@article {17868, title = {Proteomic changes in an extended-spectrum beta-lactamase-producing Escherichia coli strain under cefotaxime selection}, journal = {Journal of Integrated OMICS}, year = {2013}, month = {2013-10-09 00:00:00}, abstract = {

Proteomics can be used to study the metabolic pathways and mechanisms involved in

antimicrobial resistance. The aim of this comparative proteomic study was to establish the

overall changes in the proteome of a naturally occurring ESBL-producing E. coli strain

(C5478) stressed with its minimal inhibitory concentration (2 μg/mL) of cefotaxime,

compared to the proteome of the same strain without antimicrobial stress, by using 2-D gel

electrophoresis (2-DE) followed by matrix-assisted laser desorption/ionization time-of-flight

mass spectrometry (MALDI-TOF MS). The comparative proteomic analysis revealed that

the abundance of numerous protein species changed in the strain stressed by CTX compared

to the non-stressed wild-type strain. A total of 188 spots were excised from the 2-DE gel of

the wild-type strain, 112 of which were successfully identified by MALDI-TOF MS,

representing 110 different proteins. Concerning the 2-DE gel of the CTX-stressed bacteria,

171 spots were excised and 156 were identified, representing 143 different proteins. The

proteins identified in both strains were categorized according to their biological functions.

These proteins were involved in metabolism, protein synthesis, cell division, stress

responses, and antimicrobial resistance, among others. These findings will be helpful to

further understand not only the antimicrobial resistance mechanisms, but also the role of

wild animals as reservoirs in spreading antimicrobial-resistant bacteria into the environment.

}, keywords = {Antimicrobial resistance, ESBL-E. coli, Proteomics, stress response}, doi = {10.5584/jiomics.v2013i2013.140}, author = {Radhouani, H. and Nunes-Miranda, J. D. and Carreira, R. J. and Santos, H. M. and Pinto, L. and Monteiro, R. and Carvalho, C. and Poeta, P. and Capelo-Martinez, J. L. and Igrejas, G.} }