Evidence map›Paper›PMID 29677209›Full record

ArticlePloS one2018

Osteopontin plays a pivotal role in increasing severity of respiratory syncytial virus infection.

Viviana Sampayo-Escobar, Ryan Green, Michael B Cheung, Raminder Bedi, Subhra Mohapatra, Shyam S Mohapatra

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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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

6 authors at 1 institution in 1 country.

Viviana Sampayo-EscobarJames A Haley Veterans Affairs Hospital, Tampa, Florida, United States of America.
Ryan GreenDepartment of Molecular Medicine, University of South Florida Morsani College of Medicine, Tampa, Florida, United States of America.
Michael B CheungJames A Haley Veterans Affairs Hospital, Tampa, Florida, United States of America.
Raminder BediJames A Haley Veterans Affairs Hospital, Tampa, Florida, United States of America.
Subhra MohapatraJames A Haley Veterans Affairs Hospital, Tampa, Florida, United States of America.
Shyam S MohapatraJames A Haley Veterans Affairs Hospital, Tampa, Florida, United States of America.ORCID 0000-0001-5838-0681
University of South Florida · US

Funding

Tumor targeted engineered stem cells for treatment of lung cancerI01BX003413 · VA · JAMES A. HALEY VA MEDICAL CENTER · PI MOHAPATRA, SHYAM S, MOHAPATRA, SUBHRA · 2018 to 2022
–
BLRD VA I01 BX003413BLRD VA I01 BX003685BLRD VA IK6 BX003778BLRD VA IK6 BX004212
6 · The paper itself

Abstract

The molecular mechanisms underlying susceptibility to severe respiratory syncytial virus (RSV) infection remain poorly understood. Herein, we report on the role of osteopontin (OPN) in regulation of RSV infection in human epithelial cells and how interleukin-1 beta (IL-1β), a cytokine secreted soon after RSV infection, when persistently expressed can induce OPN expression leading to increased viral infection. We first compared OPN expression in two human epithelial cell lines: HEK-293 and HEp-2. In contrast to HEp-2, HEK-293 expresses low levels of pro-caspase-1 resulting in decreased IL-1β expression in response to RSV infection. We found a correlation between low IL-1β levels and a delay in induction of OPN expression in RSV-infected HEK-293 cells compared to HEp-2. This phenomenon could partially explain the high susceptibility of HEp-2 cells to RSV infection versus the moderate susceptibility of HEK-293 cells. Also, HEK-293 cells expressing low levels of pro-caspase-1 exhibit decreased IL-1β expression and delayed OPN expression in response to RSV infection. HEK-293 cells incubated with human rIL-1β showed a dose-dependent increase in OPN expression upon RSV infection. Also, incubation with rOPN increased RSV viral load. Moreover, HEp-2 cells or mice infected with a mucogenic RSV strain RSV-L19F showed elevated levels of OPN in contrast to mice infected with the laboratory RSV strain rA2. This correlated with elevated levels of OPN following infection with RSV-L19F compared to rA2. Together, these results demonstrate that increased OPN expression is regulated in part by IL-1β, and the interplay between IL-1β and OPN signaling may play a pivotal role in the spread of RSV infection.

Indexed as

AnimalsFemaleGene Expression RegulationHEK293 CellsHost-Pathogen InteractionsHumansHyaluronan ReceptorsInterleukin-1betaMice, Inbred C57BLMice, KnockoutOsteopontinRespiratory Syncytial VirusesRespiratory Syncytial Virus InfectionsViral LoadVirus ReplicationCD44 protein, humanHyaluronan ReceptorsInterleukin-1betaOsteopontinSPP1 protein, humanSpp1 protein, mouse

Identifiers

PMID29677209
PMCPMC5909912
OpenAlexW2767706897

What OpenQuestion holds

Textmetadata
LicenceCC0
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.