Bordetella pertussis isolates from argentinean whooping cough patients display enhanced biofilm formation capacity compared to Tohama I reference strain

Autores
Arnal, Laura; Grunert, Tom; Cattelan, Natalia; Gouw, Dann de; Villalba, María Inés; Serra, Diego Omar; Mooi, Frits R.; Ehling Schulz, Monika; Yantorno, Osvaldo Miguel
Año de publicación
2015
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Pertussis is a highly contagious disease mainly caused by Bordetella pertussis. Despite the massive use of vaccines, since the 1950s the disease has become re-emergent in 2000 with a shift in incidence from infants to adolescents and adults. Clearly, the efficacy of current cellular or acellular vaccines, formulated from bacteria grown in stirred bioreactors is limited, presenting a challenge for future vaccine development. For gaining insights into the role of B. pertussis biofilm development for host colonization and persistence within the host, we examined the biofilm forming capacity of eight argentinean clinical isolates recovered from 2001 to 2007. All clinical isolates showed an enhanced potential for biofilm formation compared to the reference strain Tohama I. We further selected the clinical isolate B. pertussis 2723, exhibiting the highest biofilm biomass production, for quantitative proteomic profiling by means of two-dimensional fluorescence difference gel electrophoresis (2D-DIGE) coupled with mass spectrometry, which was accompanied by targeted transcriptional analysis. Results revealed an elevated expression of several virulence factors, including adhesins involved in biofilm development. In addition, we observed a higher expression of energy metabolism enzymes in the clinical isolate compared to the Tohama I strain. Furthermore, all clinical isolates carried a polymorphism in the bvgS gene. This mutation was associated to an increased sensitivity to modulation and a faster rate of adhesion to abiotic surfaces. Thus, the phenotypic biofilm characteristics shown by the clinical isolates might represent an important, hitherto underestimated, adaptive strategy for host colonization and long time persistence within the host.
Facultad de Ciencias Exactas
Centro de Investigación y Desarrollo en Fermentaciones Industriales
Materia
Ciencias Exactas
Biofilm
Bordetella pertussis
Clinical isolates
Proteomic
Real time PCR
Whooping cough
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-sa/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/85736

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network_name_str SEDICI (UNLP)
spelling Bordetella pertussis isolates from argentinean whooping cough patients display enhanced biofilm formation capacity compared to Tohama I reference strainArnal, LauraGrunert, TomCattelan, NataliaGouw, Dann deVillalba, María InésSerra, Diego OmarMooi, Frits R.Ehling Schulz, MonikaYantorno, Osvaldo MiguelCiencias ExactasBiofilmBordetella pertussisClinical isolatesProteomicReal time PCRWhooping coughPertussis is a highly contagious disease mainly caused by <i>Bordetella pertussis</i>. Despite the massive use of vaccines, since the 1950s the disease has become re-emergent in 2000 with a shift in incidence from infants to adolescents and adults. Clearly, the efficacy of current cellular or acellular vaccines, formulated from bacteria grown in stirred bioreactors is limited, presenting a challenge for future vaccine development. For gaining insights into the role of <i>B. pertussis</i> biofilm development for host colonization and persistence within the host, we examined the biofilm forming capacity of eight argentinean clinical isolates recovered from 2001 to 2007. All clinical isolates showed an enhanced potential for biofilm formation compared to the reference strain Tohama I. We further selected the clinical isolate <i>B. pertussis</i> 2723, exhibiting the highest biofilm biomass production, for quantitative proteomic profiling by means of two-dimensional fluorescence difference gel electrophoresis (2D-DIGE) coupled with mass spectrometry, which was accompanied by targeted transcriptional analysis. Results revealed an elevated expression of several virulence factors, including adhesins involved in biofilm development. In addition, we observed a higher expression of energy metabolism enzymes in the clinical isolate compared to the Tohama I strain. Furthermore, all clinical isolates carried a polymorphism in the <i>bvgS</i> gene. This mutation was associated to an increased sensitivity to modulation and a faster rate of adhesion to abiotic surfaces. Thus, the phenotypic biofilm characteristics shown by the clinical isolates might represent an important, hitherto underestimated, adaptive strategy for host colonization and long time persistence within the host.Facultad de Ciencias ExactasCentro de Investigación y Desarrollo en Fermentaciones Industriales2015info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://sedici.unlp.edu.ar/handle/10915/85736enginfo:eu-repo/semantics/altIdentifier/issn/1664-302Xinfo:eu-repo/semantics/altIdentifier/doi/10.3389/fmicb.2015.01352info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:17:00Zoai:sedici.unlp.edu.ar:10915/85736Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:17:00.366SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Bordetella pertussis isolates from argentinean whooping cough patients display enhanced biofilm formation capacity compared to Tohama I reference strain
title Bordetella pertussis isolates from argentinean whooping cough patients display enhanced biofilm formation capacity compared to Tohama I reference strain
spellingShingle Bordetella pertussis isolates from argentinean whooping cough patients display enhanced biofilm formation capacity compared to Tohama I reference strain
Arnal, Laura
Ciencias Exactas
Biofilm
Bordetella pertussis
Clinical isolates
Proteomic
Real time PCR
Whooping cough
title_short Bordetella pertussis isolates from argentinean whooping cough patients display enhanced biofilm formation capacity compared to Tohama I reference strain
title_full Bordetella pertussis isolates from argentinean whooping cough patients display enhanced biofilm formation capacity compared to Tohama I reference strain
title_fullStr Bordetella pertussis isolates from argentinean whooping cough patients display enhanced biofilm formation capacity compared to Tohama I reference strain
title_full_unstemmed Bordetella pertussis isolates from argentinean whooping cough patients display enhanced biofilm formation capacity compared to Tohama I reference strain
title_sort Bordetella pertussis isolates from argentinean whooping cough patients display enhanced biofilm formation capacity compared to Tohama I reference strain
dc.creator.none.fl_str_mv Arnal, Laura
Grunert, Tom
Cattelan, Natalia
Gouw, Dann de
Villalba, María Inés
Serra, Diego Omar
Mooi, Frits R.
Ehling Schulz, Monika
Yantorno, Osvaldo Miguel
author Arnal, Laura
author_facet Arnal, Laura
Grunert, Tom
Cattelan, Natalia
Gouw, Dann de
Villalba, María Inés
Serra, Diego Omar
Mooi, Frits R.
Ehling Schulz, Monika
Yantorno, Osvaldo Miguel
author_role author
author2 Grunert, Tom
Cattelan, Natalia
Gouw, Dann de
Villalba, María Inés
Serra, Diego Omar
Mooi, Frits R.
Ehling Schulz, Monika
Yantorno, Osvaldo Miguel
author2_role author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Ciencias Exactas
Biofilm
Bordetella pertussis
Clinical isolates
Proteomic
Real time PCR
Whooping cough
topic Ciencias Exactas
Biofilm
Bordetella pertussis
Clinical isolates
Proteomic
Real time PCR
Whooping cough
dc.description.none.fl_txt_mv Pertussis is a highly contagious disease mainly caused by <i>Bordetella pertussis</i>. Despite the massive use of vaccines, since the 1950s the disease has become re-emergent in 2000 with a shift in incidence from infants to adolescents and adults. Clearly, the efficacy of current cellular or acellular vaccines, formulated from bacteria grown in stirred bioreactors is limited, presenting a challenge for future vaccine development. For gaining insights into the role of <i>B. pertussis</i> biofilm development for host colonization and persistence within the host, we examined the biofilm forming capacity of eight argentinean clinical isolates recovered from 2001 to 2007. All clinical isolates showed an enhanced potential for biofilm formation compared to the reference strain Tohama I. We further selected the clinical isolate <i>B. pertussis</i> 2723, exhibiting the highest biofilm biomass production, for quantitative proteomic profiling by means of two-dimensional fluorescence difference gel electrophoresis (2D-DIGE) coupled with mass spectrometry, which was accompanied by targeted transcriptional analysis. Results revealed an elevated expression of several virulence factors, including adhesins involved in biofilm development. In addition, we observed a higher expression of energy metabolism enzymes in the clinical isolate compared to the Tohama I strain. Furthermore, all clinical isolates carried a polymorphism in the <i>bvgS</i> gene. This mutation was associated to an increased sensitivity to modulation and a faster rate of adhesion to abiotic surfaces. Thus, the phenotypic biofilm characteristics shown by the clinical isolates might represent an important, hitherto underestimated, adaptive strategy for host colonization and long time persistence within the host.
Facultad de Ciencias Exactas
Centro de Investigación y Desarrollo en Fermentaciones Industriales
description Pertussis is a highly contagious disease mainly caused by <i>Bordetella pertussis</i>. Despite the massive use of vaccines, since the 1950s the disease has become re-emergent in 2000 with a shift in incidence from infants to adolescents and adults. Clearly, the efficacy of current cellular or acellular vaccines, formulated from bacteria grown in stirred bioreactors is limited, presenting a challenge for future vaccine development. For gaining insights into the role of <i>B. pertussis</i> biofilm development for host colonization and persistence within the host, we examined the biofilm forming capacity of eight argentinean clinical isolates recovered from 2001 to 2007. All clinical isolates showed an enhanced potential for biofilm formation compared to the reference strain Tohama I. We further selected the clinical isolate <i>B. pertussis</i> 2723, exhibiting the highest biofilm biomass production, for quantitative proteomic profiling by means of two-dimensional fluorescence difference gel electrophoresis (2D-DIGE) coupled with mass spectrometry, which was accompanied by targeted transcriptional analysis. Results revealed an elevated expression of several virulence factors, including adhesins involved in biofilm development. In addition, we observed a higher expression of energy metabolism enzymes in the clinical isolate compared to the Tohama I strain. Furthermore, all clinical isolates carried a polymorphism in the <i>bvgS</i> gene. This mutation was associated to an increased sensitivity to modulation and a faster rate of adhesion to abiotic surfaces. Thus, the phenotypic biofilm characteristics shown by the clinical isolates might represent an important, hitherto underestimated, adaptive strategy for host colonization and long time persistence within the host.
publishDate 2015
dc.date.none.fl_str_mv 2015
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/85736
url http://sedici.unlp.edu.ar/handle/10915/85736
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/1664-302X
info:eu-repo/semantics/altIdentifier/doi/10.3389/fmicb.2015.01352
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.format.none.fl_str_mv application/pdf
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