Brazilian red propolis in combination with β-lactams exerts an efficient antibacterial action over methicillin-resistant Staphylococcus aureus (MRSA) strains

Detalhes bibliográficos
Autor(a) principal: Ripari, Nicolas [UNESP]
Data de Publicação: 2023
Outros Autores: Pereira, Ana Flávia Marques [UNESP], Júnior, Ary Fernandes [UNESP], Rall, Vera Lúcia Mores [UNESP], Aldana-Mejía, Jennyfer A., Bastos, Jairo Kenupp, Sforcin, José Maurício [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1093/jambio/lxac080
http://hdl.handle.net/11449/249664
Resumo: AIMS: The antibacterial activity of red propolis extract (RPE) and brown propolis extracts (BPE) and the synergistic effect of RPE with cefoxitin (CEFO), imipenem (IMI), and ertapenem (ERTA) was evaluated in vitro against methicillin-resistant Staphylococcus aureus (MRSA) strains. METHODS AND RESULTS: MRSA ATCC 33591, community-associated (CA-MRSA) USA300, and four clinical isolates were used. A broth microdilution assay was performed to obtain inhibitory and bactericidal concentrations of BPE, RPE, CEFO, IMI, and ERTA. RPE in combination with CEFO, IMI, and ERTA was evaluated on the formation or eradication of biofilm. The bacterial relative membrane conductivity of the strains was assessed after RPE and combinations exposition. Surface/binding computational analyzes between RPE compounds and penicillin binding protein 2a (PBP2a) were performed. BPE samples had no activity against MRSA (MICs 3.2-5 g l-1; MBCs 10-15 g l-1), so the subsequent assays were carried out only with RPE and antimicrobials. RPE exerted a bacteriostatic action (MICs 0.0156-0.125 g l-1; MBCs 0.5-2 g l-1) but the combinations with IMI and ERTA showed the highest inhibition, as observed in the time-kill curve. However, the FICI index showed synergism (≥0.5) only to RPE + IMI. This combination was the most effective in inhibiting the biofilm and showed the highest values of membrane conductivity. Computational predictions indicated that RPE constituents may interact with PBP2a. CONCLUSION: RPE and RPE + IMI exerted an antibacterial and antibiofilm activity on MRSA strains probably due to membrane/wall damage and interactions with PBP2a.
id UNSP_435d4465b13f2eef628bf3ddce314239
oai_identifier_str oai:repositorio.unesp.br:11449/249664
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling Brazilian red propolis in combination with β-lactams exerts an efficient antibacterial action over methicillin-resistant Staphylococcus aureus (MRSA) strainsbiofilmmethicillin-resistant Staphylococcus aureusPBP2apropolisβ-lactam antibioticsAIMS: The antibacterial activity of red propolis extract (RPE) and brown propolis extracts (BPE) and the synergistic effect of RPE with cefoxitin (CEFO), imipenem (IMI), and ertapenem (ERTA) was evaluated in vitro against methicillin-resistant Staphylococcus aureus (MRSA) strains. METHODS AND RESULTS: MRSA ATCC 33591, community-associated (CA-MRSA) USA300, and four clinical isolates were used. A broth microdilution assay was performed to obtain inhibitory and bactericidal concentrations of BPE, RPE, CEFO, IMI, and ERTA. RPE in combination with CEFO, IMI, and ERTA was evaluated on the formation or eradication of biofilm. The bacterial relative membrane conductivity of the strains was assessed after RPE and combinations exposition. Surface/binding computational analyzes between RPE compounds and penicillin binding protein 2a (PBP2a) were performed. BPE samples had no activity against MRSA (MICs 3.2-5 g l-1; MBCs 10-15 g l-1), so the subsequent assays were carried out only with RPE and antimicrobials. RPE exerted a bacteriostatic action (MICs 0.0156-0.125 g l-1; MBCs 0.5-2 g l-1) but the combinations with IMI and ERTA showed the highest inhibition, as observed in the time-kill curve. However, the FICI index showed synergism (≥0.5) only to RPE + IMI. This combination was the most effective in inhibiting the biofilm and showed the highest values of membrane conductivity. Computational predictions indicated that RPE constituents may interact with PBP2a. CONCLUSION: RPE and RPE + IMI exerted an antibacterial and antibiofilm activity on MRSA strains probably due to membrane/wall damage and interactions with PBP2a.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Institute of Biosciences São Paulo State University (UNESP), Campus Botucatu 18618-691School of Pharmaceutical Sciences of Ribeirão Preto University of São Paulo (USP)Institute of Biosciences São Paulo State University (UNESP), Campus Botucatu 18618-691FAPESP: FAPESP-2017/04138-8Universidade Estadual Paulista (UNESP)Universidade de São Paulo (USP)Ripari, Nicolas [UNESP]Pereira, Ana Flávia Marques [UNESP]Júnior, Ary Fernandes [UNESP]Rall, Vera Lúcia Mores [UNESP]Aldana-Mejía, Jennyfer A.Bastos, Jairo KenuppSforcin, José Maurício [UNESP]2023-07-29T16:05:56Z2023-07-29T16:05:56Z2023-02-16info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1093/jambio/lxac080Journal of applied microbiology, v. 134, n. 2, 2023.1365-2672http://hdl.handle.net/11449/24966410.1093/jambio/lxac0802-s2.0-85148258772Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of applied microbiologyinfo:eu-repo/semantics/openAccess2023-07-29T16:05:56Zoai:repositorio.unesp.br:11449/249664Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:30:41.469517Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Brazilian red propolis in combination with β-lactams exerts an efficient antibacterial action over methicillin-resistant Staphylococcus aureus (MRSA) strains
title Brazilian red propolis in combination with β-lactams exerts an efficient antibacterial action over methicillin-resistant Staphylococcus aureus (MRSA) strains
spellingShingle Brazilian red propolis in combination with β-lactams exerts an efficient antibacterial action over methicillin-resistant Staphylococcus aureus (MRSA) strains
Ripari, Nicolas [UNESP]
biofilm
methicillin-resistant Staphylococcus aureus
PBP2a
propolis
β-lactam antibiotics
title_short Brazilian red propolis in combination with β-lactams exerts an efficient antibacterial action over methicillin-resistant Staphylococcus aureus (MRSA) strains
title_full Brazilian red propolis in combination with β-lactams exerts an efficient antibacterial action over methicillin-resistant Staphylococcus aureus (MRSA) strains
title_fullStr Brazilian red propolis in combination with β-lactams exerts an efficient antibacterial action over methicillin-resistant Staphylococcus aureus (MRSA) strains
title_full_unstemmed Brazilian red propolis in combination with β-lactams exerts an efficient antibacterial action over methicillin-resistant Staphylococcus aureus (MRSA) strains
title_sort Brazilian red propolis in combination with β-lactams exerts an efficient antibacterial action over methicillin-resistant Staphylococcus aureus (MRSA) strains
author Ripari, Nicolas [UNESP]
author_facet Ripari, Nicolas [UNESP]
Pereira, Ana Flávia Marques [UNESP]
Júnior, Ary Fernandes [UNESP]
Rall, Vera Lúcia Mores [UNESP]
Aldana-Mejía, Jennyfer A.
Bastos, Jairo Kenupp
Sforcin, José Maurício [UNESP]
author_role author
author2 Pereira, Ana Flávia Marques [UNESP]
Júnior, Ary Fernandes [UNESP]
Rall, Vera Lúcia Mores [UNESP]
Aldana-Mejía, Jennyfer A.
Bastos, Jairo Kenupp
Sforcin, José Maurício [UNESP]
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Ripari, Nicolas [UNESP]
Pereira, Ana Flávia Marques [UNESP]
Júnior, Ary Fernandes [UNESP]
Rall, Vera Lúcia Mores [UNESP]
Aldana-Mejía, Jennyfer A.
Bastos, Jairo Kenupp
Sforcin, José Maurício [UNESP]
dc.subject.por.fl_str_mv biofilm
methicillin-resistant Staphylococcus aureus
PBP2a
propolis
β-lactam antibiotics
topic biofilm
methicillin-resistant Staphylococcus aureus
PBP2a
propolis
β-lactam antibiotics
description AIMS: The antibacterial activity of red propolis extract (RPE) and brown propolis extracts (BPE) and the synergistic effect of RPE with cefoxitin (CEFO), imipenem (IMI), and ertapenem (ERTA) was evaluated in vitro against methicillin-resistant Staphylococcus aureus (MRSA) strains. METHODS AND RESULTS: MRSA ATCC 33591, community-associated (CA-MRSA) USA300, and four clinical isolates were used. A broth microdilution assay was performed to obtain inhibitory and bactericidal concentrations of BPE, RPE, CEFO, IMI, and ERTA. RPE in combination with CEFO, IMI, and ERTA was evaluated on the formation or eradication of biofilm. The bacterial relative membrane conductivity of the strains was assessed after RPE and combinations exposition. Surface/binding computational analyzes between RPE compounds and penicillin binding protein 2a (PBP2a) were performed. BPE samples had no activity against MRSA (MICs 3.2-5 g l-1; MBCs 10-15 g l-1), so the subsequent assays were carried out only with RPE and antimicrobials. RPE exerted a bacteriostatic action (MICs 0.0156-0.125 g l-1; MBCs 0.5-2 g l-1) but the combinations with IMI and ERTA showed the highest inhibition, as observed in the time-kill curve. However, the FICI index showed synergism (≥0.5) only to RPE + IMI. This combination was the most effective in inhibiting the biofilm and showed the highest values of membrane conductivity. Computational predictions indicated that RPE constituents may interact with PBP2a. CONCLUSION: RPE and RPE + IMI exerted an antibacterial and antibiofilm activity on MRSA strains probably due to membrane/wall damage and interactions with PBP2a.
publishDate 2023
dc.date.none.fl_str_mv 2023-07-29T16:05:56Z
2023-07-29T16:05:56Z
2023-02-16
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/10.1093/jambio/lxac080
Journal of applied microbiology, v. 134, n. 2, 2023.
1365-2672
http://hdl.handle.net/11449/249664
10.1093/jambio/lxac080
2-s2.0-85148258772
url http://dx.doi.org/10.1093/jambio/lxac080
http://hdl.handle.net/11449/249664
identifier_str_mv Journal of applied microbiology, v. 134, n. 2, 2023.
1365-2672
10.1093/jambio/lxac080
2-s2.0-85148258772
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of applied microbiology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
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
_version_ 1808128371076366336