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Pathogenic Nontuberculous Mycobacteria Resist and Inactivate Cathelicidin: Implication of a Novel Role for Polar Mycobacterial Lipids

Nontuberculous mycobacteria (NTM) are a large group of environmental organisms with worldwide distribution, but only a relatively few are known to be pathogenic. Chronic, debilitating lung disease is the most common manifestation of NTM infection, which is often refractory to treatment. The incidenc...

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Autores principales: Honda, Jennifer R., Hess, Tamara, Malcolm, Kenneth C., Ovrutsky, Alida R., Bai, Xiyuan, Irani, Vida R., Dobos, Karen M., Chan, Edward D., Flores, Sonia C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436335/
https://www.ncbi.nlm.nih.gov/pubmed/25993058
http://dx.doi.org/10.1371/journal.pone.0126994
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author Honda, Jennifer R.
Hess, Tamara
Malcolm, Kenneth C.
Ovrutsky, Alida R.
Bai, Xiyuan
Irani, Vida R.
Dobos, Karen M.
Chan, Edward D.
Flores, Sonia C.
author_facet Honda, Jennifer R.
Hess, Tamara
Malcolm, Kenneth C.
Ovrutsky, Alida R.
Bai, Xiyuan
Irani, Vida R.
Dobos, Karen M.
Chan, Edward D.
Flores, Sonia C.
author_sort Honda, Jennifer R.
collection PubMed
description Nontuberculous mycobacteria (NTM) are a large group of environmental organisms with worldwide distribution, but only a relatively few are known to be pathogenic. Chronic, debilitating lung disease is the most common manifestation of NTM infection, which is often refractory to treatment. The incidence and prevalence of NTM lung disease are increasing in the United States and in many parts of the world. Hence, a more complete understanding of NTM pathogenesis will provide the foundation to develop innovative approaches to treat this recalcitrant disease. Herein, we demonstrate that several species of NTM show broad resistance to the antimicrobial peptide, cathelicidin (LL-37). Resistance to LL-37 was not significantly different between M. avium that contain serovar-specific glycopeptidolipid (GPL, M. avium (ssGPL)) and M. avium that do not (M. avium (ΔssGPL)). Similarly, M. abscessus containing non-specific GPL (M. abscessus (nsGPL(+))) or lacking nsGPL (M. abscessus (nsGPL(-))) remained equally resistant to LL-37. These findings would support the notion that GPL are not the components responsible for NTM resistance to LL-37. Unexpectedly, the growth of M. abscessus (nsGPL(-)) increased with LL-37 or scrambled LL-37 peptide in a dose-dependent fashion. We also discovered that LL-37 exposed to NTM had reduced antimicrobial activity, and initial work indicates that this is likely due to inactivation of LL-37 by lipid component(s) of the NTM cell envelope. We conclude that pathogenic NTM resist and inactivate LL-37. The mechanism by which NTM circumvent the antimicrobial activity of LL-37 remains to be determined.
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spelling pubmed-44363352015-05-27 Pathogenic Nontuberculous Mycobacteria Resist and Inactivate Cathelicidin: Implication of a Novel Role for Polar Mycobacterial Lipids Honda, Jennifer R. Hess, Tamara Malcolm, Kenneth C. Ovrutsky, Alida R. Bai, Xiyuan Irani, Vida R. Dobos, Karen M. Chan, Edward D. Flores, Sonia C. PLoS One Research Article Nontuberculous mycobacteria (NTM) are a large group of environmental organisms with worldwide distribution, but only a relatively few are known to be pathogenic. Chronic, debilitating lung disease is the most common manifestation of NTM infection, which is often refractory to treatment. The incidence and prevalence of NTM lung disease are increasing in the United States and in many parts of the world. Hence, a more complete understanding of NTM pathogenesis will provide the foundation to develop innovative approaches to treat this recalcitrant disease. Herein, we demonstrate that several species of NTM show broad resistance to the antimicrobial peptide, cathelicidin (LL-37). Resistance to LL-37 was not significantly different between M. avium that contain serovar-specific glycopeptidolipid (GPL, M. avium (ssGPL)) and M. avium that do not (M. avium (ΔssGPL)). Similarly, M. abscessus containing non-specific GPL (M. abscessus (nsGPL(+))) or lacking nsGPL (M. abscessus (nsGPL(-))) remained equally resistant to LL-37. These findings would support the notion that GPL are not the components responsible for NTM resistance to LL-37. Unexpectedly, the growth of M. abscessus (nsGPL(-)) increased with LL-37 or scrambled LL-37 peptide in a dose-dependent fashion. We also discovered that LL-37 exposed to NTM had reduced antimicrobial activity, and initial work indicates that this is likely due to inactivation of LL-37 by lipid component(s) of the NTM cell envelope. We conclude that pathogenic NTM resist and inactivate LL-37. The mechanism by which NTM circumvent the antimicrobial activity of LL-37 remains to be determined. Public Library of Science 2015-05-18 /pmc/articles/PMC4436335/ /pubmed/25993058 http://dx.doi.org/10.1371/journal.pone.0126994 Text en © 2015 Honda et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Honda, Jennifer R.
Hess, Tamara
Malcolm, Kenneth C.
Ovrutsky, Alida R.
Bai, Xiyuan
Irani, Vida R.
Dobos, Karen M.
Chan, Edward D.
Flores, Sonia C.
Pathogenic Nontuberculous Mycobacteria Resist and Inactivate Cathelicidin: Implication of a Novel Role for Polar Mycobacterial Lipids
title Pathogenic Nontuberculous Mycobacteria Resist and Inactivate Cathelicidin: Implication of a Novel Role for Polar Mycobacterial Lipids
title_full Pathogenic Nontuberculous Mycobacteria Resist and Inactivate Cathelicidin: Implication of a Novel Role for Polar Mycobacterial Lipids
title_fullStr Pathogenic Nontuberculous Mycobacteria Resist and Inactivate Cathelicidin: Implication of a Novel Role for Polar Mycobacterial Lipids
title_full_unstemmed Pathogenic Nontuberculous Mycobacteria Resist and Inactivate Cathelicidin: Implication of a Novel Role for Polar Mycobacterial Lipids
title_short Pathogenic Nontuberculous Mycobacteria Resist and Inactivate Cathelicidin: Implication of a Novel Role for Polar Mycobacterial Lipids
title_sort pathogenic nontuberculous mycobacteria resist and inactivate cathelicidin: implication of a novel role for polar mycobacterial lipids
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436335/
https://www.ncbi.nlm.nih.gov/pubmed/25993058
http://dx.doi.org/10.1371/journal.pone.0126994
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