Evidence map›Paper›PMID 32352894›Full record

ArticleViral immunology2020

Coxsackievirus B4 Exposure Results in Variable Pattern Recognition Response in the Kidneys of Female Non-Obese Diabetic Mice Before Establishment of Diabetes.

Debra L Walter, Sarah E Benner, Rosemary J Oaks, Jean R Thuma, Ramiro Malgor, Frank L Schwartz, Karen T Coschigano, Kelly D McCall

Open access · greenAbstract read
In one paragraph

Article in Viral immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.1field-weighted citation impact, top 42% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Debra L WalterInterdisciplinary Program in Molecular and Cellular Biology, Ohio University, Athens, Ohio, USA.
Sarah E BennerInterdisciplinary Program in Molecular and Cellular Biology, Ohio University, Athens, Ohio, USA.
Rosemary J OaksProgram in Biological Sciences, Honors Tutorial College, Ohio University, Athens, Ohio, USA.
Jean R ThumaDepartment of Specialty Medicine, Heritage College of Osteopathic Medicine, Ohio University, Athens, Ohio, USA.
Ramiro MalgorInterdisciplinary Program in Molecular and Cellular Biology, Ohio University, Athens, Ohio, USA.
Frank L SchwartzDepartment of Specialty Medicine, Heritage College of Osteopathic Medicine, Ohio University, Athens, Ohio, USA.
Karen T CoschiganoInterdisciplinary Program in Molecular and Cellular Biology, Ohio University, Athens, Ohio, USA.
Kelly D McCallInterdisciplinary Program in Molecular and Cellular Biology, Ohio University, Athens, Ohio, USA.
Ohio University · USFlorida State University · US

Funding

UMass Mouse Metabolic Phenotyping Center - Metabolism CoreU2CDK093000 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KIM, JASON K · 2016 to 2021
$4.6M
NIDDK NIH HHS U2C DK093000
6 · The paper itself

Abstract

End-stage renal disease (ESRD) is described by four primary diagnoses, diabetes, hypertension, glomerulonephritis, and cystic kidney disease, all of which have viruses implicated as causative agents. Enteroviruses, such as coxsackievirus (CV), are a common genus of viruses that have been implicated in both diabetes and cystic kidney disease; however, little is known about how CVs cause kidney injury and ESRD or predispose individuals with a genetic susceptibility to type 1 diabetes (T1D) to kidney injury. This study evaluated kidney injury resulting from coxsackievirus B4 (CVB4) inoculation of non-obese diabetic (NOD) mice to glean a better understanding of how viral exposure may predispose individuals with a genetic susceptibility to T1D to kidney injury. The objectives were to assess acute and chronic kidney damage in CVB4-inoculated NOD mice without diabetes. Results indicated the presence of CVB4 RNA in the kidney for at least 14 days post-CVB4 inoculation and a coordinated pattern recognition receptor response, but the absence of an immune response or cytotoxicity. CVB4-inoculated NOD mice also had a higher propensity to develop an increase in mesangial area 17 weeks post-CVB4 inoculation. These studies identified initial gene expression changes in the kidney resulting from CVB4 exposure that may predispose to ESRD. Thus, this study provides an initial characterization of kidney injury resulting from CVB4 inoculation of mice that are genetically susceptible to developing T1D that may one day provide better therapeutic options and predictive measures for patients who are at risk for developing kidney disease from T1D.

Indexed as

Enterovirus B, HumanAnimalsCoxsackievirus InfectionsDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Disease Models, AnimalFemaleGene Expression RegulationGenetic Predisposition to DiseaseHost Microbial InteractionsHumansKidneyKidney Diseases, CysticMiceMice, Inbred NODMice, KnockoutReceptors, Pattern RecognitioncoxsackieviruskidneyNODTLR3

Identifiers

PMID32352894
PMCPMC7478222
OpenAlexW3022960122

What OpenQuestion holds

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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.