Evidence map›Paper›PMID 21807906›Full record

ArticleInfection and immunity2011

Regulation of chlamydial infection by host autophagy and vacuolar ATPase-bearing organelles.

Muhammad Yasir, Niseema D Pachikara, Xiaofeng Bao, Zui Pan, Huizhou Fan

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
8.0field-weighted citation impact, top 3% 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

38 citing papers in PubMed, 66 citations in OpenAlex.

  1. Infection and immunity · 2026
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  2. The N-terminal domain ofFrontiers in immunology · 2025
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  3. Recognition ofInfection and immunity · 2024
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  7. Autophagy: the misty lands ofFrontiers in cellular and infection microbiology · 2024
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  8. ATG9A supportsMicrobiology spectrum · 2023
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  9. Article
  10. Review
  11. [Type III secretory protein SINC ofNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2023
    Article
  12. Establishing the intracellular niche of obligate intracellular vacuolar pathogens.Frontiers in cellular and infection microbiology · 2023
    Review
  13. GSDMD-mediated pyroptosis restrains intracellularFrontiers in cellular and infection microbiology · 2023
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  14. Article
  15. Review
  16. Frontiers in immunology · 2021
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  17. Article
  18. An Ancient Molecular Arms Race:Frontiers in immunology · 2020
    Review
  19. The Macrophage Response toFrontiers in cellular and infection microbiology · 2020
    Review
  20. Review
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

5 authors at 1 institution in 1 country.

Muhammad YasirDepartment of Physiology and Biophysics, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway, NJ 08854, USA.
Niseema D Pachikara
Xiaofeng Bao
Zui Pan
Huizhou Fan
Rutgers, The State University of New Jersey · US

Funding

Peptide Deformylase Inhibitor LBM415 for Sexually Transmitted InfectionsR33AI071954 · NIAID · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI FAN, HUIZHOU · 2009 to 2011
$971k
Peptide Deformylase Inhibitor LBM415 for Sexually Transmitted InfectionsR21AI071954 · NIAID · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI FAN, HUIZHOU · 2007 to 2008
$408k
NIAID NIH HHS AI071954NIAID NIH HHS R21 AI071954NIAID NIH HHS R33 AI071954
6 · The paper itself

Abstract

As arguably the most successful parasite, Chlamydia is an obligate intracellular bacterium replicating inside a vacuole of eukaryotic host cells. The chlamydial vacuole does not fuse with the defense cell organelle lysosome. We previously showed that chlamydial infection increases markers of autophagy, an innate antimicrobial activity requiring lysosomal function. However, the work presented here demonstrates that p62, an autophagy protein that is degraded in lysosomes, either remained unchanged or increased in chlamydia-infected human epithelial, mouse fibroblast, and mouse macrophage cell lines. In addition, the activities of three lysosomal enzymes analyzed were diminished in chlamydia-infected macrophages. Bafilomycin A1 (BafA), a specific inhibitor of vacuolar ATPase (vATPase) required for lysosomal function, increased the growth of the human pathogen Chlamydia trachomatis (L2) in wild-type murine fibroblasts and macrophages but inhibited growth in the autophagy-deficient ATG5(-/-) fibroblasts. BafA exhibited only slight inhibition or no effect on L2 growth in multiple human genital epithelial cell lines. In contrast to L2, the mouse pathogen Chlamydia muridarum (MoPn) was consistently inhibited by BafA in all cell lines examined, regardless of species origin and autophagy status. Finally, L2 but not MoPn grew more efficiently in the ATG5(-/-) cells than in wild-type cells. These results suggest that there are two types of vATPase-bearing organelles that regulate chlamydial infection: one supports chlamydial infection, while the other plays a defensive role through autophagy when cells are artificially infected with certain chlamydiae that have not been adapted to the host species.

Indexed as

AutophagyAnimalsCell LineChlamydia InfectionsChlamydia muridarumChlamydia trachomatisEnzyme InhibitorsEpithelial CellsFibroblastsHeLa CellsHumansLysosomesMacrolidesMacrophagesMiceOrganellesbafilomycin A1Enzyme InhibitorsMacrolidesVacuolar Proton-Translocating ATPases

Identifiers

PMID21807906
PMCPMC3187247
OpenAlexW2116035127

What OpenQuestion holds

Textmetadata
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.