Antibacterial activity of the non-cytotoxic peptide (p-BthTX-I)2 and its serum degradation product against multidrug-resistant bacteria

Detalhes bibliográficos
Autor(a) principal: Santos-Filho, Norival A. [UNESP]
Data de Publicação: 2017
Outros Autores: Fernandes, Rafaela S., Sgardioli, Bruna F., Ramos, Matheus A. S. [UNESP], Piccoli, Julia P. [UNESP], Camargo, Ilana L. B. C., Bauab, Tais M. [UNESP], Cilli, Eduardo M. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.3390/molecules22111898
http://hdl.handle.net/11449/179358
Resumo: Antimicrobial peptides can be used systemically, however, their susceptibility to proteases is a major obstacle in peptide-based therapeutic development. In the present study, the serum stability of p-BthTX-I (KKYRYHLKPFCKK) and (p-BthTX-I)2, a p-BthTX-I disulfide-linked dimer, were analyzed by mass spectrometry and analytical high-performance liquid chromatography (HPLC). Antimicrobial activities were assessed by determining their minimum inhibitory concentrations (MIC) using cation-adjusted Mueller-Hinton broth. Furthermore, biofilm eradication and time-kill kinetics were performed. Our results showed that p-BthTX-I and (p-BthTX-I)2 were completely degraded after 25 min. Mass spectrometry showed that the primary degradation product was a peptide that had lost four lysine residues on its C-terminus region (des-Lys12/Lys13-(p-BthTX-I)2), which was stable after 24 h of incubation. The antibacterial activities of the peptides p-BthTX-I, (p-BthTX-I)2, and des-Lys12/Lys13-(p-BthTX-I)2 were evaluated against a variety of bacteria, including multidrug-resistant strains. Des-Lys12/Lys13-(p-BthTX-I)2 and (p-BthTX-I)2 degraded Staphylococcus epidermidis biofilms. Additionally, both the peptides exhibited bactericidal activities against planktonic S. epidermidis in time-kill assays. The emergence of bacterial resistance to a variety of antibiotics used in clinics is the ultimate challenge for microbial infection control. Therefore, our results demonstrated that both peptides analyzed and the product of proteolysis obtained from (p-BthTX-I)2 are promising prototypes as novel drugs to treat multidrug-resistant bacterial infections.
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spelling Antibacterial activity of the non-cytotoxic peptide (p-BthTX-I)2 and its serum degradation product against multidrug-resistant bacteria(P-BthTX-I)2Antimicrobial peptidesBiofilmMultidrug-resistant bacteriaAntimicrobial peptides can be used systemically, however, their susceptibility to proteases is a major obstacle in peptide-based therapeutic development. In the present study, the serum stability of p-BthTX-I (KKYRYHLKPFCKK) and (p-BthTX-I)2, a p-BthTX-I disulfide-linked dimer, were analyzed by mass spectrometry and analytical high-performance liquid chromatography (HPLC). Antimicrobial activities were assessed by determining their minimum inhibitory concentrations (MIC) using cation-adjusted Mueller-Hinton broth. Furthermore, biofilm eradication and time-kill kinetics were performed. Our results showed that p-BthTX-I and (p-BthTX-I)2 were completely degraded after 25 min. Mass spectrometry showed that the primary degradation product was a peptide that had lost four lysine residues on its C-terminus region (des-Lys12/Lys13-(p-BthTX-I)2), which was stable after 24 h of incubation. The antibacterial activities of the peptides p-BthTX-I, (p-BthTX-I)2, and des-Lys12/Lys13-(p-BthTX-I)2 were evaluated against a variety of bacteria, including multidrug-resistant strains. Des-Lys12/Lys13-(p-BthTX-I)2 and (p-BthTX-I)2 degraded Staphylococcus epidermidis biofilms. Additionally, both the peptides exhibited bactericidal activities against planktonic S. epidermidis in time-kill assays. The emergence of bacterial resistance to a variety of antibiotics used in clinics is the ultimate challenge for microbial infection control. Therefore, our results demonstrated that both peptides analyzed and the product of proteolysis obtained from (p-BthTX-I)2 are promising prototypes as novel drugs to treat multidrug-resistant bacterial infections.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Instituto de Química Universidade Estadual Paulista (UNESP)Instituto de Física de São Carlos USP-Universidade de São PauloFaculdade de Ciências Farmaceûticas Universidade Estadual Paulista (UNESP)Instituto de Química Universidade Estadual Paulista (UNESP)Faculdade de Ciências Farmaceûticas Universidade Estadual Paulista (UNESP)FAPESP: #2014/05538-1Universidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Santos-Filho, Norival A. [UNESP]Fernandes, Rafaela S.Sgardioli, Bruna F.Ramos, Matheus A. S. [UNESP]Piccoli, Julia P. [UNESP]Camargo, Ilana L. B. C.Bauab, Tais M. [UNESP]Cilli, Eduardo M. [UNESP]2018-12-11T17:34:51Z2018-12-11T17:34:51Z2017-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://dx.doi.org/10.3390/molecules22111898Molecules, v. 22, n. 11, 2017.1420-3049http://hdl.handle.net/11449/17935810.3390/molecules221118982-s2.0-850337770372-s2.0-85033777037.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMolecules0,855info:eu-repo/semantics/openAccess2023-11-30T06:13:55Zoai:repositorio.unesp.br:11449/179358Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T19:07:02.459834Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Antibacterial activity of the non-cytotoxic peptide (p-BthTX-I)2 and its serum degradation product against multidrug-resistant bacteria
title Antibacterial activity of the non-cytotoxic peptide (p-BthTX-I)2 and its serum degradation product against multidrug-resistant bacteria
spellingShingle Antibacterial activity of the non-cytotoxic peptide (p-BthTX-I)2 and its serum degradation product against multidrug-resistant bacteria
Santos-Filho, Norival A. [UNESP]
(P-BthTX-I)2
Antimicrobial peptides
Biofilm
Multidrug-resistant bacteria
title_short Antibacterial activity of the non-cytotoxic peptide (p-BthTX-I)2 and its serum degradation product against multidrug-resistant bacteria
title_full Antibacterial activity of the non-cytotoxic peptide (p-BthTX-I)2 and its serum degradation product against multidrug-resistant bacteria
title_fullStr Antibacterial activity of the non-cytotoxic peptide (p-BthTX-I)2 and its serum degradation product against multidrug-resistant bacteria
title_full_unstemmed Antibacterial activity of the non-cytotoxic peptide (p-BthTX-I)2 and its serum degradation product against multidrug-resistant bacteria
title_sort Antibacterial activity of the non-cytotoxic peptide (p-BthTX-I)2 and its serum degradation product against multidrug-resistant bacteria
author Santos-Filho, Norival A. [UNESP]
author_facet Santos-Filho, Norival A. [UNESP]
Fernandes, Rafaela S.
Sgardioli, Bruna F.
Ramos, Matheus A. S. [UNESP]
Piccoli, Julia P. [UNESP]
Camargo, Ilana L. B. C.
Bauab, Tais M. [UNESP]
Cilli, Eduardo M. [UNESP]
author_role author
author2 Fernandes, Rafaela S.
Sgardioli, Bruna F.
Ramos, Matheus A. S. [UNESP]
Piccoli, Julia P. [UNESP]
Camargo, Ilana L. B. C.
Bauab, Tais M. [UNESP]
Cilli, Eduardo M. [UNESP]
author2_role author
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 Santos-Filho, Norival A. [UNESP]
Fernandes, Rafaela S.
Sgardioli, Bruna F.
Ramos, Matheus A. S. [UNESP]
Piccoli, Julia P. [UNESP]
Camargo, Ilana L. B. C.
Bauab, Tais M. [UNESP]
Cilli, Eduardo M. [UNESP]
dc.subject.por.fl_str_mv (P-BthTX-I)2
Antimicrobial peptides
Biofilm
Multidrug-resistant bacteria
topic (P-BthTX-I)2
Antimicrobial peptides
Biofilm
Multidrug-resistant bacteria
description Antimicrobial peptides can be used systemically, however, their susceptibility to proteases is a major obstacle in peptide-based therapeutic development. In the present study, the serum stability of p-BthTX-I (KKYRYHLKPFCKK) and (p-BthTX-I)2, a p-BthTX-I disulfide-linked dimer, were analyzed by mass spectrometry and analytical high-performance liquid chromatography (HPLC). Antimicrobial activities were assessed by determining their minimum inhibitory concentrations (MIC) using cation-adjusted Mueller-Hinton broth. Furthermore, biofilm eradication and time-kill kinetics were performed. Our results showed that p-BthTX-I and (p-BthTX-I)2 were completely degraded after 25 min. Mass spectrometry showed that the primary degradation product was a peptide that had lost four lysine residues on its C-terminus region (des-Lys12/Lys13-(p-BthTX-I)2), which was stable after 24 h of incubation. The antibacterial activities of the peptides p-BthTX-I, (p-BthTX-I)2, and des-Lys12/Lys13-(p-BthTX-I)2 were evaluated against a variety of bacteria, including multidrug-resistant strains. Des-Lys12/Lys13-(p-BthTX-I)2 and (p-BthTX-I)2 degraded Staphylococcus epidermidis biofilms. Additionally, both the peptides exhibited bactericidal activities against planktonic S. epidermidis in time-kill assays. The emergence of bacterial resistance to a variety of antibiotics used in clinics is the ultimate challenge for microbial infection control. Therefore, our results demonstrated that both peptides analyzed and the product of proteolysis obtained from (p-BthTX-I)2 are promising prototypes as novel drugs to treat multidrug-resistant bacterial infections.
publishDate 2017
dc.date.none.fl_str_mv 2017-11-01
2018-12-11T17:34:51Z
2018-12-11T17:34:51Z
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/10.3390/molecules22111898
Molecules, v. 22, n. 11, 2017.
1420-3049
http://hdl.handle.net/11449/179358
10.3390/molecules22111898
2-s2.0-85033777037
2-s2.0-85033777037.pdf
url http://dx.doi.org/10.3390/molecules22111898
http://hdl.handle.net/11449/179358
identifier_str_mv Molecules, v. 22, n. 11, 2017.
1420-3049
10.3390/molecules22111898
2-s2.0-85033777037
2-s2.0-85033777037.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Molecules
0,855
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
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
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