Ewunkem, A.J.; Rodgers, L.; Campbell, D.; Staley, C.; Subedi, K.; Boyd, S.; Graves, J.L., Jr. Experimental Evolution of Magnetite Nanoparticle Resistance in Escherichia coli. Nanomaterials2021, 11, 790.
Ewunkem, A.J.; Rodgers, L.; Campbell, D.; Staley, C.; Subedi, K.; Boyd, S.; Graves, J.L., Jr. Experimental Evolution of Magnetite Nanoparticle Resistance in Escherichia coli. Nanomaterials 2021, 11, 790.
Ewunkem, A.J.; Rodgers, L.; Campbell, D.; Staley, C.; Subedi, K.; Boyd, S.; Graves, J.L., Jr. Experimental Evolution of Magnetite Nanoparticle Resistance in Escherichia coli. Nanomaterials2021, 11, 790.
Ewunkem, A.J.; Rodgers, L.; Campbell, D.; Staley, C.; Subedi, K.; Boyd, S.; Graves, J.L., Jr. Experimental Evolution of Magnetite Nanoparticle Resistance in Escherichia coli. Nanomaterials 2021, 11, 790.
Abstract
Experimental evolution was utilized to produce 5 magnetite nanoparticle-resistant (FeNP1-5) populations of Escherichia coli. The control populations were not exposed to magnetite nanoparticles. The 24-hour growth of these replicates was evaluated in the presence of increasing concentrations magnetite NPs as well as other ionic metals (gallium III, iron II, iron III, silver I) and antibiotics (ampicillin, chloramphenicol, rifampicin, sulfanilamide, tetracycline). Scanning electron microscope was utilized to determine cell size and shape in response to magnetite nanoparticle selection. Whole genome sequencing was carried out to determine if any genomic changes that resulted from magnetite nanoparticle resistance. After 25 days of selection magnetite resistance was evident in the FeNP treatment. The FeNP populations also showed a highly significantly (p < 0.0001) greater 24-growth as measured by optical density in metals (Fe (II), Fe (III), Ga (III), Ag and Cu II); as well as antibiotics (ampicillin, chloramphenicol, rifampicin, sulfanilamide, and tetracycline). The FeNP resistant populations also showed a significantly greater cell length compared to controls (p < 0.001). Genomic analysis of FeNP identified both polymorphisms and hard selective sweeps in the RNA polymerase genes rpoA, rpoB, and rpoC. Collectively, our results show that E. coli can rapidly evolve resistance to magnetite nanoparticles and that this result is correlated resistances to other metals and antibiotics. There were also changes in cell morphology resulting from adaptation to magnetite NPs. Thus, the various applications of magnetite nanoparticles could result in unanticipated changes in resistance to both metal and antibiotics.
Copyright:
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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