Evidence map›Paper›PMID 25285720›Full record

ArticleThe American journal of pathology2014

Lethal factor, but not edema factor, is required to cause fatal anthrax in cynomolgus macaques after pulmonary spore challenge.

Julie A Hutt, Julie A Lovchik, Melissa Drysdale, Robert L Sherwood, Trevor Brasel, Mary F Lipscomb, C Rick Lyons

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  7. Article
  8. American journal of physiology. Heart and circulatory physiology · 2019
    Article
  9. International journal of molecular sciences · 2019
    Article
  10. Review
  11. Article
  12. 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

7 authors at 2 institutions in 1 country.

Julie A HuttLovelace Respiratory Research Institute, Albuquerque, New Mexico; Center for Infectious Disease & Immunity, University of New Mexico Health Science Center, Albuquerque, New Mexico. Electronic address: jhutt@lrri.org.
Julie A LovchikCenter for Infectious Disease & Immunity, University of New Mexico Health Science Center, Albuquerque, New Mexico; Department of Internal Medicine, University of New Mexico Health Science Center, Albuquerque, New Mexico.
Melissa DrysdaleCenter for Infectious Disease & Immunity, University of New Mexico Health Science Center, Albuquerque, New Mexico; Department of Internal Medicine, University of New Mexico Health Science Center, Albuquerque, New Mexico.
Robert L SherwoodLovelace Respiratory Research Institute, Albuquerque, New Mexico.
Trevor BraselLovelace Respiratory Research Institute, Albuquerque, New Mexico.
Mary F LipscombDepartment of Pathology, University of New Mexico Health Science Center, Albuquerque, New Mexico.
C Rick LyonsCenter for Infectious Disease & Immunity, University of New Mexico Health Science Center, Albuquerque, New Mexico; Department of Internal Medicine, University of New Mexico Health Science Center, Albuquerque, New Mexico.
University of New Mexico · USLovelace Respiratory Research Institute · US

Funding

Pulmonary responses to Bioweapon Category A PathogensP01AI056295 · NIAID · UNIVERSITY OF NEW MEXICO · PI LYONS, CLIFFORD RICK · 2005 to 2009
$13.2M
NIAID NIH HHS P01 AI056295
6 · The paper itself

Abstract

Inhalational anthrax is caused by inhalation of Bacillus anthracis spores. The ability of B. anthracis to cause anthrax is attributed to the plasmid-encoded A/B-type toxins, edema toxin (edema factor and protective antigen) and lethal toxin (lethal factor and protective antigen), and a poly-d-glutamic acid capsule. To better understand the contribution of these toxins to the disease pathophysiology in vivo, we used B. anthracis Ames strain and isogenic toxin deletion mutants derived from the Ames strain to examine the role of lethal toxin and edema toxin after pulmonary spore challenge of cynomolgus macaques. Lethal toxin, but not edema toxin, was required to induce sustained bacteremia and death after pulmonary challenge with spores delivered via bronchoscopy. After intravenous challenge with bacilli to model the systemic phase of infection, lethal toxin contributed to bacterial proliferation and subsequent host death to a greater extent than edema toxin. Deletion of protective antigen resulted in greater loss of virulence after intravenous challenge with bacilli than deletion of lethal toxin or edema toxin alone. These findings are consistent with the ability of anti-protective antigen antibodies to prevent anthrax and suggest that lethal factor is the dominant toxin that contributes to the escape of significant numbers of bacilli from the thoracic cavity to cause anthrax after inhalation challenge with spores.

Indexed as

AnimalsAnthraxAntibodies, BacterialAntigens, BacterialBacillus anthracisBacterial ToxinsFemaleLungMacacaMaleRespiratory Tract InfectionsSpores, BacterialVirulenceVirulence Factorsanthrax toxinAntibodies, BacterialAntigens, BacterialBacterial ToxinsVirulence Factors

Identifiers

PMID25285720
PMCPMC4258508
OpenAlexW2134916526

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.