Evidence map›Paper›PMID 31118297›Full record

ArticlemSphere2019

Kinome-Wide RNA Interference Screening Identifies Mitogen-Activated Protein Kinases and Phosphatidylinositol Metabolism as Key Factors for Rabies Virus Infection.

Benoit Besson, Seonhee Kim, Taehee Kim, Yoonae Ko, Sangchul Lee, Florence Larrous, Jihwan Song, David Shum, Regis Grailhe, Hervé Bourhy

Open access · goldAbstract read
In one paragraph

Article in mSphere, 2019. 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
1.4field-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, 16 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

10 authors at 2 institutions in 2 countries.

Benoit BessonInstitut Pasteur, Unité Lyssavirus, épidémiologie et neuropathologie, Paris, France benoahb@gmail.com.ORCID 0000-0002-6889-0818
Seonhee KimInstitut Pasteur, Unité Lyssavirus, épidémiologie et neuropathologie, Paris, France.
Taehee KimScreening Discovery Platform, Institut Pasteur Korea, Seongnam-si, Republic of Korea.
Yoonae KoScreening Discovery Platform, Institut Pasteur Korea, Seongnam-si, Republic of Korea.
Sangchul LeeScreening Discovery Platform, Institut Pasteur Korea, Seongnam-si, Republic of Korea.
Florence LarrousInstitut Pasteur, Unité Lyssavirus, épidémiologie et neuropathologie, Paris, France.ORCID 0000-0003-0881-4263
Jihwan SongCHA Bio Complex, CHA Stem Cell Institute, Seongnam-si, Republic of Korea.
David ShumScreening Discovery Platform, Institut Pasteur Korea, Seongnam-si, Republic of Korea.
Regis GrailheScreening Discovery Platform, Institut Pasteur Korea, Seongnam-si, Republic of Korea.
Hervé BourhyInstitut Pasteur, Unité Lyssavirus, épidémiologie et neuropathologie, Paris, France.
Institut Pasteur Korea · KRInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Throughout the rabies virus (RABV) infectious cycle, host-virus interactions define its capacity to replicate, escape the immune response, and spread. As phosphorylation is a key regulatory mechanism involved in most cellular processes, kinases represent a target of choice to identify host factors required for viral replication. A kinase and phosphatase small interfering RNA (siRNA) high-content screening was performed on a fluorescent protein-recombinant field isolate (Tha RABV). We identified 57 high-confidence key host factors important for RABV replication with a readout set at 18 h postinfection and 73 with a readout set at 36 h postinfection, including 24 common factors at all stages of the infection. Amongst them, gene clusters of the most prominent pathways were determined. Up to 15 mitogen-activated protein kinases (MAPKs) and effectors, including MKK7 (associated with Jun N-terminal protein kinase [JNK] signalization) and DUSP5, as well as 17 phosphatidylinositol (PI)-related proteins, including PIP5K1C and MTM1, were found to be involved in the later stage of RABV infection. The importance of these pathways was further validated, as small molecules Ro 31-8820 and PD 198306 inhibited RABV replication in human neurons.

Indexed as

Host Microbial InteractionsRNA InterferenceCell LineHigh-Throughput Screening AssaysHumansMetabolic Networks and PathwaysMitogen-Activated Protein KinasesPhosphatidylinositolsRabies virusSmall Molecule LibrariesVirus ReplicationMitogen-Activated Protein KinasesPhosphatidylinositolsSmall Molecule Librariesdrug screeninginositol phosphate phosphatasesmitogen-activated protein kinasesrabiesRNA interference

Identifiers

PMID31118297
PMCPMC6531879
OpenAlexW2946217735

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.