| Literature DB >> 31237481 |
Fernanda Cristina Bergamo Alves1, Mariana Albano1, Bruna Fernanda Murbach Teles Andrade1, Jéssica Luana Chechi1, Ana Flávia Marques Pereira1, Alessandra Furlanetto1, Vera Lúcia Mores Rall1, Ana Angélica Henrique Fernandes2, Lucilene Delazari Dos Santos3,4, Lidiane Nunes Barbosa5, Ary Fernandes Junior1,6.
Abstract
We investigated the responses and mechanisms of action of methicillin-resistant Staphylococcus aureus (MRSA) metabolism when exposed under sublethal concentrations of the synergistic antibacterial combination of nisin + oxacillin (¼ of maximum sublethal concentration) and sublethal concentrations of oxacillin only and nisin only. A total of 135 proteins were identified, showing an alteration in the expression of 85 proteins when treatment was compared with untreated bacteria (control). When the bacteria were treated using the combination, there was an increase in the expression of proteins related to resistance (e.g., beta-lactamase) and also in the ones involved in protein synthesis, and there was a decrease in the expression of proteins related to stress and alterations in proteins related to bacterial energy metabolism. Bacterial oxidative stress showed that the combination was able to induce oxidative stress (p < 0.05) and increase enzyme activities and lipid hydroperoxide levels compared with individual treatments. The analysis of cell ultrastructure showed damage in MRSA, especially on the bacterial wall and the plasma membrane, with cell lysis and death. Thus, the changes caused by these treatments affected different proteins related to the bacterial biological processes and signaling pathways such as cell division, structure, stress, regulation, bacterial resistance, protein synthesis, gene expression, energetic metabolism, and virulence. It was observed that synergism among antimicrobials has high potential in therapeutic use and may reduce the required amounts of antibacterial substances in addition to being effective on different targets in bacterial cells.Entities:
Keywords: LC-MS/MS; antimicrobial peptide; bacterial resistance; oxidative stress; synergism; transmission electron microscopy
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Year: 2019 PMID: 31237481 DOI: 10.1089/mdr.2019.0038
Source DB: PubMed Journal: Microb Drug Resist ISSN: 1076-6294 Impact factor: 3.431