Evidence map›Paper›PMID 25993058›Full record

ArticlePloS one2015

Pathogenic nontuberculous mycobacteria resist and inactivate cathelicidin: implication of a novel role for polar mycobacterial lipids.

Jennifer R Honda, Tamara Hess, Kenneth C Malcolm, Alida R Ovrutsky, Xiyuan Bai, Vida R Irani, Karen M Dobos, Edward D Chan, Sonia C Flores

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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

  1. Trial
  2. Article
  3. International journal of molecular sciences · 2025
    Review
  4. Article
  5. Article
  6. Virulence Mechanisms ofFrontiers in microbiology · 2022
    Review
  7. Review
  8. Article
  9. Time to Expand the Picture of Mycobacterial Lipids: Spotlight on Nontuberculous Mycobacteria.American journal of respiratory cell and molecular biology · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Molecular basis of mycobacterial survival in macrophages.Cellular and molecular life sciences : CMLS · 2017
    Review
  14. Treatment of Non-Tuberculous Mycobacterial Lung Disease.Current treatment options in infectious diseases · 2016
    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

9 authors at 6 institutions in 1 country.

Jennifer R HondaDepartment of Medicine, Division of Pulmonary Sciences and Critical Care Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States of America; National Jewish Health, Denver, Colorado, United States of America; Denver Veterans Affairs Medical Center, Denver, Colorado, United States of America.
Tamara HessDepartment of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, United States of America.
Kenneth C MalcolmDepartment of Medicine, Division of Pulmonary Sciences and Critical Care Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States of America; National Jewish Health, Denver, Colorado, United States of America.
Alida R OvrutskyNational Jewish Health, Denver, Colorado, United States of America; Denver Veterans Affairs Medical Center, Denver, Colorado, United States of America.
Xiyuan BaiNational Jewish Health, Denver, Colorado, United States of America; Denver Veterans Affairs Medical Center, Denver, Colorado, United States of America.
Vida R IraniDepartment of Biology, Indiana University of Pennsylvania, Indiana, Pennsylvania, United States of America.
Karen M DobosDepartment of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, United States of America.
Edward D ChanDepartment of Medicine, Division of Pulmonary Sciences and Critical Care Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States of America; National Jewish Health, Denver, Colorado, United States of America; Denver Veterans Affairs Medical Center, Denver, Colorado, United States of America.
Sonia C FloresDepartment of Medicine, Division of Pulmonary Sciences and Critical Care Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States of America.
Colorado State University · USDenver VA Medical Center · USUniversity of Colorado Anschutz Medical Campus · USIndiana University of Pennsylvania · USNational Jewish Health · USUniversity of Colorado Denver · US

Funding

MULTIDISCIPLINARY RESPIRATORY DISEASES RESEARCH TRAININGT32HL007085 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI ELLEN L BURNHAM, LISA A MAIER · 1985 to 2026
$21.6M
UNIVERSITY OF COLORADO HIV RESEARCH TRAINING PROGRAMT32AI007447 · NIAID · UNIVERSITY OF COLORADO DENVER · PI CAMPBELL, THOMAS B. · 1992 to 2016
$2.8M
Role of redox status in HIV-1 Tat-mediated inflammationR01HL059785 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI FLORES, SONIA CASTRO · 1997 to 2006
$2.2M
NHLBI NIH HHS 3R01HL059785-09S1NHLBI NIH HHS R01 HL059785NHLBI NIH HHS T32 HL007085NHLBI NIH HHS T32 HL 7085-83NIAID NIH HHS T32 AI007447NIAID NIH HHS T32-AI007447-19
6 · The paper itself

Abstract

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. aviumssGPL) and M. avium that do not (M. aviumΔssGPL). Similarly, M. abscessus containing non-specific GPL (M. abscessusnsGPL(+)) or lacking nsGPL (M. abscessusnsGPL(-)) 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. abscessusnsGPL(-) 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.

Indexed as

Lipid MetabolismLipidsAnti-Bacterial AgentsAntimicrobial Cationic PeptidesCathelicidinsDrug Resistance, BacterialHumansMicrobial Sensitivity TestsMycobacterium Infections, NontuberculousNontuberculous MycobacteriaAnti-Bacterial AgentsAntimicrobial Cationic PeptidesCathelicidinsLipids

Identifiers

PMID25993058
PMCPMC4436335
OpenAlexW1525208545

What OpenQuestion holds

Textmetadata
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.