Proteomic Analyses Reveal New Insights on the Antimicrobial Mechanisms of Chitosan Biopolymers and Their Nanosized Particles against Escherichia coli

Detalhes bibliográficos
Autor(a) principal: Gomes, Laidson P.
Data de Publicação: 2019
Outros Autores: Anjo, Sandra I., Manadas, Bruno, Coelho, Ana V., Paschoalin, Vania M F
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/106214
https://doi.org/10.3390/ijms21010225
Resumo: The well-known antimicrobial effects of chitosan (CS) polymers make them a promising adjuvant in enhancing antibiotic effectiveness against human pathogens. However, molecular CS antimicrobial mechanisms remain unclear, despite the insights presented in the literature. Thus, the aim of the present study was to depict the molecular effects implicated in the interaction of low or medium molecular mass CS polymers and their nanoparticle-counterparts against Escherichia coli. The differential E. coli proteomes sensitized to either CS polymers or nanoparticles were investigated by nano liquid chromatography-mass spectrometry (micro-LC-MS/MS). A total of 127 proteins differentially expressed in CS-sensitized bacteria were predominantly involved in (i) structural functions associated to the stability of outer membrane, (ii) increment of protein biosynthesis due to high abundance of ribosomal proteins and (iii) activation of biosynthesis of amino acid and purine metabolism pathways. Antibacterial activity of CS polymers/nanoparticles seems to be triggered by the outer bacterial membrane disassembly, leading to increased protein biosynthesis by diverting the metabolic flux to amino acid and purine nucleotides supply. Understanding CS-antibacterial molecular effects can be valuable to optimize the use of CS-based nanomaterials in food decontamination, and may represent a breakthrough on CS nanocapsules-drug delivery devices for novel antibiotics, as the chitosan-disassembly of bacteria cell membranes can potentialize antibiotic effects.
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spelling Proteomic Analyses Reveal New Insights on the Antimicrobial Mechanisms of Chitosan Biopolymers and Their Nanosized Particles against Escherichia coliantibiotic e ectanti-microbial molecular mechanismchitosan polymergene ontologyKEGGmetaboanalystmicro-LC-MS/MSSTRING analysisultrasonicated-cs nanoparticlesAnti-Bacterial AgentsBacterial Outer Membrane ProteinsChitosanEscherichia coliNanoparticlesProteomeThe well-known antimicrobial effects of chitosan (CS) polymers make them a promising adjuvant in enhancing antibiotic effectiveness against human pathogens. However, molecular CS antimicrobial mechanisms remain unclear, despite the insights presented in the literature. Thus, the aim of the present study was to depict the molecular effects implicated in the interaction of low or medium molecular mass CS polymers and their nanoparticle-counterparts against Escherichia coli. The differential E. coli proteomes sensitized to either CS polymers or nanoparticles were investigated by nano liquid chromatography-mass spectrometry (micro-LC-MS/MS). A total of 127 proteins differentially expressed in CS-sensitized bacteria were predominantly involved in (i) structural functions associated to the stability of outer membrane, (ii) increment of protein biosynthesis due to high abundance of ribosomal proteins and (iii) activation of biosynthesis of amino acid and purine metabolism pathways. Antibacterial activity of CS polymers/nanoparticles seems to be triggered by the outer bacterial membrane disassembly, leading to increased protein biosynthesis by diverting the metabolic flux to amino acid and purine nucleotides supply. Understanding CS-antibacterial molecular effects can be valuable to optimize the use of CS-based nanomaterials in food decontamination, and may represent a breakthrough on CS nanocapsules-drug delivery devices for novel antibiotics, as the chitosan-disassembly of bacteria cell membranes can potentialize antibiotic effects.This research was funded by Fundação Carlos Chagas Filho de Apoio à Pesquisa do Estado do Rio de Janeiro—FAPERJ Grants: Pos-doc Nota 10 program, PDR-10-E-26/202.319/2017; CNE, E-26/203.039/2015; CNE, E-26/202.815/2018; Sediadas E-26/010002864/2014 and Nottinghan/Birminghan, E-26/010.002673/2014. This study was partially supported by: Project LISBOA-01-0145-FEDER-007660 (Microbiologia Molecular, Estrutural e Celular) funded by FEDER funds through COMPETE2020—Programa Operacional Competitividade e Internacionalização (POCI), by ONEIDA project (LISBOA-01-0145-FEDER-016417) co-funded by FEEI—“Fundos Europeus Estruturais e de Investimento” from “Programa Operacional Regional Lisboa 2020” and by national funds through “FCT—Fundação para a Ciência e a Tecnologia”. This work was partially supported by: by the European Regional Development Fund (ERDF) through the COMPETE 2020—Operational Programme for Competitiveness and Internationalisation and Portuguese national funds via FCT – Fundação para a Ciência e a Tecnologia, I.P., OE FCT/MCTES (PIDDAC) under projects: POCI-01-0145-FEDER-007440 (strategic project UID/NEU/04539/2019) and POCI-01-0145-FEDER-029311 (ref.: PTDC/BTM-TEC/29311/2017).MDPI2019-12-28info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/106214http://hdl.handle.net/10316/106214https://doi.org/10.3390/ijms21010225eng1422-0067Gomes, Laidson P.Anjo, Sandra I.Manadas, BrunoCoelho, Ana V.Paschoalin, Vania M Finfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-04-06T10:19:51Zoai:estudogeral.uc.pt:10316/106214Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:22:42.116545Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Proteomic Analyses Reveal New Insights on the Antimicrobial Mechanisms of Chitosan Biopolymers and Their Nanosized Particles against Escherichia coli
title Proteomic Analyses Reveal New Insights on the Antimicrobial Mechanisms of Chitosan Biopolymers and Their Nanosized Particles against Escherichia coli
spellingShingle Proteomic Analyses Reveal New Insights on the Antimicrobial Mechanisms of Chitosan Biopolymers and Their Nanosized Particles against Escherichia coli
Gomes, Laidson P.
antibiotic e ect
anti-microbial molecular mechanism
chitosan polymer
gene ontology
KEGG
metaboanalyst
micro-LC-MS/MS
STRING analysis
ultrasonicated-cs nanoparticles
Anti-Bacterial Agents
Bacterial Outer Membrane Proteins
Chitosan
Escherichia coli
Nanoparticles
Proteome
title_short Proteomic Analyses Reveal New Insights on the Antimicrobial Mechanisms of Chitosan Biopolymers and Their Nanosized Particles against Escherichia coli
title_full Proteomic Analyses Reveal New Insights on the Antimicrobial Mechanisms of Chitosan Biopolymers and Their Nanosized Particles against Escherichia coli
title_fullStr Proteomic Analyses Reveal New Insights on the Antimicrobial Mechanisms of Chitosan Biopolymers and Their Nanosized Particles against Escherichia coli
title_full_unstemmed Proteomic Analyses Reveal New Insights on the Antimicrobial Mechanisms of Chitosan Biopolymers and Their Nanosized Particles against Escherichia coli
title_sort Proteomic Analyses Reveal New Insights on the Antimicrobial Mechanisms of Chitosan Biopolymers and Their Nanosized Particles against Escherichia coli
author Gomes, Laidson P.
author_facet Gomes, Laidson P.
Anjo, Sandra I.
Manadas, Bruno
Coelho, Ana V.
Paschoalin, Vania M F
author_role author
author2 Anjo, Sandra I.
Manadas, Bruno
Coelho, Ana V.
Paschoalin, Vania M F
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Gomes, Laidson P.
Anjo, Sandra I.
Manadas, Bruno
Coelho, Ana V.
Paschoalin, Vania M F
dc.subject.por.fl_str_mv antibiotic e ect
anti-microbial molecular mechanism
chitosan polymer
gene ontology
KEGG
metaboanalyst
micro-LC-MS/MS
STRING analysis
ultrasonicated-cs nanoparticles
Anti-Bacterial Agents
Bacterial Outer Membrane Proteins
Chitosan
Escherichia coli
Nanoparticles
Proteome
topic antibiotic e ect
anti-microbial molecular mechanism
chitosan polymer
gene ontology
KEGG
metaboanalyst
micro-LC-MS/MS
STRING analysis
ultrasonicated-cs nanoparticles
Anti-Bacterial Agents
Bacterial Outer Membrane Proteins
Chitosan
Escherichia coli
Nanoparticles
Proteome
description The well-known antimicrobial effects of chitosan (CS) polymers make them a promising adjuvant in enhancing antibiotic effectiveness against human pathogens. However, molecular CS antimicrobial mechanisms remain unclear, despite the insights presented in the literature. Thus, the aim of the present study was to depict the molecular effects implicated in the interaction of low or medium molecular mass CS polymers and their nanoparticle-counterparts against Escherichia coli. The differential E. coli proteomes sensitized to either CS polymers or nanoparticles were investigated by nano liquid chromatography-mass spectrometry (micro-LC-MS/MS). A total of 127 proteins differentially expressed in CS-sensitized bacteria were predominantly involved in (i) structural functions associated to the stability of outer membrane, (ii) increment of protein biosynthesis due to high abundance of ribosomal proteins and (iii) activation of biosynthesis of amino acid and purine metabolism pathways. Antibacterial activity of CS polymers/nanoparticles seems to be triggered by the outer bacterial membrane disassembly, leading to increased protein biosynthesis by diverting the metabolic flux to amino acid and purine nucleotides supply. Understanding CS-antibacterial molecular effects can be valuable to optimize the use of CS-based nanomaterials in food decontamination, and may represent a breakthrough on CS nanocapsules-drug delivery devices for novel antibiotics, as the chitosan-disassembly of bacteria cell membranes can potentialize antibiotic effects.
publishDate 2019
dc.date.none.fl_str_mv 2019-12-28
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/106214
http://hdl.handle.net/10316/106214
https://doi.org/10.3390/ijms21010225
url http://hdl.handle.net/10316/106214
https://doi.org/10.3390/ijms21010225
dc.language.iso.fl_str_mv eng
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