are closely related to the ColE1 replication initiation RNAs. Polymerase chain reaction assays, developed to detect the sul2-strA-strB gene cluster in this context, identified a streptomycin and sulphonamide resistance plasmid, pCERC2, identical to pCERC1 without the dfrA14 cassette in two further E. coli isolates. Bioinformatic analysis revealed plasmids similar to pCERC1 and two more members of this family. One, the probable progenitor, carries only the sul2 gene adjacent to the small mobile element CR2. The other has a variant resistance gene cluster that has evolved from pCERC2 via acquisition of the tet(A) tetracycline resistance determinant. pCERC1 and pCERC2 have been detected in many countries, indicating a global distribution and appear to have been circulating in Gram-negative bacteria for more than 25 years.
从健康成年人体内筛选出共生大肠杆菌,检测其携带的抗生素抗性基因。两株不相关的菌株携带 sul2 磺胺类抗性基因和 strAB 链霉素抗性基因,strA 基因中带有 dfrA14 三嗪类抗生素抗性基因盒,对甲氧苄啶和磺胺甲恶唑具有抗性。回收并测序了携带这些抗性基因的 6.8kb 质粒 pCERC1。构建了缺失突变体,并将 pCERC1 的复制区限制在一个携带与 ColE1 复制起始 RNA 密切相关的 RNA 基因的 1kb 片段上。设计了聚合酶链反应检测该基因簇的方法,鉴定出两个进一步的大肠杆菌分离株中存在与 pCERC1 相同但不携带 dfrA14 盒的链霉素和磺胺抗性质粒 pCERC2。生物信息学分析揭示了与 pCERC1 相似的质粒和该家族的另外两个成员。一个可能是原始质粒,仅携带 sul2 基因,紧邻小型移动元件 CR2。另一个具有变异的抗性基因簇,是通过从 pCERC2 获得 tet(A) 四环素抗性决定簇而进化而来的。pCERC1 和 pCERC2 已在许多国家检测到,表明其具有全球分布,并可能在革兰氏阴性菌中传播了 25 年以上。