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A sensitive colorimetric assay for identification of Acinetobacter baumannii using unmodified gold nanoparticles

机译:使用未修饰的金纳米粒子鉴定鲍曼不动杆菌的灵敏比色法

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摘要

Aims: Acinetobacter baumannii is a global health problem, which threatens many healthcare settings. The current study aims to develop a detection assay for Ac. baumannii using unmodified gold nanoparticles (AuNPs). Methods and Results: Fifty-three Ac. baumannii clinical isolates were collected from Egyptian hospitals. Bacterial isolation and biochemical identification of isolates were carried out followed by DNA extraction using boiling method and PCR amplification of the 23S-16S rRNA intergenic spacer sequences (ITS). AuNPs were synthesized using citrate reduction method. Detection and optimization of Ac. baumannii amplicons using unmodified spherical AuNPs were performed using species-specific DNA oligonucleotide. The nano-gold assay was able to colorimetrically detect and distinguish Ac. baumannii from other Gram-negative bacteria. The turnaround time of the assay is about 2 h including sample treatment and amplification. The assay detection limit is 0.8125 ng of DNA. Conclusions: The developed colorimetric assay is sensitive, fast and reliable and can be used for identification of Ac. baumannii. Significance and Impact of the Study: There is a need to develop robust, rapid, and specific methods for detection of Ac. baumannii isolated from clinical specimens. The developed nanogold assay prototype allows sensitive, specific and rapid detection of amplified DNA of A. baumannii and represents a reliable diagnostic tool to aid routine laboratory identification of this pathogen
机译:目的:鲍曼不动杆菌是一个全球性的健康问题,威胁着许多医疗机构。当前的研究旨在开发一种Ac检测方法。使用未修饰的金纳米粒子(AuNP)的鲍曼氏菌。方法和结果:53 Ac。鲍曼氏菌临床分离株是从埃及医院收集的。进行细菌分离和分离物的生化鉴定,然后使用煮沸法进行DNA提取和23S-16S rRNA基因间隔子序列(ITS)的PCR扩增。使用柠檬酸盐还原法合成AuNP。 Ac的检测和优化。使用未修饰的球形AuNPs进行的鲍曼氏扩增子是使用物种特异性DNA寡核苷酸进行的。纳米金测定能够比色检测和区分Ac。来自其他革兰氏阴性细菌的鲍曼不动杆菌。测定的周转时间约为2小时,包括样品处理和扩增。分析检测限为0.8125 ng DNA。结论:开发的比色法灵敏,快速,可靠,可用于鉴定Ac。鲍曼尼研究的意义和影响:有必要开发一种健壮,快速且特定的方法来检测Ac。从临床标本中分离出鲍曼氏菌。开发的纳米金检测原型可以灵敏,特异和快速地检测鲍曼不动杆菌的扩增DNA,并代表一种可靠的诊断工具,有助于常规实验室鉴定该病原体

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