Evidence map›Paper›PMID 35215992›Full record

ArticleViruses2022

Rapid SARS-CoV-2 Intra-Host and Within-Household Emergence of Novel Haplotypes.

Laura Manuto, Marco Grazioli, Andrea Spitaleri, Paolo Fontana, Luca Bianco, Luigi Bertolotti, Martina Bado, Giorgia Mazzotti, Federico Bianca, Francesco Onelia and 11 more

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. SARS-CoV-2 mutant spectrum complexity is an epidemiologically evolvable trait.Proceedings of the National Academy of Sciences of the United States of America · 2025
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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

21 authors at 6 institutions in 2 countries.

Laura ManutoDepartment of Molecular Medicine, University of Padova, 35121 Padua, Italy.
Marco GrazioliDepartment of Molecular Medicine, University of Padova, 35121 Padua, Italy.
Andrea SpitaleriCenter for Omics Sciences, IRCCS San Raffaele Institute, 20132 Milan, Italy.ORCID 0000-0003-3012-3557
Paolo FontanaResearch and Innovation Center, Edmund Mach Foundation, 38098 San Michele all'Adige, Italy.ORCID 0000-0002-4523-4818
Luca BiancoResearch and Innovation Center, Edmund Mach Foundation, 38098 San Michele all'Adige, Italy.ORCID 0000-0002-0196-8422
Luigi BertolottiDepartment of Veterinary Sciences, University of Torino, Grugliasco, 10095 Turin, Italy.
Martina BadoDepartment of Molecular Medicine, University of Padova, 35121 Padua, Italy.
Giorgia MazzottiDepartment of Molecular Medicine, University of Padova, 35121 Padua, Italy.
Federico BiancaDepartment of Molecular Medicine, University of Padova, 35121 Padua, Italy.
Francesco OneliaDepartment of Molecular Medicine, University of Padova, 35121 Padua, Italy.
Giovanni LorenzinEmerging Bacterial Pathogens Unit, Division of Immunology, Transplantation and Infectious Diseases, IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.
Fabio SimeoniCenter for Omics Sciences, IRCCS San Raffaele Institute, 20132 Milan, Italy.
Dejan LazarevicCenter for Omics Sciences, IRCCS San Raffaele Institute, 20132 Milan, Italy.ORCID 0000-0003-4527-290X
Elisa FranchinDepartment of Molecular Medicine, University of Padova, 35121 Padua, Italy.
Claudia Del VecchioDepartment of Molecular Medicine, University of Padova, 35121 Padua, Italy.ORCID 0000-0001-5645-9126
Ilaria DorigattiMRC Centre for Global Infectious Disease Analysis, Imperial College London, London SW7 2BX, UK.ORCID 0000-0001-9959-0706
Giovanni TononCenter for Omics Sciences, IRCCS San Raffaele Institute, 20132 Milan, Italy.
Daniela Maria CirilloEmerging Bacterial Pathogens Unit, Division of Immunology, Transplantation and Infectious Diseases, IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.ORCID 0000-0001-6415-1535
Enrico LavezzoDepartment of Molecular Medicine, University of Padova, 35121 Padua, Italy.ORCID 0000-0002-3902-8356
Andrea CrisantiDepartment of Molecular Medicine, University of Padova, 35121 Padua, Italy.
Stefano ToppoDepartment of Molecular Medicine, University of Padova, 35121 Padua, Italy.ORCID 0000-0002-0246-3119
University of Padua · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITVita-Salute San Raffaele University · ITFondazione Edmund Mach · ITImperial College London · GBUniversity of Turin · IT

Funding

European Union's Horizon 2020 research and innovation programme No 874735 (VEO)Fondazione Umberto Veronesi Misura Ricerca Covid 19, year 2020Medical Research Council MC_PC_19012Medical Research Council MR/R015600/1University of Padova and the Department of Molecular Medicine PRID/SID 2020University of Padova and the Department of Molecular Medicine STARS-CoG ISS-MYTHUniversity of Padova and the Department of Molecular Medicine TOPP_PRIV20_01University of Padova and the Department of Molecular Medicine TOPP_SID19_01
6 · The paper itself

Abstract

In February 2020, the municipality of Vo', a small town near Padua (Italy) was quarantined due to the first coronavirus disease 19 (COVID-19)-related death detected in Italy. To investigate the viral prevalence and clinical features, the entire population was swab tested in two sequential surveys. Here we report the analysis of 87 viral genomes, which revealed that the unique ancestor haplotype introduced in Vo' belongs to lineage B, carrying the mutations G11083T and G26144T. The viral sequences allowed us to investigate the viral evolution while being transmitted within and across households and the effectiveness of the non-pharmaceutical interventions implemented in Vo'. We report, for the first time, evidence that novel viral haplotypes can naturally arise intra-host within an interval as short as two weeks, in approximately 30% of the infected individuals, regardless of symptom severity or immune system deficiencies. Moreover, both phylogenetic and minimum spanning network analyses converge on the hypothesis that the viral sequences evolved from a unique common ancestor haplotype that was carried by an index case. The lockdown extinguished both the viral spread and the emergence of new variants.

Indexed as

Family CharacteristicsGenome, ViralHaplotypesCommunicable Disease ControlCOVID-19Evolution, MolecularHost Microbial InteractionsHumansItalyMutationPhylogenySARS-CoV-2Spike Glycoprotein, CoronavirusSpike Glycoprotein, Coronavirusepidemiologyintra-host haplotypeslongitudinal analysisminimum spanning networkNGS sequencingphylogenetic analysisSARS-CoV-2viral genomics

Identifiers

PMID35215992
PMCPMC8877413
OpenAlexW4213183821

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.