Evidence map›Paper›PMID 39282343›Full record

ArticlebioRxiv : the preprint server for biology2024

EFFECT OF GENOTYPE AND AGE ON A DEFINED MICROBIOTA IN GNOTOBIOTIC SCID PIGLETS.

Katherine M Widmer, Faith Rahic-Seggerman, Ahlea Forster, Amanda Ahrens-Kress, Mary Sauer, Shankumar Mooyottu, Akhil Vinithakumari, Aaron Dunkerson-Kurzhumov, Brett Sponseller, Matti Kiupel and 2 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Katherine M WidmerDepartment of Animal Science, Iowa State University, Ames, IA 50011, USA.
Faith Rahic-SeggermanDepartment of Animal Science, Iowa State University, Ames, IA 50011, USA.
Ahlea ForsterDepartment of Animal Science, Iowa State University, Ames, IA 50011, USA.
Amanda Ahrens-KressLaboratory Animal Resources, Iowa State University, Ames, IA 50011, USA.
Mary SauerLaboratory Animal Resources, Iowa State University, Ames, IA 50011, USA.
Shankumar MooyottuDepartment of Veterinary Pathology, College of Veterinary Medicine, Iowa State University, Ames, IA 50011, USA.
Akhil VinithakumariDepartment of Veterinary Pathology, College of Veterinary Medicine, Iowa State University, Ames, IA 50011, USA.
Aaron Dunkerson-KurzhumovDepartment of Veterinary Pathology, College of Veterinary Medicine, Iowa State University, Ames, IA 50011, USA.
Brett SponsellerDepartment of Veterinary Microbiology and Preventive Medicine, College of Veterinary Medicine, Iowa State University, Ames, IA 50011, USA.
Matti KiupelDepartment of Pathobiology and Diagnostic Investigation, College of Veterinary Medicine, Michigan State University, East Lansing, MI 48824, USA.
Stephan Schmitz-EsserDepartment of Animal Science, Iowa State University, Ames, IA 50011, USA.
Christopher K TuggleDepartment of Animal Science, Iowa State University, Ames, IA 50011, USA.

Funding

Developing second generation SCID pig models: filling the gaps to improve translation of therapeutics in regenerative medicineR24OD028748 · OD · IOWA STATE UNIVERSITY · PI Christopher Tuggle · 2020 to 2026
$4.7M
NIH HHS R24 OD028748
6 · The paper itself

Abstract

Severe combined immunodeficient (SCID) individuals lack functional T and B lymphocytes, leading to a deficient adaptive immune system. SCID pigs are a unique large animal biomedical model as they possess many similarities to humans, allowing for the collection of translatable data in regenerative medicine, cancer, and other biomedical research topics. While many studies suggest early gut microbiota development is necessary for developing the intestinal barrier and immune system, these animals are often cesarian section derived, leaving them uncolonized for normal intestinal microflora. The hypothesis was that an increase in complexity of microbiota inoculum will allow for more stability in the composition of the gut microbiota of SCID piglets. This was tested across multiple litters of SCID piglets with three different defined microbiota consortium (2-strain, 6-strain, 7-strain). All piglets received their designated defined microbiota by oral gavage immediately after birth and again 24 hours later. There was no effect of SCID genotype on the composition of the gut microbiota, but there was a significant effect due to piglet age. Additionally, all three defined microbiota consortia were deemed safe to use in SCID piglets, and the 7-strain microbiota was the most stable over time. Based on these results, the 7-strain defined microbiota will be added to the SCID pig husbandry protocol, allowing for a more reproducible model.

Identifiers

PMID39282343
PMCPMC11398413

What OpenQuestion holds

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Registered trials

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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.