Evidence map›Paper›PMID 35463975›Full record

ArticleBioMed research international2022

Adaptive Evolution of the Fox Coronavirus Based on Genome-Wide Sequence Analysis.

Chunyu Feng, Yuting Liu, Guangqi Lyu, Songyang Shang, Hongyue Xia, Junpeng Zhang, David M Irwin, Zhe Wang, Shuyi Zhang

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. 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

9 authors at 2 institutions in 2 countries.

Chunyu FengCollege of Animal Science and Veterinary Medicine, Shenyang Agricultural University, Shenyang 110866, China.ORCID https://orcid.org/0000-0002-0268-7526
Yuting LiuCollege of Animal Science and Veterinary Medicine, Shenyang Agricultural University, Shenyang 110866, China.ORCID https://orcid.org/0000-0002-3451-470X
Guangqi LyuCollege of Animal Science and Veterinary Medicine, Shenyang Agricultural University, Shenyang 110866, China.ORCID https://orcid.org/0000-0002-4025-4086
Songyang ShangCollege of Animal Science and Veterinary Medicine, Shenyang Agricultural University, Shenyang 110866, China.ORCID https://orcid.org/0000-0003-4494-4321
Hongyue XiaAgricultural Development Service Center of Hunnan District, Shenyang 110000, China.ORCID https://orcid.org/0000-0002-8355-5399
Junpeng ZhangCollege of Animal Science and Veterinary Medicine, Shenyang Agricultural University, Shenyang 110866, China.
David M IrwinDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada M5S 1A8.
Zhe WangCollege of Animal Science and Veterinary Medicine, Shenyang Agricultural University, Shenyang 110866, China.ORCID https://orcid.org/0000-0002-8166-1059
Shuyi ZhangCollege of Animal Science and Veterinary Medicine, Shenyang Agricultural University, Shenyang 110866, China.ORCID https://orcid.org/0000-0001-6582-5319
Shenyang Agricultural University · CNUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To report the first complete fox coronavirus (CoV) genome sequence obtained through genome-wide amplifications and to understand the adaptive evolution of fox CoV. Methods: Anal swab samples were collected from 35 foxes to detect the presence of CoV and obtain the virus sequence. Phylogenetic analysis was conducted using MrBayes. The possibility of recombination within these sequences was assessed using GARD. Analysis of the levels of selection pressure experienced by these sequences was assessed using methods on both the PAML and Data Monkey platforms. Results: Of the 35 samples, two were positive, and complete genome sequences for the viruses were obtained. Phylogenetic analysis, using Bayesian methods, of these sequences, together with other CoV sequences, revealed that the fox CoV sequences clustered with canine coronavirus (CCoV) sequences, with sequences from other carnivores more distantly related. In contrast to the feline, ferret and mink CoV sequences that clustered into species-specific clades, the fox CoV fell within the CCoV clade. Minimal evidence for recombination was found among the sequences. A total of 7, 3, 14, and 2 positively selected sites were identified in the M, N, S, and 7B genes, respectively, with 99, 111, and 581 negatively selected sites identified in M, N, and S genes, respectively. Conclusion: The complete genome sequence of fox CoV has been obtained for the first time. The results suggest that the genome sequence of fox CoV may have experienced adaptive evolution in the genes replication, entry, and virulence. The number of sites in each gene that experienced negative selection is far greater than the number that underwent positive selection, suggesting that most of the sequence is highly conserved and important for viral survive. However, positive selection at a few sites likely aided these viruses to adapt to new environments.

Indexed as

CoronavirusCoronavirus, CanineCoronavirus InfectionsAnimalsBayes TheoremCatsDogsFerretsGenome, ViralPhylogenySequence Analysis, DNA

Identifiers

PMID35463975
PMCPMC9020971
OpenAlexW4223960641

What OpenQuestion holds

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LicenceCC BY
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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.