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产质粒介导喹诺酮类耐药决定因子的临床肺炎克雷伯菌分离株中β-内酰胺酶和 16S rRNA 甲基化酶基因的流行率。

Prevalence of β-lactamases and 16S rRNA methylase genes amongst clinical Klebsiella pneumoniae isolates carrying plasmid-mediated quinolone resistance determinants.

机构信息

Department of Microbiology, Chinese PLA General Hospital, 28# Fuxing Road, Beijing 100853, China.

出版信息

Int J Antimicrob Agents. 2011 Apr;37(4):352-5. doi: 10.1016/j.ijantimicag.2010.12.018. Epub 2011 Mar 3.

Abstract

To characterise the prevalence of β-lactamases and 16S rRNA methylase genes amongst clinical Klebsiella pneumoniae isolates carrying plasmid-mediated quinolone resistance (PMQR) determinants in China, 59 non-duplicate K. pneumoniae isolates harbouring at least one PMQR gene were screened for common β-lactamases and 16S rRNA methylases genes. The genetic relatedness of the isolates was analysed by pulsed-field gel electrophoresis (PFGE). Most of PMQR gene-positive isolates carried no substitutions within the quinolone resistance-determining regions (QRDRs) or single point mutation in GyrA or ParC. Over one-half (52.5%) of the isolates exhibited decreased susceptibility to ciprofloxacin [minimum inhibitory concentration (MIC)=0.5-2 μg/mL] or low-level resistance to ciprofloxacin (MIC=4-8 μg/mL). qnr, aac(6')-Ib-cr and qepA were positive in 52 (88.1%), 16 (27.1%) and 3 (5.1%) isolates, respectively. The identified genes for β-lactamases were distributed as follows: bla(TEM), 50.8%; bla(SHV), 91.5%; bla(CTX-M), 55.9%; bla(DHA), 59.3%; and bla(OXA-1), 22.1%. armA and rmtB were detected in 16.9% and 3.4% of isolates, respectively. All qnrB were detected in DHA-producing K. pneumoniae. Approximately 81.3%, 68.8% and 43.8% of aac(6')-Ib-cr carrying isolates produced OXA-1, DHA and ArmA, respectively. In conclusion, owing to few QRDR substitutions, most of the PMQR gene-carrying K. pneumoniae isolates exhibited low-level resistance to fluoroquinolones. qnr appears to be the predominant PMQR gene and it presented a significant correlation with bla(SHV), bla(CTX-M) and bla(DHA), whereas aac(6')-Ib-cr exhibited a close relationship with bla(OXA-1), bla(DHA) and armA. qepA was rarely detected in this study.

摘要

为了描述在中国携带质粒介导的喹诺酮耐药(PMQR)决定因子的临床肺炎克雷伯菌分离株中β-内酰胺酶和 16S rRNA 甲基酶基因的流行情况,筛选了 59 株至少携带一种 PMQR 基因的非重复肺炎克雷伯菌分离株,以检测常见的β-内酰胺酶和 16S rRNA 甲基酶基因。通过脉冲场凝胶电泳(PFGE)分析分离株的遗传相关性。大多数 PMQR 基因阳性分离株在喹诺酮耐药决定区(QRDRs)内没有取代或在 GyrA 或 ParC 中只有单个点突变。超过一半(52.5%)的分离株对环丙沙星的敏感性降低[最小抑菌浓度(MIC)=0.5-2μg/ml]或对环丙沙星的低水平耐药(MIC=4-8μg/ml)。qnr、aac(6')-Ib-cr 和 qepA 在 52(88.1%)、16(27.1%)和 3(5.1%)株中阳性,分别。鉴定的β-内酰胺酶基因分布如下:bla(TEM),50.8%;bla(SHV),91.5%;bla(CTX-M),55.9%;bla(DHA),59.3%;bla(OXA-1),22.1%。armA 和 rmtB 在 16.9%和 3.4%的分离株中分别检测到。所有 qnrB 均在 DHA 产生的肺炎克雷伯菌中检出。携带 aac(6')-Ib-cr 的分离株中分别有 81.3%、68.8%和 43.8%产生 OXA-1、DHA 和 ArmA。总之,由于 QRDR 取代较少,大多数携带 PMQR 基因的肺炎克雷伯菌分离株对氟喹诺酮类药物表现出低水平耐药。qnr 似乎是主要的 PMQR 基因,它与 bla(SHV)、bla(CTX-M)和 bla(DHA)呈显著相关性,而 aac(6')-Ib-cr 与 bla(OXA-1)、bla(DHA)和 armA 密切相关。本研究中很少检测到 qepA。

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