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亚胺培南耐药铜绿假单胞菌的金属β-内酰胺酶检测 被引量:23
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作者 余广超 徐霖 +7 位作者 袁广卿 张甜 陈康 蒋岗 姜余琴 许沙沙 常彦敏 曹开源 《中国抗生素杂志》 CAS CSCD 北大核心 2011年第3期223-227,共5页
目的了解金属β-内酰胺酶在广州地区铜绿假单胞菌中的流行状况及其流行亚型,完善广州地区金属β-内酰胺酶的分子流行病学资料。方法采用双纸片协同法和双纸片增效法对164株亚胺培南耐药的铜绿假单胞菌筛选金属β-内酰胺酶表型阳性的菌株... 目的了解金属β-内酰胺酶在广州地区铜绿假单胞菌中的流行状况及其流行亚型,完善广州地区金属β-内酰胺酶的分子流行病学资料。方法采用双纸片协同法和双纸片增效法对164株亚胺培南耐药的铜绿假单胞菌筛选金属β-内酰胺酶表型阳性的菌株,采用PCR检测5类金属β-内酰胺酶的编码基因(IMP家族、VIM家族、GIM-1、SPM-1和SIM-1),利用生物信息学的方法对检测到的金属β-内酰胺酶亚型进行比对分析并制作分子进化树。结果 164株亚胺培南耐药的铜绿假单胞菌中筛选出22株金属β-内酰胺酶表型阳性的菌株,IMP阳性15株(9.1%),其中11株为IMP-9亚型,另外4株携带一个新的亚型,命名为IMP-25,VIM阳性5株(3.0%),均为VIM-2亚型,未检测到GIM-1、SPM-1和SIM-1型金属β-内酰胺酶。结论广州地区铜绿假单胞菌产金属β-内酰胺酶的基因型已经出现多型化的特征,同时存在IMP型和VIM型金属β-内酰胺酶的流行,本次研究发现了一个新的金属β-内酰胺酶亚型(IMP-25),为IMP家族金属β-内酰胺酶的多样性及其分子流行病学资料提供了新的信息。 展开更多
关键词 铜绿假单胞菌 金属β-内酰胺酶 耐药基因
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耐亚胺培南铜绿假单胞菌的金属β-内酰胺酶检测 被引量:9
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作者 唐慧琴 陈定强 吴爱武 《中国卫生检验杂志》 北大核心 2014年第6期831-833,共3页
目的了解耐亚胺培南铜绿假单胞菌产金属β-内酰胺酶(MBL)的分离率以及编码MBL的基因型别。方法采用双纸片协同试验结合增强试验对116株耐亚胺培南铜绿假单胞菌进行MBL的表型检测,同时采用多重PCR及普通PCR进行MBL的编码基因(包括VIM型,... 目的了解耐亚胺培南铜绿假单胞菌产金属β-内酰胺酶(MBL)的分离率以及编码MBL的基因型别。方法采用双纸片协同试验结合增强试验对116株耐亚胺培南铜绿假单胞菌进行MBL的表型检测,同时采用多重PCR及普通PCR进行MBL的编码基因(包括VIM型,IMP型,SPM型,GIM型,NDM型,SIM型,DIM型,AIM型)检测。结果116株耐亚胺培南铜绿单胞菌中筛选出7株(6%)MBL表型阳性的菌株,用分子生物学的方法也检测出7株金属酶基因阳性的菌株(6%),其中VIM基因阳性的有2株(1.7%),IMP基因阳性的有5株(4.3%),其他基因型均阴性;经过测序和比对分析发现2株菌携带的MBL基因型为VIM-2,5株菌所携带的MBL基因型为IMP-9。结论此次检测铜绿假单胞菌金属β-内酰胺酶的基因型以IMP-9型和VIM-2型流行为主,尚未发现其他型别的基因型。 展开更多
关键词 铜绿假单胞菌 金属β-内酰胺酶 耐药基因 表型
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Evaluation of Disk Potentiation Test (DPT) and Double Disk Synergy Test (DDST) for The Detection of Metallo-β-Lactamases (MBLs) in Clinical Isolates of Bangladesh
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作者 Sumon Kumar Das Afzal Sheikh +4 位作者 Nikhat Ara Suma Mita Biswas Abhinandan Chowdhury Fatimah Az Zahra Chaman Ara Keya 《Advances in Infectious Diseases》 2023年第4期609-626,共18页
Objective: Increasing the emergence of Metallo-β-lactamase (MBL) producing gram-negative bacteria and their dexterous horizontal transmission demands rapid and accurate detection. This study was conducted to determin... Objective: Increasing the emergence of Metallo-β-lactamase (MBL) producing gram-negative bacteria and their dexterous horizontal transmission demands rapid and accurate detection. This study was conducted to determine a suitable method to promptly detect MBL-producing gram-negative bacteria. Methods: A total of 103 gram-negative bacteria were identified from various clinical samples at a tertiary care hospital in Dhaka city. MBL producers were detected by two phenotypic methods, the Disk Potentiation Test (DPT) and the Double Disk Synergy Test (DDST) based on β-lactam chelator combinations where EDTA/SMA has been used as an inhibitor and Imipenem, Ceftazidime as substrates. Results: 103 isolates which were identified as Escherichia coli spp, Klebsiella spp, Pseudomonas spp, Acinetobacter spp, Proteus spp, Providencia spp were found to be multidrug-resistant in antibiogram test. Isolates showed complete resistance (100%) to Imipenem, Meropenem, and Amoxiclav. The highest carbapenem-resistant etiological agents were Acinetobacter spp 40 (38.8%) followed by Pseudomonas spp 27 (26.2%), Klebsiella spp 26 (25.2%), Escherichia coli 8 (7.8%), Proteus spp 1 (1%) and Providencia spp 1 (1%). DPT method detected significantly (p = 0.000009) a higher number of MBL-producers (Imipenem with 0.5 M EDTA n = 61, 59.2% & Ceftazidime with 0.5 M EDTA n = 56, 54.4%) compared to the DDST method (Imipenem -0.5 M EDTA n = 43, 41.7%, Imipenem – SMA n = 38, 36.9% & Ceftazidime -0.5 M EDTA n = 15, 14.6%). Conclusion: Pieces of evidence suggest that DPT is a more sensitive method than DDST and could be recommended for identifying MBL-producing bacteria in Bangladeshi hospitals for the proper management of patients, to reduce time constraints and treatment costs. 展开更多
关键词 Disk Potentiation Test (DPT) Double Disk Synergy Test (DDST) metallo-β-lactamase (mbl) Sodium Mercaptoacetate (SMA) and Ethylenediaminetetraacetic Acid (EDTA)
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