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首页> 外文期刊>Journal of Clinical Microbiology >Identification of clinical isolates of indole-positive Klebsiella spp., including Klebsiella planticola, and a genetic and molecular analysis of their beta-lactamases.
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Identification of clinical isolates of indole-positive Klebsiella spp., including Klebsiella planticola, and a genetic and molecular analysis of their beta-lactamases.

机译:鉴定吲哚阳性克雷伯菌属的种,包括植物克雷伯菌,并对它们的β-内酰胺酶进行遗传和分子分析。

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In a collection of 43 indole-positive Klebsiella clinical isolates, which were initially identified as Klebsiella oxytoca, there were 18 isolates which exhibited a pattern characteristic of extended-spectrum beta-lactamase (ESBL) resistance. This study aimed to confirm their identity by biochemical tests and by PCR and to determine the genetic basis for their resistance to the beta-lactams and broad-spectrum cephalosporins. Chromosomal beta-lactamase genes were analyzed by PCR, and plasmid-mediated beta-lactamase genes were analyzed by conjugation and transformation. There were 39 isolates which grew on melezitose but failed to grow on 3-hydroxybutyrate, confirming them as K. oxytoca. PCR analysis of their beta-lactamase genes divided these isolates into two groups, the bla(OXY-1) group and the bla(OXY-2) group. Each group had beta-lactamases with different isoelectric points; the bla(OXY-1) group had beta-lactamases with isoelectric points at 7.2, 7.8, 8.2, and 8.8, and the more common bla(OXY-2) group had beta-lactamases with pIs at 5.2, 5.4 (TEM-1), 5.7, 5.9, 6.4, and 6.8. A pI of 5.2 was the most frequently detected and accounted for 59% of all the bla(OXY-2) beta-lactamases. Hyperproduction of clavulanate-inhibited chromosomal beta-lactamases was detected in 17 K. oxytoca isolates, resulting in an ESBL phenotype. K. oxytoca isolates having a plasmid-mediated genetic basis for their ESBL phenotype were not found, confirming that, in K. oxytoca, plasmids are rarely involved in conferring resistance to the newer cephalosporins. Four isolates proved to be isolates of K. planticola in which the beta-lactamase genes failed to react with the primers used in the PCR. One K. planticola isolate contained a transferable plasmid harboring the SHV-5 beta-lactamase gene and showed an ESBL phenotype, while the other non-ESBL K. planticola isolates contained chromosomal beta-lactamases with isoelectric points at 7.2, 7.7, and 7.9 plus 7.2.
机译:在最初被鉴定为产酸克雷伯菌的43种吲哚阳性克雷伯菌临床分离株中,有18种表现出对广谱β-内酰胺酶(ESBL)耐药的特征性菌株。这项研究旨在通过生化测试和PCR来确认其身份,并确定其对β-内酰胺类和广谱头孢菌素的耐药性的遗传基础。通过PCR分析染色体β-内酰胺酶基因,并通过缀合和转化分析质粒介导的β-内酰胺酶基因。有39个分离物在松三糖上生长,但在3-羟基丁酸酯上不能生长,证实它们是产氧假丝酵母。其β-内酰胺酶基因的PCR分析将这些分离物分为两组,bla(OXY-1)组和bla(OXY-2)组。每组具有不同等电点的β-内酰胺酶。 bla(OXY-1)组的β-内酰胺酶的等电点分别为7.2、7.8、8.2和8.8,更常见的bla(OXY-2)组的β-内酰胺酶的pIs分别为5.2、5.4(TEM-1 ),5.7、5.9、6.4和6.8。 pI值为5.2,是最常检测到的,占所有bla(OXY-2)β-内酰胺酶的59%。在17个催产克氏杆菌分离物中检测到了克拉维酸抑制的染色体β-内酰胺酶的过量生产,从而导致了ESBL表型。未发现具有其ESBL表型具有质粒介导的遗传基础的催产克氏菌分离株,这证实在催产克氏杆菌中,质粒很少涉及赋予对较新的头孢菌素的抗性。四个分离株被证明是K. planticola的分离株,其中β-内酰胺酶基因无法与PCR中使用的引物反应。一个植物分离株含有一个带有SHV-5β-内酰胺酶基因的可转移质粒,表现出ESBL表型,而其他非ESBL植物分离株则含有等电点分别为7.2、7.7和7.9的染色体β-内酰胺酶。 7.2。

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