Evidence map›Paper›PMID 39861802›Full record

ArticleViruses2024

Development of Primer Panels for Whole-Genome Amplification and Sequencing of Human Seasonal Coronaviruses: hCoV-OC43, hCoV-HKU1, hCoV-229E, and hCoV-NL63.

Tamila Musaeva, Artem Fadeev, Maria Pisareva, Veronika Eder, Andrey Ksenafontov, Margarita Korzhanova, Valery Tsvetkov, Alexander Perederiy, Irina Kiseleva, Daria Danilenko and 2 more

Abstract read
In one paragraph

Article in Viruses, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

12 authors.

Tamila MusaevaSmorodintsev Research Institute of Influenza, 197376 Saint Petersburg, Russia.ORCID 0000-0002-3050-1936
Artem FadeevSmorodintsev Research Institute of Influenza, 197376 Saint Petersburg, Russia.ORCID 0000-0003-3558-3261
Maria PisarevaSmorodintsev Research Institute of Influenza, 197376 Saint Petersburg, Russia.ORCID 0000-0002-1499-9957
Veronika EderSmorodintsev Research Institute of Influenza, 197376 Saint Petersburg, Russia.ORCID 0000-0002-9970-3325
Andrey KsenafontovSmorodintsev Research Institute of Influenza, 197376 Saint Petersburg, Russia.
Margarita KorzhanovaSmorodintsev Research Institute of Influenza, 197376 Saint Petersburg, Russia.ORCID 0000-0003-2512-2517
Valery TsvetkovSmorodintsev Research Institute of Influenza, 197376 Saint Petersburg, Russia.ORCID 0000-0001-5195-9316
Alexander PerederiySmorodintsev Research Institute of Influenza, 197376 Saint Petersburg, Russia.ORCID 0000-0002-5961-1856
Irina KiselevaInstitute of Experimental Medicine, 197022 Saint Petersburg, Russia.ORCID 0000-0002-3892-9873
Daria DanilenkoSmorodintsev Research Institute of Influenza, 197376 Saint Petersburg, Russia.ORCID 0000-0001-6174-0836
Dmitry LioznovSmorodintsev Research Institute of Influenza, 197376 Saint Petersburg, Russia.ORCID 0000-0003-3643-7354
Andrey KomissarovSmorodintsev Research Institute of Influenza, 197376 Saint Petersburg, Russia.

Funding

Ministry of Health of the Russian Federation #TVKQ-2024-0003 "Complex approach to genetic characterization and early identifications of pathogens with epidemic and pandemic potential using metagenomic sequencing"
6 · The paper itself

Abstract

Human seasonal coronaviruses (hCoVs) are a group of viruses that affect the upper respiratory tract. While seasonal patterns and the annual variability of predominant hCoV species are well-documented, their genetic and species diversity in St. Petersburg and across Russia remains largely unexplored. In this study, we developed a two-pool, long-amplicon (900-1100 bp) PCR primer panel for the whole-genome sequencing of four seasonal hCoV species. The panel was validated using nasopharyngeal swab samples collected within the Global Influenza Hospital Surveillance Network (GIHSN) project. Over a period of six epidemiological seasons from 2017 to 2023, we retrospectively analyzed 14,704 nasopharyngeal swabs collected from patients hospitalized in St. Petersburg clinics. Of these samples, 5010 (34.07%) tested positive for respiratory viruses, with 424 (2.88% of all samples) identified as seasonal human coronaviruses. The assessment of species diversity showed that predominant hCoV species alternate between seasons. Whole-genome sequences for 85 seasonal human coronaviruses (hCoVs) with >70% genome coverage were obtained, including 23 hCoV-OC43, 6 hCoV-HKU1, 39 hCoV-229E, and 17 hCoV-NL63. These represent the first near-complete genomes of seasonal hCoVs from the Russian Federation, addressing a significant gap in the genomic epidemiology of these viruses. A detailed phylogenetic analysis of the sequenced genomes was conducted, highlighting the emergence of hCoV-229E subclades 7b.1 and 7b.2, which carry numerous substitutions in the Spike protein. Additionally, we sequenced a historical hCoV-229E isolate collected in the USSR in 1979, the oldest sequenced 229E virus from Eurasia, and demonstrated that it belongs to Genotype 2. The newly developed PCR-based sequencing protocol for seasonal hCoVs is straightforward and well-suited for genomic surveillance, providing a valuable tool to enhance our understanding of the genetic diversity of human seasonal coronaviruses.

Indexed as

CoronavirusCoronavirus InfectionsDNA PrimersGenome, ViralWhole Genome SequencingCoronavirus 229E, HumanCoronavirus OC43, HumanGenetic VariationHumansNasopharynxPhylogenyRetrospective StudiesRussiaSeasonsDNA Primersacute respiratory infectionshCoV-229EhCoV-HKU1hCoV-NL63hCoV-OC43human seasonal coronavirusesmolecular virologyviruses

Identifiers

PMID39861802
PMCPMC11768711

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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.