Abstract

Acinetobacter baumannii is a remarkable microorganism known for its diversity of habitat and its multi-drug resistance, resulting in hard-to-treat infections. Thus, a sensitive method for the identification and detection of Acinetobacter baumannii is vital. However, current methods used for the detection of pathogens have not improved in the past decades and suffer from long process times and low detection limits. A cheap, quick, and easy detection mechanism is needed. In this work, we successfully prepared indium phosphide quantum dots with a zinc sulphide shell, conjugated to a targeting aptamer ligand, to specifically label Acinetobacter baumannii. The system retained both the photophysical properties of the quantum dots and the folded structure and molecular recognition function of the aptamer, therefore successfully targeting Acinetobacter baumannii. Confocal microscopy and transmission electron microscopy showed the fluorescent quantum dots surrounding the Acinetobacter baumannii cells confirming the specificity of the aptamer conjugated to indium phosphide quantum dots with a zinc sulphide shell. Controls were undertaken with a different bacteria species, showing no binding of the aptamer conjugated quantum dots. Our strategy offers a novel method to detect bacteria and engineer a scalable platform for fluorescence detection, therefore improving current methods and allowing for better treatment.

Highlights

  • The current state of the world and the ongoing fight against the coronavirus disease2019 (COVID-19) demonstrates that the study of microbes is far from developed

  • The ligand exchange procedure adapted by Yong et al produced mercaptosuccinic acid (MSA) conjugated quantum dots (QDs) (QDs-MSA) resulting in a carboxylic acid functionality [26]

  • The QDs-MSA were water soluble and the terminal carboxylic groups from the MSA allowed for the formation of an amide covalent bond via the amine functionalised aptamers (QDs-aptamer)

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Summary

Introduction

The current state of the world and the ongoing fight against the coronavirus disease2019 (COVID-19) demonstrates that the study of microbes is far from developed. A. baumannii is a Gram-negative bacteria capable of causing both community and health-care associated infections [3,4,5]. The organism’s ability to survive under a wide range of environmental conditions and to persist for extended periods of time on surfaces make it a frequent cause of outbreaks [7,8,9]. It is responsible for many infections including pneumonia, meningitis, urinary tract infections and wound infections [6,10,11]. A sensitive method for the identification and the detection of A. baumannii is crucial to preventing the spread of infections

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