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Development of a Serum-Free Medium To Aid Large-Scale Production of Mycoplasma-Based Therapies

To assist in the advancement of the large-scale production of safe Mycoplasma vaccines and other Mycoplasma-based therapies, we developed a culture medium free of animal serum and other animal components for Mycoplasma pneumoniae growth. By establishing a workflow method to systematically test diffe...

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Autores principales: Burgos, Raul, Garcia-Ramallo, Eva, Shaw, Daniel, Lluch-Senar, Maria, Serrano, Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10269708/
https://www.ncbi.nlm.nih.gov/pubmed/37097155
http://dx.doi.org/10.1128/spectrum.04859-22
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author Burgos, Raul
Garcia-Ramallo, Eva
Shaw, Daniel
Lluch-Senar, Maria
Serrano, Luis
author_facet Burgos, Raul
Garcia-Ramallo, Eva
Shaw, Daniel
Lluch-Senar, Maria
Serrano, Luis
author_sort Burgos, Raul
collection PubMed
description To assist in the advancement of the large-scale production of safe Mycoplasma vaccines and other Mycoplasma-based therapies, we developed a culture medium free of animal serum and other animal components for Mycoplasma pneumoniae growth. By establishing a workflow method to systematically test different compounds and concentrations, we provide optimized formulations capable of supporting serial passaging and robust growth reaching 60 to 70% of the biomass obtained in rich medium. Global transcriptomic and proteomic analysis showed minor physiological changes upon cell culture in the animal component-free medium, supporting its suitability for the production of M. pneumoniae-based therapies. The major contributors to growth performance were found to be glucose as a carbon source, glycerol, cholesterol, and phospholipids as a source of fatty acids. Bovine serum albumin or cyclodextrin (in the animal component-free medium) were required as lipid carriers to prevent lipid toxicity. Connaught Medical Research Laboratories medium (CMRL) used to simplify medium preparation as a source of amino acids, nucleotide precursors, vitamins, and other cofactors could be substituted by cysteine. In fact, the presence of protein hydrolysates such as yeastolate or peptones was found to be essential and preferred over free amino acids, except for the cysteine. Supplementation of nucleotide precursors and vitamins is not strictly necessary in the presence of yeastolate, suggesting that this animal origin-free hydrolysate serves as an efficient source for these compounds. Finally, we adapted the serum-free medium formulation to support growth of Mycoplasma hyopneumoniae, a swine pathogen for which inactivated whole-cell vaccines are available. IMPORTANCE Mycoplasma infections have a significant negative impact on both livestock production and human health. Vaccination is often the first option to control disease and alleviate the economic impact that some Mycoplasma infections cause on milk production, weight gain, and animal health. The fastidious nutrient requirements of these bacteria, however, challenges the industrial production of attenuated or inactivated whole-cell vaccines, which depends on the use of animal serum and other animal raw materials. Apart from their clinical relevance, some Mycoplasma species have become cellular models for systems and synthetic biology, owing to the small size of their genomes and the absence of a cell wall, which offers unique opportunities for the secretion and delivery of biotherapeutics. This study proposes medium formulations free of serum and animal components with the potential of supporting large-scale production upon industrial optimization, thus contributing to the development of safe vaccines and other Mycoplasma-based therapies.
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spelling pubmed-102697082023-06-16 Development of a Serum-Free Medium To Aid Large-Scale Production of Mycoplasma-Based Therapies Burgos, Raul Garcia-Ramallo, Eva Shaw, Daniel Lluch-Senar, Maria Serrano, Luis Microbiol Spectr Research Article To assist in the advancement of the large-scale production of safe Mycoplasma vaccines and other Mycoplasma-based therapies, we developed a culture medium free of animal serum and other animal components for Mycoplasma pneumoniae growth. By establishing a workflow method to systematically test different compounds and concentrations, we provide optimized formulations capable of supporting serial passaging and robust growth reaching 60 to 70% of the biomass obtained in rich medium. Global transcriptomic and proteomic analysis showed minor physiological changes upon cell culture in the animal component-free medium, supporting its suitability for the production of M. pneumoniae-based therapies. The major contributors to growth performance were found to be glucose as a carbon source, glycerol, cholesterol, and phospholipids as a source of fatty acids. Bovine serum albumin or cyclodextrin (in the animal component-free medium) were required as lipid carriers to prevent lipid toxicity. Connaught Medical Research Laboratories medium (CMRL) used to simplify medium preparation as a source of amino acids, nucleotide precursors, vitamins, and other cofactors could be substituted by cysteine. In fact, the presence of protein hydrolysates such as yeastolate or peptones was found to be essential and preferred over free amino acids, except for the cysteine. Supplementation of nucleotide precursors and vitamins is not strictly necessary in the presence of yeastolate, suggesting that this animal origin-free hydrolysate serves as an efficient source for these compounds. Finally, we adapted the serum-free medium formulation to support growth of Mycoplasma hyopneumoniae, a swine pathogen for which inactivated whole-cell vaccines are available. IMPORTANCE Mycoplasma infections have a significant negative impact on both livestock production and human health. Vaccination is often the first option to control disease and alleviate the economic impact that some Mycoplasma infections cause on milk production, weight gain, and animal health. The fastidious nutrient requirements of these bacteria, however, challenges the industrial production of attenuated or inactivated whole-cell vaccines, which depends on the use of animal serum and other animal raw materials. Apart from their clinical relevance, some Mycoplasma species have become cellular models for systems and synthetic biology, owing to the small size of their genomes and the absence of a cell wall, which offers unique opportunities for the secretion and delivery of biotherapeutics. This study proposes medium formulations free of serum and animal components with the potential of supporting large-scale production upon industrial optimization, thus contributing to the development of safe vaccines and other Mycoplasma-based therapies. American Society for Microbiology 2023-04-25 /pmc/articles/PMC10269708/ /pubmed/37097155 http://dx.doi.org/10.1128/spectrum.04859-22 Text en Copyright © 2023 Burgos et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Burgos, Raul
Garcia-Ramallo, Eva
Shaw, Daniel
Lluch-Senar, Maria
Serrano, Luis
Development of a Serum-Free Medium To Aid Large-Scale Production of Mycoplasma-Based Therapies
title Development of a Serum-Free Medium To Aid Large-Scale Production of Mycoplasma-Based Therapies
title_full Development of a Serum-Free Medium To Aid Large-Scale Production of Mycoplasma-Based Therapies
title_fullStr Development of a Serum-Free Medium To Aid Large-Scale Production of Mycoplasma-Based Therapies
title_full_unstemmed Development of a Serum-Free Medium To Aid Large-Scale Production of Mycoplasma-Based Therapies
title_short Development of a Serum-Free Medium To Aid Large-Scale Production of Mycoplasma-Based Therapies
title_sort development of a serum-free medium to aid large-scale production of mycoplasma-based therapies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10269708/
https://www.ncbi.nlm.nih.gov/pubmed/37097155
http://dx.doi.org/10.1128/spectrum.04859-22
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