Generation and selection of antibodies for a novel immunochromatographic lateral flow test to rapidly identify OXA-23-like-mediated carbapenem resistance in Acinetobacter baumannii

J Med Microbiol. 2019 Jul;68(7):1021-1032. doi: 10.1099/jmm.0.001015. Epub 2019 Jun 12.

Abstract

Introduction: The spread of carbapenem-resistant Acinetobacter baumannii has led to a worldwide healthcare problem. Carbapenem resistance in A. baumannii is mainly mediated by the acquisition of the carbapenem-hydrolyzing oxacillinase OXA-23. The phenotypic detection of carbapenem-producing A. baumannii is challenging and time-consuming. Hence, there is an unmet medical need for reliable and rapid diagnostic tools to detect OXA-23-producing Acinetobacter isolates to enable successful patient management.

Aim: Development of an immunochromatographic lateral flow test (ICT) for the rapid and reliable detection of OXA-23-producing carbapenem-resistant Acinetobacter isolates.

Methodology: For the development of an antibody-based ICT, we generated anti-OXA-23 monoclonal antibodies (MoAbs) and screened them sequentially for their ability to bind native OXA-23. Selected OXA-23-specific MoAbs were tested in different combinations for their capacity to capture and detect OXA-23His6 by sandwich enzyme-linked immunosorbent assay (ELISA) and ICT. A well-characterized collection of carbapenem-resistant Acinetobacter isolates with defined carbapenem resistance mechanisms were used to evaluate the specificity of the final OXA-23 ICT prototype.

Results: The antibody pairs best suited for the sandwich ELISA format did not match the best pairs in the ICT format selected during the development process of the final prototype OXA-23 ICT. This prototype was able to differentiate between OXA-23 subfamily-mediated carbapenem resistance and carbapenem-resistant Acinetobacter isolates overexpressing other OXAs with 100 % specificity and a turnaround time of 20 min from culture plate to result.

Conclusion: With this rapid detection assay one can save 12-48 h of diagnostic time, which could help avoid inappropriate use of carbapenems and enable earlier intervention to control the transmission of OXA-23-producing carbapenem-resistant Acinetobacter isolates to other patients and healthcare workers.

Keywords: Acinetobacter baumannii; OXA-23; carbapenem resistance; diagnostic; immunochromatographic lateral flow test (ICT); oxacillinase.

MeSH terms

  • Acinetobacter baumannii / drug effects
  • Acinetobacter baumannii / enzymology
  • Acinetobacter baumannii / immunology
  • Acinetobacter baumannii / isolation & purification*
  • Animals
  • Anti-Bacterial Agents / metabolism
  • Anti-Bacterial Agents / pharmacology*
  • Antibodies, Monoclonal / immunology
  • Antibodies, Monoclonal / metabolism
  • Bacterial Proteins
  • Carbapenems / metabolism
  • Carbapenems / pharmacology*
  • Cloning, Molecular
  • Drug Resistance, Multiple, Bacterial*
  • Female
  • Gene Expression Regulation, Bacterial
  • Immunoassay / methods*
  • Mice
  • Microbial Sensitivity Tests
  • beta-Lactamases / genetics
  • beta-Lactamases / immunology
  • beta-Lactamases / metabolism

Substances

  • Anti-Bacterial Agents
  • Antibodies, Monoclonal
  • Bacterial Proteins
  • Carbapenems
  • beta-Lactamases