Evidence map›Paper›PMID 25675351›Full record

ArticlePloS one2015

Mycobacterium abscessus morphotype comparison in a murine model.

Lindsay J Caverly, Silvia M Caceres, Cori Fratelli, Carrie Happoldt, Kelley M Kidwell, Kenneth C Malcolm, Jerry A Nick, David P Nichols

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.2field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Interplay ofVirulence · 2025
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  4. The role of colony morphotype in shaping gene essentiality inProceedings of the National Academy of Sciences of the United States of America · 2025
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  6. An alveolus lung-on-a-chip model ofbioRxiv : the preprint server for biology · 2025
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  7. Insights on the Pathogenesis ofJournal of clinical medicine · 2025
    Review
  8. Article
  9. Review
  10. Review
  11. The roles of neutrophils in non-tuberculous mycobacterial pulmonary disease.Annals of clinical microbiology and antimicrobials · 2023
    Review
  12. Alternatives to Antibiotics againstAntibiotics (Basel, Switzerland) · 2022
    Review
  13. Article
  14. Article
  15. Virulence Mechanisms ofFrontiers in microbiology · 2022
    Review
  16. Review
  17. Review
  18. Rufomycin Exhibits Dual Effects AgainstFrontiers in microbiology · 2021
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Lindsay J CaverlyDepartment of Pediatrics, University of Michigan, Ann Arbor, Michigan, United States of America.
Silvia M CaceresDepartment of Medicine, National Jewish Health, Denver, Colorado, United States of America.
Cori FratelliDepartment of Pediatrics, National Jewish Health, Denver, Colorado, United States of America.
Carrie HappoldtDepartment of Pediatrics, National Jewish Health, Denver, Colorado, United States of America.
Kelley M KidwellDepartment of Biostatistics, University of Michigan, Ann Arbor, Michigan, United States of America.
Kenneth C MalcolmDepartment of Medicine, National Jewish Health, Denver, Colorado, United States of America; Department of Medicine, University of Colorado Denver, Aurora, Colorado, United States of America.
Jerry A NickDepartment of Medicine, National Jewish Health, Denver, Colorado, United States of America; Department of Medicine, University of Colorado Denver, Aurora, Colorado, United States of America.
David P NicholsDepartment of Medicine, National Jewish Health, Denver, Colorado, United States of America; Department of Pediatrics, National Jewish Health, Denver, Colorado, United States of America; Department of Medicine, University of Colorado Denver, Aurora, Colorado, United States of America.
National Jewish Health · USUniversity of Colorado Denver · USMichigan United · US

Funding

Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
Advancing Child Health Through Cellular and Molecular BiologyK12HD028820 · NICHD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Donna M. Martin · 2002 to 2026
$9.2M
ACADEMIC TRAINING PROGRAM IN PEDIATRIC PULMONARY DISEASET32HL007670 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI ABMAN, STEVEN HERBERT · 1988 to 2019
$5.9M
Colorado Clinical and Translational Sciences InstituteKL2TR001080 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$2.6M
Colorado Clinical and Translational Science Institute (KL2)KL2TR000156 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2012 to 2013
$521k
NCATS NIH HHS KL2 TR000156NCATS NIH HHS KL2 TR001080NCATS NIH HHS UL1 TR001082NHLBI NIH HHS T32 HL007670NHLBI NIH HHS T32HL007670NICHD NIH HHS K12 HD028820NICHD NIH HHS K12HD028820
6 · The paper itself

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.

Indexed as

AnimalsBacterial LoadBronchoalveolar Lavage FluidCytokinesDisease Models, AnimalLungMacrophagesMiceMycobacterium Infections, NontuberculousNeutrophilsNontuberculous MycobacteriaSpleenCytokines

Identifiers

PMID25675351
PMCPMC4326282
OpenAlexW2082467209

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.