Longitudinal Evolution of the Pseudomonas-Derived Cephalosporinase (PDC) Structure and Activity in a Cystic Fibrosis Patient Treated with β-Lactams

Autores
Colque, Claudia A.; Albarracín Orio, Andrea Georgina; Tomatis, Pablo Emiliano; Dotta, Gina; Moreno, Diego M.; Hedemann, Laura Gabriela; Hickman, Rachel; Madsen Sommer, Lea Mette; Feliziani, Sofía; Moyano, Alejandro José; Bonomo, Robert; Johansen, Helle Krogh; Molin, Søren; Vila, Alejandro; Smania, Andrea M.
Año de publicación
2022
Idioma
español castellano
Tipo de recurso
artículo
Estado
versión aceptada
Descripción
Traditional studies on the evolution of antibiotic resistance development use approaches that can range from laboratory-based experimental studies, to epidemiological surveillance, to sequencing of clinical isolates. However, evolutionary trajectories also depend on the environment in which selection takes place, compelling the need to more deeply investigate the impact of environmental complexities and their dynamics over time. Herein, we explored the within-patient adaptive long-term evolution of a Pseudomonas aeruginosa hypermutator lineage in the airways of a cystic fibrosis (CF) patient by performing a chronological tracking of mutations that occurred in different subpopulations; our results demonstrated parallel evolution events in the chromosomally encoded class C b-lactamase (blaPDC). These multiple mutations within blaPDC shaped diverse coexisting alleles, whose frequency dynamics responded to the changing antibiotic selective pressures for more than 26 years of chronic infection. Importantly, the combination of the cumulative mutations in blaPDC provided structural and functional protein changes that resulted in a continuous enhancement of its catalytic efficiency and high level of cephalosporin resistance. This evolution was linked to the persistent treatment with ceftazidime, which we demonstrated selected for variants with robust catalytic activity against this expanded-spectrum cephalosporin. A “gain of function” of collateral resistance toward ceftolozane, a more recently introduced cephalosporin that was not prescribed to this patient, was also observed, and the biochemical basis of this cross-resistance phenomenon was elucidated. This work unveils the evolutionary trajectories paved by bacteria toward a multidrug-resistant phenotype, driven by decades of antibiotic treatment in the natural CF environmental setting.
Fil: Colque, Claudia A. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina
Fil: Albarracín Orio, Andrea Georgina. Universidad Católica de Córdoba. Facultad de Ciencias Agropecuarias; Argentina
Fil: Tomatis, Pablo Emiliano. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina
Fil: Dotta, Gina. Universidad Nacional de Rosario. Instituto de Biología Molecular; Argentina
Fil: Moreno, Diego M. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina
Fil: Hedemann, Laura Gabriela. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina
Fil: Hickman, Rachel. Technical University of Denmark; Dinamarca
Fil: Madsen Sommer, Lea Mette. Technical University of Denmark; Dinamarca
Fil: Feliziani, Sofía. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina
Fil: Moyano, Alejandro José. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina
Fil: Bonomo, Robert. Case Western Reserve University; Estados Unidos
Fil: Johansen, Helle Krogh. University of Copenhagen; Dinamarca
Fil: Molin, Søren. Technical University of Denmark; Dinamarca
Fil: Vila, Alejandro. niversidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina
Fil: Smania, Andrea M. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina
Fuente
Colque, Claudia A. ORCID: https://orcid.org/0000-0002-9027-4747 , Albarracín Orio, Andrea Georgina ORCID: https://orcid.org/0000-0002-4722-1439 , Tomatis, Pablo Emiliano ORCID: https://orcid.org/0000-0002-1126-8200 , Dotta, Gina ORCID: https://orcid.org/0000-0003-1023-1606 , Moreno, Diego M. ORCID: https://orcid.org/0000-0001-5493-8537 , Hedemann, Laura Gabriela ORCID: https://orcid.org/0000-0002-6667-6500 , Hickman, Rachel ORCID: https://orcid.org/0000-0002-0290-1836 , Madsen Sommer, Lea Mette ORCID: https://orcid.org/0000-0002-1622-6691 , Feliziani, Sofía, Moyano, Alejandro José ORCID: https://orcid.org/0000-0002-4976-7611 , Bonomo, Robert ORCID: https://orcid.org/0000-0002-3299-894X , Johansen, Helle Krogh ORCID: https://orcid.org/0000-0003-0268-3717 , Molin, Søren ORCID: https://orcid.org/0000-0002-7973-2639 , Vila, Alejandro ORCID: https://orcid.org/0000-0002-7978-3233 and Smania, Andrea M. (2022) Longitudinal Evolution of the Pseudomonas-Derived Cephalosporinase (PDC) Structure and Activity in a Cystic Fibrosis Patient Treated with β-Lactams. mBio, 13 (5).
Materia
R Medicina (General)
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by/4.0/deed.es
Repositorio
Producción Académica (UCC)
Institución
Universidad Católica de Córdoba
OAI Identificador
oai:pa.bibdigital.uccor.edu.ar:3687

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network_name_str Producción Académica (UCC)
spelling Longitudinal Evolution of the Pseudomonas-Derived Cephalosporinase (PDC) Structure and Activity in a Cystic Fibrosis Patient Treated with β-LactamsColque, Claudia A.Albarracín Orio, Andrea GeorginaTomatis, Pablo EmilianoDotta, GinaMoreno, Diego M.Hedemann, Laura GabrielaHickman, RachelMadsen Sommer, Lea MetteFeliziani, SofíaMoyano, Alejandro JoséBonomo, RobertJohansen, Helle KroghMolin, SørenVila, AlejandroSmania, Andrea M.R Medicina (General)Traditional studies on the evolution of antibiotic resistance development use approaches that can range from laboratory-based experimental studies, to epidemiological surveillance, to sequencing of clinical isolates. However, evolutionary trajectories also depend on the environment in which selection takes place, compelling the need to more deeply investigate the impact of environmental complexities and their dynamics over time. Herein, we explored the within-patient adaptive long-term evolution of a Pseudomonas aeruginosa hypermutator lineage in the airways of a cystic fibrosis (CF) patient by performing a chronological tracking of mutations that occurred in different subpopulations; our results demonstrated parallel evolution events in the chromosomally encoded class C b-lactamase (blaPDC). These multiple mutations within blaPDC shaped diverse coexisting alleles, whose frequency dynamics responded to the changing antibiotic selective pressures for more than 26 years of chronic infection. Importantly, the combination of the cumulative mutations in blaPDC provided structural and functional protein changes that resulted in a continuous enhancement of its catalytic efficiency and high level of cephalosporin resistance. This evolution was linked to the persistent treatment with ceftazidime, which we demonstrated selected for variants with robust catalytic activity against this expanded-spectrum cephalosporin. A “gain of function” of collateral resistance toward ceftolozane, a more recently introduced cephalosporin that was not prescribed to this patient, was also observed, and the biochemical basis of this cross-resistance phenomenon was elucidated. This work unveils the evolutionary trajectories paved by bacteria toward a multidrug-resistant phenotype, driven by decades of antibiotic treatment in the natural CF environmental setting.Fil: Colque, Claudia A. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; ArgentinaFil: Albarracín Orio, Andrea Georgina. Universidad Católica de Córdoba. Facultad de Ciencias Agropecuarias; ArgentinaFil: Tomatis, Pablo Emiliano. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; ArgentinaFil: Dotta, Gina. Universidad Nacional de Rosario. Instituto de Biología Molecular; ArgentinaFil: Moreno, Diego M. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; ArgentinaFil: Hedemann, Laura Gabriela. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; ArgentinaFil: Hickman, Rachel. Technical University of Denmark; DinamarcaFil: Madsen Sommer, Lea Mette. Technical University of Denmark; DinamarcaFil: Feliziani, Sofía. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; ArgentinaFil: Moyano, Alejandro José. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; ArgentinaFil: Bonomo, Robert. Case Western Reserve University; Estados UnidosFil: Johansen, Helle Krogh. University of Copenhagen; DinamarcaFil: Molin, Søren. Technical University of Denmark; DinamarcaFil: Vila, Alejandro. niversidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; ArgentinaFil: Smania, Andrea M. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina2022-09-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://pa.bibdigital.ucc.edu.ar/3687/1/A_Colque_Albarrac%C3%ADnOrio_Tomatis_Dotta_Moreno_Hedemann_Hickman_Sommer_Feliziani_Moyano_Bonomo_Johansen_Molin_Vila_Smania.pdf Colque, Claudia A. ORCID: https://orcid.org/0000-0002-9027-4747 <https://orcid.org/0000-0002-9027-4747>, Albarracín Orio, Andrea Georgina ORCID: https://orcid.org/0000-0002-4722-1439 <https://orcid.org/0000-0002-4722-1439>, Tomatis, Pablo Emiliano ORCID: https://orcid.org/0000-0002-1126-8200 <https://orcid.org/0000-0002-1126-8200>, Dotta, Gina ORCID: https://orcid.org/0000-0003-1023-1606 <https://orcid.org/0000-0003-1023-1606>, Moreno, Diego M. ORCID: https://orcid.org/0000-0001-5493-8537 <https://orcid.org/0000-0001-5493-8537>, Hedemann, Laura Gabriela ORCID: https://orcid.org/0000-0002-6667-6500 <https://orcid.org/0000-0002-6667-6500>, Hickman, Rachel ORCID: https://orcid.org/0000-0002-0290-1836 <https://orcid.org/0000-0002-0290-1836>, Madsen Sommer, Lea Mette ORCID: https://orcid.org/0000-0002-1622-6691 <https://orcid.org/0000-0002-1622-6691>, Feliziani, Sofía, Moyano, Alejandro José ORCID: https://orcid.org/0000-0002-4976-7611 <https://orcid.org/0000-0002-4976-7611>, Bonomo, Robert ORCID: https://orcid.org/0000-0002-3299-894X <https://orcid.org/0000-0002-3299-894X>, Johansen, Helle Krogh ORCID: https://orcid.org/0000-0003-0268-3717 <https://orcid.org/0000-0003-0268-3717>, Molin, Søren ORCID: https://orcid.org/0000-0002-7973-2639 <https://orcid.org/0000-0002-7973-2639>, Vila, Alejandro ORCID: https://orcid.org/0000-0002-7978-3233 <https://orcid.org/0000-0002-7978-3233> and Smania, Andrea M. (2022) Longitudinal Evolution of the Pseudomonas-Derived Cephalosporinase (PDC) Structure and Activity in a Cystic Fibrosis Patient Treated with β-Lactams. mBio, 13 (5). reponame:Producción Académica (UCC)instname:Universidad Católica de Córdobaspahttp://pa.bibdigital.ucc.edu.ar/3687/info:eu-repo/semantics/altIdentifier/doi/0.1128/mbio.01663-22info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/4.0/deed.es2025-10-16T10:06:27Zoai:pa.bibdigital.uccor.edu.ar:3687instacron:UCCInstitucionalhttp://pa.bibdigital.uccor.edu.ar/Universidad privadaNo correspondehttp://pa.bibdigital.uccor.edu.ar/cgi/oai2bibdir@uccor.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:27182025-10-16 10:06:28.218Producción Académica (UCC) - Universidad Católica de Córdobafalse
dc.title.none.fl_str_mv Longitudinal Evolution of the Pseudomonas-Derived Cephalosporinase (PDC) Structure and Activity in a Cystic Fibrosis Patient Treated with β-Lactams
title Longitudinal Evolution of the Pseudomonas-Derived Cephalosporinase (PDC) Structure and Activity in a Cystic Fibrosis Patient Treated with β-Lactams
spellingShingle Longitudinal Evolution of the Pseudomonas-Derived Cephalosporinase (PDC) Structure and Activity in a Cystic Fibrosis Patient Treated with β-Lactams
Colque, Claudia A.
R Medicina (General)
title_short Longitudinal Evolution of the Pseudomonas-Derived Cephalosporinase (PDC) Structure and Activity in a Cystic Fibrosis Patient Treated with β-Lactams
title_full Longitudinal Evolution of the Pseudomonas-Derived Cephalosporinase (PDC) Structure and Activity in a Cystic Fibrosis Patient Treated with β-Lactams
title_fullStr Longitudinal Evolution of the Pseudomonas-Derived Cephalosporinase (PDC) Structure and Activity in a Cystic Fibrosis Patient Treated with β-Lactams
title_full_unstemmed Longitudinal Evolution of the Pseudomonas-Derived Cephalosporinase (PDC) Structure and Activity in a Cystic Fibrosis Patient Treated with β-Lactams
title_sort Longitudinal Evolution of the Pseudomonas-Derived Cephalosporinase (PDC) Structure and Activity in a Cystic Fibrosis Patient Treated with β-Lactams
dc.creator.none.fl_str_mv Colque, Claudia A.
Albarracín Orio, Andrea Georgina
Tomatis, Pablo Emiliano
Dotta, Gina
Moreno, Diego M.
Hedemann, Laura Gabriela
Hickman, Rachel
Madsen Sommer, Lea Mette
Feliziani, Sofía
Moyano, Alejandro José
Bonomo, Robert
Johansen, Helle Krogh
Molin, Søren
Vila, Alejandro
Smania, Andrea M.
author Colque, Claudia A.
author_facet Colque, Claudia A.
Albarracín Orio, Andrea Georgina
Tomatis, Pablo Emiliano
Dotta, Gina
Moreno, Diego M.
Hedemann, Laura Gabriela
Hickman, Rachel
Madsen Sommer, Lea Mette
Feliziani, Sofía
Moyano, Alejandro José
Bonomo, Robert
Johansen, Helle Krogh
Molin, Søren
Vila, Alejandro
Smania, Andrea M.
author_role author
author2 Albarracín Orio, Andrea Georgina
Tomatis, Pablo Emiliano
Dotta, Gina
Moreno, Diego M.
Hedemann, Laura Gabriela
Hickman, Rachel
Madsen Sommer, Lea Mette
Feliziani, Sofía
Moyano, Alejandro José
Bonomo, Robert
Johansen, Helle Krogh
Molin, Søren
Vila, Alejandro
Smania, Andrea M.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv R Medicina (General)
topic R Medicina (General)
dc.description.none.fl_txt_mv Traditional studies on the evolution of antibiotic resistance development use approaches that can range from laboratory-based experimental studies, to epidemiological surveillance, to sequencing of clinical isolates. However, evolutionary trajectories also depend on the environment in which selection takes place, compelling the need to more deeply investigate the impact of environmental complexities and their dynamics over time. Herein, we explored the within-patient adaptive long-term evolution of a Pseudomonas aeruginosa hypermutator lineage in the airways of a cystic fibrosis (CF) patient by performing a chronological tracking of mutations that occurred in different subpopulations; our results demonstrated parallel evolution events in the chromosomally encoded class C b-lactamase (blaPDC). These multiple mutations within blaPDC shaped diverse coexisting alleles, whose frequency dynamics responded to the changing antibiotic selective pressures for more than 26 years of chronic infection. Importantly, the combination of the cumulative mutations in blaPDC provided structural and functional protein changes that resulted in a continuous enhancement of its catalytic efficiency and high level of cephalosporin resistance. This evolution was linked to the persistent treatment with ceftazidime, which we demonstrated selected for variants with robust catalytic activity against this expanded-spectrum cephalosporin. A “gain of function” of collateral resistance toward ceftolozane, a more recently introduced cephalosporin that was not prescribed to this patient, was also observed, and the biochemical basis of this cross-resistance phenomenon was elucidated. This work unveils the evolutionary trajectories paved by bacteria toward a multidrug-resistant phenotype, driven by decades of antibiotic treatment in the natural CF environmental setting.
Fil: Colque, Claudia A. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina
Fil: Albarracín Orio, Andrea Georgina. Universidad Católica de Córdoba. Facultad de Ciencias Agropecuarias; Argentina
Fil: Tomatis, Pablo Emiliano. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina
Fil: Dotta, Gina. Universidad Nacional de Rosario. Instituto de Biología Molecular; Argentina
Fil: Moreno, Diego M. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina
Fil: Hedemann, Laura Gabriela. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina
Fil: Hickman, Rachel. Technical University of Denmark; Dinamarca
Fil: Madsen Sommer, Lea Mette. Technical University of Denmark; Dinamarca
Fil: Feliziani, Sofía. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina
Fil: Moyano, Alejandro José. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina
Fil: Bonomo, Robert. Case Western Reserve University; Estados Unidos
Fil: Johansen, Helle Krogh. University of Copenhagen; Dinamarca
Fil: Molin, Søren. Technical University of Denmark; Dinamarca
Fil: Vila, Alejandro. niversidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina
Fil: Smania, Andrea M. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina
description Traditional studies on the evolution of antibiotic resistance development use approaches that can range from laboratory-based experimental studies, to epidemiological surveillance, to sequencing of clinical isolates. However, evolutionary trajectories also depend on the environment in which selection takes place, compelling the need to more deeply investigate the impact of environmental complexities and their dynamics over time. Herein, we explored the within-patient adaptive long-term evolution of a Pseudomonas aeruginosa hypermutator lineage in the airways of a cystic fibrosis (CF) patient by performing a chronological tracking of mutations that occurred in different subpopulations; our results demonstrated parallel evolution events in the chromosomally encoded class C b-lactamase (blaPDC). These multiple mutations within blaPDC shaped diverse coexisting alleles, whose frequency dynamics responded to the changing antibiotic selective pressures for more than 26 years of chronic infection. Importantly, the combination of the cumulative mutations in blaPDC provided structural and functional protein changes that resulted in a continuous enhancement of its catalytic efficiency and high level of cephalosporin resistance. This evolution was linked to the persistent treatment with ceftazidime, which we demonstrated selected for variants with robust catalytic activity against this expanded-spectrum cephalosporin. A “gain of function” of collateral resistance toward ceftolozane, a more recently introduced cephalosporin that was not prescribed to this patient, was also observed, and the biochemical basis of this cross-resistance phenomenon was elucidated. This work unveils the evolutionary trajectories paved by bacteria toward a multidrug-resistant phenotype, driven by decades of antibiotic treatment in the natural CF environmental setting.
publishDate 2022
dc.date.none.fl_str_mv 2022-09-08
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/acceptedVersion
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info:ar-repo/semantics/articulo
format article
status_str acceptedVersion
dc.identifier.none.fl_str_mv http://pa.bibdigital.ucc.edu.ar/3687/1/A_Colque_Albarrac%C3%ADnOrio_Tomatis_Dotta_Moreno_Hedemann_Hickman_Sommer_Feliziani_Moyano_Bonomo_Johansen_Molin_Vila_Smania.pdf
url http://pa.bibdigital.ucc.edu.ar/3687/1/A_Colque_Albarrac%C3%ADnOrio_Tomatis_Dotta_Moreno_Hedemann_Hickman_Sommer_Feliziani_Moyano_Bonomo_Johansen_Molin_Vila_Smania.pdf
dc.language.none.fl_str_mv spa
language spa
dc.relation.none.fl_str_mv http://pa.bibdigital.ucc.edu.ar/3687/
info:eu-repo/semantics/altIdentifier/doi/0.1128/mbio.01663-22
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
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eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0/deed.es
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv Colque, Claudia A. ORCID: https://orcid.org/0000-0002-9027-4747 <https://orcid.org/0000-0002-9027-4747>, Albarracín Orio, Andrea Georgina ORCID: https://orcid.org/0000-0002-4722-1439 <https://orcid.org/0000-0002-4722-1439>, Tomatis, Pablo Emiliano ORCID: https://orcid.org/0000-0002-1126-8200 <https://orcid.org/0000-0002-1126-8200>, Dotta, Gina ORCID: https://orcid.org/0000-0003-1023-1606 <https://orcid.org/0000-0003-1023-1606>, Moreno, Diego M. ORCID: https://orcid.org/0000-0001-5493-8537 <https://orcid.org/0000-0001-5493-8537>, Hedemann, Laura Gabriela ORCID: https://orcid.org/0000-0002-6667-6500 <https://orcid.org/0000-0002-6667-6500>, Hickman, Rachel ORCID: https://orcid.org/0000-0002-0290-1836 <https://orcid.org/0000-0002-0290-1836>, Madsen Sommer, Lea Mette ORCID: https://orcid.org/0000-0002-1622-6691 <https://orcid.org/0000-0002-1622-6691>, Feliziani, Sofía, Moyano, Alejandro José ORCID: https://orcid.org/0000-0002-4976-7611 <https://orcid.org/0000-0002-4976-7611>, Bonomo, Robert ORCID: https://orcid.org/0000-0002-3299-894X <https://orcid.org/0000-0002-3299-894X>, Johansen, Helle Krogh ORCID: https://orcid.org/0000-0003-0268-3717 <https://orcid.org/0000-0003-0268-3717>, Molin, Søren ORCID: https://orcid.org/0000-0002-7973-2639 <https://orcid.org/0000-0002-7973-2639>, Vila, Alejandro ORCID: https://orcid.org/0000-0002-7978-3233 <https://orcid.org/0000-0002-7978-3233> and Smania, Andrea M. (2022) Longitudinal Evolution of the Pseudomonas-Derived Cephalosporinase (PDC) Structure and Activity in a Cystic Fibrosis Patient Treated with β-Lactams. mBio, 13 (5).
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instname_str Universidad Católica de Córdoba
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