Ultrasensitive and rapid identification of ESRI developer- and piperacillin/tazobactam-resistant Escherichia coli by the MALDIpiptaz test

Emerg Microbes Infect. 2022 Dec;11(1):2034-2044. doi: 10.1080/22221751.2022.2113746.

Abstract

Background: The excessive use of piperacillin/tazobactam (P/T) has promoted the emergence of P/T-resistant Enterobacterales. We reported that in Escherichia coli, P/T contributes to the development of extended-spectrum resistance to β-lactam/β-lactamase inhibitor (BL/BLI) (ESRI) in isolates that are P/T susceptible but have low-level resistance to BL/BLI. Currently, the detection of P/T resistance relying on conventional methods is time-consuming. To overcome this issue, we developed a cost-effective test based on MALDI-MS technology, called MALDIpiptaz, which aims to detect P/T resistance and ESRI developers in E. coli.

Methods: We used automated Clover MS Data Analysis software to analyse the protein profile spectra obtained by MALDI-MS from a collection of 248 E. coli isolates (91 P/T-resistant, 81 ESRI developers and 76 P/T-susceptible). This software allowed to preprocess all the spectra to build different peak matrices that were analysed by machine learning algorithms.

Results: We demonstrated that MALDIpiptaz can efficiently and rapidly (15 min) discriminate between P/T-resistant, ESRI developer and P/T-susceptible isolates and allowed the correct classification between ESRI developers from their isogenic resistance to P/T.

Conclusion: The combination of excellent performance and cost-effectiveness are all desirable attributes, allowing the MALDIpiptaz test to be a useful tool for the rapid determination of P/T resistance in clinically relevant E. coli isolates.

Keywords: Escherichia coli; Piperacillin; algorithm; beta-lactamase; beta-lactamase inhibitor; machine learning; resistance; tazobactam.

MeSH terms

  • Anti-Bacterial Agents
  • Escherichia coli Infections*
  • Escherichia coli*
  • Humans
  • Microbial Sensitivity Tests
  • Piperacillin, Tazobactam Drug Combination
  • beta-Lactamases

Substances

  • Anti-Bacterial Agents
  • Piperacillin, Tazobactam Drug Combination
  • beta-Lactamases

Grants and funding

This study was supported by the [Proyectos de Investigación en Salud, Instituto de Salud Carlos III, Ministerio de Ciencia, Innovación y Universidades of Spain] under grant [number PI19/01009] cofinanced by European Development Regional Fund “A way to achieve Europe”, operative program Intelligent Growth 2014-2020. Y.S. was supported by the [subprograma Miguel Servet Tipo II, Instituto de Salud Carlos III, Ministerio de Ciencia e Innovación of Spain] under grant [number CP20/00018]. A.R.-V. was supported by the [subprograma Juan Rodés, Instituto de Salud Carlos III, Ministerio de Ciencia e Innovación of Spain] under grant [number JR20/00023].