Please use this identifier to cite or link to this item: https://doi.org/10.3389/fmicb.2019.02973
Title: Overexpression of AmpC Promotes Bacteriophage Lysis of Ampicillin-Resistant Escherichia coli
Authors: Wang, S.
Yin, B. 
Yu, L.
Dang, M. 
Guo, Z.
Yan, G.
Hu, D.
Gu, J.
Du, C.
Feng, X.
Han, W.
Adam, Y.Y. 
Sun, C.
Bossé, J.T.
Lei, L.
Keywords: AmpC
ampicillin
antibiotic resistance
bacteriophage
E. coli
Issue Date: 2020
Publisher: Frontiers Media S.A.
Citation: Wang, S., Yin, B., Yu, L., Dang, M., Guo, Z., Yan, G., Hu, D., Gu, J., Du, C., Feng, X., Han, W., Adam, Y.Y., Sun, C., Bossé, J.T., Lei, L. (2020). Overexpression of AmpC Promotes Bacteriophage Lysis of Ampicillin-Resistant Escherichia coli. Frontiers in Microbiology 10 : 2973. ScholarBank@NUS Repository. https://doi.org/10.3389/fmicb.2019.02973
Rights: Attribution 4.0 International
Abstract: Infections caused by antibiotic-resistant Escherichia coli are a threat to human and animal health globally. Phage therapy has made great progress for the treatment of drug-resistant infections, but it is still unclear whether E. coli resistance to antibiotics could change the lysis ability of phages. In this study, we demonstrate that over expression of AmpC, an important ?-lactamase for ampicillin resistance, promotes lysis of E. coli by phage utilizing OmpA as a receptor. E. coli strains expressing more AmpC showed higher levels of OmpA, an E. coli outer membrane protein known to serve as a receptor for T-even phages, which resulted in increased adsorption and lysis by the phage tested in this study. These data demonstrate that increased ampicillin resistance can increase the sensitivity of E. coli to some lytic phage, which provides evidence for the feasibility of synergistic application of phage and antibiotics. © Copyright © 2020 Wang, Yin, Yu, Dang, Guo, Yan, Hu, Gu, Du, Feng, Han, Adam, Sun, Bossé and Lei.
Source Title: Frontiers in Microbiology
URI: https://scholarbank.nus.edu.sg/handle/10635/196215
ISSN: 1664-302X
DOI: 10.3389/fmicb.2019.02973
Rights: Attribution 4.0 International
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