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Isolation, characterization, and antibacterial activity of lytic bacteriophage against methicillin-resistant Staphylococcus aureus causing bedsore and diabetic wounds

BACKGROUND AND OBJECTIVES: Phage therapy has gained interest as an alternative treatment for methicillin-resistant Staphylococcus aureus (MRSA) infections. The purpose of this study was to isolate and characterize an effective bacteriophage against isolates of MRSA. MATERIALS AND METHODS: Bacterioph...

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Autores principales: Rezaei, Zeinab, Elikaei, Ameneh, Barzi, Seyed Mahmoud, Shafiei, Morvarid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723423/
https://www.ncbi.nlm.nih.gov/pubmed/36531807
http://dx.doi.org/10.18502/ijm.v14i5.10967
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author Rezaei, Zeinab
Elikaei, Ameneh
Barzi, Seyed Mahmoud
Shafiei, Morvarid
author_facet Rezaei, Zeinab
Elikaei, Ameneh
Barzi, Seyed Mahmoud
Shafiei, Morvarid
author_sort Rezaei, Zeinab
collection PubMed
description BACKGROUND AND OBJECTIVES: Phage therapy has gained interest as an alternative treatment for methicillin-resistant Staphylococcus aureus (MRSA) infections. The purpose of this study was to isolate and characterize an effective bacteriophage against isolates of MRSA. MATERIALS AND METHODS: Bacteriophage was isolated from hospital sewage. Lytic activity and the titers of phage lysates were measured using spot test and double-layer plaque assay. The phage characterization was determined through transmission electron microscopy. Adsorption rate, host range and stability tests were investigated. The latent period and burst size were estimated from a one-step growth curve. The effect of bacteriophage against MRSA biofilms was determined and Real-time PCR was used to assess the effects of the bacteriophage on the expression of the biofilm-associated genes. RESULTS: TEM results showed that the phage resembled the Cystoviridae family. Its latent period was 30 min, corresponding to about 71/43 phage particles per infected cell. The phage had a broad host range and it was most stable at 37°C and pH 7. It was sensitive to NaCl concentrations. The expressions of the biofilm-associated genes were significantly reduced in the presence of the phage. CONCLUSION: The isolated phage was effective against MRSA strains and it can be an optional strategy of controlling biofilm development.
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spelling pubmed-97234232022-12-15 Isolation, characterization, and antibacterial activity of lytic bacteriophage against methicillin-resistant Staphylococcus aureus causing bedsore and diabetic wounds Rezaei, Zeinab Elikaei, Ameneh Barzi, Seyed Mahmoud Shafiei, Morvarid Iran J Microbiol Original Article BACKGROUND AND OBJECTIVES: Phage therapy has gained interest as an alternative treatment for methicillin-resistant Staphylococcus aureus (MRSA) infections. The purpose of this study was to isolate and characterize an effective bacteriophage against isolates of MRSA. MATERIALS AND METHODS: Bacteriophage was isolated from hospital sewage. Lytic activity and the titers of phage lysates were measured using spot test and double-layer plaque assay. The phage characterization was determined through transmission electron microscopy. Adsorption rate, host range and stability tests were investigated. The latent period and burst size were estimated from a one-step growth curve. The effect of bacteriophage against MRSA biofilms was determined and Real-time PCR was used to assess the effects of the bacteriophage on the expression of the biofilm-associated genes. RESULTS: TEM results showed that the phage resembled the Cystoviridae family. Its latent period was 30 min, corresponding to about 71/43 phage particles per infected cell. The phage had a broad host range and it was most stable at 37°C and pH 7. It was sensitive to NaCl concentrations. The expressions of the biofilm-associated genes were significantly reduced in the presence of the phage. CONCLUSION: The isolated phage was effective against MRSA strains and it can be an optional strategy of controlling biofilm development. Tehran University of Medical Sciences 2022-10 /pmc/articles/PMC9723423/ /pubmed/36531807 http://dx.doi.org/10.18502/ijm.v14i5.10967 Text en Copyright © 2022 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
Rezaei, Zeinab
Elikaei, Ameneh
Barzi, Seyed Mahmoud
Shafiei, Morvarid
Isolation, characterization, and antibacterial activity of lytic bacteriophage against methicillin-resistant Staphylococcus aureus causing bedsore and diabetic wounds
title Isolation, characterization, and antibacterial activity of lytic bacteriophage against methicillin-resistant Staphylococcus aureus causing bedsore and diabetic wounds
title_full Isolation, characterization, and antibacterial activity of lytic bacteriophage against methicillin-resistant Staphylococcus aureus causing bedsore and diabetic wounds
title_fullStr Isolation, characterization, and antibacterial activity of lytic bacteriophage against methicillin-resistant Staphylococcus aureus causing bedsore and diabetic wounds
title_full_unstemmed Isolation, characterization, and antibacterial activity of lytic bacteriophage against methicillin-resistant Staphylococcus aureus causing bedsore and diabetic wounds
title_short Isolation, characterization, and antibacterial activity of lytic bacteriophage against methicillin-resistant Staphylococcus aureus causing bedsore and diabetic wounds
title_sort isolation, characterization, and antibacterial activity of lytic bacteriophage against methicillin-resistant staphylococcus aureus causing bedsore and diabetic wounds
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723423/
https://www.ncbi.nlm.nih.gov/pubmed/36531807
http://dx.doi.org/10.18502/ijm.v14i5.10967
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