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Additive Effects of Cyclic Peptide [R4W4] When Added Alongside Azithromycin and Rifampicin against Mycobacterium avium Infection

Mycobacterium avium (M. avium), a type of nontuberculous mycobacteria (NTM), poses a risk for pulmonary infections and disseminated infections in immunocompromised individuals. Conventional treatment consists of a 12-month regimen of the first-line antibiotics rifampicin and azithromycin. However, t...

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Autores principales: Kelley, Melissa, Sasaninia, Kayvan, Abnousian, Arbi, Badaoui, Ali, Owens, James, Beever, Abrianna, Kachour, Nala, Tiwari, Rakesh Kumar, Venketaraman, Vishwanath
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10459066/
https://www.ncbi.nlm.nih.gov/pubmed/37624017
http://dx.doi.org/10.3390/pathogens12081057
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author Kelley, Melissa
Sasaninia, Kayvan
Abnousian, Arbi
Badaoui, Ali
Owens, James
Beever, Abrianna
Kachour, Nala
Tiwari, Rakesh Kumar
Venketaraman, Vishwanath
author_facet Kelley, Melissa
Sasaninia, Kayvan
Abnousian, Arbi
Badaoui, Ali
Owens, James
Beever, Abrianna
Kachour, Nala
Tiwari, Rakesh Kumar
Venketaraman, Vishwanath
author_sort Kelley, Melissa
collection PubMed
description Mycobacterium avium (M. avium), a type of nontuberculous mycobacteria (NTM), poses a risk for pulmonary infections and disseminated infections in immunocompromised individuals. Conventional treatment consists of a 12-month regimen of the first-line antibiotics rifampicin and azithromycin. However, the treatment duration and low antibiotic tolerability present challenges in the treatment of M. avium infection. Furthermore, the emergence of multidrug-resistant mycobacterium strains prompts a need for novel treatments against M. avium infection. This study aims to test the efficacy of a novel antimicrobial peptide, cyclic [R4W4], alongside the first-line antibiotics azithromycin and rifampicin in reducing M. avium survival. Colony-forming unit (CFU) counts were assessed after treating M. avium cultures with varying concentrations of cyclic [R4W4] alone or in conjunction with azithromycin or rifampicin 3 h and 4 days post-treatment. M. avium growth was significantly reduced 4 days after cyclic [R4W4] single treatment. Additionally, cyclic [R4W4]–azithromycin and cyclic [R4W4]–rifampicin combination treatments at specific concentrations significantly reduced M. avium survival 3 h and 4 days post-treatment compared with single antibiotic treatment alone. These findings demonstrate cyclic [R4W4] as a potent treatment method against M. avium and provide insight into novel therapeutic approaches against mycobacterium infections.
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spelling pubmed-104590662023-08-27 Additive Effects of Cyclic Peptide [R4W4] When Added Alongside Azithromycin and Rifampicin against Mycobacterium avium Infection Kelley, Melissa Sasaninia, Kayvan Abnousian, Arbi Badaoui, Ali Owens, James Beever, Abrianna Kachour, Nala Tiwari, Rakesh Kumar Venketaraman, Vishwanath Pathogens Article Mycobacterium avium (M. avium), a type of nontuberculous mycobacteria (NTM), poses a risk for pulmonary infections and disseminated infections in immunocompromised individuals. Conventional treatment consists of a 12-month regimen of the first-line antibiotics rifampicin and azithromycin. However, the treatment duration and low antibiotic tolerability present challenges in the treatment of M. avium infection. Furthermore, the emergence of multidrug-resistant mycobacterium strains prompts a need for novel treatments against M. avium infection. This study aims to test the efficacy of a novel antimicrobial peptide, cyclic [R4W4], alongside the first-line antibiotics azithromycin and rifampicin in reducing M. avium survival. Colony-forming unit (CFU) counts were assessed after treating M. avium cultures with varying concentrations of cyclic [R4W4] alone or in conjunction with azithromycin or rifampicin 3 h and 4 days post-treatment. M. avium growth was significantly reduced 4 days after cyclic [R4W4] single treatment. Additionally, cyclic [R4W4]–azithromycin and cyclic [R4W4]–rifampicin combination treatments at specific concentrations significantly reduced M. avium survival 3 h and 4 days post-treatment compared with single antibiotic treatment alone. These findings demonstrate cyclic [R4W4] as a potent treatment method against M. avium and provide insight into novel therapeutic approaches against mycobacterium infections. MDPI 2023-08-18 /pmc/articles/PMC10459066/ /pubmed/37624017 http://dx.doi.org/10.3390/pathogens12081057 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kelley, Melissa
Sasaninia, Kayvan
Abnousian, Arbi
Badaoui, Ali
Owens, James
Beever, Abrianna
Kachour, Nala
Tiwari, Rakesh Kumar
Venketaraman, Vishwanath
Additive Effects of Cyclic Peptide [R4W4] When Added Alongside Azithromycin and Rifampicin against Mycobacterium avium Infection
title Additive Effects of Cyclic Peptide [R4W4] When Added Alongside Azithromycin and Rifampicin against Mycobacterium avium Infection
title_full Additive Effects of Cyclic Peptide [R4W4] When Added Alongside Azithromycin and Rifampicin against Mycobacterium avium Infection
title_fullStr Additive Effects of Cyclic Peptide [R4W4] When Added Alongside Azithromycin and Rifampicin against Mycobacterium avium Infection
title_full_unstemmed Additive Effects of Cyclic Peptide [R4W4] When Added Alongside Azithromycin and Rifampicin against Mycobacterium avium Infection
title_short Additive Effects of Cyclic Peptide [R4W4] When Added Alongside Azithromycin and Rifampicin against Mycobacterium avium Infection
title_sort additive effects of cyclic peptide [r4w4] when added alongside azithromycin and rifampicin against mycobacterium avium infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10459066/
https://www.ncbi.nlm.nih.gov/pubmed/37624017
http://dx.doi.org/10.3390/pathogens12081057
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