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Whole Slide Imaging for High-Throughput Sensing Antibiotic Resistance at Single-Bacterium Level and Its Application to Rapid Antibiotic Susceptibility Testing

机译:用于高通量感测单细菌水平的抗生素抗性的整体滑动成像及其在快速抗生素易感测试中的应用

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摘要

Since conventional culture-based antibiotic susceptibility testing (AST) methods are too time-consuming (typically 24−72 h), rapid AST is urgently needed for preventing the increasing emergence and spread of antibiotic resistant infections. Although several phenotypic antibiotic resistance sensing modalities are able to reduce the AST time to a few hours or less, concerning the biological heterogeneity, their accuracy or limit of detection are limited by low throughput. Here, we present a rapid AST method based on whole slide imaging (WSI)-enabled high-throughput sensing antibiotic resistance at single-bacterium level. The time for determining the minimum inhibitory concentration (MIC) was theoretically shortest, which ensures that the growth of each individual cell present in a large population is inhibited. As a demonstration, our technique was able to sense the growth of at least several thousand bacteria at single-cell level. Reliable MIC of Enterobacter cloacae against gentamicin was obtained within 1 h, while the gold standard broth dilution method required at least 16 h for the same result. In addition, the application of our method prevails over other imaging-based AST approaches in allowing rapid and accurate determination of antibiotic susceptibility for phenotypically heterogeneous samples, in which the number of antibiotic resistant cells was negligible compared to that of the susceptible cells. Hence, our method shows great promise for both rapid AST determination and point-of-care testing of complex clinical bacteria isolates.
机译:由于常规的培养基抗生素敏感性测试(AST)方法太耗了(通常为24-72小时),因此迫切需要快速AST,以防止抗生素抗性感染的增加和​​传播。尽管有几种表型抗生素抗性感测模型能够将AST时间减少到几小时或更小,但关于生物异质性,它们的准确性或检测的极限受到低通量的限制。在这里,我们在单细菌水平下呈现基于整体滑动成像(WSI)的高通量感测抗生素抗生素抗生素抗生素抗生素抗生素的快速AST方法。确定最小抑制浓度(MIC)的时间是理论上最短的,这确保了抑制了大群中存在的每个单独细胞的生长。作为演示,我们的技术能够在单细胞层面感受至少几千个细菌的生长。在1小时内获得肠杆菌肝脏对庆大霉素的可靠性MIC,而金标准肉汤稀释方法在相同的结果中需要至少16小时。此外,我们的方法应用于其他基于成像的AST方法,允许快速准确地测定表型异构样品的抗生素敏感性,其中抗生素抗性细胞的数量与敏感细胞相比可忽略不计。因此,我们的方法对复杂临床细菌分离株的快速AST测定和护理点测试表现出了很大的承诺。

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