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      Mycobacterium abscessus Morphotype Comparison in a Murine Model

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          Abstract

          Pulmonary infections with Mycobacterium abscessus ( M. abscessus) are increasingly prevalent in patients with lung diseases such as cystic fibrosis. M. abscessus exists in two morphotypes, smooth and rough, but the impact of morphotype on virulence is unclear. We developed an immune competent mouse model of pulmonary M. abscessus infection and tested the differences in host inflammatory response between the morphotypes of M. abscessus. Smooth and rough morphotypes of M. abscessus were isolated from the same American Type Culture Collection strain. Wild type and cystic fibrosis mice were intratracheally inoculated with known quantities of M. abscessus suspended in fibrin plugs. At the time of sacrifice lung and splenic tissues and bronchoalveolar lavage fluid were collected and cultured. Bronchoalveolar lavage fluid was analyzed for leukocyte count, differential and cytokine expression. Pulmonary infection with M. abscessus was present at both 3 days and 14 days post-inoculation in all groups at greater levels than systemic infection. Inoculation with M. abscessus rough morphotype resulted in more bronchoalveolar lavage fluid neutrophils compared to smooth morphotype at 14 days post-inoculation in both wild type (p = 0.01) and cystic fibrosis (p<0.01) mice. Spontaneous in vivo conversion from smooth to rough morphotype occurred in 12/57 (21%) of mice. These mice trended towards greater weight loss than mice in which morphotype conversion did not occur. In the described fibrin plug model of M. abscessus infection, pulmonary infection with minimal systemic dissemination is achieved with both smooth and rough morphotypes. In this model M. abscessus rough morphotype causes a greater host inflammatory response than the smooth based on bronchoalveolar lavage fluid neutrophil levels.

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          Most cited references29

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          Chronic Mycobacterium abscessus infection and lung function decline in cystic fibrosis.

          Although nontuberculous mycobacteria (NTM) are recognized pathogens in cystic fibrosis (CF), associations with clinical outcomes remain unclear. Microbiological data was obtained from 1216 CF patients over 8years (481+/-55patients/year). Relationships to clinical outcomes were examined in the subset (n=271, 203+/-23 patients/year) with longitudinal data. Five hundred thirty-six of 4862 (11%) acid-fast bacilli (AFB) cultures grew NTM, with Mycobacterium abscessus (n=298, 55.6%) and Mycobacterium avium complex (n=190, 35.4%) most common. Associated bacterial cultures grew Stenotrophomonas or Aspergillus species more often when NTM were isolated (18.2% vs. 8.4% and 13.9% vs. 7.2%, respectively, p<0.01). After controlling for confounders, patients with chronic M. abscessus infection had greater rates of lung function decline than those with no NTM infection (-2.52 vs. -1.64% predicted FEV(1)/year, p<0.05). NTM infection is common in CF and associated with particular pathogens. Chronic M. abscessus infection is associated with increased lung function decline. Copyright (c) 2009 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
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            Respiratory outbreak of Mycobacterium abscessus subspecies massiliense in a lung transplant and cystic fibrosis center.

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              Mouse models of cystic fibrosis: phenotypic analysis and research applications.

              Genetically modified mice have been studied for more than fifteen years as models of cystic fibrosis (CF). The large amount of experimental data generated illuminates the complex multi-organ pathology of CF and raises new questions relevant to human disease. CF mice have also been used to test experimental therapies prior to clinical trials. This review recapitulates the major phenotypic traits of CF mice and highlights important new findings including aberrant alveolar macrophages, bone and cartilage abnormalities and abnormal bioactive lipid metabolism. Novel data are presented on the intestinal and nasal physiology of F508del-CFTR CF mice backcrossed onto different genetic backgrounds. Caveats, and sources of variability including age, gender and animal husbandry, are discussed. Interspecies differences limit comparison of lung pathology in CF mice to the human disease. The recent development of genetically modified pigs and ferrets heralds the application of more advanced animal models to CF research and drug development. Copyright © 2011 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                12 February 2015
                2015
                : 10
                : 2
                : e0117657
                Affiliations
                [1 ]Department of Pediatrics, University of Michigan, Ann Arbor, Michigan, United States of America
                [2 ]Department of Medicine, National Jewish Health, Denver, Colorado, United States of America
                [3 ]Department of Pediatrics, National Jewish Health, Denver, Colorado, United States of America
                [4 ]Department of Biostatistics, University of Michigan, Ann Arbor, Michigan, United States of America
                [5 ]Department of Medicine, University of Colorado Denver, Aurora, Colorado, United States of America
                The Hospital for Sick Children and The University of Toronto, CANADA
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: LJC KCM JAN DPN. Performed the experiments: LJC SMC CF CH DPN. Analyzed the data: LJC KMK JAN DPN. Contributed reagents/materials/analysis tools: LJC SMC KMK KCM JAN DPN. Wrote the paper: LJC SMC KMK KCM JAN DPN.

                Article
                PONE-D-14-31955
                10.1371/journal.pone.0117657
                4326282
                25675351
                4b2b5735-ca8e-4daf-9601-6c63a4ca50b8
                Copyright @ 2015

                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 credited

                History
                : 16 July 2014
                : 30 December 2014
                Page count
                Figures: 8, Tables: 0, Pages: 18
                Funding
                Funding provided by Cystic fibrosis foundation, www.cff.org: grant number CAVERL13D0 to author: LJC, National Institute of Health, www.nih.gov: grant numbers K12HD028820, T32HL007670 to author: LJC, grant number KL2 TR000156 to author: DPN and Charles Woodson Fund for Clinical Research, www.charleswoodsonfoundation.org to author: KK. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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                Research Article
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