摘要
为了探求院内感染革兰氏阴性杆菌产生超广谱β内酰胺酶的基因决定机制,我们采用DNA斑点杂交技术对所选临床分离的产β内酰胺的大肠埃希氏菌、克雷伯氏菌等进行了其质粒介导的β内酰胺酶基因类型分析。对20株菌质粒用TEM1探针检测的结果如下:11株大肠埃希氏菌全与TEM1探针杂交;6株肺炎克雷伯氏菌有3株与TEM1探针杂交;1株已证明含有SHV2超广谱β内酰胺酶的日勾维肠杆菌未与TEM1探针杂交;2株不动杆菌有1株(溶血不动杆菌)与TEM1探针杂交。
To detect the genic mechanism of ExtendedSpectrum βlactamase(Esbla)in clinical nosocomial gram negative isolates.DNA blotting hybridization was used to analyse plasmids of 20 isolates which produced βlactamase including E.Coli,K.Pneumoniae etc.The results show that 11 E.Coli are TEM1 probe positive;3 of 6 K.pneumoniae have TEM fragment;1 E.gergoviae which has been proved to have SHV2 Esbla was TEM1 negative and 2 acintobacter can't hybridize with TEM1 probe.
出处
《华西医学》
CAS
1998年第1期102-104,共3页
West China Medical Journal