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Isolation and immunogenicity of extracted outer membrane vesicles from Pseudomonas aeruginosa under antibiotics treatment conditions

BACKGROUND AND OBJECTIVES: Different types of antibiotics have been indicated to enhance the secretion of OMVs from Pseudomonas aeruginosa. We aimed to investigate the effect of meropenem and amikacin antibiotics on inducing the secretion of OMVs and immunologic features in P. aeruginosa. MATERIALS...

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Autores principales: Hadadi-Fishani, Mehdi, Najar-Peerayeh, Shahin, Siadat, Seyed Davar, Sekhavati, Mohammad, Mobarez, Ashraf Mohabati
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8816698/
https://www.ncbi.nlm.nih.gov/pubmed/35222861
http://dx.doi.org/10.18502/ijm.v13i6.8087
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author Hadadi-Fishani, Mehdi
Najar-Peerayeh, Shahin
Siadat, Seyed Davar
Sekhavati, Mohammad
Mobarez, Ashraf Mohabati
author_facet Hadadi-Fishani, Mehdi
Najar-Peerayeh, Shahin
Siadat, Seyed Davar
Sekhavati, Mohammad
Mobarez, Ashraf Mohabati
author_sort Hadadi-Fishani, Mehdi
collection PubMed
description BACKGROUND AND OBJECTIVES: Different types of antibiotics have been indicated to enhance the secretion of OMVs from Pseudomonas aeruginosa. We aimed to investigate the effect of meropenem and amikacin antibiotics on inducing the secretion of OMVs and immunologic features in P. aeruginosa. MATERIALS AND METHODS: The OMVs were prepared from P. aeruginosa under hypervesiculation condition (treatment with amikacin and meropenem), and extraction was carried out by the sequential ultracentrifugation. Physicochemical features of extracted OMVs were evaluated by electron microscopy and SDS-PAGE. To quantify antibody synthesis and function after immunization with OMV, we used ELISA, serum bactericidal activity, and opsonophagocytosis. Production of cytokines from splenocytes of immunized mice was measured with ELISA. RESULTS: Specific-antibody IgG production, particularly IgG1 subclass, increased in mice primed with hypervesiculation-derived OMVs compared to normal condition-derived OMVs. Serum bactericidal activity and opsonophagocytosis of secreted antibody was enhanced in mice primed with hypervesiculation-derived OMVs. Investigation of cytokine production showed the upregulation of IL-8, IL-12, IL-17, and TNF-α and downregulation of IL-10. CONCLUSION: Based on our findings, OMVs production can be increased by treating P. aeruginosa with amikacin and meropenem antibiotics. Moreover, hypervesiculation-derived OMV scan possibly activate the humoral and cellular immune response more than normal OMVs.
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spelling pubmed-88166982022-02-25 Isolation and immunogenicity of extracted outer membrane vesicles from Pseudomonas aeruginosa under antibiotics treatment conditions Hadadi-Fishani, Mehdi Najar-Peerayeh, Shahin Siadat, Seyed Davar Sekhavati, Mohammad Mobarez, Ashraf Mohabati Iran J Microbiol Original Article BACKGROUND AND OBJECTIVES: Different types of antibiotics have been indicated to enhance the secretion of OMVs from Pseudomonas aeruginosa. We aimed to investigate the effect of meropenem and amikacin antibiotics on inducing the secretion of OMVs and immunologic features in P. aeruginosa. MATERIALS AND METHODS: The OMVs were prepared from P. aeruginosa under hypervesiculation condition (treatment with amikacin and meropenem), and extraction was carried out by the sequential ultracentrifugation. Physicochemical features of extracted OMVs were evaluated by electron microscopy and SDS-PAGE. To quantify antibody synthesis and function after immunization with OMV, we used ELISA, serum bactericidal activity, and opsonophagocytosis. Production of cytokines from splenocytes of immunized mice was measured with ELISA. RESULTS: Specific-antibody IgG production, particularly IgG1 subclass, increased in mice primed with hypervesiculation-derived OMVs compared to normal condition-derived OMVs. Serum bactericidal activity and opsonophagocytosis of secreted antibody was enhanced in mice primed with hypervesiculation-derived OMVs. Investigation of cytokine production showed the upregulation of IL-8, IL-12, IL-17, and TNF-α and downregulation of IL-10. CONCLUSION: Based on our findings, OMVs production can be increased by treating P. aeruginosa with amikacin and meropenem antibiotics. Moreover, hypervesiculation-derived OMV scan possibly activate the humoral and cellular immune response more than normal OMVs. Tehran University of Medical Sciences 2021-12 /pmc/articles/PMC8816698/ /pubmed/35222861 http://dx.doi.org/10.18502/ijm.v13i6.8087 Text en Copyright © 2021 The Authors. Published by Tehran University of Medical Sciences https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International license (https://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited.
spellingShingle Original Article
Hadadi-Fishani, Mehdi
Najar-Peerayeh, Shahin
Siadat, Seyed Davar
Sekhavati, Mohammad
Mobarez, Ashraf Mohabati
Isolation and immunogenicity of extracted outer membrane vesicles from Pseudomonas aeruginosa under antibiotics treatment conditions
title Isolation and immunogenicity of extracted outer membrane vesicles from Pseudomonas aeruginosa under antibiotics treatment conditions
title_full Isolation and immunogenicity of extracted outer membrane vesicles from Pseudomonas aeruginosa under antibiotics treatment conditions
title_fullStr Isolation and immunogenicity of extracted outer membrane vesicles from Pseudomonas aeruginosa under antibiotics treatment conditions
title_full_unstemmed Isolation and immunogenicity of extracted outer membrane vesicles from Pseudomonas aeruginosa under antibiotics treatment conditions
title_short Isolation and immunogenicity of extracted outer membrane vesicles from Pseudomonas aeruginosa under antibiotics treatment conditions
title_sort isolation and immunogenicity of extracted outer membrane vesicles from pseudomonas aeruginosa under antibiotics treatment conditions
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8816698/
https://www.ncbi.nlm.nih.gov/pubmed/35222861
http://dx.doi.org/10.18502/ijm.v13i6.8087
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