Evidence map›Paper›PMID 37894036›Full record

ArticleMicroorganisms2023

Detection of SARS-CoV-2 Δ426 ORF8 Deletion Mutant Cluster in NGS Screening.

Riccardo Cecchetto, Emil Tonon, Nicoletta Medaina, Giona Turri, Erica Diani, Pier Paolo Piccaluga, Angela Salomoni, Michela Conti, Evelina Tacconelli, Anna Lagni and 3 more

Abstract read
In one paragraph

Article in Microorganisms, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. 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

13 authors.

Riccardo CecchettoMicrobiology Section, Department of Diagnostic and Public Health, University of Verona, 37134 Verona, Italy.ORCID 0009-0000-5189-8867
Emil TononMicrobiology Section, Department of Diagnostic and Public Health, University of Verona, 37134 Verona, Italy.
Nicoletta MedainaUOC Microbiology Unit, AOUI Verona, 37134 Verona, Italy.
Giona TurriUOC Microbiology Unit, AOUI Verona, 37134 Verona, Italy.
Erica DianiMicrobiology Section, Department of Diagnostic and Public Health, University of Verona, 37134 Verona, Italy.ORCID 0000-0002-1373-7533
Pier Paolo PiccalugaHematopathology Section, Department of Experimental, Diagnostic, and Experimental Medicine, Bologna University, 40126 Bologna, Italy.ORCID 0000-0002-9432-0595
Angela SalomoniIstituto Zooprofilattico Sperimentale delle Venezie, Legnaro, 35020 Padua, Italy.
Michela ContiInfectious Diseases Section, Department of Diagnostic and Public Health, University of Verona, 37134 Verona, Italy.
Evelina TacconelliInfectious Diseases Section, Department of Diagnostic and Public Health, University of Verona, 37134 Verona, Italy.
Anna LagniMicrobiology Section, Department of Diagnostic and Public Health, University of Verona, 37134 Verona, Italy.ORCID 0009-0005-1044-3109
Virginia LottiMicrobiology Section, Department of Diagnostic and Public Health, University of Verona, 37134 Verona, Italy.ORCID 0000-0002-5746-3810
Mosé FavaratoMolecular Diagnostics and Genetics, AULSS 3 Serenissima, 30174 Venice, Italy.
Davide GibelliniMicrobiology Section, Department of Diagnostic and Public Health, University of Verona, 37134 Verona, Italy.

Funding

Fondazione Cariverona ENACT project VIRO-COVID
6 · The paper itself

Abstract

Next-generation sequencing (NGS) from SARS-CoV-2-positive swabs collected during the last months of 2022 revealed a large deletion spanning ORF7b and ORF8 (426 nt) in six patients infected with the BA.5.1 Omicron variant. This extensive genome loss removed a large part of these two genes, maintaining in frame the first 22 aminoacids of ORF7b and the last three aminoacids of ORF8. Interestingly, the deleted region was flanked by two small repeats, which were likely involved in the formation of a hairpin structure. Similar rearrangements, comparable in size and location to the deletion, were also identified in 15 sequences in the NCBI database. In this group, seven out of 15 cases from the USA and Switzerland presented both the BA.5.1 variant and the same 426 nucleotides deletion. It is noteworthy that three out of six cases were detected in patients with immunodeficiency, and it is conceivable that this clinical condition could promote the replication and selection of these mutations.

Indexed as

deletiongenomic surveillanceNGSSARS-CoV-2variants

Identifiers

PMID37894036
PMCPMC10609088

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.