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国家自然科学基金(31060348)

作品数:3 被引量:10H指数:2
相关作者:周学章贾芳张仁参更多>>
相关机构:宁夏大学更多>>
发文基金:国家自然科学基金宁夏回族自治区科技厅科技攻关项目国家重点基础研究发展计划更多>>
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宁夏牛源克雷伯菌和大肠埃希菌分离株产超广谱β-内酰胺酶基因型检测被引量:3
2010年
为了解宁夏牛源产超广谱β-内酰胺酶(ESBLs)肺炎克雷伯菌(Klebsiella pneumonia)和大肠埃希菌(Esche-richia coli)的耐药性和基因型分布,采用美国临床实验室标准化研究所(CLSI)2008年推荐的双纸片确证试验,对宁夏地区100株克雷伯菌和大肠埃希菌进行产ESBLs确定,并采用PCR扩增法和克隆测序法对产ESBLs菌株进行基因分型.结果显示,宁夏地区有42株产ESBLs菌株,阳性率为42%;其中31株菌扩增呈阳性,产TEM型菌17株,产SHV型菌14株,产CTX型菌15株;同时产3种基因型菌1株,同时产2种基因型菌13株,产单一基因型菌17株,分别占产ESBLs菌株的2.38%,30.95%,40.48%;多表现为多重耐药.
周学章张仁参贾芳吴彦虎
关键词:克雷伯菌大肠埃希菌超广谱Β-内酰胺酶基因型
SHV-12型超广谱β-内酰胺酶的原核表达及免疫原性分析被引量:1
2011年
利用PCR技术扩增了SHV-12 ESBLs目的基因,并将目的基因亚克隆到表达载体pET-28a(+)中,获得重组质粒pET-28a-SHV-12转化于表达菌株BL21(DE3)中诱导表达,表达蛋白纯化后经SDS-PAGE电泳分析.结果表明,目的蛋白SHV-12 ESBLs相对分子质量为30 KDa,经蛋白质印迹检测证明具有特异性条带,经头孢硝基噻吩显色反应表明获得了有活力的ESBLs,包涵体作为免疫抗原免疫Balb/c小鼠,3次免疫后利用间接ELISA法测定免疫效价达到1∶106.获得了可靠而稳定的免疫原.
贾芳周学章
关键词:抗体效价
Total Alkaloids from Sophora Alopecuroides L.Increase Susceptibility of Extended-Spectrum β-Lactamases Producing Escherichia coli Isolates to Cefotaxime and Ceftazidime被引量:6
2013年
Objective: To evaluate the antimicrobial activity of total alkaloids extracted from Sophorea alopecuroides L. (TASA) against clinical isolated extended-spectrum beta-lactamases (ESBLs) producing Escherichia coil (E.. coil) strains. Methods: The antibacterial activity of TASA either itself or in combination with cefotaxime (CTX) or ceftazidime (CAZ) was investigated by using the microbroth dilution method and phenotypic confirmatory disk diffusion test against three clinical isolated ESBLs-producing E. coil strains; the interactions of TASA and C'I'X or CAZ were ascertained by evaluating the fractional inhibitory concentration index (FICI). Results: The antibacterial activity of either TASA itself or in combination with C'IX or CAZ was found. The minimum inhibitory concentration (MICs) of TASA against the ESBLs producing isolates was 12.5 mg/mL. In the combinations with a sub-inhibitory concentration of TASA, a synergistic effect on CTX and CAZ against the ESBLs producing isolates was observed. Similarly, the isolates exposed to lower dose of TASA yielded an increased susceptibility to CTX and CAZ by 8-16 folds determined by microdilution assay. Moreover, enzymatic detection of ESBLs demonstrated that TASA induced reversal resistance to CTX and CAZ partially by a mechanism of inhibition of ESBLs activity in these isolates. Additionally, in the tested isolates following the exposure of TASA, molecular analysis verified the SHV-type beta-lactamase encoding ESBL gene in these isolates, and no mutation was introduced into the ESBL gene. Conclusions: These results suggest that TASA could be used as a source of natural compound with pharmacological activity of reversal resistance to antimicrobial agent. These findings also indicated that the application of the TASA in combination with antibiotics might prove useful in the control and treatment of infectious diseases caused by the ESBLs producing enterobacteriaceae.
周学章贾芳刘晓明杨聪赵莉王玉炯
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