Evidence map›Paper›PMID 33202558›Full record

ArticleViruses2020

Genomic Diversity and Evolution of Quasispecies in Newcastle Disease Virus Infections.

Archana Jadhav, Lele Zhao, Weiwei Liu, Chan Ding, Venugopal Nair, Sebastian E Ramos-Onsins, Luca Ferretti

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2020. 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
1.6field-weighted citation impact, top 15% 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, 20 citations in OpenAlex.

  1. Article
  2. Article
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  9. Review
  10. Review detection of Newcastle disease virus.Frontiers in veterinary science · 2022
    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

7 authors at 4 institutions in 3 countries.

Archana JadhavViral Oncogenesis Group, The Pirbright Institute, Pirbright, Woking GU24 0NF, Surrey, UK.
Lele ZhaoNuffield Department of Medicine, Li Ka Shing Centre for Health Information and Discovery, Big Data Institute, University of Oxford, Oxford OX3 7LF, UK.
Weiwei LiuDepartment of Avian Infectious Diseases, Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Science, Shanghai 200241, China.
Chan DingDepartment of Avian Infectious Diseases, Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Science, Shanghai 200241, China.
Venugopal NairViral Oncogenesis Group, The Pirbright Institute, Pirbright, Woking GU24 0NF, Surrey, UK.ORCID 0000-0002-8255-516X
Sebastian E Ramos-OnsinsPlant and Animal Genomics, Centre de Recerca en Agrigenòmica (CRAG) CSIC-IRTA-UAB-UB, 08193 Bellaterra, Spain.ORCID 0000-0002-1776-140X
Luca FerrettiNuffield Department of Medicine, Li Ka Shing Centre for Health Information and Discovery, Big Data Institute, University of Oxford, Oxford OX3 7LF, UK.
Shanghai Veterinary Research Institute · CNThe Pirbright Institute · GBUniversity of Oxford · GBCenter for Research in Agricultural Genomics · ES

Funding

Biotechnology and Biological Sciences Research Council BBS/E/I/00007032, BBS/E/I/00007039, BB/R007896, BBS/OS/NW/000007Biotechnology and Biological Sciences Research Council BBS/E/I/00007039
6 · The paper itself

Abstract

Newcastle disease virus (NDV) infections are well known to harbour quasispecies, due to the error-prone nature of the RNA polymerase. Quasispecies variants in the fusion cleavage site of the virus are known to significantly change its virulence. However, little is known about the genomic patterns of diversity and selection in NDV viral swarms. We analyse deep sequencing data from in vitro and in vivo NDV infections to uncover the genomic patterns of diversity and the signatures of selection within NDV swarms. Variants in viruses from in vitro samples are mostly localised in non-coding regions and 3' and 5' untranslated regions (3'UTRs or 5'UTRs), while in vivo samples contain an order of magnitude more variants. We find different patterns of genomic divergence and diversity among NDV genotypes, as well as differences in the genomic distribution of intra-host variants among in vitro and in vivo infections of the same strain. The frequency spectrum shows clear signatures of intra-host purifying selection in vivo on the matrix protein (M) coding gene and positive or diversifying selection on nucleocapsid (NP) and haemagglutinin-neuraminidase (HN). The comparison between within-host polymorphisms and phylogenetic divergence reveals complex patterns of selective pressure on the NDV genome at between- and within-host level. The M sequence is strongly constrained both between and within hosts, fusion protein (F) coding gene is under intra-host positive selection, and NP and HN show contrasting patterns: HN RNA sequence is positively selected between hosts while its protein sequence is positively selected within hosts, and NP is under intra-host positive selection at the RNA level and negative selection at the protein level.

Indexed as

Evolution, MolecularGenetic VariationAnimalsCell LineChick EmbryoChickensGenome, ViralGenomicsGenotypeHemagglutininsHigh-Throughput Nucleotide SequencingHost-Pathogen InteractionsNeuraminidaseNewcastle DiseaseNewcastle disease virusPhylogenyHemagglutininsNeuraminidaseRNA, ViralViral Proteinsdeep sequencinggenetic diversitygenetic variabilityintra-host variabilityMcDonald–Kreitman testNewcastle disease virusquasispeciesTajima’s D

Identifiers

PMID33202558
PMCPMC7698180
OpenAlexW3101606742

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.