Cargando…

A Rapid Method for Performing a Multivariate Optimization of Phage Production Using the RCCD Approach

Bacteriophages can be used in various applications, from the classical approach as substitutes for antibiotics (phage therapy) to new biotechnological uses, i.e., as a protein delivery vehicle, a diagnostic tool for specific strains of bacteria (phage typing), or environmental bioremediation. The de...

Descripción completa

Detalles Bibliográficos
Autores principales: Silva, Jessica, Dias, Roberto, Junior, José Ivo, Marcelino, Maraísa, Silva, Mirelly, Carmo, Adriele, Sousa, Maira, Silva, Cynthia, de Paula, Sergio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8468216/
https://www.ncbi.nlm.nih.gov/pubmed/34578135
http://dx.doi.org/10.3390/pathogens10091100
_version_ 1784573607730479104
author Silva, Jessica
Dias, Roberto
Junior, José Ivo
Marcelino, Maraísa
Silva, Mirelly
Carmo, Adriele
Sousa, Maira
Silva, Cynthia
de Paula, Sergio
author_facet Silva, Jessica
Dias, Roberto
Junior, José Ivo
Marcelino, Maraísa
Silva, Mirelly
Carmo, Adriele
Sousa, Maira
Silva, Cynthia
de Paula, Sergio
author_sort Silva, Jessica
collection PubMed
description Bacteriophages can be used in various applications, from the classical approach as substitutes for antibiotics (phage therapy) to new biotechnological uses, i.e., as a protein delivery vehicle, a diagnostic tool for specific strains of bacteria (phage typing), or environmental bioremediation. The demand for bacteriophage production increases daily, and studies that improve these production processes are necessary. This study evaluated the production of a T4-like bacteriophage vB_EcoM-UFV09 (an E. coli-infecting phage with high potential for reducing environmental biofilms) in seven types of culture media (Luria–Bertani broth and the M9 minimal medium with six different carbon sources) employing four cultivation variables (temperature, incubation time, agitation, and multiplicity of infection). For this purpose, the rotatable central composite design (RCCD) methodology was used, combining and comparing all parameters to determine the ideal conditions for starting to scale up the production process. We used the RCCD to set up the experimental design by combining the cultivation parameters in a specific and systematic way. Despite the high number of conditions evaluated, the results showed that when specific conditions were utilized, viral production was effective even when using a minimal medium, such as M9/glucose, which is less expensive and can significantly reduce costs during large-scale phage production.
format Online
Article
Text
id pubmed-8468216
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-84682162021-09-27 A Rapid Method for Performing a Multivariate Optimization of Phage Production Using the RCCD Approach Silva, Jessica Dias, Roberto Junior, José Ivo Marcelino, Maraísa Silva, Mirelly Carmo, Adriele Sousa, Maira Silva, Cynthia de Paula, Sergio Pathogens Article Bacteriophages can be used in various applications, from the classical approach as substitutes for antibiotics (phage therapy) to new biotechnological uses, i.e., as a protein delivery vehicle, a diagnostic tool for specific strains of bacteria (phage typing), or environmental bioremediation. The demand for bacteriophage production increases daily, and studies that improve these production processes are necessary. This study evaluated the production of a T4-like bacteriophage vB_EcoM-UFV09 (an E. coli-infecting phage with high potential for reducing environmental biofilms) in seven types of culture media (Luria–Bertani broth and the M9 minimal medium with six different carbon sources) employing four cultivation variables (temperature, incubation time, agitation, and multiplicity of infection). For this purpose, the rotatable central composite design (RCCD) methodology was used, combining and comparing all parameters to determine the ideal conditions for starting to scale up the production process. We used the RCCD to set up the experimental design by combining the cultivation parameters in a specific and systematic way. Despite the high number of conditions evaluated, the results showed that when specific conditions were utilized, viral production was effective even when using a minimal medium, such as M9/glucose, which is less expensive and can significantly reduce costs during large-scale phage production. MDPI 2021-08-29 /pmc/articles/PMC8468216/ /pubmed/34578135 http://dx.doi.org/10.3390/pathogens10091100 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Silva, Jessica
Dias, Roberto
Junior, José Ivo
Marcelino, Maraísa
Silva, Mirelly
Carmo, Adriele
Sousa, Maira
Silva, Cynthia
de Paula, Sergio
A Rapid Method for Performing a Multivariate Optimization of Phage Production Using the RCCD Approach
title A Rapid Method for Performing a Multivariate Optimization of Phage Production Using the RCCD Approach
title_full A Rapid Method for Performing a Multivariate Optimization of Phage Production Using the RCCD Approach
title_fullStr A Rapid Method for Performing a Multivariate Optimization of Phage Production Using the RCCD Approach
title_full_unstemmed A Rapid Method for Performing a Multivariate Optimization of Phage Production Using the RCCD Approach
title_short A Rapid Method for Performing a Multivariate Optimization of Phage Production Using the RCCD Approach
title_sort rapid method for performing a multivariate optimization of phage production using the rccd approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8468216/
https://www.ncbi.nlm.nih.gov/pubmed/34578135
http://dx.doi.org/10.3390/pathogens10091100
work_keys_str_mv AT silvajessica arapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach
AT diasroberto arapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach
AT juniorjoseivo arapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach
AT marcelinomaraisa arapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach
AT silvamirelly arapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach
AT carmoadriele arapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach
AT sousamaira arapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach
AT silvacynthia arapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach
AT depaulasergio arapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach
AT silvajessica rapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach
AT diasroberto rapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach
AT juniorjoseivo rapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach
AT marcelinomaraisa rapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach
AT silvamirelly rapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach
AT carmoadriele rapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach
AT sousamaira rapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach
AT silvacynthia rapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach
AT depaulasergio rapidmethodforperformingamultivariateoptimizationofphageproductionusingtherccdapproach