Evidence map›Paper›PMID 31623214›Full record

ArticleViruses2019

Geographical Variability Affects CCHFV Detection by RT-PCR: A Tool for In-Silico Evaluation of Molecular Assays.

Cesare E M Gruber, Barbara Bartolini, Concetta Castilletti, Ali Mirazimi, Roger Hewson, Iva Christova, Tatjana Avšič, Roland Grunow, Anna Papa, María P Sánchez-Seco and 5 more

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  4. Review
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  6. Crimean-Congo haemorrhagic fever virus.Nature reviews. Microbiology · 2023
    Review
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  8. 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

15 authors at 10 institutions in 9 countries.

Cesare E M GruberNational Institute for Infectious Diseases (INMI) "L. Spallanzani" IRCCS, WHO Collaborating Center for clinical care, diagnosis, response and training on Highly Infectious Diseases, 00149 Rome, Italy. cesare.gruber@inmi.it.
Barbara BartoliniNational Institute for Infectious Diseases (INMI) "L. Spallanzani" IRCCS, WHO Collaborating Center for clinical care, diagnosis, response and training on Highly Infectious Diseases, 00149 Rome, Italy. barbara.bartolini@inmi.it.
Concetta CastillettiNational Institute for Infectious Diseases (INMI) "L. Spallanzani" IRCCS, WHO Collaborating Center for clinical care, diagnosis, response and training on Highly Infectious Diseases, 00149 Rome, Italy. concetta.castilletti@inmi.it.
Ali MirazimiPublic Health agency of Sweden, 17182 Solna, Sweden. ali.mirazimi@folkhalsomyndigheten.se.
Roger HewsonPublic Health England, National Infection Service WHO Collaborating Centre for Virus Reference and Research (Special Pathogens) Porton Down, Salisbury SP40JG, UK. Roger.Hewson@hpa.org.uk.
Iva ChristovaNational Reference Laboratory on Vector-Borne Pathogens, Leptospira and Listeria, Microbiology Department, National Center of Infectious and Parasitic Diseases, 1504 Sofia, Bulgaria. iva_christova@yahoo.com.
Tatjana AvšičFaculty of Medicine, Institute of Microbiology and Immunology, 1000 Ljubljana, Slovenia. Tatjana.Avsic@mf.uni-lj.si.
Roland GrunowCentre for Biological Threats and Special Pathogens, Highly Pathogenic Microorganisms (ZBS 2), Robert Koch Institute, 13353 Berlin, Germany. GrunowR@rki.de.
Anna PapaDepartment of Microbiology, Medical School, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece. annap@med.auth.gr.
María P Sánchez-SecoNational Centre of Microbiology, Institute of Health "Carlos III", Majadahonda, 28220 Madrid, Spain. paz.sanchez@isciii.es.
Marion KopmansErasmus MC, Department of Viroscience, WHO Collaborating Centre for arbovirus and viral hemorrhagic fever reference and research, 3015 CN Rotterdam, The Netherlands. m.koopmans@erasmusmc.nl.
Giuseppe IppolitoNational Institute for Infectious Diseases (INMI) "L. Spallanzani" IRCCS, WHO Collaborating Center for clinical care, diagnosis, response and training on Highly Infectious Diseases, 00149 Rome, Italy. giuseppe.ippolito@inmi.it.
Maria R CapobianchiNational Institute for Infectious Diseases (INMI) "L. Spallanzani" IRCCS, WHO Collaborating Center for clinical care, diagnosis, response and training on Highly Infectious Diseases, 00149 Rome, Italy. maria.capobianchi@inmi.it.
Chantal B E M ReuskenErasmus MC, Department of Viroscience, WHO Collaborating Centre for arbovirus and viral hemorrhagic fever reference and research, 3015 CN Rotterdam, The Netherlands. c.reusken@erasmusmc.nl.
Antonino Di CaroNational Institute for Infectious Diseases (INMI) "L. Spallanzani" IRCCS, WHO Collaborating Center for clinical care, diagnosis, response and training on Highly Infectious Diseases, 00149 Rome, Italy. antonino.dicaro@inmi.it.
Center for Prevention and Treatment of Infections · USAristotle University of Thessaloniki · GRErasmus University Rotterdam · NLInstitute of Oncology Ljubljana · SIInstituto de Salud Carlos III · ESNational Center of Infectious and Parasitic Diseases · BGNational Institute for Public Health and the Environment · NLPublic Health Agency of Sweden · SEPublic Health England · GBRobert Koch Institute · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Crimean-Congo hemorrhagic fever virus (CCHFV) is considered to be a major emerging infectious threat, according to the WHO R&D blueprint. A wide range of CCHFV molecular assays have been developed, employing varied primer/probe combinations. The high genetic variability of CCHFV often hampers the efficacy of available molecular tests and can affect their diagnostic potential. Recently, increasing numbers of complete CCHFV genomic sequences have become available, allowing a better appreciation of the genomic evolution of this virus. We summarized the current knowledge on molecular methods and developed a new bioinformatics tool to evaluate the existing assays for CCHFV detection, with a special focus on strains circulating in different geographical areas. Twenty-two molecular methods and 181 sequences of CCHFV were collected, respectively, from PubMed and GenBank databases. Up to 28 mismatches between primers and probes of each assay and CCHFV strains were detected through in-silico PCR analysis. Combinations of up to three molecular methods markedly decreased the number of mismatches within most geographic areas. These results supported the good practice of CCHFV detection of performing more than one assay, aimed for different sequence targets. The choice of the most appropriate tests must take into account patient's travel history and geographic distribution of the different CCHFV strains.

Indexed as

Computational BiologyGenetic VariationSoftwareComputer SimulationGeographyHemorrhagic Fever, CrimeanHemorrhagic Fever Virus, Crimean-CongoHumansMolecular Diagnostic TechniquesPhylogenyReverse Transcriptase Polymerase Chain ReactionSensitivity and Specificityarthropod-borne virusCCHFVCrimean–Congo hemorrhagic fever virusemerging diseaseslaboratory preparednessmolecular detection

Identifiers

PMID31623214
PMCPMC6833031
OpenAlexW2981275244

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.