Evidence map›Paper›PMID 29377961›Full record

ArticlePloS one2018

Shared and organism-specific host responses to childhood diarrheal diseases revealed by whole blood transcript profiling.

Hannah A DeBerg, Mussaret B Zaidi, Matthew C Altman, Prasong Khaenam, Vivian H Gersuk, Freddy D Campos, Iza Perez-Martinez, Mario Meza-Segura, Damien Chaussabel, Jacques Banchereau and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 17% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 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

12 authors at 5 institutions in 2 countries.

Hannah A DeBergBenaroya Research Institute at Virginia Mason, Seattle, Washington, United States of America.ORCID 0000-0002-5263-158X
Mussaret B ZaidiInfectious Diseases Research Unit, and Pediatric Emergency Department, Hospital General O'Horan, Mérida, Yucatán, Mexico.
Matthew C AltmanBenaroya Research Institute at Virginia Mason, Seattle, Washington, United States of America.
Prasong KhaenamBenaroya Research Institute at Virginia Mason, Seattle, Washington, United States of America.
Vivian H GersukBenaroya Research Institute at Virginia Mason, Seattle, Washington, United States of America.
Freddy D CamposInfectious Diseases Research Unit, and Pediatric Emergency Department, Hospital General O'Horan, Mérida, Yucatán, Mexico.
Iza Perez-MartinezDepartment of Molecular Biomedicine, CINVESTAV-IPN, México DF, México.
Mario Meza-SeguraDepartment of Molecular Biomedicine, CINVESTAV-IPN, México DF, México.
Damien ChaussabelBenaroya Research Institute at Virginia Mason, Seattle, Washington, United States of America.
Jacques BanchereauThe Jackson Laboratory for Genomic Medicine, Farmington, Connecticut, United States of America.
Teresa Estrada-GarciaDepartment of Molecular Biomedicine, CINVESTAV-IPN, México DF, México.
Peter S LinsleyBenaroya Research Institute at Virginia Mason, Seattle, Washington, United States of America.
Benaroya Research InstituteCentro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional · MXJackson Laboratory · USMichigan United · USUniversity of Washington · US

Funding

Blood Transcriptional Biomarker Profiles for Category B PathogensU01AI082110 · NIAID · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI LINSLEY, PETER S · 2009 to 2013
$6.3M
NIAID NIH HHS U01 AI082110
6 · The paper itself

Abstract

Globally, diarrheal diseases are a leading cause of death in children under five and disproportionately affect children in developing countries. Children who contract diarrheal diseases are rarely screened to identify the etiologic agent due to time and cost considerations associated with pathogen-specific screening and hence pathogen-directed therapy is uncommon. The development of biomarkers to rapidly identify underlying pathogens could improve treatment options and clinical outcomes in childhood diarrheal diseases. Here, we perform RNA sequencing on blood samples collected from children evaluated in an emergency room setting with diarrheal disease where the pathogen(s) present are known. We determine host response gene signatures specific to Salmonella, Shigella and rotavirus, but not E. coli, infections that distinguish them from each other and from healthy controls. Specifically, we observed differential expression of genes related to chemokine receptors or inflammasome signaling in Shigella cases, such as CCR3, CXCR8, and NLRC4, and interferon response genes, such as IFI44 and OASL, in rotavirus cases. Our findings add insight into the host peripheral immune response to these pathogens, and suggest strategies and limitations for the use host response transcript signatures for diagnosing the etiologic agent of childhood diarrheal diseases.

Indexed as

Gene Expression ProfilingChildDiarrheaGastrointestinal DiseasesHumansRNA, MessengerRotavirusShigellaRNA, Messenger

Identifiers

PMID29377961
PMCPMC5788382
OpenAlexW2786793629

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.