Evidence map›Paper›PMID 21437287›Full record

ArticlePloS one2011

Bacillus anthracis protease InhA increases blood-brain barrier permeability and contributes to cerebral hemorrhages.

Dhritiman V Mukherjee, Jessica H Tonry, Kwang Sik Kim, Nalini Ramarao, Taissia G Popova, Charles Bailey, Serguei Popov, Myung-Chul Chung

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Anthrax Meningoencephalitis and Intracranial Hemorrhage.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2022
    Review
  6. Review
  7. Article
  8. Toxins · 2020
    Article
  9. Article
  10. TheMicrobiology spectrum · 2019
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Iron and zinc exploitation during bacterial pathogenesis.Metallomics : integrated biometal science · 2015
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  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

8 authors at 3 institutions in 2 countries.

Dhritiman V MukherjeeNational Center for Biodefense and Infectious Diseases, Department of Molecular and Microbiology, George Mason University, Manassas, Virginia, United States of America.
Jessica H Tonry
Kwang Sik Kim
Nalini Ramarao
Taissia G Popova
Charles Bailey
Serguei Popov
Myung-Chul Chung
George Mason University · USJohns Hopkins Medicine · USMicrobiologie de l’alimentation au service de la santé · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hemorrhagic meningitis is a fatal complication of anthrax, but its pathogenesis remains poorly understood. The present study examined the role of B. anthracis-secreted metalloprotease InhA on monolayer integrity and permeability of human brain microvasculature endothelial cells (HBMECs) which constitute the blood-brain barrier (BBB). Treatment of HBMECs with purified InhA resulted in a time-dependent decrease in trans-endothelial electrical resistance (TEER) accompanied by zonula occluden-1 (ZO-1) degradation. An InhA-expressing B. subtilis exhibited increased permeability of HBMECs, which did not occur with the isogenic inhA deletion mutant (ΔinhA) of B. anthracis, compared with the corresponding wild-type strain. Mice intravenously administered with purified InhA or nanoparticles-conjugated to InhA demonstrated a time-dependent Evans Blue dye extravasation, leptomeningeal thickening, leukocyte infiltration, and brain parenchymal distribution of InhA indicating BBB leakage and cerebral hemorrhage. Mice challenged with vegetative bacteria of the ΔinhA strain of B. anthracis exhibited a significant decrease in leptomeningeal thickening compared to the wildtype strain. Cumulatively, these findings indicate that InhA contributes to BBB disruption associated with anthrax meningitis through proteolytic attack on the endothelial tight junctional protein zonula occluden (ZO)-1.

Indexed as

AnimalsAnthraxBacillus anthracisBacterial ProteinsBlood-Brain BarrierBlotting, WesternCerebral HemorrhageCytoplasmElectric ImpedanceEndothelial CellsFemaleHumansMembrane ProteinsMetalloproteasesMiceMutant ProteinsBacterial ProteinsMembrane ProteinsMetalloproteasesMutant ProteinsPhosphoproteinsTJP1 protein, humanTjp1 protein, mouseZonula Occludens-1 Protein

Identifiers

PMID21437287
PMCPMC3060093
OpenAlexW2091196779

What OpenQuestion holds

Textmetadata
LicenceCC0
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.