Evidence map›Paper›PMID 33409849›Full record

ArticleAnnals of biomedical engineering2021

A Millifluidic Perfusion Cassette for Studying the Pathogenesis of Enteric Infections Using Ex-Vivo Organoids.

Reid L Wilson, Sarah A Hewes, Anubama Rajan, Shih-Ching Lin, Carolyn Bomidi, Takanori Iida, Mary K Estes, Anthony W Maresso, K Jane Grande-Allen

Open access · greenAbstract read
In one paragraph

Article in Annals of biomedical engineering, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. 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

9 authors at 2 institutions in 1 country.

Reid L Wilson *Department of Bioengineering, Rice University, 6100 Main St, MS-142, Houston, TX, 77005, USA.
Sarah A Hewes *Department of Bioengineering, Rice University, 6100 Main St, MS-142, Houston, TX, 77005, USA.
Anubama RajanDepartment of Molecular Virology and Microbiology, Baylor College of Medicine, One Baylor Plaza, Houston, TX, 77030, USA.
Shih-Ching LinDepartment of Molecular Virology and Microbiology, Baylor College of Medicine, One Baylor Plaza, Houston, TX, 77030, USA.
Carolyn BomidiDepartment of Molecular Virology and Microbiology, Baylor College of Medicine, One Baylor Plaza, Houston, TX, 77030, USA.
Takanori IidaDepartment of Bioengineering, Rice University, 6100 Main St, MS-142, Houston, TX, 77005, USA.
Mary K EstesDepartment of Molecular Virology and Microbiology, Baylor College of Medicine, One Baylor Plaza, Houston, TX, 77030, USA.
Anthony W MaressoDepartment of Molecular Virology and Microbiology, Baylor College of Medicine, One Baylor Plaza, Houston, TX, 77030, USA.
K Jane Grande-AllenDepartment of Bioengineering, Rice University, 6100 Main St, MS-142, Houston, TX, 77005, USA. grande@rice.edu.ORCID http://orcid.org/0000-0003-1533-3767
Baylor College of Medicine · USRice University · US

Funding

Tissue Analysis & Molecular Imaging CoreP30DK056338 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI Geoffrey A Preidis · 2001 to 2026
$28.3M
Novel Platforms for Human Intestinal Enteroids: Matrix, Mechanics, and TopographyU19AI116497 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI GRANDE-ALLEN, KATHRYN JANE · 2015 to 2025
$13.2M
Novel biomaterial and biomechanical platforms for modeling the small intestineF30DK108541 · NIDDK · RICE UNIVERSITY · PI WILSON, REID LAURENCE · 2016 to 2019
$164k
Cancer Prevention and Research Institute of Texas RP160283NIAID NIH HHS U19 AI116497NIDDK NIH HHS F30 DK108541NIDDK NIH HHS P30 DK056338NIH HHS F30 DK108541NIH HHS U19 AI116497
6 · The paper itself

Abstract

To generate physiologically-relevant experimental models, the study of enteric diarrheal diseases is turning increasingly to advanced in vitro models that combine ex vivo, stem cell-derived "organoid" cell lines with bioengineered culture environments that expose them to mechanical stimuli, such as fluid flow. However, such approaches require considerable technical expertise with both microfabrication and organoid culture, and are, therefore, inaccessible to many researchers. For this reason, we have developed a perfusion system that is simple to fabricate, operate, and maintain. Its dimensions approximate the volume and cell culture area of traditional 96-well plates and allow the incorporation of fastidious primary, stem cell-derived cell lines with only minimal adaptation of their established culture techniques. We show that infections with enteroaggregative E. coli and norovirus, common causes of infectious diarrhea, in the system display important differences from static models, and in some ways better recreate the pathophysiology of in vivo infections. Furthermore, commensal strains of bacteria can be added alongside the pathogens to simulate the effects of a host microbiome on the infectious process. For these reasons, we believe that this perfusion system is a powerful, yet easily accessible tool for studying host-pathogen interactions in the human intestine.

Indexed as

Caliciviridae InfectionsEscherichia coliEscherichia coli InfectionsGastrointestinal DiseasesNorovirusOrgan Culture TechniquesAdultBiofilmsCells, CulturedEscherichia coli ProteinsFimbriae ProteinsHost-Pathogen InteractionsHumansIntestine, SmallMucinsOrganoidsEscherichia coli ProteinsFimbriae ProteinsMucinsVirulence FactorsBacteriaDynamicEnteroidEscherichia coliMicrobiomeMicrofluidicNorovirusOrganoidShear

Identifiers

PMID33409849
PMCPMC8012234
OpenAlexW3119476034

What OpenQuestion holds

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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.