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Effect of fetal and adult bovine serum on pyocyanin production in Pseudomonas aeruginosa isolated from clinical and soil samples

OBJECTIVE(S): Pyocyanin is a blue-greenish redox-active pigment, produced by Pseudomonas aeruginosa, with a wide range of biological and biotechnological applications. Pyocyanin biosynthesis is regulated by the quorum-sensing (QS) system in which the expression of QS genes and QS-controlled virulenc...

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Autores principales: Moayedi, Aylin, Nowroozi, Jamileh, Sepahy, Abbas Akhavan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722993/
https://www.ncbi.nlm.nih.gov/pubmed/29238468
http://dx.doi.org/10.22038/IJBMS.2017.9621
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author Moayedi, Aylin
Nowroozi, Jamileh
Sepahy, Abbas Akhavan
author_facet Moayedi, Aylin
Nowroozi, Jamileh
Sepahy, Abbas Akhavan
author_sort Moayedi, Aylin
collection PubMed
description OBJECTIVE(S): Pyocyanin is a blue-greenish redox-active pigment, produced by Pseudomonas aeruginosa, with a wide range of biological and biotechnological applications. Pyocyanin biosynthesis is regulated by the quorum-sensing (QS) system in which the expression of QS genes and QS-controlled virulence genes may be affected by serum as a complex medium. In the current study, effects of adult bovine serum (ABS) and fetal bovine serum (FBS) on the production of pyocyanin were examined in order to develop it. MATERIALS AND METHODS: The presence of pyocyanin-producing specific genes and proteins in clinical and soil isolates of P. aeruginosa was confirmed using PCR and SDS-PAGE. Isolates were inoculated to media containing different concentrations of complement-active/-inactivated ABS or FBS and pyocyanin concentration was measured by spectrophotometry. Extracted pigment was characterized by using UV-Visible spectrophotometry. Titration of ABS antibodies against studied isolates was performed by the tube agglutination test. RESULTS: Adding ABS to P. aeruginosa culture medium decreased pyocyanin production compared to the control, while its production increased in FBS-containing media (113.21±2.581 vs. 55.26±0.827 μg.ml(-1) and 126.80±2.036 vs. 30.56±0.382 μg.ml(-1) of C(11) and E(8) pyocyanin concentration in the presence of 10% FBS vs. control, respectively). CONCLUSION: In this study, due to the presence of inhibitors such as complement proteins and antibodies in ABS samples, the use of FBS devoid of antibodies was effective to increase pyocyanin production in studied isolates.
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spelling pubmed-57229932017-12-13 Effect of fetal and adult bovine serum on pyocyanin production in Pseudomonas aeruginosa isolated from clinical and soil samples Moayedi, Aylin Nowroozi, Jamileh Sepahy, Abbas Akhavan Iran J Basic Med Sci Original Article OBJECTIVE(S): Pyocyanin is a blue-greenish redox-active pigment, produced by Pseudomonas aeruginosa, with a wide range of biological and biotechnological applications. Pyocyanin biosynthesis is regulated by the quorum-sensing (QS) system in which the expression of QS genes and QS-controlled virulence genes may be affected by serum as a complex medium. In the current study, effects of adult bovine serum (ABS) and fetal bovine serum (FBS) on the production of pyocyanin were examined in order to develop it. MATERIALS AND METHODS: The presence of pyocyanin-producing specific genes and proteins in clinical and soil isolates of P. aeruginosa was confirmed using PCR and SDS-PAGE. Isolates were inoculated to media containing different concentrations of complement-active/-inactivated ABS or FBS and pyocyanin concentration was measured by spectrophotometry. Extracted pigment was characterized by using UV-Visible spectrophotometry. Titration of ABS antibodies against studied isolates was performed by the tube agglutination test. RESULTS: Adding ABS to P. aeruginosa culture medium decreased pyocyanin production compared to the control, while its production increased in FBS-containing media (113.21±2.581 vs. 55.26±0.827 μg.ml(-1) and 126.80±2.036 vs. 30.56±0.382 μg.ml(-1) of C(11) and E(8) pyocyanin concentration in the presence of 10% FBS vs. control, respectively). CONCLUSION: In this study, due to the presence of inhibitors such as complement proteins and antibodies in ABS samples, the use of FBS devoid of antibodies was effective to increase pyocyanin production in studied isolates. Mashhad University of Medical Sciences 2017-12 /pmc/articles/PMC5722993/ /pubmed/29238468 http://dx.doi.org/10.22038/IJBMS.2017.9621 Text en Copyright: © Iranian Journal of Basic Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Moayedi, Aylin
Nowroozi, Jamileh
Sepahy, Abbas Akhavan
Effect of fetal and adult bovine serum on pyocyanin production in Pseudomonas aeruginosa isolated from clinical and soil samples
title Effect of fetal and adult bovine serum on pyocyanin production in Pseudomonas aeruginosa isolated from clinical and soil samples
title_full Effect of fetal and adult bovine serum on pyocyanin production in Pseudomonas aeruginosa isolated from clinical and soil samples
title_fullStr Effect of fetal and adult bovine serum on pyocyanin production in Pseudomonas aeruginosa isolated from clinical and soil samples
title_full_unstemmed Effect of fetal and adult bovine serum on pyocyanin production in Pseudomonas aeruginosa isolated from clinical and soil samples
title_short Effect of fetal and adult bovine serum on pyocyanin production in Pseudomonas aeruginosa isolated from clinical and soil samples
title_sort effect of fetal and adult bovine serum on pyocyanin production in pseudomonas aeruginosa isolated from clinical and soil samples
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722993/
https://www.ncbi.nlm.nih.gov/pubmed/29238468
http://dx.doi.org/10.22038/IJBMS.2017.9621
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