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813. Combination of N-Acetyl-Cysteine With Clarithromycin Against Mycobacterium avium Infection

BACKGROUND: N-Acetyl-cysteine (NAC) is widely used in patients with chronic pulmonary diseases. In previous studies, its antimicrobacterial and antimycobacterial effects have been reported. Among its effect in Mycobacteria, it has been mainly studied in Mycobacterium tuberculosis. Here, we examined...

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Autores principales: Shiozawa, Ayako, Kajiwara, Chiaki, Ishii, Yoshikazu, Tateda, Kazuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254830/
http://dx.doi.org/10.1093/ofid/ofy210.820
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author Shiozawa, Ayako
Kajiwara, Chiaki
Ishii, Yoshikazu
Tateda, Kazuhiro
author_facet Shiozawa, Ayako
Kajiwara, Chiaki
Ishii, Yoshikazu
Tateda, Kazuhiro
author_sort Shiozawa, Ayako
collection PubMed
description BACKGROUND: N-Acetyl-cysteine (NAC) is widely used in patients with chronic pulmonary diseases. In previous studies, its antimicrobacterial and antimycobacterial effects have been reported. Among its effect in Mycobacteria, it has been mainly studied in Mycobacterium tuberculosis. Here, we examined whether NAC has antibiotic activity against M. avium. METHODS: The antimycobacterial effect of NAC was assessed in JCM 15430 M. avium strain infected A-549 (human lung epithelial cells) and MH-S (mouse alveolar macrophages). These cells were infected with M. avium at multiplicity of infection of 10 for 1 hours, washed and then cultivated for 5 days. Bacterial uptake was evaluated at 0 days and 5 days of cultivation. For the NAC treatment group, 5% FBS medium with 10 mM NAC was used as culture medium. We also tested its effect in combination with clarithromycin in vivo. BALB/c mice were infected intranasally with M. avium, and were given NAC (400 mg/kg) or clarithromycin (100 mg/kg) or both by gavage daily for 6 days. On day 7 of infection, lungs were harvested and CFU, cytokines and antimicrobial peptides were measured. RESULTS: NAC treatment of M. avium-infected A-549 and MH-S resulted in a significant reduction of mycobacterial loads (P = 0.014 and P = 0.014). In vivo, NAC treatment resulted in a significant reduction of mycobacterial loads in the lungs of M. avium-infected mice (P = 0.007). When in combination with clarithromycin, we also had an additional reduction (vs. clarithromycin monotherapy; P = 0.001). Several antimicrobial peptides significantly increased when treated with NAC and clarithromycin combination therapy. CONCLUSION: NAC exhibits potent anti-mycobacterial effects and may limit M. avium infection. In addition with clarithromycin, it showed an additive effect in reduction of mycobacterial loads. Interestingly, in our study, several antimicrobial peptides increased significantly which may be one of the possibility on how NAC is involved in antimycobacterial effects. These results indicate that NAC may be an additional option in treating M. avium-infected patients in future, along with its classical drug regimens containing clarithromycin. DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-62548302018-11-28 813. Combination of N-Acetyl-Cysteine With Clarithromycin Against Mycobacterium avium Infection Shiozawa, Ayako Kajiwara, Chiaki Ishii, Yoshikazu Tateda, Kazuhiro Open Forum Infect Dis Abstracts BACKGROUND: N-Acetyl-cysteine (NAC) is widely used in patients with chronic pulmonary diseases. In previous studies, its antimicrobacterial and antimycobacterial effects have been reported. Among its effect in Mycobacteria, it has been mainly studied in Mycobacterium tuberculosis. Here, we examined whether NAC has antibiotic activity against M. avium. METHODS: The antimycobacterial effect of NAC was assessed in JCM 15430 M. avium strain infected A-549 (human lung epithelial cells) and MH-S (mouse alveolar macrophages). These cells were infected with M. avium at multiplicity of infection of 10 for 1 hours, washed and then cultivated for 5 days. Bacterial uptake was evaluated at 0 days and 5 days of cultivation. For the NAC treatment group, 5% FBS medium with 10 mM NAC was used as culture medium. We also tested its effect in combination with clarithromycin in vivo. BALB/c mice were infected intranasally with M. avium, and were given NAC (400 mg/kg) or clarithromycin (100 mg/kg) or both by gavage daily for 6 days. On day 7 of infection, lungs were harvested and CFU, cytokines and antimicrobial peptides were measured. RESULTS: NAC treatment of M. avium-infected A-549 and MH-S resulted in a significant reduction of mycobacterial loads (P = 0.014 and P = 0.014). In vivo, NAC treatment resulted in a significant reduction of mycobacterial loads in the lungs of M. avium-infected mice (P = 0.007). When in combination with clarithromycin, we also had an additional reduction (vs. clarithromycin monotherapy; P = 0.001). Several antimicrobial peptides significantly increased when treated with NAC and clarithromycin combination therapy. CONCLUSION: NAC exhibits potent anti-mycobacterial effects and may limit M. avium infection. In addition with clarithromycin, it showed an additive effect in reduction of mycobacterial loads. Interestingly, in our study, several antimicrobial peptides increased significantly which may be one of the possibility on how NAC is involved in antimycobacterial effects. These results indicate that NAC may be an additional option in treating M. avium-infected patients in future, along with its classical drug regimens containing clarithromycin. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6254830/ http://dx.doi.org/10.1093/ofid/ofy210.820 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Shiozawa, Ayako
Kajiwara, Chiaki
Ishii, Yoshikazu
Tateda, Kazuhiro
813. Combination of N-Acetyl-Cysteine With Clarithromycin Against Mycobacterium avium Infection
title 813. Combination of N-Acetyl-Cysteine With Clarithromycin Against Mycobacterium avium Infection
title_full 813. Combination of N-Acetyl-Cysteine With Clarithromycin Against Mycobacterium avium Infection
title_fullStr 813. Combination of N-Acetyl-Cysteine With Clarithromycin Against Mycobacterium avium Infection
title_full_unstemmed 813. Combination of N-Acetyl-Cysteine With Clarithromycin Against Mycobacterium avium Infection
title_short 813. Combination of N-Acetyl-Cysteine With Clarithromycin Against Mycobacterium avium Infection
title_sort 813. combination of n-acetyl-cysteine with clarithromycin against mycobacterium avium infection
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254830/
http://dx.doi.org/10.1093/ofid/ofy210.820
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