Foglia Gessica, Del Grosso Maria, Vignaroli Carla, Bagnarelli Patrizia, Varaldo Pietro E, Pantosti Annalisa, Biavasco Francesca
Department of Microbiology and Biomedical Sciences, Università Politecnica delle Marche, Via Ranieri, Monte d'Ago, 60131 Ancona, Italy.
J Antimicrob Chemother. 2003 Nov;52(5):772-5. doi: 10.1093/jac/dkg445. Epub 2003 Sep 30.
Four Enterococcus gallinarum isolates, all highly resistant to vancomycin, were studied in order to investigate their relationship and to gain insight into the molecular events responsible for their acquired resistance.
Extensive molecular analysis was performed to compare the four E. gallinarum isolates and their Tn1546-like elements.
The four strains had very similar random amplified polymorphic DNA (RAPD) patterns and different but related PFGE profiles. Genotypic analysis demonstrated that all carried both vanC-1 and vanA genes. Using a vanA probe, no hybridization was detected to plasmid DNA, whereas hybridization to different SmaI fragments of the four strains was obtained with total DNA. Amplification and sequencing experiments showed that all four strains carried a Tn1546-like element that contained the orf2, vanR, vanS, vanH, vanA and vanX genes and was flanked at both ends by oppositely oriented IS1216V sequences. On the left side of the vanA cluster, all lacked IRL, and all had, upstream from orf2, 1029 bp of the 3' end of orf1. On the right side, one of the strains lacked vanY, vanZ and IRR, whereas in one of the other three there was an IS1542 element inserted within the vanZ gene. In one strain, an additional IS1216V element was inserted in the intergenic region vanX-vanY.
This is the first study providing a molecular analysis of chromosomal Tn1546-like elements (possibly composite transposons) associated with high-level vancomycin resistance in human and animal strains of E. gallinarum. These molecular findings, together with those from PFGE and RAPD, suggest that the four E. gallinarum isolates are related and might have a common ancestor.
对4株均对万古霉素高度耐药的鹑鸡肠球菌分离株进行研究,以调查它们之间的关系,并深入了解导致其获得性耐药的分子事件。
进行了广泛的分子分析,以比较这4株鹑鸡肠球菌分离株及其Tn1546样元件。
这4株菌株具有非常相似的随机扩增多态性DNA(RAPD)图谱和不同但相关的脉冲场凝胶电泳(PFGE)图谱。基因型分析表明,所有菌株均携带vanC-1和vanA基因。使用vanA探针,未检测到与质粒DNA的杂交,而用总DNA与这4株菌株的不同SmaI片段进行杂交时获得了杂交信号。扩增和测序实验表明,所有4株菌株均携带一个Tn1546样元件,该元件包含orf2、vanR、vanS、vanH、vanA和vanX基因,两端侧翼为方向相反的IS1216V序列。在vanA基因簇的左侧,所有菌株均缺乏IRL,并且在orf2上游均具有orf1 3'端的1029 bp。在右侧,其中一株菌株缺乏vanY、vanZ和IRR,而在另外三株中的一株中,vanZ基因内插入了一个IS1542元件。在一株菌株中,vanX-vanY基因间区域插入了一个额外的IS1216V元件。
这是第一项对与人及动物来源的鹑鸡肠球菌高水平万古霉素耐药相关的染色体Tn1546样元件(可能为复合转座子)进行分子分析的研究。这些分子研究结果,连同PFGE和RAPD的结果,表明这4株鹑鸡肠球菌分离株具有相关性,可能有一个共同的祖先。