Evidence map›Paper›PMID 37870692›Full record

ArticleInfectious diseases and therapy2023

Mutations in Coding and Non-Coding Regions in Varicella-Zoster Virus Causing Fatal Hemorrhagic Fever Without Rash in an Immunocompetent Patient: Case Report.

Juan Camacho, Anabel Negredo, Bartolomé Carrilero, Manuel Segovia, Antonio Moreno, Francisco Pozo, Juan-Emilio Echevarría, José-Manuel Echevarría, M Paz Sánchez-Seco, David Tarragó

Open access · goldAbstract read
In one paragraph

Article in Infectious diseases and therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Hybrid capture shotgun sequencing detected unexpected viruses in the cerebrospinal fluid of children with acute meningitis and encephalitis.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2024
    Article
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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

10 authors at 2 institutions in 1 country.

Juan CamachoNational Center for Microbiology, Instituto de Salud Carlos III, Madrid, Spain.
Anabel NegredoNational Center for Microbiology, Instituto de Salud Carlos III, Madrid, Spain.
Bartolomé CarrileroVirgen de la Arrixaca Hospital, Murcia, Spain.
Manuel SegoviaVirgen de la Arrixaca Hospital, Murcia, Spain.
Antonio MorenoVirgen de la Arrixaca Hospital, Murcia, Spain.
Francisco PozoNational Center for Microbiology, Instituto de Salud Carlos III, Madrid, Spain.
Juan-Emilio EchevarríaNational Center for Microbiology, Instituto de Salud Carlos III, Madrid, Spain.
José-Manuel EchevarríaNational Center for Microbiology, Instituto de Salud Carlos III, Madrid, Spain.
M Paz Sánchez-SecoNational Center for Microbiology, Instituto de Salud Carlos III, Madrid, Spain.
David TarragóNational Center for Microbiology, Instituto de Salud Carlos III, Madrid, Spain. davtarrago@isciii.es.ORCID http://orcid.org/0000-0002-1298-3089
Instituto de Salud Carlos III · ESHospital Universitario Virgen de la Arrixaca · ES

Funding

Instituto de Salud Carlos III MPY1372/12
6 · The paper itself

Abstract

introductionWe report the case of a fatal hemorrhagic varicella primary infection in an immunocompetent man and whole-genome characterization of the virus for the investigation of biomarkers of virulence. CASE: A 38-year-old patient born in Nigeria presented to the emergency department with abdominal pain and subsequently developed fatal hemorrhagic disease without skin rash. Extensive laboratory tests including serology and PCR for arenaviruses, bunyaviruses and ebolaviruses were negative. Varicella-zoster virus (VZV) PCR of sera, liver and spleen tissue samples from autopsy revealed the presence of VZV DNA. Primary infection by varicella-zoster virus with hemorrhagic manifestations was diagnosed after virological testing. The VZV genome was sequenced using a mWGS approach. Bioinformatic analysis showed 53 mutations across the genome, 33 of them producing non-synonymous variants affecting up to 14 genes. Some of them, such as ORF11 and ORF 62, encoded for essential functions related to skin or neurotropism. To our knowledge, the mutations reported here have never been described in a VZV causing such a devastating outcome. DISCUSSION: In immunocompetent patients, viral factors should be considered in patients with uncommon symptoms or severe diseases. Some relevant mutations revealed by using whole genome sequencing (WGS) directly from clinical samples may be involved in this case and deserves further investigation.

conclusionDifferential diagnosis of varicella-zoster virus in immunocompetent adults should be considered among patients with suspected VHF, even if the expected vesicular rash is not present at admission and does not arise thereafter. Whole genome sequencing of strains causing uncommon symptoms and/or mortality is needed for epidemiological surveillance and further characterization of putative markers of virulence. Additionally, this report highlights the recommendation for a VZV vaccination policy in non-immunized migrants from developing countries.

Indexed as

Hemorrhagic feverMetagenomic whole genome sequencing (mWGS)Single-nucleotide polymorphism (SNP)Varicella-zoster virusVaricella-zoster virus cell tropismVaricella-zoster virus cladesVaricella-zoster virus mutationsVaricella-zoster virus virulence

Identifiers

PMID37870692
PMCPMC10651560
OpenAlexW4387865451

What OpenQuestion holds

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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.