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革兰氏阴性菌门把手污染物中超广谱β-内酰胺酶的基因特征在奥巴西·奥纳班琼大学教学医院,萨盖姆,奥贡州。

Genotypic characterization of extended spectrum beta-lactamase in gram negative bacterial contaminants of some door handles in Olabisi Onabanjo University Teaching Hospital, Sagamu, Ogun state.

机构信息

Department of Pharmaceutical Microbiology, Faculty of Pharmacy, Olabisi Onabanjo University, Sagamu, Ogun state.

Department of Medical Microbiology and Parasitology, Olabisi Onabanjo University Teaching Hospital, Sagamu, Ogun state.

出版信息

Afr Health Sci. 2023 Jun;23(2):208-218. doi: 10.4314/ahs.v23i2.23.

Abstract

BACKGROUND

Nosocomial infections due to cross-transmission by microorganisms from inanimate surfaces have become a recognized public health problem.

OBJECTIVES

This research was carried out to detect bacterial contaminants of door handles and their production of extended spectrum beta-lactamase (ESBL) in Olabisi Onabanjo University Teaching Hospital.

METHODS

Seventy door handles from twenty-seven sections of Olabisi Onabanjo University Teaching Hospital were swabbed and inoculated on different culture media. The isolates were identified using standard microbiological procedures. Susceptibility of the isolates to eleven antibiotics was determined by Kirby- Bauer disc diffusion test. Phenotypic detection of ESBL was determined by modified double disc synergy test (MDDST) followed by PCR amplification of ESBL- encoding genes.

RESULTS

Forty-four (62.9%) out of 70 door swabs were positive for bacterial growth. was the most common isolate (22.9%). Multidrug resistance was observed in 15(79.0%) and 20(69%) of Gram positive and Gram-negative isolates, respectively. Coagulase negative staphylococci, and species were totally resistant to ceftazidime (100%). PCR amplification of ESBL-genes revealed the presence of blaTEM blaCTX -M and blaSHV in 4(14.3%), 2(7.2%) and 1(3.6%) isolate, respectively.

CONCLUSION

This study revealed that door handles of different sections in hospital environment were contaminated by multidrug resistant Gram-negative bacteria encoding ESBL genes.

摘要

背景

由于微生物从无生命表面的交叉传播而导致的医院感染已成为公认的公共卫生问题。

目的

本研究旨在检测拉各斯大学教学医院门把手的细菌污染物及其产生的扩展谱β-内酰胺酶(ESBL)。

方法

从拉各斯大学教学医院的 27 个科室中采集了 70 个门把手进行拭子采样,并接种在不同的培养基上。使用标准微生物学程序对分离物进行鉴定。采用 Kirby-Bauer 纸片扩散试验测定分离物对 11 种抗生素的敏感性。通过改良的双碟协同试验(MDDST)检测 ESBL 的表型,并通过 ESBL 编码基因的 PCR 扩增来检测 ESBL。

结果

70 个门把手拭子中,有 44 个(62.9%)呈细菌生长阳性。 是最常见的分离株(22.9%)。革兰氏阳性和革兰氏阴性分离株中分别有 15 株(79.0%)和 20 株(69%)表现出多药耐药性。凝固酶阴性葡萄球菌、 和 对头孢他啶(100%)完全耐药。ESBL 基因的 PCR 扩增显示,4 株(14.3%)、2 株(7.2%)和 1 株(3.6%)分离株分别携带 blaTEM、blaCTX-M 和 blaSHV 基因。

结论

本研究表明,医院环境中不同科室的门把手被携带 ESBL 基因的多药耐药性革兰氏阴性细菌污染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf0/10782325/73e9eb9ab89b/AFHS2302-0208Fig1.jpg

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