Evidence map›Paper›PMID 17440430›Full record

ArticleThe pharmacogenomics journal2008

Rat survival to anthrax lethal toxin is likely controlled by a single gene.

S H Nye, A L Wittenburg, D L Evans, J A O'Connor, R J Roman, H J Jacob

Abstract read
PubMed Publisher
In one paragraph

Article in The pharmacogenomics journal, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. TheMicrobiology spectrum · 2019
    Review
  2. American journal of physiology. Heart and circulatory physiology · 2019
    Article
  3. Anthrax and the inflammasome.Microbes and infection · 2012
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. 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

6 authors at 2 institutions in 1 country.

S H NyePhysioGenix Inc., 10437 Innovation Drive, Milwaukee, WI 53226, USA. snye@physiogenix.com
A L Wittenburg
D L Evans
J A O'Connor
R J Roman
H J Jacob
PhysioGenix (United States) · USMedical College of Wisconsin · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We examined whether survival of different rat strains administered anthrax lethal toxin is genetically determined. A reproducible test population of first filial generation hybrid rats was bred based on the susceptibility of progenitors to anthrax lethal toxin and to maximize genetic diversity across the strains. These rats were then tested with varying doses of anthrax lethal toxin. We found that all 'sensitive' strains died within 2 h following systemic administration of 240 mug/kg lethal toxin, while one strain survived following a five times higher dose (1.4 mg/kg). The ability of lethal toxin to lyse macrophage cultures derived from the bone marrow of these strains corresponded with in vivo results. We conclude that a rat test population can detect strain differences in response to anthrax lethal toxin. Survival is influenced by the host genome background and is likely due to a single gene with a recessive mode of inheritance.

Indexed as

AnimalsAntigens, BacterialBacterial ToxinsBreedingCells, CulturedCell SeparationDrug ResistanceGenomeMacrophagesMaleRatsRats, Inbred F344Rats, Inbred LewRats, Inbred WKYSpecies SpecificitySurvival Analysisanthrax toxinAntigens, BacterialBacterial Toxins

Identifiers

PMID17440430
OpenAlexW2003103524

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.