Evidence map›Paper›PMID 34732811›Full record

ArticleCommunications biology2021

Aggregation state of Mycobacterium tuberculosis impacts host immunity and augments pulmonary disease pathology.

Afsal Kolloli, Ranjeet Kumar, Pooja Singh, Anshika Narang, Gilla Kaplan, Alex Sigal, Selvakumar Subbian

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. EmergentInfection and immunity · 2024
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  6. Immune Responses toBiomedicines · 2024
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  7. Article
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  9. Review
  10. BCGΔBCG1419c increased memory CD8Scientific reports · 2022
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  11. Liposomal Glutathione Helps to MitigateAntioxidants (Basel, Switzerland) · 2022
    Article
  12. Article
  13. The Dark Side of the COVID-19 Treatments onMediterranean journal of hematology and infectious diseases · 2022
    Review
  14. Article
  15. AggregatedFrontiers in microbiology · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 3 countries.

Afsal KolloliThe Public Health Research Institute at New Jersey Medical School, Rutgers University, Newark, NJ, 07103, USA.
Ranjeet KumarThe Public Health Research Institute at New Jersey Medical School, Rutgers University, Newark, NJ, 07103, USA.
Pooja SinghThe Public Health Research Institute at New Jersey Medical School, Rutgers University, Newark, NJ, 07103, USA.
Anshika NarangThe Public Health Research Institute at New Jersey Medical School, Rutgers University, Newark, NJ, 07103, USA.
Gilla KaplanUniversity of Cape Town, Cape Town, 7925, South Africa.
Alex SigalAfrica Health Research Institute, Durban, 4013, South Africa.
Selvakumar SubbianThe Public Health Research Institute at New Jersey Medical School, Rutgers University, Newark, NJ, 07103, USA. subbiase@njms.rutgers.edu.ORCID 0000-0003-2021-8632
Rutgers, The State University of New Jersey · USMax Planck Institute for Infection Biology · DEUniversity of Cape Town · ZA

Funding

Project 5 Nano-micro Hybrid Fibrous Materials for Containment Removal and Site RemediationP42ES027723 · NIEHS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ANTONY, VEENA B. · 2020 to 2024
$6.7M
Bill and Melinda Gates Foundation (Bill & Melinda Gates Foundation) OPP1116944NIEHS NIH HHS P42 ES027723
6 · The paper itself

Abstract

In vitro phagocytosis of Mycobacterium tuberculosis (Mtb) aggregates (Mtb-AG), rather than similar numbers of single bacilli (Mtb-SC), induces host macrophage death and favors bacterial growth. Here, we examined whether aggregation contributes to enhanced Mtb pathogenicity in vivo in rabbit lungs. Rabbits were exposed to infectious aerosols containing mainly Mtb-AG or Mtb-SC. The lung bacterial load, systemic immune response, histology, and immune cell composition were investigated over time. Genome-wide transcriptome analysis, cellular and tissue-level assays, and immunofluorescent imaging were performed on lung tissue to define and compare immune activation and pathogenesis between Mtb-AG and Mtb-SC infection. Lung bacillary loads, disease scores, lesion size, and structure were significantly higher in Mtb-AG than Mtb-SC infected animals. Differences in immune cell distribution and activation were noted in the lungs of the two groups of infected animals. Consistently larger lung granulomas with large aggregates of Mtb, extensive necrotic foci, and elevated matrix metalloproteases expression were observed in Mtb-AG infected rabbits. Our findings suggest that bacillary aggregation increases Mtb fitness for improved growth and accelerates lung inflammation and infected host cell death, thereby exacerbating disease pathology in the lungs.

Indexed as

Adaptive ImmunityHost-Pathogen InteractionsImmunity, InnatePhagocytosisAnimalsFemaleLung DiseasesMycobacterium tuberculosisRabbits

Identifiers

PMID34732811
PMCPMC8566596
OpenAlexW3209702849

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.