Evidence map›Paper›PMID 34079533›Full record

ArticleFrontiers in microbiology2021

Paracrine IFN Response Limits ZIKV Infection in Human Sertoli Cells.

Daniel P Strange, Boonyanudh Jiyarom, Hooman Sadri-Ardekani, Lisa H Cazares, Tara A Kenny, Michael D Ward, Saguna Verma

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 10 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

7 authors at 3 institutions in 1 country.

Daniel P StrangeDepartment of Tropical Medicine, Medical Microbiology, and Pharmacology, John A. Burns School of Medicine, University of Hawai'i at Mãnoa, Honolulu, HI, United States.
Boonyanudh JiyaromDepartment of Tropical Medicine, Medical Microbiology, and Pharmacology, John A. Burns School of Medicine, University of Hawai'i at Mãnoa, Honolulu, HI, United States.
Hooman Sadri-ArdekaniWake Forest Institute for Regenerative Medicine, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Lisa H CazaresSystems and Structural Biology Division, Protein Sciences Branch, U.S. Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Tara A KennySystems and Structural Biology Division, Protein Sciences Branch, U.S. Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Michael D WardSystems and Structural Biology Division, Protein Sciences Branch, U.S. Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Saguna VermaDepartment of Tropical Medicine, Medical Microbiology, and Pharmacology, John A. Burns School of Medicine, University of Hawai'i at Mãnoa, Honolulu, HI, United States.
United States Army Medical Research Institute of Infectious Diseases · USUniversity of Hawaiʻi at Mānoa · USForest Institute · US

Funding

Human 3D testicular organoids as a model to dissect cell-type specific tropism and immune response to Zika virusR21AI140248 · NIAID · UNIVERSITY OF HAWAII AT MANOA · PI SADRI, HOOMAN, VERMA, SAGUNA · 2018 to 2019
$438k
Under attack: Modulation of the blood-testes barrier by Zika virusR21AI129465 · NIAID · UNIVERSITY OF HAWAII AT MANOA · PI VERMA, SAGUNA · 2017 to 2018
$424k
NIAID NIH HHS R21 AI129465NIAID NIH HHS R21 AI140248
6 · The paper itself

Abstract

Zika virus (ZIKV) is unique among mosquito-borne flaviviruses in its ability to be sexually transmitted. The testes have been implicated as sites of long-term ZIKV replication, and our previous studies have identified Sertoli cells (SC), the nurse cells of the seminiferous epithelium that govern spermatogenesis, as major targets of ZIKV infection. To improve our understanding of the interaction of ZIKV with human SC, we analyzed ZIKV-induced proteome changes in these cells using high-throughput liquid chromatography-tandem mass spectrometry (LC-MS/MS). Our data demonstrated that interferon (IFN) signaling was the most significantly enriched pathway and the antiviral proteins MX1 and IFIT1 were among the top upregulated proteins in SC following ZIKV infection. The dynamic between IFN response and ZIKV infection kinetics in SC remains unclear, therefore we further determined whether MX1 and IFIT1 serve as antiviral effectors against ZIKV. We found that increased levels of MX1 at the later time points of infection coincided with diminished ZIKV infection while the silencing of

Indexed as

host-ZIKV interactionIFIT1IFN responseISGsMX1Sertoli cellstestesZIKV

Identifiers

PMID34079533
PMCPMC8165286
OpenAlexW3160955915

What Socratic 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 Socratic graph.