Development of Resistance in <i>Escherichia coli</i> ATCC25922 under Exposure of Sub-Inhibitory Concentration of Olaquindox

• Main Authors: Yufeng Gu, Shuge Wang, Lulu Huang, Wei Sa, Jun Li, Junhong Huang, Menghong Dai, Guyue Cheng
• Format: Article
• Language: English
• Published: MDPI AG 2020-11-01
• Series: Antibiotics
• Subjects: <i>E. coli</i>; olaquindox; resistance; sub-inhibitory concentration; transcriptome sequencing; whole genome sequencing
• Online Access: https://www.mdpi.com/2079-6382/9/11/791

Quinoxaline1,4-di-<i>N</i>-oxides (QdNOs) are a class of important antibacterial drugs of veterinary use, of which the drug resistance mechanism has not yet been clearly explained. This study investigated the molecular mechanism of development of resistance in <i>Escherichia coli</i> (<i>E. coli</i>) under the pressure of sub-inhibitory concentration (sub-MIC) of olaquindox (OLA), a representative QdNOs drug. In vitro challenge of <i>E. coli</i> with 1/100× MIC to 1/2× MIC of OLA showed that the bacteria needed a longer time to develop resistance and could only achieve low to moderate levels of resistance as well as form weak biofilms. The transcriptomic and genomic profiles of the resistant <i>E. coli</i> induced by sub-MIC of OLA demonstrated that genes involved in tricarboxylic acid cycle, oxidation-reduction process, biofilm formation, and efflux pumps were up-regulated, while genes involved in DNA repair and outer membrane porin were down-regulated. Mutation rates were significantly increased in the sub-MIC OLA-treated bacteria and the mutated genes were mainly involved in the oxidation-reduction process, DNA repair, and replication. The SNPs were found in <i>degQ</i>, <i>ks71A</i>, <i>vgrG</i>, <i>bigA</i>, <i>cusA</i>, and <i>DR76_-4702</i> genes, which were covered in both transcriptomic and genomic profiles. This study provides new insights into the resistance mechanism of QdNOs and increases the current data pertaining to the development of bacterial resistance under the stress of antibacterials at sub-MIC concentrations.