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Catheter-associated Mycobacterium intracellulare biofilm infection in C3HeB/FeJ mice
Non-tuberculosis mycobacterial (NTM) diseases are steadily increasing in prevalence and mortality worldwide. Mycobacterium avium and M. intracellulare, the two major pathogens of NTM diseases, are resistant to antibiotics, and chlorine, necessitating their capacity to survive in natural environments...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10564925/ https://www.ncbi.nlm.nih.gov/pubmed/37816786 http://dx.doi.org/10.1038/s41598-023-44403-0 |
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author | Yamamoto, Kentaro Tsujimura, Yusuke Ato, Manabu |
author_facet | Yamamoto, Kentaro Tsujimura, Yusuke Ato, Manabu |
author_sort | Yamamoto, Kentaro |
collection | PubMed |
description | Non-tuberculosis mycobacterial (NTM) diseases are steadily increasing in prevalence and mortality worldwide. Mycobacterium avium and M. intracellulare, the two major pathogens of NTM diseases, are resistant to antibiotics, and chlorine, necessitating their capacity to survive in natural environments (e.g. soil and rivers) and disinfected municipal water. They can also form biofilms on artificial surfaces to provide a protective barrier and habitat for bacilli, which can cause refractory systemic disseminated NTM disease. Therefore, preventing biofilm formation by these pathogens is crucial; however, not many in vivo experimental systems and studies on NTM biofilm infection are available. This study develops a mouse model of catheter-associated systemic disseminated disease caused by M. intracellulare that reproduces the pathophysiology of catheter-associated infections observed in patients undergoing peritoneal dialysis. In addition, the bioluminescence system enabled noninvasive visualization of the amount and distribution of bacilli in vivo and conveniently examine the efficacy of antimicrobials. Furthermore, the cellulose-based biofilms, which were extensively formed in the tissue surrounding the catheter insertion site, reduced drug therapy effectiveness. Overall, this study provides insights into the cause of the drug resistance of NTM and may guide the development of new therapies for NTM diseases. |
format | Online Article Text |
id | pubmed-10564925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105649252023-10-12 Catheter-associated Mycobacterium intracellulare biofilm infection in C3HeB/FeJ mice Yamamoto, Kentaro Tsujimura, Yusuke Ato, Manabu Sci Rep Article Non-tuberculosis mycobacterial (NTM) diseases are steadily increasing in prevalence and mortality worldwide. Mycobacterium avium and M. intracellulare, the two major pathogens of NTM diseases, are resistant to antibiotics, and chlorine, necessitating their capacity to survive in natural environments (e.g. soil and rivers) and disinfected municipal water. They can also form biofilms on artificial surfaces to provide a protective barrier and habitat for bacilli, which can cause refractory systemic disseminated NTM disease. Therefore, preventing biofilm formation by these pathogens is crucial; however, not many in vivo experimental systems and studies on NTM biofilm infection are available. This study develops a mouse model of catheter-associated systemic disseminated disease caused by M. intracellulare that reproduces the pathophysiology of catheter-associated infections observed in patients undergoing peritoneal dialysis. In addition, the bioluminescence system enabled noninvasive visualization of the amount and distribution of bacilli in vivo and conveniently examine the efficacy of antimicrobials. Furthermore, the cellulose-based biofilms, which were extensively formed in the tissue surrounding the catheter insertion site, reduced drug therapy effectiveness. Overall, this study provides insights into the cause of the drug resistance of NTM and may guide the development of new therapies for NTM diseases. Nature Publishing Group UK 2023-10-10 /pmc/articles/PMC10564925/ /pubmed/37816786 http://dx.doi.org/10.1038/s41598-023-44403-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yamamoto, Kentaro Tsujimura, Yusuke Ato, Manabu Catheter-associated Mycobacterium intracellulare biofilm infection in C3HeB/FeJ mice |
title | Catheter-associated Mycobacterium intracellulare biofilm infection in C3HeB/FeJ mice |
title_full | Catheter-associated Mycobacterium intracellulare biofilm infection in C3HeB/FeJ mice |
title_fullStr | Catheter-associated Mycobacterium intracellulare biofilm infection in C3HeB/FeJ mice |
title_full_unstemmed | Catheter-associated Mycobacterium intracellulare biofilm infection in C3HeB/FeJ mice |
title_short | Catheter-associated Mycobacterium intracellulare biofilm infection in C3HeB/FeJ mice |
title_sort | catheter-associated mycobacterium intracellulare biofilm infection in c3heb/fej mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10564925/ https://www.ncbi.nlm.nih.gov/pubmed/37816786 http://dx.doi.org/10.1038/s41598-023-44403-0 |
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