Evidence map›Paper›PMID 34905574›Full record

ArticlePloS one2021

Local occurrence and fast spread of B.1.1.7 lineage: A glimpse into Friuli Venezia Giulia.

Catia Mio, Chiara Dal Secco, Stefania Marzinotto, Claudio Bruno, Santa Pimpo, Elena Betto, Martina Bertoni, Corrado Pipan, Emanuela Sozio, Carlo Tascini and 2 more

Abstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Catia MioDepartment of Medicine (DAME), University of Udine, Udine, Italy.ORCID 0000-0002-6245-8266
Chiara Dal SeccoDepartment of Medicine (DAME), University of Udine, Udine, Italy.
Stefania MarzinottoDepartment of Laboratory Medicine, University Hospital of Udine, Udine, Italy.
Claudio BrunoDepartment of Medicine (DAME), University of Udine, Udine, Italy.
Santa PimpoDepartment of Medicine (DAME), University of Udine, Udine, Italy.
Elena BettoDepartment of Laboratory Medicine, University Hospital of Udine, Udine, Italy.
Martina BertoniDepartment of Laboratory Medicine, University Hospital of Udine, Udine, Italy.
Corrado PipanDepartment of Medicine (DAME), University of Udine, Udine, Italy.
Emanuela SozioInfectious Diseases Clinic, University Hospital of Udine, Udine, Italy.ORCID 0000-0001-6247-5958
Carlo TasciniDepartment of Medicine (DAME), University of Udine, Udine, Italy.
Giuseppe DamanteDepartment of Medicine (DAME), University of Udine, Udine, Italy.
Francesco CurcioDepartment of Medicine (DAME), University of Udine, Udine, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In-depth study of the entire SARS-CoV-2 genome has uncovered many mutations, which have replaced the lineage that characterized the first wave of infections all around the world. In December 2020, the outbreak of variant of concern (VOC) 202012/01 (lineage B.1.1.7) in the United Kingdom defined a turning point during the pandemic, immediately posing a worldwide threat on the Covid-19 vaccination campaign. Here, we reported the evolution of B.1.1.7 lineage-related infections, analyzing samples collected from January 1st 2021, until April 15th 2021, in Friuli Venezia Giulia, a northeastern region of Italy. A cohort of 1508 nasopharyngeal swabs was analyzed by High Resolution Melting (HRM) and 479 randomly selected samples underwent Next Generation Sequencing analysis (NGS), uncovering a steady and continuous accumulation of B.1.1.7 lineage-related specimens, joined by sporadic cases of other known lineages (i.e. harboring the Spike glycoprotein p.E484K mutation). All the SARS-CoV-2 genome has been analyzed in order to highlight all the rare mutations that may eventually result in a new variant of interest. This work suggests that a thorough monitoring of the SARS-CoV-2 genome by NGS is essential to contain any new variant that could jeopardize all the efforts that have been made so far to resolve the emergence of the pandemic.

Indexed as

COVID-19Disease OutbreaksHigh-Throughput Nucleotide SequencingHumansItalyNasopharynxPhylogenyPhylogeographyRNA, ViralSARS-CoV-2Sequence Analysis, RNAUnited KingdomRNA, Viral

Identifiers

PMID34905574
PMCPMC8670677

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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.