Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Pneumonia I: Introduction01:30

Pneumonia I: Introduction

184
Pneumonia is an acute respiratory infection that targets the lungs, specifically the alveoli. These tiny air sacs, essential for oxygen exchange, become engorged with pus and fluid, severely hindering breathing, decreasing oxygen absorption, and causing significant pain and discomfort during respiration.
Risk Factors
Various factors influence the likelihood of developing pneumonia. Age plays a crucial role, with infants, children under two, and individuals over 65 at increased risk due to their...
184

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Characteristics of severe disease in granulomatous lymphocytic interstitial lung disease: a retrospective cohort study.

ERJ open research·2026
Same author

Quantitative lung tissue functional analysis for pulmonary adverse event risk assessment prior to thoracic radiotherapy.

Physics and imaging in radiation oncology·2026
Same author

Toll-like receptor 5 protects against murine lung fibrosis through reduced dysbiosis, and <i>TLR5</i> deficiency is associated with human IPF.

Science translational medicine·2026
Same author

Gut microbiota associate with disease severity and survival in idiopathic pulmonary fibrosis.

American journal of respiratory and critical care medicine·2026
Same author

Targeted lung <i>Lactobacillus johnsonii</i> intervention alleviates virus-induced fibrosis post-HCT through PD-L1/PD-1 signaling.

Science advances·2026
Same author

A Quantitative Imaging Measure of Progressive Pulmonary Fibrosis.

American journal of respiratory and critical care medicine·2025

Related Experiment Video

Updated: May 10, 2025

Studying Microbial Communities In Vivo: A Model of Host-mediated Interaction Between Candida Albicans and Pseudomonas Aeruginosa in the Airways
06:43

Studying Microbial Communities In Vivo: A Model of Host-mediated Interaction Between Candida Albicans and Pseudomonas Aeruginosa in the Airways

Published on: January 13, 2016

8.4K

The lung microbiome in interstitial lung disease.

Sheridan G Mikhail1, David N O'Dwyer1,2

  • 1Division of Pulmonary and Critical Care Medicine, Dept. of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USA.

Breathe (Sheffield, England)
|April 21, 2025
PubMed
Summary

The lung microbiome, particularly bacterial burden, is altered in idiopathic pulmonary fibrosis (IPF) and linked to mortality. Further research is needed to understand its role in other interstitial lung diseases (ILDs) and the oral-lung/gut-lung axes.

More Related Videos

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
04:44

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease

Published on: June 16, 2020

19.6K
Growing a Cystic Fibrosis-Relevant Polymicrobial Biofilm to Probe Community Phenotypes
03:53

Growing a Cystic Fibrosis-Relevant Polymicrobial Biofilm to Probe Community Phenotypes

Published on: April 19, 2024

428

Related Experiment Videos

Last Updated: May 10, 2025

Studying Microbial Communities In Vivo: A Model of Host-mediated Interaction Between Candida Albicans and Pseudomonas Aeruginosa in the Airways
06:43

Studying Microbial Communities In Vivo: A Model of Host-mediated Interaction Between Candida Albicans and Pseudomonas Aeruginosa in the Airways

Published on: January 13, 2016

8.4K
Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
04:44

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease

Published on: June 16, 2020

19.6K
Growing a Cystic Fibrosis-Relevant Polymicrobial Biofilm to Probe Community Phenotypes
03:53

Growing a Cystic Fibrosis-Relevant Polymicrobial Biofilm to Probe Community Phenotypes

Published on: April 19, 2024

428

Area of Science:

  • Pulmonary Medicine
  • Microbiology
  • Immunology

Background:

  • Interstitial lung disease (ILD) is a chronic lung condition with poorly understood pathogenesis.
  • Idiopathic pulmonary fibrosis (IPF), a common ILD, has a poor prognosis and involves dysregulated immune responses.
  • The lung microbiome is a key regulator of immunity and clinical outcomes in ILD.

Purpose of the Study:

  • To review studies on the lung microbiome's role in IPF pathogenesis.
  • To explore the potential influence of the oral and gut microbiomes on ILD.
  • To highlight the need for further research into the oral-lung and gut-lung axes in ILD.

Main Methods:

  • Literature review of observational lung microbiome studies in ILD patients.
  • Analysis of existing data on bacterial burden in IPF lungs.
  • Discussion of proposed mechanisms involving oral and gut microbiomes.

Main Results:

  • Elevated bacterial burden in the lungs of IPF patients is a consistent finding.
  • Increased lung bacterial burden in IPF predicts mortality.
  • Limited understanding exists regarding the lung microbiome's role in non-IPF ILDs.

Conclusions:

  • The lung microbiome plays a role in IPF pathogenesis, with increased bacterial load being a key factor.
  • The oral-lung and gut-lung axes are potential contributors to ILD pathogenesis.
  • More research is essential to elucidate the complex interactions within the lung microbiome and its impact on ILD progression.