Evidence map›Paper›PMID 42215729›Full record

ReviewNature reviews. Microbiology2026

Infection cycles of viruses of the phylum Nucleocytoviricota.

Chantal Abergel, Jônatas Santos Abrahão, Fasseli Coulibaly, Matthias Fischer, Sandra Jeudy, Roland L Knorr, Mart Krupovic, Matthieu Legendre, Daniel Pérez-Núñez, Chisom Nwokolo and 5 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Why did some viruses evolve to be giants while others did not?Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. 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

15 authors.

Chantal AbergelAix-Marseille University, Centre National de la Recherche Scientifique, Information Génomique & Structurale (IGS), Unité Mixte de Recherche (Institut de Microbiologie de la Méditerranée), IM2B Institute, Marseille, France.ORCID http://orcid.org/0000-0003-1875-4049
Jônatas Santos AbrahãoUniversidade Federal de Minas Gerais, Department of Microbiology, Instituto de Ciências Biológicas, Belo Horizonte, Brazil.
Fasseli CoulibalyDepartment of Biochemistry and Molecular Biology and Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.ORCID http://orcid.org/0000-0003-3380-2117
Matthias FischerProtist Virology, Max Planck Institute for Marine Microbiology, Bremen, Germany.
Sandra JeudyAix-Marseille University, Centre National de la Recherche Scientifique, Information Génomique & Structurale (IGS), Unité Mixte de Recherche (Institut de Microbiologie de la Méditerranée), IM2B Institute, Marseille, France.
Roland L KnorrFaculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.ORCID http://orcid.org/0000-0002-6747-0088
Mart KrupovicInstitut Pasteur, Université Paris Cité, Cell Biology and Virology of Archaea Unit, Paris, France.ORCID http://orcid.org/0000-0001-5486-0098
Matthieu LegendreAix-Marseille University, Centre National de la Recherche Scientifique, Information Génomique & Structurale (IGS), Unité Mixte de Recherche (Institut de Microbiologie de la Méditerranée), IM2B Institute, Marseille, France.ORCID http://orcid.org/0000-0002-8413-2910
Daniel Pérez-NúñezMicrobes in Health and Welfare Department, Centro de Biología Molecular Severo Ochoa (CBM), CSIC-UAM, Madrid, Spain.
Chisom NwokoloAix-Marseille University, Centre National de la Recherche Scientifique, Information Génomique & Structurale (IGS), Unité Mixte de Recherche (Institut de Microbiologie de la Méditerranée), IM2B Institute, Marseille, France.
Victória QueirozUniversidade Federal de Minas Gerais, Department of Microbiology, Instituto de Ciências Biológicas, Belo Horizonte, Brazil.
Alain SchmittAix-Marseille University, Centre National de la Recherche Scientifique, Information Génomique & Structurale (IGS), Unité Mixte de Recherche (Institut de Microbiologie de la Méditerranée), IM2B Institute, Marseille, France.ORCID http://orcid.org/0000-0002-3565-8692
James L Van EttenDepartment of Plant Pathology and Nebraska Center for Virology, University of Nebraska-Lincoln, Lincoln, NE, USA.ORCID http://orcid.org/0000-0002-5063-0049
Anouk WillemsenCentre for Microbiology and Environmental Systems Science, Division of Microbial Ecology, University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0002-8511-3244
Hugo BisioAix-Marseille University, Centre National de la Recherche Scientifique, Information Génomique & Structurale (IGS), Unité Mixte de Recherche (Institut de Microbiologie de la Méditerranée), IM2B Institute, Marseille, France. hugo.bisio@igs.cnrs-mrs.fr.ORCID http://orcid.org/0000-0002-4585-8874

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The phylum Nucleocytoviricota, formerly known as nucleocytoplasmic large DNA viruses (NCLDVs), comprises evolutionarily related viruses with remarkably diverse genome sizes, coding capacities and virion morphologies. These viruses infect hosts across the eukaryotic tree of life, from protists to humans, and are believed to have emerged during the early stages of eukaryotic evolution. How the basic aspects of virus-host interaction have evolved in different lineages and whether they share a conserved infection cycle remain unclear. In this Review, we synthesize the information on the infection cycles of model representatives from the major orders within the phylum, revealing both shared traits and lineage-specific innovations. We compare the information available for the extensively studied poxviruses, asfiviruses, iridoviruses and chloroviruses with insights from the rapidly expanding literature on the mimiviruses, pandoraviruses, marseilleviruses and pithoviruses. We provide an overview of the molecular details underlying the key stages of Nucleocytoviricota infection cycles: entry via membrane fusion, formation of viral factories organized via phase separation, genome replication, virion morphogenesis through a crescent intermediate, and egress. We highlight outstanding questions in the field, unify concepts across traditionally separated research areas, and provide a conceptual framework to guide future cell biology studies on large double-stranded DNA viruses.

Indexed as

DNA VirusesAnimalsGenome, ViralHost-Pathogen InteractionsHumansVirionVirus Replication

Identifiers

What Socratic holds

Textmetadata
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 Socratic graph.