Evidence map›Paper›PMID 36077122›Full record

ArticleInternational journal of molecular sciences2022

Ultrastructural Characterization of Human Bronchial Epithelial Cells during SARS-CoV-2 Infection: Morphological Comparison of Wild-Type and CFTR-Modified Cells.

Flavia Merigo, Virginia Lotti, Paolo Bernardi, Anita Conti, Andrea Di Clemente, Marco Ligozzi, Anna Lagni, Claudio Sorio, Andrea Sbarbati, Davide Gibellini

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. 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
0.8field-weighted citation impact, top 28% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

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

10 authors at 1 institution in 1 country.

Flavia MerigoAnatomy and Histology Section, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, 37134 Verona, Italy.ORCID 0000-0002-6919-7169
Virginia LottiMicrobiology Section, Department of Diagnostic and Public Health, University of Verona, 37134 Verona, Italy.ORCID 0000-0002-5746-3810
Paolo BernardiAnatomy and Histology Section, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, 37134 Verona, Italy.
Anita ContiAnatomy and Histology Section, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, 37134 Verona, Italy.
Andrea Di ClementeMicrobiology Section, Department of Diagnostic and Public Health, University of Verona, 37134 Verona, Italy.
Marco LigozziMicrobiology 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.
Claudio SorioGeneral Pathology Section, Department of Medicine, University of Verona, 37134 Verona, Italy.ORCID 0000-0003-2739-4014
Andrea SbarbatiAnatomy and Histology Section, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, 37134 Verona, Italy.
Davide GibelliniMicrobiology Section, Department of Diagnostic and Public Health, University of Verona, 37134 Verona, Italy.
University of Verona · IT

Funding

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

Abstract

SARS-CoV-2 replicates in host cell cytoplasm. People with cystic fibrosis, considered at risk of developing severe symptoms of COVID-19, instead, tend to show mild symptoms. We, thus, analyzed at the ultrastructural level the morphological effects of SARS-CoV-2 infection on wild-type (WT) and F508del (ΔF) CFTR-expressing CFBE41o- cells at early and late time points post infection. We also investigated ACE2 expression through immune-electron microscopy. At early times of infection, WT cells exhibited double-membrane vesicles, representing typical replicative structures, with granular and vesicular content, while at late time points, they contained vesicles with viral particles. ∆F cells exhibited double-membrane vesicles with an irregular shape and degenerative changes and at late time of infection, showed vesicles containing viruses lacking a regular structure and a well-organized distribution. ACE2 was expressed at the plasma membrane and present in the cytoplasm only at early times in WT, while it persisted even at late times of infection in ΔF cells. The autophagosome content also differed between the cells: in WT cells, it comprised vesicles associated with virus-containing structures, while in ΔF cells, it comprised ingested material for lysosomal digestion. Our data suggest that CFTR-modified cells infected with SARS-CoV-2 have impaired organization of normo-conformed replicative structures.

Indexed as

COVID-19Angiotensin-Converting Enzyme 2Cystic Fibrosis Transmembrane Conductance RegulatorEpithelial CellsHumansSARS-CoV-2Angiotensin-Converting Enzyme 2CFTR protein, humanCystic Fibrosis Transmembrane Conductance RegulatorACE2CFTRcystic fibrosisdouble-membrane vesicles (DMVs)SARS-CoV-2 virustransmission electron microscopy (TEM)

Identifiers

PMID36077122
PMCPMC9455986
OpenAlexW4293537772

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.