1,8-cineole as an antimicrobial and antibiofilm agent against multidrug resistant Klebsiella pneumoniae

Autores
Vázquez, Nicolás Martín; Moreno, Silvia; Galvan, Estela Maria
Año de publicación
2021
Idioma
inglés
Tipo de recurso
documento de conferencia
Estado
versión publicada
Descripción
Klebsiella pneumoniae is a common cause of antimicrobial-resistant opportunistic infections in hospitalized patients, including urinary tract infections. The emergence of multidrug-resistant (MDR) strains producing extended-spectrum β-lactamases (ESBL) and/or carbapenemases, in combination with the capacity to produce biofilm has created additional problems in providing adequate antibiotic treatment of urinary tract infections. Biofilms are complex bacterial communities adhered to biotic or abiotic surfaces that are surrounded by an extracellular matrix composed of exopolysaccharides, proteins and nucleic acids that give them differential phenotypic properties associated with greater resistance to antibiotics. 1,8-cineole, one of the main components of Rosmarinus officinalis volatile oil, has shown antimicrobial activity against non-MDR Gram negative bacteria (including K. pneumoniae) during planktonic growth. Here, we evaluated the antimicrobial and antibiofilm activity of 1,8-cineole against planktonic and pre-formed mature biofilms of non-MDR and MDR ESBL-producing K. pneumoniae clinical strains isolated from urinary tract infections. Killing curves were performed in planktonic cultures by adding 1% (v/v) 1,8-cineole for 5-180 min and counting viable cells (cfu/ml). Results showed variable decrease of K. pneumoniae viability (ranging from 0.5 to 4 log reduction) after phytochemical treatment, not related to their antibiotic resistance profile. Regarding biofilms, all tested strains formed robust biomass after 48 h, as determined by crystal violet staining (Abs 595nm > 1). One-hour treatment with 1% (v/v) 1,8-cineole partially disrupted biofilm biomasses (34 to 62% reduction in crystal violet staining). Additionally, a variable decrease in cell viability (between 0,5 and 4 log reduction of ufc/cm2 ) was observed by viable cell counting, regardless if they were or not MDR. Two MDR ESBL-producing K. pneumoniae strains, presenting different susceptibility to 1,8-cineole, were chosen to study their extracellular matrix in biofilms by confocal laser scanning microscopy after calcofluor white staining. Noteworthy, differences in the extracellular matrix structure were observed between strains, that could account for differences in 1,8-cineole susceptibility. Altogether, our results show that some antibiotic-sensitive and MDR ESBL-producing K. pneumoniae isolates were sensitive to 1,8-cineole exposure and support the efficacy of 1,8-cineole as a potential antimicrobial agent for the treatment of planktonic and biofilm-associated infections caused by MDR K. pneumoniae.
Fil: Vázquez, Nicolás Martín. Universidad Maimónides. Área de Investigaciones Biomédicas y Biotecnológicas. Centro de Estudios Biomédicos, Biotecnológicos, Ambientales y de Diagnóstico; Argentina. Laboratorio de Biotecnologia Bacteriana.; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Moreno, Silvia. Universidad Maimónides. Área de Investigaciones Biomédicas y Biotecnológicas. Centro de Estudios Biomédicos, Biotecnológicos, Ambientales y de Diagnóstico; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Galvan, Estela Maria. Laboratorio de Biotecnologia Bacteriana.; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
LVII Annual Meeting of the Argentine Society for Biochemistry and Molecular Biology Research; XVI Annual Meeting of the Argentinean Society for General Microbiology
Ciudad Autónoma de Buenos Aires
Argentina
Sociedad Argentina de Bioquímica e Investigación en Biología Molecular
Sociedad Argentina de Microbiología General
Materia
KLEBSIELLA PNEUMONIAE
BIOFILM
PHYTOCHEMICAL AS ANTIBIOFILM
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/158719

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repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling 1,8-cineole as an antimicrobial and antibiofilm agent against multidrug resistant Klebsiella pneumoniaeVázquez, Nicolás MartínMoreno, SilviaGalvan, Estela MariaKLEBSIELLA PNEUMONIAEBIOFILMPHYTOCHEMICAL AS ANTIBIOFILMhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Klebsiella pneumoniae is a common cause of antimicrobial-resistant opportunistic infections in hospitalized patients, including urinary tract infections. The emergence of multidrug-resistant (MDR) strains producing extended-spectrum β-lactamases (ESBL) and/or carbapenemases, in combination with the capacity to produce biofilm has created additional problems in providing adequate antibiotic treatment of urinary tract infections. Biofilms are complex bacterial communities adhered to biotic or abiotic surfaces that are surrounded by an extracellular matrix composed of exopolysaccharides, proteins and nucleic acids that give them differential phenotypic properties associated with greater resistance to antibiotics. 1,8-cineole, one of the main components of Rosmarinus officinalis volatile oil, has shown antimicrobial activity against non-MDR Gram negative bacteria (including K. pneumoniae) during planktonic growth. Here, we evaluated the antimicrobial and antibiofilm activity of 1,8-cineole against planktonic and pre-formed mature biofilms of non-MDR and MDR ESBL-producing K. pneumoniae clinical strains isolated from urinary tract infections. Killing curves were performed in planktonic cultures by adding 1% (v/v) 1,8-cineole for 5-180 min and counting viable cells (cfu/ml). Results showed variable decrease of K. pneumoniae viability (ranging from 0.5 to 4 log reduction) after phytochemical treatment, not related to their antibiotic resistance profile. Regarding biofilms, all tested strains formed robust biomass after 48 h, as determined by crystal violet staining (Abs 595nm > 1). One-hour treatment with 1% (v/v) 1,8-cineole partially disrupted biofilm biomasses (34 to 62% reduction in crystal violet staining). Additionally, a variable decrease in cell viability (between 0,5 and 4 log reduction of ufc/cm2 ) was observed by viable cell counting, regardless if they were or not MDR. Two MDR ESBL-producing K. pneumoniae strains, presenting different susceptibility to 1,8-cineole, were chosen to study their extracellular matrix in biofilms by confocal laser scanning microscopy after calcofluor white staining. Noteworthy, differences in the extracellular matrix structure were observed between strains, that could account for differences in 1,8-cineole susceptibility. Altogether, our results show that some antibiotic-sensitive and MDR ESBL-producing K. pneumoniae isolates were sensitive to 1,8-cineole exposure and support the efficacy of 1,8-cineole as a potential antimicrobial agent for the treatment of planktonic and biofilm-associated infections caused by MDR K. pneumoniae.Fil: Vázquez, Nicolás Martín. Universidad Maimónides. Área de Investigaciones Biomédicas y Biotecnológicas. Centro de Estudios Biomédicos, Biotecnológicos, Ambientales y de Diagnóstico; Argentina. Laboratorio de Biotecnologia Bacteriana.; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Moreno, Silvia. Universidad Maimónides. Área de Investigaciones Biomédicas y Biotecnológicas. Centro de Estudios Biomédicos, Biotecnológicos, Ambientales y de Diagnóstico; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Galvan, Estela Maria. Laboratorio de Biotecnologia Bacteriana.; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaLVII Annual Meeting of the Argentine Society for Biochemistry and Molecular Biology Research; XVI Annual Meeting of the Argentinean Society for General MicrobiologyCiudad Autónoma de Buenos AiresArgentinaSociedad Argentina de Bioquímica e Investigación en Biología MolecularSociedad Argentina de Microbiología GeneralTech Science Press2021info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectCongresoJournalhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/1587191,8-cineole as an antimicrobial and antibiofilm agent against multidrug resistant Klebsiella pneumoniae; LVII Annual Meeting of the Argentine Society for Biochemistry and Molecular Biology Research; XVI Annual Meeting of the Argentinean Society for General Microbiology; Ciudad Autónoma de Buenos Aires; Argentina; 2021; 114-1140327-95451667-5746CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://congresos.g2consultora.com/congreso-conjunto-saib-samige-2021/info:eu-repo/semantics/altIdentifier/url/http://www.saib.org.ar/sites/default/files/TSP_BIOCELL_46213-SAIB-SAMIGE%202021.pdfNacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:41:29Zoai:ri.conicet.gov.ar:11336/158719instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:41:29.568CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv 1,8-cineole as an antimicrobial and antibiofilm agent against multidrug resistant Klebsiella pneumoniae
title 1,8-cineole as an antimicrobial and antibiofilm agent against multidrug resistant Klebsiella pneumoniae
spellingShingle 1,8-cineole as an antimicrobial and antibiofilm agent against multidrug resistant Klebsiella pneumoniae
Vázquez, Nicolás Martín
KLEBSIELLA PNEUMONIAE
BIOFILM
PHYTOCHEMICAL AS ANTIBIOFILM
title_short 1,8-cineole as an antimicrobial and antibiofilm agent against multidrug resistant Klebsiella pneumoniae
title_full 1,8-cineole as an antimicrobial and antibiofilm agent against multidrug resistant Klebsiella pneumoniae
title_fullStr 1,8-cineole as an antimicrobial and antibiofilm agent against multidrug resistant Klebsiella pneumoniae
title_full_unstemmed 1,8-cineole as an antimicrobial and antibiofilm agent against multidrug resistant Klebsiella pneumoniae
title_sort 1,8-cineole as an antimicrobial and antibiofilm agent against multidrug resistant Klebsiella pneumoniae
dc.creator.none.fl_str_mv Vázquez, Nicolás Martín
Moreno, Silvia
Galvan, Estela Maria
author Vázquez, Nicolás Martín
author_facet Vázquez, Nicolás Martín
Moreno, Silvia
Galvan, Estela Maria
author_role author
author2 Moreno, Silvia
Galvan, Estela Maria
author2_role author
author
dc.subject.none.fl_str_mv KLEBSIELLA PNEUMONIAE
BIOFILM
PHYTOCHEMICAL AS ANTIBIOFILM
topic KLEBSIELLA PNEUMONIAE
BIOFILM
PHYTOCHEMICAL AS ANTIBIOFILM
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Klebsiella pneumoniae is a common cause of antimicrobial-resistant opportunistic infections in hospitalized patients, including urinary tract infections. The emergence of multidrug-resistant (MDR) strains producing extended-spectrum β-lactamases (ESBL) and/or carbapenemases, in combination with the capacity to produce biofilm has created additional problems in providing adequate antibiotic treatment of urinary tract infections. Biofilms are complex bacterial communities adhered to biotic or abiotic surfaces that are surrounded by an extracellular matrix composed of exopolysaccharides, proteins and nucleic acids that give them differential phenotypic properties associated with greater resistance to antibiotics. 1,8-cineole, one of the main components of Rosmarinus officinalis volatile oil, has shown antimicrobial activity against non-MDR Gram negative bacteria (including K. pneumoniae) during planktonic growth. Here, we evaluated the antimicrobial and antibiofilm activity of 1,8-cineole against planktonic and pre-formed mature biofilms of non-MDR and MDR ESBL-producing K. pneumoniae clinical strains isolated from urinary tract infections. Killing curves were performed in planktonic cultures by adding 1% (v/v) 1,8-cineole for 5-180 min and counting viable cells (cfu/ml). Results showed variable decrease of K. pneumoniae viability (ranging from 0.5 to 4 log reduction) after phytochemical treatment, not related to their antibiotic resistance profile. Regarding biofilms, all tested strains formed robust biomass after 48 h, as determined by crystal violet staining (Abs 595nm > 1). One-hour treatment with 1% (v/v) 1,8-cineole partially disrupted biofilm biomasses (34 to 62% reduction in crystal violet staining). Additionally, a variable decrease in cell viability (between 0,5 and 4 log reduction of ufc/cm2 ) was observed by viable cell counting, regardless if they were or not MDR. Two MDR ESBL-producing K. pneumoniae strains, presenting different susceptibility to 1,8-cineole, were chosen to study their extracellular matrix in biofilms by confocal laser scanning microscopy after calcofluor white staining. Noteworthy, differences in the extracellular matrix structure were observed between strains, that could account for differences in 1,8-cineole susceptibility. Altogether, our results show that some antibiotic-sensitive and MDR ESBL-producing K. pneumoniae isolates were sensitive to 1,8-cineole exposure and support the efficacy of 1,8-cineole as a potential antimicrobial agent for the treatment of planktonic and biofilm-associated infections caused by MDR K. pneumoniae.
Fil: Vázquez, Nicolás Martín. Universidad Maimónides. Área de Investigaciones Biomédicas y Biotecnológicas. Centro de Estudios Biomédicos, Biotecnológicos, Ambientales y de Diagnóstico; Argentina. Laboratorio de Biotecnologia Bacteriana.; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Moreno, Silvia. Universidad Maimónides. Área de Investigaciones Biomédicas y Biotecnológicas. Centro de Estudios Biomédicos, Biotecnológicos, Ambientales y de Diagnóstico; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Galvan, Estela Maria. Laboratorio de Biotecnologia Bacteriana.; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
LVII Annual Meeting of the Argentine Society for Biochemistry and Molecular Biology Research; XVI Annual Meeting of the Argentinean Society for General Microbiology
Ciudad Autónoma de Buenos Aires
Argentina
Sociedad Argentina de Bioquímica e Investigación en Biología Molecular
Sociedad Argentina de Microbiología General
description Klebsiella pneumoniae is a common cause of antimicrobial-resistant opportunistic infections in hospitalized patients, including urinary tract infections. The emergence of multidrug-resistant (MDR) strains producing extended-spectrum β-lactamases (ESBL) and/or carbapenemases, in combination with the capacity to produce biofilm has created additional problems in providing adequate antibiotic treatment of urinary tract infections. Biofilms are complex bacterial communities adhered to biotic or abiotic surfaces that are surrounded by an extracellular matrix composed of exopolysaccharides, proteins and nucleic acids that give them differential phenotypic properties associated with greater resistance to antibiotics. 1,8-cineole, one of the main components of Rosmarinus officinalis volatile oil, has shown antimicrobial activity against non-MDR Gram negative bacteria (including K. pneumoniae) during planktonic growth. Here, we evaluated the antimicrobial and antibiofilm activity of 1,8-cineole against planktonic and pre-formed mature biofilms of non-MDR and MDR ESBL-producing K. pneumoniae clinical strains isolated from urinary tract infections. Killing curves were performed in planktonic cultures by adding 1% (v/v) 1,8-cineole for 5-180 min and counting viable cells (cfu/ml). Results showed variable decrease of K. pneumoniae viability (ranging from 0.5 to 4 log reduction) after phytochemical treatment, not related to their antibiotic resistance profile. Regarding biofilms, all tested strains formed robust biomass after 48 h, as determined by crystal violet staining (Abs 595nm > 1). One-hour treatment with 1% (v/v) 1,8-cineole partially disrupted biofilm biomasses (34 to 62% reduction in crystal violet staining). Additionally, a variable decrease in cell viability (between 0,5 and 4 log reduction of ufc/cm2 ) was observed by viable cell counting, regardless if they were or not MDR. Two MDR ESBL-producing K. pneumoniae strains, presenting different susceptibility to 1,8-cineole, were chosen to study their extracellular matrix in biofilms by confocal laser scanning microscopy after calcofluor white staining. Noteworthy, differences in the extracellular matrix structure were observed between strains, that could account for differences in 1,8-cineole susceptibility. Altogether, our results show that some antibiotic-sensitive and MDR ESBL-producing K. pneumoniae isolates were sensitive to 1,8-cineole exposure and support the efficacy of 1,8-cineole as a potential antimicrobial agent for the treatment of planktonic and biofilm-associated infections caused by MDR K. pneumoniae.
publishDate 2021
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1,8-cineole as an antimicrobial and antibiofilm agent against multidrug resistant Klebsiella pneumoniae; LVII Annual Meeting of the Argentine Society for Biochemistry and Molecular Biology Research; XVI Annual Meeting of the Argentinean Society for General Microbiology; Ciudad Autónoma de Buenos Aires; Argentina; 2021; 114-114
0327-9545
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0327-9545
1667-5746
CONICET Digital
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