TY - JOUR
T1 - A large chromosomal inversion affects antimicrobial sensitivity of Escherichia coli to sodium deoxycholate
AU - Le, Vuong Van Hung
AU - León-Quezada, Rayén Ignacia
AU - Biggs, Patrick J
AU - Rakonjac, Jasna
PY - 2022/8
Y1 - 2022/8
N2 - Resistance to antimicrobials is normally caused by mutations in the drug targets or genes involved in antimicrobial activation or expulsion. Here we show that an Escherichia coli strain, named DOC14, selected for increased resistance to the bile salt sodium deoxycholate, has no mutations in any ORF, but instead has a 2.1 Mb chromosomal inversion. The breakpoints of the inversion are two inverted copies of an IS5 element. Besides lowering deoxycholate susceptibility, the IS5-mediated chromosomal inversion in the DOC14 mutant was found to increase bacterial survival upon exposure to ampicillin and vancomycin, and sensitize the cell to ciprofloxacin and meropenem, but does not affect bacterial growth or cell morphology in a rich medium in the absence of antibacterial molecules. Overall, our findings support the notion that a large chromosomal inversion can benefit bacterial cells under certain conditions, contributing to genetic variability available for selection during evolution. The DOC14 mutant paired with its isogenic parental strain form a useful model as bacterial ancestors in evolution experiments to study how a large chromosomal inversion influences the evolutionary trajectory in response to various environmental stressors.
AB - Resistance to antimicrobials is normally caused by mutations in the drug targets or genes involved in antimicrobial activation or expulsion. Here we show that an Escherichia coli strain, named DOC14, selected for increased resistance to the bile salt sodium deoxycholate, has no mutations in any ORF, but instead has a 2.1 Mb chromosomal inversion. The breakpoints of the inversion are two inverted copies of an IS5 element. Besides lowering deoxycholate susceptibility, the IS5-mediated chromosomal inversion in the DOC14 mutant was found to increase bacterial survival upon exposure to ampicillin and vancomycin, and sensitize the cell to ciprofloxacin and meropenem, but does not affect bacterial growth or cell morphology in a rich medium in the absence of antibacterial molecules. Overall, our findings support the notion that a large chromosomal inversion can benefit bacterial cells under certain conditions, contributing to genetic variability available for selection during evolution. The DOC14 mutant paired with its isogenic parental strain form a useful model as bacterial ancestors in evolution experiments to study how a large chromosomal inversion influences the evolutionary trajectory in response to various environmental stressors.
KW - Anti-Bacterial Agents/pharmacology
KW - Chromosome Inversion
KW - Deoxycholic Acid/pharmacology
KW - Drug Resistance, Bacterial
KW - Escherichia coli
KW - Escherichia coli Infections/microbiology
KW - Humans
KW - Microbial Sensitivity Tests
U2 - 10.1099/mic.0.001232
DO - 10.1099/mic.0.001232
M3 - Journal article
C2 - 35960647
SN - 1350-0872
VL - 168
JO - Microbiology
JF - Microbiology
IS - 8
ER -