Evidence map›Paper›PMID 26262637›Full record

ArticleViruses2015

Genetic Characterization of the Belgian Nephropathogenic Infectious Bronchitis Virus (NIBV) Reference Strain B1648.

Vishwanatha R A P Reddy, Sebastiaan Theuns, Inge D M Roukaerts, Mark Zeller, Jelle Matthijnssens, Hans J Nauwynck

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
5.0field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 40 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

6 authors at 2 institutions in 1 country.

Vishwanatha R A P ReddyLaboratory of Virology, Department of Virology, Parasitology and Immunology,Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, B-9820 Merelbeke, Belgium. Reddy.Vishwanatha@ugent.be.
Sebastiaan TheunsLaboratory of Virology, Department of Virology, Parasitology and Immunology,Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, B-9820 Merelbeke, Belgium. Sebastiaan.Theuns@UGent.be.
Inge D M RoukaertsLaboratory of Virology, Department of Virology, Parasitology and Immunology,Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, B-9820 Merelbeke, Belgium. inge.roukaerts@UGent.be.
Mark ZellerRega Institute for Medical Research, Laboratory of Clinical Virology, Department of Microbiologyand Immunology, KU Leuven-University of Leuven, Minderbroedersstraat 10, BE-3000 Leuven, Belgium. mark.zeller@uzleuven.be.
Jelle MatthijnssensRega Institute for Medical Research, Laboratory of Clinical Virology, Department of Microbiologyand Immunology, KU Leuven-University of Leuven, Minderbroedersstraat 10, BE-3000 Leuven, Belgium. jelle.matthijnssens@uzleuven.be.
Hans J NauwynckLaboratory of Virology, Department of Virology, Parasitology and Immunology,Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, B-9820 Merelbeke, Belgium. Hans.Nauwynck@ugent.be.
Ghent University · BERega Institute for Medical Research · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The virulent nephropathogenic infectious bronchitis virus (NIBV) strain B1648 was first isolated in 1984, in Flanders, Belgium. Despite intensive vaccination, B1648 and its variants are still circulating in Europe and North Africa. Here, the full-length genome of this Belgian NIBV reference strain was determined by next generation sequencing (NGS) to understand its evolutionary relationship with other IBV strains, and to identify possible genetic factors that may be associated with the nephropathogenicity. Thirteen open reading frames (ORFs) were predicted in the B1648 strain (51UTR-1a-1b-S-3a-3b-E-M-4b-4c-5a-5b-N-6b-31UTR). ORFs 4b, 4c and 6b, which have been rarely reported in literature, were present in B1648 and most of the other IBV complete genomes. According to phylogenetic analysis of the full-length genome, replicase transcriptase complex, spike protein, partial S1 gene and M protein, B1648 strain clustered with the non-Massachusetts type strains NGA/A116E7/2006, UKr 27-11, QX-like ITA/90254/2005, QX-like CK/SWE/0658946/10, TN20/00, RF-27/99, RF/06/2007 and SLO/266/05. Based on the partial S1 fragment, B1648 clustered with the strains TN20/00, RF-27/99, RF/06/2007 and SLO/266/05 and, further designated as B1648 genotype. The full-length genome of B1648 shared the highest sequence homology with UKr 27-11, Gray, JMK, and NGA/A116E7/2006 (91.2% to 91.6%) and was least related with the reference Beaudette and Massachusetts strains (89.7%). Nucleotide and amino acid sequence analyses indicated that B1648 strain may have played an important role in the evolution of IBV in Europe and North Africa. Further, the nephropathogenicity determinants might be located on the 1a, spike, M and accessory proteins (3a, 3b, 4b, 4c, 5a, 5b and 6b). Overall, strain B1648 is distinct from all the strains reported so far in Europe and other parts of the world.

Indexed as

Genome, ViralAnimalsBelgiumChickensCluster AnalysisCoronavirus InfectionsEvolution, MolecularGenetic VariationHigh-Throughput Nucleotide SequencingInfectious bronchitis virusMolecular Sequence DataOpen Reading FramesPhylogenyPoultry DiseasesRNA, ViralSequence Analysis, DNARNA, ViralB1648chickenIBVnephropathogenicnonstructural protein

Identifiers

PMID26262637
PMCPMC4576188
OpenAlexW2142083428

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Registered trials

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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.