Handwerger S, Skoble J
Laboratory of Microbiology, Rockefeller University, New York, New York 10021, USA.
Antimicrob Agents Chemother. 1995 Nov;39(11):2446-53. doi: 10.1128/AAC.39.11.2446.
A clinical isolate of Enterococcus faecium that contains a chromosomally encoded vanA gene cluster, Tn1546::IS1251, transferred vancomycin resistance to the plasmid-free strain Enterococcus faecalis JH2-2 during filter matings. Hybridization of a vanHAXY probe to SmaI restriction-digested genomic DNA separated by pulsed-field gel electrophoresis showed that the vanA gene cluster was located on a 40-kb fragment in the original donor strain and on fragments of different sizes (150 to 450 kb) in the transconjugants. No hybridization to vanA gene cluster probes was obtained with plasmid DNA preparations from the donor or transconjugants. These results suggested that in each case, the van genes had integrated into the recipient chromosome. The transconjugants in turn could act as donors of vancomycin resistance, and resistance was transferable to a Rec- recipient. The results of restriction analyses and DNA hybridizations of genomic DNA from the donor and transconjugants were consistent with the transfer of a mobile element that includes the 12.3-kb Tn1546::IS1251 gene cluster and at least 13 kb of additional DNA. This element has been tentatively designated Tn5482. DNA sequence analysis of a fragment predicted to contain the left end of Tn5482 revealed two insertion sequence-like elements: IS1216V and an apparently truncated IS3-like element. Restriction mapping and DNA hybridization patterns of the van gene clusters of three additional clinical isolates from New York City showed an element similar to Tn5482. Transfer of Tn5482 and related elements may be involved in dissemination of vancomycin resistance.
一株含有染色体编码的vanA基因簇Tn1546::IS1251的屎肠球菌临床分离株,在滤膜交配过程中将万古霉素耐药性转移至无质粒的屎肠球菌菌株JH2-2。用vanHAXY探针与经脉冲场凝胶电泳分离的SmaI酶切基因组DNA杂交,结果显示vanA基因簇在原始供体菌株中位于一个40kb的片段上,而在接合子中位于不同大小(150至450kb)的片段上。从供体或接合子制备的质粒DNA与vanA基因簇探针未获得杂交信号。这些结果表明,在每种情况下,van基因已整合到受体染色体中。这些接合子继而可作为万古霉素耐药性的供体,且耐药性可转移至Rec-受体。对供体和接合子的基因组DNA进行限制性分析和DNA杂交的结果与一个移动元件的转移情况相符,该移动元件包括12.3kb的Tn1546::IS1251基因簇以及至少13kb的额外DNA。这个元件被暂定为Tn5482。对一个预计包含Tn5482左端的片段进行DNA序列分析,发现了两个插入序列样元件:IS1216V和一个明显截短的IS3样元件。对来自纽约市的另外三株临床分离株的van基因簇进行限制性图谱分析和DNA杂交模式分析,结果显示存在一个与Tn5482相似的元件。Tn5482及相关元件的转移可能参与了万古霉素耐药性的传播。