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2019-10-16Zeitschriftenartikel DOI: 10.25646/6543
Geographical Variability Affects CCHFV Detection by RT–PCR: A Tool for In-Silico Evaluation of Molecular Assays
dc.contributor.authorGruber, Cesare E. M.
dc.contributor.authorBartolini, Barbara
dc.contributor.authorCastilletti, Concetta
dc.contributor.authorMirazimi, Ali
dc.contributor.authorHewson, Roger
dc.contributor.authorChristova, Iva
dc.contributor.authorAvšič, Tatjana
dc.contributor.authorGrunow, Roland
dc.contributor.authorPapa, Anna
dc.contributor.authorSánchez-Seco, Maria P.
dc.contributor.authorKoopmans, Marion
dc.contributor.authorIppolito, Giuseppe
dc.contributor.authorCapobianchi, Maria R.
dc.contributor.authorReusken, Chantal B. E. M.
dc.contributor.authorAntonino, Di Caro
dc.date.accessioned2020-03-17T07:24:10Z
dc.date.available2020-03-17T07:24:10Z
dc.date.issued2019-10-16none
dc.identifier.other10.3390/v11100953
dc.identifier.urihttp://edoc.rki.de/176904/6512
dc.description.abstractThe 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.eng
dc.language.isoengnone
dc.publisherRobert Koch-Institut
dc.rights(CC BY 3.0 DE) Namensnennung 3.0 Deutschlandger
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/de/
dc.subjectCCHFVeng
dc.subjectmolecular detectioneng
dc.subjectCrimean–Congo hemorrhagic fever viruseng
dc.subjectarthropod-borne viruseng
dc.subjectlaboratory preparednesseng
dc.subjectemerging diseaseseng
dc.subject.ddc610 Medizin und Gesundheitnone
dc.titleGeographical Variability Affects CCHFV Detection by RT–PCR: A Tool for In-Silico Evaluation of Molecular Assaysnone
dc.typearticle
dc.identifier.urnurn:nbn:de:kobv:0257-176904/6512-5
dc.identifier.doihttp://dx.doi.org/10.25646/6543
dc.type.versionpublishedVersionnone
local.edoc.container-titleVirusesnone
local.edoc.type-nameZeitschriftenartikel
local.edoc.container-typeperiodical
local.edoc.container-type-nameZeitschrift
local.edoc.container-urlhttps://www.mdpi.com/1999-4915/11/10/953none
local.edoc.container-publisher-nameMolecular Diversity Preservation International (MDPI)none
local.edoc.container-volume11none
local.edoc.container-issue10none
local.edoc.container-year2019none
local.edoc.container-firstpage1none
local.edoc.container-lastpage14none
local.edoc.rki-departmentZentrum für Biologische Gefahren und Spezielle Pathogenenone
dc.description.versionPeer Reviewednone

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