Specific detection of antibiotic-resistant bacteria using CRISPR/Cas9 induced isothermal exponential amplification reaction (IEXPAR)

化学 细菌 环介导等温扩增 清脆的 抗生素 微生物学 DNA 生物化学 基因 遗传学 生物
作者
Ke Qin,Pengbo Zhang,Zhengping Li
出处
期刊:Talanta [Elsevier]
卷期号:253: 124045-124045 被引量:8
标识
DOI:10.1016/j.talanta.2022.124045
摘要

The prevalence of antibiotic-resistant bacterial infections has raised great social concern and even aggravated the burden of public healthcare systems worldwide. Simple, rapid, highly sensitive and specific detection of antibiotic-resistant bacteria is urgently needed for guiding proper antibiotic treatment. Herein, we demonstrate a novel strategy to specifically distinguish and detect antibiotic-resistant bacteria using CRISPR/Cas9 induced isothermal exponential amplification reaction (IEXPAR). Through the specific recognition and cleavage of CRISPR/Cas9 system, the antibiotic-resistant genes can be digested into two short segments with free 3ʹ-OH end. Using one of the cleaved DNA as target to design IEXPAR template (Xʹ-Y-Xʹ), highly efficient exponential amplification of IEXPAR can be triggered, resulting in the direct detection of antibiotic-resistant genes under isothermal condition with high accuracy and rapidness. While for antibiotic-sensitive bacteria, CRISPR/Cas9 system cannot cleave any DNA due to the absence of antibiotic-resistant genes and no subsequent amplification reaction occurs which ensures the high specificity of our method. Further applying our method to the detection of real biological samples, the specific discrimination of antibiotic-resistant bacteria from antibiotic-sensitive bacteria is realized even with large amounts of DNA interferents. In consideration of the distinct advantages of rapid, high specificity and facile operation, this CRISPR/Cas9-induced IEXPAR assay may serve as an efficient and convenient tool for the accurate detection of antibiotic-resistant bacteria in complex biological samples. • A CRISPR/Cas9 induced isothermal exponential amplification reaction is developed. • CRISPR/Cas9 can specifically recognize and cleave antibiotic-resistant genes. • One of the cleaved genes can trigger IEXPAR using simply designed template. • Antibiotic-resistant bacteria can directly discriminate from other bacteria. • This method has applied to the detection of antibiotic-resistant bacteria in biological samples.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Ava应助佳丽采纳,获得10
刚刚
Xicuws发布了新的文献求助10
2秒前
刘刘溜完成签到 ,获得积分10
3秒前
SciGPT应助眼睛大傲之采纳,获得10
3秒前
ccrr完成签到 ,获得积分10
3秒前
付创发布了新的文献求助30
4秒前
研友_ng9Mg8完成签到,获得积分10
4秒前
情怀应助砂浆黏你采纳,获得20
6秒前
科研通AI5应助Kemmy采纳,获得10
6秒前
8秒前
蜜雪冰城完成签到,获得积分10
8秒前
科研通AI5应助move采纳,获得10
9秒前
科研通AI2S应助陈小鬼采纳,获得10
10秒前
可爱的函函应助qks采纳,获得10
11秒前
11秒前
11秒前
王小明发布了新的文献求助10
12秒前
星辰大海应助卡哇伊骨头采纳,获得10
12秒前
科研通AI5应助单薄的咖啡采纳,获得10
13秒前
牛角尖完成签到,获得积分10
13秒前
14秒前
汉堡包应助jackdu采纳,获得10
14秒前
我是老大应助兴奋巧凡采纳,获得10
16秒前
无私绿兰完成签到 ,获得积分10
17秒前
大方梦安发布了新的文献求助10
17秒前
Lucas应助奶油布丁采纳,获得10
18秒前
wylbdhj发布了新的文献求助10
19秒前
梅子完成签到 ,获得积分10
20秒前
ID8发布了新的文献求助10
21秒前
22秒前
DrJiang完成签到,获得积分10
23秒前
Tony完成签到,获得积分10
25秒前
传奇3应助rebecka采纳,获得10
26秒前
搜集达人应助眼睛大天思采纳,获得10
26秒前
jingjun_Li发布了新的文献求助10
27秒前
28秒前
领导范儿应助swordlee采纳,获得10
28秒前
秋荆完成签到,获得积分10
28秒前
31秒前
31秒前
高分求助中
Continuum Thermodynamics and Material Modelling 3000
Production Logging: Theoretical and Interpretive Elements 2700
Mechanistic Modeling of Gas-Liquid Two-Phase Flow in Pipes 2500
Structural Load Modelling and Combination for Performance and Safety Evaluation 800
Conference Record, IAS Annual Meeting 1977 610
Interest Rate Modeling. Volume 3: Products and Risk Management 600
Interest Rate Modeling. Volume 2: Term Structure Models 600
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 量子力学 光电子学 冶金
热门帖子
关注 科研通微信公众号,转发送积分 3555360
求助须知:如何正确求助?哪些是违规求助? 3130973
关于积分的说明 9389383
捐赠科研通 2830472
什么是DOI,文献DOI怎么找? 1556047
邀请新用户注册赠送积分活动 726376
科研通“疑难数据库(出版商)”最低求助积分说明 715738