Evidence map›Paper›PMID 24990203›Full record

ArticleThe Journal of infectious diseases2015

An animal model of a newly emerging human ehrlichiosis.

Tais Berelli Saito, Nagaraja R Thirumalapura, Thomas R Shelite, Dedeke Rockx-Brouwer, Vsevolod L Popov, David H Walker

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Detection ofVector borne and zoonotic diseases (Larchmont, N.Y.) · 2023
    Article
  5. Article
  6. Review
  7. Applied and environmental microbiology · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Co-Feeding Transmission of the Ehrlichia muris-Like Agent to Mice (Mus musculus).Vector borne and zoonotic diseases (Larchmont, N.Y.) · 2016
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Tais Berelli SaitoDepartment of Pathology, University of Texas Medical Branch at Galveston.
Nagaraja R ThirumalapuraDepartment of Pathology, University of Texas Medical Branch at Galveston.
Thomas R SheliteDepartment of Pathology, University of Texas Medical Branch at Galveston.
Dedeke Rockx-BrouwerDepartment of Pathology, University of Texas Medical Branch at Galveston.
Vsevolod L PopovDepartment of Pathology, University of Texas Medical Branch at Galveston.
David H WalkerDepartment of Pathology, University of Texas Medical Branch at Galveston.
The University of Texas Medical Branch at Galveston · US

Funding

Vector-host-pathogen interface in monocytotropic ehrlichiosisR21AI102304 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI WALKER, DAVID H · 2012 to 2013
$409k
Immunity to Ehrlichial InfectionsK22AI089973 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI THIRUMALAPURA, NAGARAJA RAMAVADHANI · 2012 to 2013
$269k
NIAID NIH HHS AI089973NIAID NIH HHS AI102304NIAID NIH HHS K22 AI089973NIAID NIH HHS R21 AI102304
6 · The paper itself

Abstract

backgroundHuman ehrlichioses are emerging life-threatening diseases transmitted by ticks. Animal models have been developed to study disease development; however, there is no valid small animal model that uses a human ehrlichial pathogen. The objective of this study was to develop a mouse model for ehrlichiosis with the newly discovered human pathogen, Ehrlichia muris-like agent (EMLA).

methodsThree strains of mice were inoculated with different doses of EMLA by the intravenous, intraperitoneal, or intradermal route and evaluated for clinical and pathologic changes during the course of infection.

resultsEMLA infected C57Bl/6, BALB/c, and C3H/HeN mice and induced lethal or persistent infection in a route- and dose-dependent manner. The clinical chemistry and hematologic changes were similar to those of human infection by Ehrlichia chaffeensis or EMLA. Bacterial distribution in tissues differed after intradermal infection, compared with the distribution after intravenous or intraperitoneal injection. Lethal infection did not cause remarkable pathologic changes, but it caused fluid imbalance. EMLA infection of endothelium and mononuclear cells likely plays a role in the severe outcome.

conclusionsThe EMLA mouse model mimics human infection and can be used to study pathogenesis and immunity and for development of a vector transmission model of ehrlichiosis.

Indexed as

AnimalsDisease Models, AnimalEhrlichia chaffeensisEhrlichiosisFemaleHumansMiceMice, Inbred BALB CMice, Inbred C3HMice, Inbred C57BLTicksEhrlichia muris-likeehrlichiosisemerging infectious diseasehuman pathogentick-borne disease

Identifiers

PMID24990203
PMCPMC4351372
OpenAlexW2141305060

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.