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The antibacterial activity and toxin production control of bee venom in mouse MRSA pneumonia model

BACKGROUND: The current antimicrobial therapy is still important for the treatment of pneumonia due to MRSA infection, but there are some limitations, including the route of administration, side effect profile, and increased microbial resistance patterns. Therefore, we investigated whether BV, which...

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Autores principales: Kong, Ryong, Lee, Young-Seob, Kang, Dam-Hee, Wang, Shu, Li, Qianqian, Kwon, Dong-Yeul, Kang, Ok-Hwa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7385961/
https://www.ncbi.nlm.nih.gov/pubmed/32718325
http://dx.doi.org/10.1186/s12906-020-02991-8
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author Kong, Ryong
Lee, Young-Seob
Kang, Dam-Hee
Wang, Shu
Li, Qianqian
Kwon, Dong-Yeul
Kang, Ok-Hwa
author_facet Kong, Ryong
Lee, Young-Seob
Kang, Dam-Hee
Wang, Shu
Li, Qianqian
Kwon, Dong-Yeul
Kang, Ok-Hwa
author_sort Kong, Ryong
collection PubMed
description BACKGROUND: The current antimicrobial therapy is still important for the treatment of pneumonia due to MRSA infection, but there are some limitations, including the route of administration, side effect profile, and increased microbial resistance patterns. Therefore, we investigated whether BV, which shows a strong antimicrobial effect against MRSA, would be effective in a pneumonia model. METHODS: In vitro, we checked MIC, qRT-PCR, western blot, ELISA, LDH-assay. In vivo, we checked survival rate, gross pathological change, histopathology, lung bacterial clearance assay, and the expression of inflammatory related gene. RESULTS: The minimum inhibitory concentration of BV against MRSA is 15.6 μg/ml by broth dilution method. The production of toxins and related gene were reduced by BV in MRSA. The secretion of cytokines were decreased by treatment with BV in 264.7 RAW macrophages stimulated by MRSA Also, BV protected A549 from pathogenicity of MRSA. Bee venom reduced the number of bacteria in the lungs and alleviated the symptoms of MRSA-induced pneumonia in mouse. CONCLUSION: BV inhibited the virulence of the bacterium and the number of bacterial cells present in lung tissue, thereby alleviating the symptoms of pneumonia in mice. This study suggested that BV may be a candidate substance for the treatment of pneumonia caused by MRSA infection.
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spelling pubmed-73859612020-07-30 The antibacterial activity and toxin production control of bee venom in mouse MRSA pneumonia model Kong, Ryong Lee, Young-Seob Kang, Dam-Hee Wang, Shu Li, Qianqian Kwon, Dong-Yeul Kang, Ok-Hwa BMC Complement Med Ther Research Article BACKGROUND: The current antimicrobial therapy is still important for the treatment of pneumonia due to MRSA infection, but there are some limitations, including the route of administration, side effect profile, and increased microbial resistance patterns. Therefore, we investigated whether BV, which shows a strong antimicrobial effect against MRSA, would be effective in a pneumonia model. METHODS: In vitro, we checked MIC, qRT-PCR, western blot, ELISA, LDH-assay. In vivo, we checked survival rate, gross pathological change, histopathology, lung bacterial clearance assay, and the expression of inflammatory related gene. RESULTS: The minimum inhibitory concentration of BV against MRSA is 15.6 μg/ml by broth dilution method. The production of toxins and related gene were reduced by BV in MRSA. The secretion of cytokines were decreased by treatment with BV in 264.7 RAW macrophages stimulated by MRSA Also, BV protected A549 from pathogenicity of MRSA. Bee venom reduced the number of bacteria in the lungs and alleviated the symptoms of MRSA-induced pneumonia in mouse. CONCLUSION: BV inhibited the virulence of the bacterium and the number of bacterial cells present in lung tissue, thereby alleviating the symptoms of pneumonia in mice. This study suggested that BV may be a candidate substance for the treatment of pneumonia caused by MRSA infection. BioMed Central 2020-07-27 /pmc/articles/PMC7385961/ /pubmed/32718325 http://dx.doi.org/10.1186/s12906-020-02991-8 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Kong, Ryong
Lee, Young-Seob
Kang, Dam-Hee
Wang, Shu
Li, Qianqian
Kwon, Dong-Yeul
Kang, Ok-Hwa
The antibacterial activity and toxin production control of bee venom in mouse MRSA pneumonia model
title The antibacterial activity and toxin production control of bee venom in mouse MRSA pneumonia model
title_full The antibacterial activity and toxin production control of bee venom in mouse MRSA pneumonia model
title_fullStr The antibacterial activity and toxin production control of bee venom in mouse MRSA pneumonia model
title_full_unstemmed The antibacterial activity and toxin production control of bee venom in mouse MRSA pneumonia model
title_short The antibacterial activity and toxin production control of bee venom in mouse MRSA pneumonia model
title_sort antibacterial activity and toxin production control of bee venom in mouse mrsa pneumonia model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7385961/
https://www.ncbi.nlm.nih.gov/pubmed/32718325
http://dx.doi.org/10.1186/s12906-020-02991-8
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