Rapid antibiotic screening based on E. coli apoptosis using a potentiometric sensor array

Copyright © 2024 Elsevier B.V. All rights reserved..

Phenotypic antimicrobial susceptibility testing enables reliable antibiotic screening but requires multiple strategies to identify each phenotypic change induced by different bactericidal mechanisms. Bacteria apoptosis with typical phenotypic features has never been explored for antibiotic screening. Herein, we developed an antibiotic screening method based on the measurement of antibiotic-induced phosphatidylserine (PS) exposure of apoptotic bacteria. Phosphatidylserine externalization of E. coli that can be widely used as an apoptosis marker for antibiotics with different antibacterial mechanisms was explored. A positively charged PS-binding peptide was immobilized on magnetic beads (MBs) to recognize and capture apoptotic E. coli with PS externalization. Apoptotic E. coli binding led to the charge or charge density change of MBs-peptide, resulting in a potential change on a magneto-controlled polymeric membrane potentiometric sensor. Based on the detection of apoptotic E. coli killed by antibiotics, antibiotic screening for different classes of antibiotics and silver nanoparticles was achieved within 1.5 h using a potentiometric sensor array. This approach enables sensitive, general, and time-saving antibiotic screening, and may open up a new path for antibiotic susceptibility testing.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:1297

Enthalten in:

Analytica chimica acta - 1297(2024) vom: 08. März, Seite 342378

Sprache:

Englisch

Beteiligte Personen:

Zhang, Han [VerfasserIn]
Mou, Junsong [VerfasserIn]
Ding, Jiawang [VerfasserIn]
Qin, Wei [VerfasserIn]

Links:

Volltext

Themen:

3M4G523W1G
Anti-Bacterial Agents
Antibiotic screening
Bacteria apoptosis
Journal Article
Peptide
Peptides
Phosphatidylserines
Potentiometric detection
Silver

Anmerkungen:

Date Completed 06.03.2024

Date Revised 06.03.2024

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.aca.2024.342378

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM369281047