Abstract

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.

Highlights

  • Due to the overuse and misuse of antibiotics, the increasing emergence and spread of antibioticresistant bacteria in human infections, such as methicillin-resistant S. aureus (MRSA), vancomycin-resistant enterococci (VRE), extended-spectrum beta-lactamase (ESBL)- and carbapenemase-producers, has become a global threat to public health [1,2,3,4,5,6]

  • To obtain an image encompassing a large population of single cells, “sandwich” slides with great bacterial cultivability that we previously customized for whole slide imaging (WSI) was employed [39]

  • We demonstrated a novel rapid and accurate antibiotic susceptibility testing (AST) method established on WSI, which enabled high-throughput analysis of single-cell growth rates regardless of the variations in the size and shape of bacteria

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Summary

Introduction

Due to the overuse and misuse of antibiotics, the increasing emergence and spread of antibioticresistant bacteria in human infections, such as methicillin-resistant S. aureus (MRSA), vancomycin-resistant enterococci (VRE), extended-spectrum beta-lactamase (ESBL)- and carbapenemase-producers, has become a global threat to public health [1,2,3,4,5,6]. The most widely accepted AST methods, such as broth/agar dilution and Kirby-Bauer disk diffusion, are based on the observation of visible bacterial growth in the presence of antibiotics [9]. These conventional methods are routinely used and cost-effective, but they typically require at least 24–72 h for reliable readout [10]. Such delay leads to the empirical use of antibiotics and consequent increase in mortality [11,12]. For patients with septic shock, initiation of inappropriate antimicrobial treatment results in a five-fold

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