Comparative Proteomics of Methicillin-Resistant Staphylococcus aureus Subjected to Synergistic Effects of the Lantibiotic Nisin and Oxacillin

Detalhes bibliográficos
Autor(a) principal: Bergamo Alves, Fernanda Cristina [UNESP]
Data de Publicação: 2019
Outros Autores: Albano, Mariana [UNESP], Murbach Teles Andrade, Bruna Fernanda [UNESP], Chechi, Jessica Luana [UNESP], Marques Pereira, Ana Flavia [UNESP], Furlanetto, Alessandra [UNESP], Mores Rall, Vera Lucia [UNESP], Henrique Fernandes, Ana Angelica [UNESP], Santos, Lucilene Delazari dos [UNESP], Barbosa, Lidiane Nunes, Fernandes Junior, Ary [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1089/mdr.2019.0038
http://hdl.handle.net/11449/185854
Resumo: 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 (1/4 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.
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spelling Comparative Proteomics of Methicillin-Resistant Staphylococcus aureus Subjected to Synergistic Effects of the Lantibiotic Nisin and Oxacillinantimicrobial peptidebacterial resistancesynergismLC-MS/MSoxidative stresstransmission electron microscopyWe 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 (1/4 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.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Sao Paulo State Univ UNESP, IBB, Dept Microbiol & Immunol, BR-18618691 Botucatu, SP, BrazilSao Paulo State Univ UNESP, IBB, Dept Chem & Biochem, Botucatu, SP, BrazilSao Paulo State Univ UNESP, Botucatu Med Sch FMB, Grad Program Trop Dis, Botucatu, SP, BrazilSao Paulo State Univ UNESP, Ctr Study Venom & Venomous Anim CEVAP, Botucatu, SP, BrazilUniv Paranaense UNIPAR, Grad Program Anim Sci Emphasis Bioact Prod, Umuarama, BrazilSao Paulo State Univ UNESP, IBB, Elect Microscopy Ctr, Botucatu, SP, BrazilSao Paulo State Univ UNESP, IBB, Dept Microbiol & Immunol, BR-18618691 Botucatu, SP, BrazilSao Paulo State Univ UNESP, IBB, Dept Chem & Biochem, Botucatu, SP, BrazilSao Paulo State Univ UNESP, Botucatu Med Sch FMB, Grad Program Trop Dis, Botucatu, SP, BrazilSao Paulo State Univ UNESP, Ctr Study Venom & Venomous Anim CEVAP, Botucatu, SP, BrazilSao Paulo State Univ UNESP, IBB, Elect Microscopy Ctr, Botucatu, SP, BrazilFAPESP: 2015/14278-6Mary Ann Liebert, IncUniversidade Estadual Paulista (Unesp)Univ Paranaense UNIPARBergamo Alves, Fernanda Cristina [UNESP]Albano, Mariana [UNESP]Murbach Teles Andrade, Bruna Fernanda [UNESP]Chechi, Jessica Luana [UNESP]Marques Pereira, Ana Flavia [UNESP]Furlanetto, Alessandra [UNESP]Mores Rall, Vera Lucia [UNESP]Henrique Fernandes, Ana Angelica [UNESP]Santos, Lucilene Delazari dos [UNESP]Barbosa, Lidiane NunesFernandes Junior, Ary [UNESP]2019-10-04T12:39:10Z2019-10-04T12:39:10Z2019-06-25info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article11http://dx.doi.org/10.1089/mdr.2019.0038Microbial Drug Resistance. New Rochelle: Mary Ann Liebert, Inc, 11 p., 2019.1076-6294http://hdl.handle.net/11449/18585410.1089/mdr.2019.0038WOS:0004733051000013368404126695911Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMicrobial Drug Resistanceinfo:eu-repo/semantics/openAccess2021-10-22T18:13:15Zoai:repositorio.unesp.br:11449/185854Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-22T18:13:15Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Comparative Proteomics of Methicillin-Resistant Staphylococcus aureus Subjected to Synergistic Effects of the Lantibiotic Nisin and Oxacillin
title Comparative Proteomics of Methicillin-Resistant Staphylococcus aureus Subjected to Synergistic Effects of the Lantibiotic Nisin and Oxacillin
spellingShingle Comparative Proteomics of Methicillin-Resistant Staphylococcus aureus Subjected to Synergistic Effects of the Lantibiotic Nisin and Oxacillin
Bergamo Alves, Fernanda Cristina [UNESP]
antimicrobial peptide
bacterial resistance
synergism
LC-MS/MS
oxidative stress
transmission electron microscopy
title_short Comparative Proteomics of Methicillin-Resistant Staphylococcus aureus Subjected to Synergistic Effects of the Lantibiotic Nisin and Oxacillin
title_full Comparative Proteomics of Methicillin-Resistant Staphylococcus aureus Subjected to Synergistic Effects of the Lantibiotic Nisin and Oxacillin
title_fullStr Comparative Proteomics of Methicillin-Resistant Staphylococcus aureus Subjected to Synergistic Effects of the Lantibiotic Nisin and Oxacillin
title_full_unstemmed Comparative Proteomics of Methicillin-Resistant Staphylococcus aureus Subjected to Synergistic Effects of the Lantibiotic Nisin and Oxacillin
title_sort Comparative Proteomics of Methicillin-Resistant Staphylococcus aureus Subjected to Synergistic Effects of the Lantibiotic Nisin and Oxacillin
author Bergamo Alves, Fernanda Cristina [UNESP]
author_facet Bergamo Alves, Fernanda Cristina [UNESP]
Albano, Mariana [UNESP]
Murbach Teles Andrade, Bruna Fernanda [UNESP]
Chechi, Jessica Luana [UNESP]
Marques Pereira, Ana Flavia [UNESP]
Furlanetto, Alessandra [UNESP]
Mores Rall, Vera Lucia [UNESP]
Henrique Fernandes, Ana Angelica [UNESP]
Santos, Lucilene Delazari dos [UNESP]
Barbosa, Lidiane Nunes
Fernandes Junior, Ary [UNESP]
author_role author
author2 Albano, Mariana [UNESP]
Murbach Teles Andrade, Bruna Fernanda [UNESP]
Chechi, Jessica Luana [UNESP]
Marques Pereira, Ana Flavia [UNESP]
Furlanetto, Alessandra [UNESP]
Mores Rall, Vera Lucia [UNESP]
Henrique Fernandes, Ana Angelica [UNESP]
Santos, Lucilene Delazari dos [UNESP]
Barbosa, Lidiane Nunes
Fernandes Junior, Ary [UNESP]
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Univ Paranaense UNIPAR
dc.contributor.author.fl_str_mv Bergamo Alves, Fernanda Cristina [UNESP]
Albano, Mariana [UNESP]
Murbach Teles Andrade, Bruna Fernanda [UNESP]
Chechi, Jessica Luana [UNESP]
Marques Pereira, Ana Flavia [UNESP]
Furlanetto, Alessandra [UNESP]
Mores Rall, Vera Lucia [UNESP]
Henrique Fernandes, Ana Angelica [UNESP]
Santos, Lucilene Delazari dos [UNESP]
Barbosa, Lidiane Nunes
Fernandes Junior, Ary [UNESP]
dc.subject.por.fl_str_mv antimicrobial peptide
bacterial resistance
synergism
LC-MS/MS
oxidative stress
transmission electron microscopy
topic antimicrobial peptide
bacterial resistance
synergism
LC-MS/MS
oxidative stress
transmission electron microscopy
description 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 (1/4 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.
publishDate 2019
dc.date.none.fl_str_mv 2019-10-04T12:39:10Z
2019-10-04T12:39:10Z
2019-06-25
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1089/mdr.2019.0038
Microbial Drug Resistance. New Rochelle: Mary Ann Liebert, Inc, 11 p., 2019.
1076-6294
http://hdl.handle.net/11449/185854
10.1089/mdr.2019.0038
WOS:000473305100001
3368404126695911
url http://dx.doi.org/10.1089/mdr.2019.0038
http://hdl.handle.net/11449/185854
identifier_str_mv Microbial Drug Resistance. New Rochelle: Mary Ann Liebert, Inc, 11 p., 2019.
1076-6294
10.1089/mdr.2019.0038
WOS:000473305100001
3368404126695911
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Microbial Drug Resistance
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 11
dc.publisher.none.fl_str_mv Mary Ann Liebert, Inc
publisher.none.fl_str_mv Mary Ann Liebert, Inc
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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