阴沟肠杆菌

此外，从环境样品中提取总DNA，通过杂交检测模型初步检测环境中阴沟肠杆菌的DNA浓度。

Furthermore , The DNA concentration of Enterobacter cloacae was detected in the total extracted DNA from environment .

各类抗生素对阴沟肠杆菌的抗菌活性分析

Clinical analysis of antibiotics ′ antimicrobial activity to Enterobacter cloacae

粪产碱菌和阴沟肠杆菌与水稻联合共生的固~（15）N2作用

~ ( 15 ) n_2 fixation of Alcaligenes faecalis and Enterobacter cloacae associated with rice plant

结论：阴沟肠杆菌与沙门菌F群有交叉凝集。

Conclusion : Enterobacter cloacae and Salmonella F group can cross agglutination .

产新型β-内酰胺酶阴沟肠杆菌的耐药性及RAPD分型分析

Analysis of drug resistance and RAPD genotyping of Enterobacter cloacae producing new β - lactamases

采用ERICPCR分型方法分析我院产ESBLs阴沟肠杆菌的流行特征。

ERIC PCR typing was used to investigate the epidemiological characteristics of ESBLs producing strains .

我们根据文献报道，通过PrimerPremier5.0软件设计了实验所需的阴沟肠杆菌和表皮葡萄球菌的捕获探针，识别探针以及目标探针的DNA序列。

The sequences of Enterobacter cloacae and staphylococcus epidermidis genes were designed using software Primer Premier 5.0 according to the literature .

结果：检出一株生化试验符合阴沟肠杆菌，与沙门菌F群血清发生强凝集反应的阴沟肠杆菌。

Results : One strain separated can agglutinate serum of Salmonella F group , but has the same biochemical characterization with Enterobacter cloacae .

AmpC酶和ESBLs介导的阴沟肠杆菌耐药

Resistance Mediated by AmpC β - Lactamase and ESBLs in Enterobacter Cloacae

结果在本组样本的47株阴沟肠杆菌临床分离株中，ESBLs的检出率为38.3%；

RESULTS In this sample , the productive rate of ESBLs was 38.3 % .

阴沟肠杆菌AmpC酶阳性菌株中整合子参与的多重耐药

Integron involved drug-resistant mechanism in AmpC enzyme positive Enterobacter cloacae clinical strains

多重耐药阴沟肠杆菌临床分离株ESBLs基因型别和分子流行病学分析

Multidrug-resistant Clinical Enterobacter cloacae Isolates : Analysis of Their ESBLs Gene Types and Molecular Epidemiology

高产AmpC酶阴沟肠杆菌的耐药性及同源性分析

Highly Producing AmpC Enzymes Enterobacter cloacae : Its Multiple Resistance and Homology Analysis

阴沟肠杆菌B8发酵液对植物的促生作用和IAA分析

Promoting plant growth and IAA analysis of Enterobacter cloacae B8 fermentation liquid

阴沟肠杆菌产AmpC酶菌和非产酶菌的耐药性研究

Study on the drug-resistance of Enterobacter cloacae producing AmpC and non producing AmpC enzyme

结果表型筛选法对58株阴沟肠杆菌检测的结果显示产ESBLs菌株的检出率为34.48%（20/58）。

Results Results of phenotype screening test showed 20 strains ( 34.48 % ) produced ESBLs enzymes .

阴沟肠杆菌可产生染色体介导的诱导型C类头孢菌素酶即AmpC酶，这一点对于临床治疗成败和抗生素的合理应用具有重要意义。

Enterobacter cloacae may produce chromosome-mediated inducible class C cephalosporinase , named AmpC enzyme which is important to clinical therapy and reasonable usage of antibiotic .

用纸片双抑制剂平行抑制试验分析阴沟肠杆菌AmpC酶

Analysis of AmpC enzyme in Enterobacter cloacae isolates by disk double inhibitor parallel inhibit test

K-B法和三维分析法测定阴沟肠杆菌AmpC酶结果分析

Kirby-Bauer Method and Three-dimensional Test Detected AmpC Enzyme in Enterobacter cloacae : Analysis of Results

产AmpC酶阴沟肠杆菌的耐药性及耐药结构基因的序列分析

Nucleotide Sequence Analysis of AmpC Structure Gene of Strains of Enterobacter Cloacae Producing Ampc and Its Resistance

ESBLs在大肠埃希菌、肺炎克雷伯菌和阴沟肠杆菌中的检出率及耐药情况比较

Comparison of detection and resistant rates of ESBLs among Escherichia coli , Klebsiella pneumoniae and Enterobacter cloacae isolates in China

阴沟肠杆菌AmpC酶检测及对酶抑制剂复合制剂稳定性研究

Detection of AmpC β - Lactamases from Enterobacter cloacae and Study of Stability to Compound Agents of Enzyme Inhibitors

β-内酰胺类抗生素对阴沟肠杆菌高产AmpC酶突变的选择作用

Potential of Six β - Lactams to Select Mutants with Depressed AmpC β - Lactamase Synthesis from Enterobacter cloacae

目的研究南昌地区大肠埃希菌、肺炎克雷伯菌和阴沟肠杆菌产ESBLs情况及耐药谱；检测三种细菌产PER－1型ESBLs的情况以及产PER－1型ESBLs菌株的耐药特点；

Study on PER-1 type ESBLs produced by Enterobacteriaceae is necessary Objective To investigate the prevalence of ESBLs in Escherichia coli Klebsiella pneumonia and Enterobact cloacae and their antimicrobial-resistance profile ;

VAP的主要致病菌为肺炎克雷伯菌、铜绿假单胞菌、不动杆菌属、阴沟肠杆菌。

Klebsiella pneumoniae , ~ Pseudomonas aeruginosa , Acinetobacter spp , and Enterobacter cloacae were the main pathogenic bacteria of VAP .

Thr70残基替换对阴沟肠杆菌AmpC酶底物特性的影响

Effect of The Substitution of Threonine at Residue 70 in Enterobacter cloacae AmpC β - lactamase on Its Substrate Specificity

国内首次发现携带耶尔森菌HPI毒力岛irp~（-2）基因的阴沟肠杆菌

Identification of HIP virulent irp ~ ( - 2 ) gene of Yersinia Yersinia enterocolitica in Enterobacter cloacae

结论表型筛选法是一种结果可靠、操作快速简便、适于微生物实验室常规开展的检测阴沟肠杆菌产AmpC酶的方法。

Conclusions Phenotype screening test is reliable to detect AmpC β - lactamase and easy to use in department of microbiology .

目的了解阴沟肠杆菌产AmpC酶的状况及对酶抑制剂复合制剂的稳定性。

OBJECTIVE To investigate the production of AmpC β lactamases from Enterobacter cloacae and the stability to the compound agents of enzyme inhibitors .

目的分析导致高产AmpC酶阴沟肠杆菌感染的临床危险因素。

OBJECTIVE To investigate the clinical factors of Enterobacter cloacae infections with high-level AmpC β - lactamase . METHODS The cases infected by E.