Evidence map›Paper›PMID 29325778›Full record

ArticleVirology2018

Nonstructural proteins nsp2TF and nsp2N of porcine reproductive and respiratory syndrome virus (PRRSV) play important roles in suppressing host innate immune responses.

Y Li, P Shang, D Shyu, C Carrillo, P Naraghi-Arani, Crystal J Jaing, G J Renukaradhya, A E Firth, E J Snijder, Y Fang

Abstract read
In one paragraph

Article in Virology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–field-weighted citation impact
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

33 citing papers in PubMed.

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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.

Y LiDepartment of Diagnostic Medicine and Pathobiology, Kansas State Veterinary Diagnostic Laboratory, College of Veterinary Medicine, Kansas State University, Manhattan, KS 66506, USA.
P ShangDepartment of Diagnostic Medicine and Pathobiology, Kansas State Veterinary Diagnostic Laboratory, College of Veterinary Medicine, Kansas State University, Manhattan, KS 66506, USA.
D ShyuFood Animal Health Research Program (FAHRP), Veterinary Preventive Medicine, The Ohio State University, Wooster, OH 44691, USA.
C CarrilloPhysical & Life Sciences Directorate, Lawrence Livermore National Laboratory, Livermore, CA 94550, USA.
P Naraghi-AraniPhysical & Life Sciences Directorate, Lawrence Livermore National Laboratory, Livermore, CA 94550, USA.
Crystal J JaingPhysical & Life Sciences Directorate, Lawrence Livermore National Laboratory, Livermore, CA 94550, USA.
G J RenukaradhyaFood Animal Health Research Program (FAHRP), Veterinary Preventive Medicine, The Ohio State University, Wooster, OH 44691, USA.
A E FirthDepartment of Pathology, University of Cambridge, Cambridge CB2 1QP, United Kingdom.
E J SnijderMolecular Virology Laboratory, Department of Medical Microbiology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
Y FangDepartment of Diagnostic Medicine and Pathobiology, Kansas State Veterinary Diagnostic Laboratory, College of Veterinary Medicine, Kansas State University, Manhattan, KS 66506, USA. Electronic address: yfang@vet.k-state.edu.

Funding

Wellcome TrustWellcome Trust 106207
6 · The paper itself

Abstract

Recently, we identified a unique -2/-1 ribosomal frameshift mechanism in PRRSV, which yields two truncated forms of nonstructural protein (nsp) 2 variants, nsp2TF and nsp2N. Here, in vitro expression of individual PRRSV nsp2TF and nsp2N demonstrated their ability to suppress cellular innate immune responses in transfected cells. Two recombinant viruses were further analyzed, in which either nsp2TF was C-terminally truncated (vKO1) or expression of both nsp2TF and nsp2N was knocked out (vKO2). Host cellular mRNA profiling showed that a panel of cellular immune genes, in particular those involved in innate immunity, was upregulated in cells infected with vKO1 and vKO2. Compared to the wild-type virus, vKO1 and vKO2 expedited the IFN-α response and increased NK cell cytotoxicity, and subsequently enhanced T cell immune responses in infected pigs. Our data strongly implicate nsp2TF/nsp2N in arteriviral immune evasion and demonstrate that nsp2TF/nsp2N-deficient PRRSV is less capable of counteracting host innate immune responses.

Indexed as

AnimalsCell LineChlorocebus aethiopsGene Expression RegulationImmunity, InnatePorcine Reproductive and Respiratory SyndromePorcine respiratory and reproductive syndrome virusRNA, MessengerSwineUp-RegulationViral Nonstructural ProteinsRNA, MessengerViral Nonstructural ProteinsInnate immune responsensp2Nnsp2TFPRRSVRibosomal frameshift

Identifiers

PMID29325778
PMCPMC5884420

What OpenQuestion holds

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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.