用于观察患者样本中革兰氏阳性细菌的远红外荧光探针

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL ACS Infectious Diseases Pub Date : 2024-04-17 DOI:10.1021/acsinfecdis.4c00060
Krittapas Jantarug, Vishwachi Tripathi, Benedict Morin, Aya Iizuka, Richard Kuehl, Mario Morgenstern, Martin Clauss, Nina Khanna, Dirk Bumann and Pablo Rivera-Fuentes*, 
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引用次数: 0

摘要

在高收入国家,革兰氏阳性细菌,尤其是金黄色葡萄球菌(S. aureus),是导致死亡的主要细菌原因,可引起身体各部位的侵入性感染。这些感染会导致长期住院、巨大的经济负担、严重的治疗失败和高死亡率。迄今为止,人们对各种感染期间金黄色葡萄球菌在人体内停留的具体位置了解有限。因此,金黄色葡萄球菌的可视化在微生物研究中具有重要意义。在此,我们报告了一种远红外荧光探针的开发和验证情况,该探针可用于检测人体深部感染活检组织中的革兰氏阳性细菌,重点是葡萄球菌。这种探针在人体组织中显示出较强的荧光和较低的背景,优于目前的金黄色葡萄球菌检测工具。演示了几种应用,包括固定细胞和活细胞成像、流式细胞术和超分辨率细菌成像。
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A Far-Red Fluorescent Probe to Visualize Gram-Positive Bacteria in Patient Samples

Gram-positive bacteria, in particular Staphylococcus aureus (S. aureus), are the leading bacterial cause of death in high-income countries and can cause invasive infections at various body sites. These infections are associated with prolonged hospital stays, a large economic burden, considerable treatment failure, and high mortality rates. So far, there is only limited knowledge about the specific locations where S. aureus resides in the human body during various infections. Hence, the visualization of S. aureus holds significant importance in microbiological research. Herein, we report the development and validation of a far-red fluorescent probe to detect Gram-positive bacteria, with a focus on staphylococci, in human biopsies from deep-seated infections. This probe displays strong fluorescence and low background in human tissues, outperforming current tools for S. aureus detection. Several applications are demonstrated, including fixed- and live-cell imaging, flow cytometry, and super-resolution bacterial imaging.

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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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