Evidence map›Paper›PMID 34986139›Full record

ArticlePLoS neglected tropical diseases2022

Comparison of percutaneous vs oral infection of hamsters with the hookworm Ancylostoma ceylanicum: Parasite development, pathology and primary immune response.

Richard D Bungiro, Lisa M Harrison, Blaise Dondji, Michael Cappello

Open access · goldAbstract readComparative Study
In one paragraph

Article in PLoS neglected tropical diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 56% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

4 authors at 2 institutions in 1 country.

Richard D BungiroDepartment of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, United States of America.
Lisa M HarrisonDepartment of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, United States of America.ORCID https://orcid.org/0000-0001-5983-4112
Blaise DondjiLaboratory of Cellular Immunology and Parasitology, Department of Biological Sciences, Central Washington University, Ellensburg, Washington, United States of America.
Michael CappelloDepartment of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, United States of America.ORCID https://orcid.org/0000-0003-2255-8833
Yale University · USCentral Washington University · US

Funding

The role of MIF in hookworm infection and diseaseR01AI058980 · NIAID · YALE UNIVERSITY · PI CAPPELLO, MICHAEL · 2005 to 2009
$2.1M
Emerging benzimidazole resistance in human hookwormsR01AI132452 · NIAID · YALE UNIVERSITY · PI CAPPELLO, MICHAEL · 2017 to 2021
$2.1M
The molecular pathogenesis of hookworm anemiaR01AI047929 · NIAID · YALE UNIVERSITY · PI CAPPELLO, MICHAEL · 2002 to 2005
$1.4M
NIAID NIH HHS R01 AI132452
6 · The paper itself

Abstract

backgroundHundreds of millions of people in poor countries continue to suffer from disease caused by bloodfeeding hookworms. While mice and rats are not reliably permissive hosts for any human hookworm species, adult Golden Syrian hamsters are fully permissive for the human and animal pathogen Ancylostoma ceylanicum. Similar to humans, hamsters may be infected with A. ceylanicum third-stage larvae orally or percutaneously. Oral infection typically leads to consistent worm yields in hamsters but may not accurately reflect the clinical and immunological manifestations of human infection resulting from skin penetration. METHODOLOGY/PRINCIPAL

findingsIn this study we compared host responses following percutaneous infection to those utilizing an established oral infection protocol. Infected hamsters exhibited a dose-dependent pathology, with 1000 percutaneous larvae (L3) causing anemia and adult worm recovery comparable to that of 50 orally administered L3. A delayed arrival and maturity of worms in the intestine was observed, as was variation in measured cellular immune responses. A long-term study found that the decline in blood hemoglobin was more gradual and did not reach levels as low, with the nadir of disease coming later in percutaneously infected hamsters. Both groups exhibited moderate growth delay, an effect that was more persistent in the percutaneously infected group. Fecal egg output also peaked later and at lower levels in the percutaneously infected animals. In contrast to orally infected hamsters, antibody titers to larval antigens continued to increase throughout the course of the experiment in the percutaneous group. CONCLUSIONS/SIGNIFICANCE: These results demonstrate that the route of infection with A. ceylanicum impacts disease pathogenesis, as well as humoral and cellular immune responses in an experimental setting. These data further validate the utility of the Golden Syrian hamster as a model of both oral and percutaneous infection with human hookworms.

Indexed as

AncylostomaAncylostomiasisAnimalsCricetinaeDisease Models, AnimalHemoglobinsMaleMesocricetusMouthSkinHemoglobins

Identifiers

PMID34986139
PMCPMC8765627
OpenAlexW4206476559

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.