利用中继反应化学发光测定法快速检测细菌对β-内酰胺类抗生素的耐药性

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL ACS Infectious Diseases Pub Date : 2024-05-31 DOI:10.1021/acsinfecdis.3c00682
Zheng Ma, Runqiu Liu, Jie Wang, Tao Yu, Yingqiu Zou, Fangfang Chen, Cui Cui, Huixin Yang and Hexin Xie*, 
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引用次数: 0

摘要

由β-内酰胺酶引起的细菌耐药性已成为全球公共卫生的一大威胁,严重削弱了β-内酰胺类抗生素的疗效,而β-内酰胺类抗生素是目前最广泛使用的治疗传染性疾病的药物。为了快速检测细菌对β-内酰胺类抗生素,尤其是特定类型的β-内酰胺类抗生素的耐药性,我们在此报告一种中继反应化学发光测定法。这种检测方法主要由两种试剂组成:β-内酰胺笼型噻吩酚和对噻吩酚敏感的化学发光报告物,这两种试剂在合成上都是可行的。β-内酰胺酶对 β-内酰胺的选择性水解导致游离苯硫酚的释放,然后以中继方式触发化学发光信号的发射。目前已合成了三种硫酚笼型β-内酰胺类药物,分别是头孢噻吩、头孢他啶和美罗培南的结构类似物。将这种检测方法与这些 β-内酰胺类抗生素类似物结合使用,可以快速检测出表达 β-内酰胺类抗生素的耐药细菌,而且还能提供细菌耐药范围的详细信息。
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Rapid Detection of Bacterial Resistance to β-Lactam Antibiotics with a Relay-Response Chemiluminescence Assay

Bacterial resistance caused by β-lactamases has been a major threat to public health around the world, seriously weakening the efficacy of β-lactam antibiotics, the most widely used therapeutic agents against infectious diseases. To detect the bacterial resistance to β-lactam antibiotics, particularly specific type of β-lactam antibiotics, in a rapid manner, we report herein a relay-response chemiluminescence assay. This assay mainly consists of two reagents: a β-lactam-caged thiophenol and a thiophenol-sensitive chemiluminescence reporter, both of which are synthetically feasible. The selective hydrolysis of β-lactam by β-lactamase leads to the releasing of free thiophenol, which then triggers the emission of a chemiluminescence signal in a relay manner. Three thiophenol-caged β-lactams, structural analogues of cephalothin, cefotaxime, and meropenem, respectively, have been synthesized. And the application of this assay with these analogues of β-lactam antibiotics allows fast detection of β-lactamase-expressing resistant bacteria and, more impressively, provides detailed information on the resistant scope of bacteria.

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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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