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Optimizing Propagation of Staphylococcus aureus Infecting Bacteriophage vB_SauM-phiIPLA-RODI on Staphylococcus xylosus Using Response Surface Methodology

The use of bacteriophages for killing pathogenic bacteria is a feasible alternative to antibiotics and disinfectants. To obtain the large quantities of phages required for this application, large-scale production of bacteriophages must be optimized. This study aims to define conditions that maximize...

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Autores principales: González-Menéndez, Eva, Arroyo-López, Francisco Noé, Martínez, Beatriz, García, Pilar, Garrido-Fernández, Antonio, Rodríguez, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923447/
https://www.ncbi.nlm.nih.gov/pubmed/29584701
http://dx.doi.org/10.3390/v10040153
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author González-Menéndez, Eva
Arroyo-López, Francisco Noé
Martínez, Beatriz
García, Pilar
Garrido-Fernández, Antonio
Rodríguez, Ana
author_facet González-Menéndez, Eva
Arroyo-López, Francisco Noé
Martínez, Beatriz
García, Pilar
Garrido-Fernández, Antonio
Rodríguez, Ana
author_sort González-Menéndez, Eva
collection PubMed
description The use of bacteriophages for killing pathogenic bacteria is a feasible alternative to antibiotics and disinfectants. To obtain the large quantities of phages required for this application, large-scale production of bacteriophages must be optimized. This study aims to define conditions that maximize the phage yield of the virulent and polyvalent staphylococcal bacteriophage vB_SauM-phiIPLA-RODI in broth culture, using the food-grade species Staphylococcus xylosus as the host strain to reduce the risk of growing massive quantities of pathogenic bacteria and therefore, to ensure the safety of the final phage stock. The effect of four variables, namely initial bacterial concentration (5.66–8.40 log(10) colony-forming unit (CFU)/mL), initial phage concentration (5–8 log(10) plaque-forming unit (PFU)/mL), temperature (21–40 °C) and agitation (20–250 rpm), on phage yield (response) was studied by using response surface methodology (RSM). Successive experimental designs showed that agitation did not significantly impact phage yield, while temperature did have a significant effect, with 38 °C being the optimum for phage propagation. The results allowed the design of a model to describe phage yield as a function of the initial bacterial and phage concentrations at fixed agitation (135 rpm), and optimum temperature (38 °C). The maximum experimental phage yield obtained was 9.3 log(10) PFU/mL, while that predicted by the model under the optimized conditions (7.07 log(10) CFU/mL initial bacterial population and 6.00 log(10) PFU/mL initial phage titer) was 9.25 ± 0.30 log(10) PFU/mL, with the desirability of 0.96. This yield is comparable to that obtained when the phage was propagated on the original host, Staphylococcus aureus. Bacteriophage phiIPLA-RODI showed the same host range and very similar biofilm removal ability regardless of the staphylococcal species used for its propagation. The results presented in this study show the suitability of using a food-grade strain of S. xylosus for the propagation of S. aureus infecting phages and the application of RSM to define the optimal propagation conditions.
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spelling pubmed-59234472018-05-03 Optimizing Propagation of Staphylococcus aureus Infecting Bacteriophage vB_SauM-phiIPLA-RODI on Staphylococcus xylosus Using Response Surface Methodology González-Menéndez, Eva Arroyo-López, Francisco Noé Martínez, Beatriz García, Pilar Garrido-Fernández, Antonio Rodríguez, Ana Viruses Article The use of bacteriophages for killing pathogenic bacteria is a feasible alternative to antibiotics and disinfectants. To obtain the large quantities of phages required for this application, large-scale production of bacteriophages must be optimized. This study aims to define conditions that maximize the phage yield of the virulent and polyvalent staphylococcal bacteriophage vB_SauM-phiIPLA-RODI in broth culture, using the food-grade species Staphylococcus xylosus as the host strain to reduce the risk of growing massive quantities of pathogenic bacteria and therefore, to ensure the safety of the final phage stock. The effect of four variables, namely initial bacterial concentration (5.66–8.40 log(10) colony-forming unit (CFU)/mL), initial phage concentration (5–8 log(10) plaque-forming unit (PFU)/mL), temperature (21–40 °C) and agitation (20–250 rpm), on phage yield (response) was studied by using response surface methodology (RSM). Successive experimental designs showed that agitation did not significantly impact phage yield, while temperature did have a significant effect, with 38 °C being the optimum for phage propagation. The results allowed the design of a model to describe phage yield as a function of the initial bacterial and phage concentrations at fixed agitation (135 rpm), and optimum temperature (38 °C). The maximum experimental phage yield obtained was 9.3 log(10) PFU/mL, while that predicted by the model under the optimized conditions (7.07 log(10) CFU/mL initial bacterial population and 6.00 log(10) PFU/mL initial phage titer) was 9.25 ± 0.30 log(10) PFU/mL, with the desirability of 0.96. This yield is comparable to that obtained when the phage was propagated on the original host, Staphylococcus aureus. Bacteriophage phiIPLA-RODI showed the same host range and very similar biofilm removal ability regardless of the staphylococcal species used for its propagation. The results presented in this study show the suitability of using a food-grade strain of S. xylosus for the propagation of S. aureus infecting phages and the application of RSM to define the optimal propagation conditions. MDPI 2018-03-27 /pmc/articles/PMC5923447/ /pubmed/29584701 http://dx.doi.org/10.3390/v10040153 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
González-Menéndez, Eva
Arroyo-López, Francisco Noé
Martínez, Beatriz
García, Pilar
Garrido-Fernández, Antonio
Rodríguez, Ana
Optimizing Propagation of Staphylococcus aureus Infecting Bacteriophage vB_SauM-phiIPLA-RODI on Staphylococcus xylosus Using Response Surface Methodology
title Optimizing Propagation of Staphylococcus aureus Infecting Bacteriophage vB_SauM-phiIPLA-RODI on Staphylococcus xylosus Using Response Surface Methodology
title_full Optimizing Propagation of Staphylococcus aureus Infecting Bacteriophage vB_SauM-phiIPLA-RODI on Staphylococcus xylosus Using Response Surface Methodology
title_fullStr Optimizing Propagation of Staphylococcus aureus Infecting Bacteriophage vB_SauM-phiIPLA-RODI on Staphylococcus xylosus Using Response Surface Methodology
title_full_unstemmed Optimizing Propagation of Staphylococcus aureus Infecting Bacteriophage vB_SauM-phiIPLA-RODI on Staphylococcus xylosus Using Response Surface Methodology
title_short Optimizing Propagation of Staphylococcus aureus Infecting Bacteriophage vB_SauM-phiIPLA-RODI on Staphylococcus xylosus Using Response Surface Methodology
title_sort optimizing propagation of staphylococcus aureus infecting bacteriophage vb_saum-phiipla-rodi on staphylococcus xylosus using response surface methodology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923447/
https://www.ncbi.nlm.nih.gov/pubmed/29584701
http://dx.doi.org/10.3390/v10040153
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