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Epidemiological Survey of Amoxicillin-Clavulanate Resistance and Corresponding Molecular Mechanisms in Escherichia coli Isolates in France: New Genetic Features of blaTEM Genes

机译:法国大肠埃希菌对阿莫西林-克拉维酸耐药性及其分子机制的流行病学调查:blaTEM基因的新遗传特征

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摘要

Amoxicillin-clavulanate resistance (MIC >16 μg/ml) and the corresponding molecular mechanisms were prospectively studied in Escherichia coli over a 3-year period (1996 to 1998) in 14 French hospitals. The overall frequency of resistant E. coli isolates remained stable at about 5% over this period. The highest frequency of resistant isolates (10 to 15%) was observed, independently of the year, among E. coli isolated from lower respiratory tract samples, and the isolation rate of resistant strains was significantly higher in surgical wards than in medical wards in 1998 (7.8 versus 2.8%). The two most frequent mechanisms of resistance for the 3 years were the hyperproduction of the chromosomal class C β-lactamase (48, 38.4, and 39.7%) and the production of inhibitor-resistant TEM (IRT) enzymes (30.4, 37.2, and 41.2%). By using the single-strand conformational polymorphism–PCR technique and sequencing methods, we determined that 59 IRT enzymes corresponded to previously described IRT enzymes whereas 8 were new. Three of these new enzymes derived from TEM-1 by only one amino acid substitution (Ser130Gly, Arg244Gly, and Asn276Asp), whereas three others derived by two amino acid substitutions (Met69Leu and Arg244Ser, Met69Leu and Ile127Val, and Met69Val and Arg275Gln). The two remaining new IRTs showed three amino acid substitutions (Met69Val, Trp165Arg, and Asn276Asp and Met69Ile, Trp165Cys, and Arg275Gln). New genetic features were also found in blaTEM genes, namely, blaTEM-1B with either the promoters Pa and Pb, P4, or a promoter displaying a C→G transversion at position 3 of the −35 consensus sequence and new blaTEM genes, notably one encoding TEM-1 but possessing the silent mutations originally described in blaTEM-2 and then in some blaTEM-encoding IRT enzymes.
机译:前三年在法国14家医院对大肠埃希菌-克拉维酸耐药性(MIC> 16μg/ ml)和相应的分子机制进行了前瞻性研究,研究期为3年(1996年至1998年)。在此期间,抗性大肠杆菌分离株的总频率保持稳定在大约5%。从下呼吸道样本中分离出的大肠杆菌中,耐药菌的分离率最高(10-15%),与年份无关,并且在1998年,外科病房中耐药菌株的分离率明显高于医学病房。 (7.8比2.8%)。三年中最常见的两种耐药机制是染色体C类β-内酰胺酶的过量生产(48%,38.4%和39.7%)和抑制剂抗性TEM(IRT)酶的产量(30.4、37.2和41.2) %)。通过使用单链构象多态性-PCR技术和测序方法,我们确定59种IRT酶对应于先前描述的IRT酶,而8种是新的。这些新酶中的三种仅通过一个氨基酸取代而衍生自TEM-1(Ser130Gly,Arg244Gly和Asn276Asp),而其他三个则通过两个氨基酸替代而衍生(Met69Leu和Arg244Ser,Met69Leu和Ile127Val,Met69Val和Arg275Gln)。其余两个新的IRT显示了三个氨基酸取代(Met69Val,Trp165Arg和Asn276Asp和Met69Ile,Trp165Cys和Arg275Gln)。在blaTEM基因中也发现了新的遗传特征,即具有启动子Pa和Pb,P4或在-35共有序列第3位显示C→G反转的启动子的blaTEM-1B和新的blaTEM基因,特别是一个编码TEM-1,但具有最初在blaTEM-2和随后在某些blaTEM编码IRT酶中描述的沉默突变。

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