Evidence map›Paper›PMID 27733686›Full record

ArticleThe Journal of biological chemistry2016

Targeting a Novel RNA-Protein Interaction for Therapeutic Intervention of Hantavirus Disease.

Nilshad N Salim, Safder S Ganaie, Anuradha Roy, Subbiah Jeeva, Mohammad A Mir

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Hantavirus Induced Kidney Disease.Frontiers in medicine · 2021
    Review
  5. Article
  6. Article
  7. Vaccines and Therapeutics Against Hantaviruses.Frontiers in microbiology · 2019
    Review
  8. Article
  9. Review
  10. Article
  11. Development of High-Throughput Screening Assay for Antihantaviral Therapeutics.SLAS discovery : advancing life sciences R & D · 2017
    Article
  12. Article
  13. Review
  14. Article
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

5 authors at 4 institutions in 1 country.

Nilshad N SalimFrom the Kansas University Medical Center, Kansas City, Kansas 66160.
Safder S GanaieFrom the Kansas University Medical Center, Kansas City, Kansas 66160.
Anuradha Roythe University of Kansas, Lawrence, Kansas 66045, and.
Subbiah Jeevathe College of Veterinary Medicine, Western University of Health Sciences, Pomona, California 91766.
Mohammad A Mirthe College of Veterinary Medicine, Western University of Health Sciences, Pomona, California 91766. Electronic address: mmir@westernu.edu.
Western University of Health Sciences · USUniversity Hospital and Clinics · USUniversity Medical Center · USUniversity of Kansas · US

Funding

Synthetic Chemical Biology CoreP20GM113117 · NIGMS · UNIVERSITY OF KANSAS LAWRENCE · PI OROZCO, ROBIN C. · 2016 to 2025
$23.9M
Identification and characterization of inhibitors for hantavirus replicationR01AI095236 · NIAID · UNIVERSITY OF KANSAS MEDICAL CENTER · PI MIR, MOHAMMAD A · 2011 to 2013
$1.1M
Characterization of hantavirus N protein-mediated translation mechanismR21AI097355 · NIAID · UNIVERSITY OF KANSAS MEDICAL CENTER · PI MIR, MOHAMMAD A · 2012 to 2013
$415k
NIAID NIH HHS R01 AI095236NIAID NIH HHS R21 AI097355NIGMS NIH HHS P20 GM113117
6 · The paper itself

Abstract

An evolutionarily conserved sequence at the 5' terminus of hantaviral genomic RNA plays an important role in viral transcription initiation and packaging of the viral genome into viral nucleocapsids. Interaction of viral nucleocapsid protein (N) with this conserved sequence facilitates mRNA translation by a unique N-mediated translation strategy. Whereas this evolutionarily conserved sequence facilitates virus replication with the assistance of N in eukaryotic hosts having multifaceted antiviral defense, we demonstrate its interaction with N presents a novel target for therapeutic intervention of hantavirus disease. Using a high throughput screening approach, we identified three lead inhibitors that bind and induce structural perturbations in N. The inhibitors interrupt N-RNA interaction and abrogate both viral genomic RNA synthesis and N-mediated translation strategy without affecting the canonical translation machinery of the host cell. The inhibitors are well tolerated by cells and inhibit hantavirus replication with the same potency as ribavarin, a commercially available antiviral. We report the identification of a unique chemical scaffold that disrupts a critical RNA-protein interaction in hantaviruses and holds promise for the development of the first anti-hantaviral therapeutic with broad spectrum antiviral activity.

Indexed as

Antiviral AgentsHantavirus InfectionsHeLa CellsHumansHuman Umbilical Vein Endothelial CellsNucleocapsid ProteinsOrthohantavirusRNA, ViralAntiviral AgentsNucleocapsid ProteinsRNA, Viralantiviral agentRNA virustranslation controlviral replicationviral transcription

Identifiers

PMID27733686
PMCPMC5114419
OpenAlexW2530480355

What Socratic holds

Textmetadata
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.