Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/47771
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dc.contributor.authorTokgun O.-
dc.contributor.authorCaliskan A.-
dc.contributor.authorCoskun C.-
dc.contributor.authorTokgun P.E.-
dc.contributor.authorAkca H.-
dc.date.accessioned2023-01-09T21:29:59Z-
dc.date.available2023-01-09T21:29:59Z-
dc.date.issued2021-
dc.identifier.issn2036-6590-
dc.identifier.urihttps://doi.org/10.3855/JIDC.14560-
dc.identifier.urihttps://hdl.handle.net/11499/47771-
dc.description.abstractIntroduction: Coronaviruses which are single-stranded RNAs, are members of a large family of viruses that may be important pathogens for humans. SARS-CoV-2 was found to cause the severe respiratory syndrome, and on January 22, 2020 first human-to-human transmission was reported. We aimed to reveal the complete genomes of 19 SARS-CoV-2 isolates from Denizli province and identify Turkish patients' genetic similarities. Methodology: 15 samples with the highest viral loads resulting from RT-PCR were selected for NGS analysis. Fifteen SARS-CoV-2 complete genome sequences were then subjected to phylogenetic analysis and uploaded to the GISAID database. Phylogenetic trees were constructed by the Neighbor-Joining method using MEGAX software. Results: Whole-genome sequencing of the viral RNA samples revealed 32 missense, 21 synonymous, and 4 non-coding alleles. In all samples c.1-25C>T (5'UTR), c.14144C>T (ORF1ab), c.2772C>T (ORF1ab) and c.1841A>G(S) mutations were detected. Phylogenetic analysis revealed that most of the present study's genomes are in 20B clade while the two are in 20A. The phylogenetic tree constructed with all complete SARS-CoV-2 genomes of Turkey showed that the viruses were spread nearly homogenous on eastern (around Kars) and western (around Istanbul) sides. Conclusions: Here, we reported the viral genomes in Denizli comprehensively for the first time. We identified 11 rare missense mutations in the virus compared to the reference genome. Phylogenetic analysis revealed that while most of our isolates were similar to European sequences, some had different sublineages depending on their genomic variants. Copyright © 2021 Tokgun et al.en_US
dc.description.sponsorship2020HZDP023en_US
dc.description.sponsorshipThis study was supported by the Scientific Research Coordination Unit of Pamukkale University under the project number “2020HZDP023”.en_US
dc.language.isoenen_US
dc.publisherJournal of Infection in Developing Countriesen_US
dc.relation.ispartofJournal of Infection in Developing Countriesen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCladeen_US
dc.subjectCoronavirusesen_US
dc.subjectLineageen_US
dc.subjectNgsen_US
dc.subjectSars-cov-2en_US
dc.subjectadolescenten_US
dc.subjectadulten_US
dc.subjectageden_US
dc.subjectArticleen_US
dc.subjectchilden_US
dc.subjectclinical articleen_US
dc.subjectcoronavirus disease 2019en_US
dc.subjectDNA extractionen_US
dc.subjectfemaleen_US
dc.subjectgene frequencyen_US
dc.subjectgene mutationen_US
dc.subjectgene sequenceen_US
dc.subjectgenetic similarityen_US
dc.subjectgenome analysisen_US
dc.subjectgenotypeen_US
dc.subjecthigh throughput sequencingen_US
dc.subjecthumanen_US
dc.subjectillumina sequencingen_US
dc.subjectmaleen_US
dc.subjectmiddle ageden_US
dc.subjectmissense mutationen_US
dc.subjectmultiplex polymerase chain reactionen_US
dc.subjectnasopharyngeal swaben_US
dc.subjectneighbor joining methoden_US
dc.subjectopen reading frameen_US
dc.subjectphylogenyen_US
dc.subjectreal time reverse transcription polymerase chain reactionen_US
dc.subjectRNA isolationen_US
dc.subjectSevere acute respiratory syndrome coronavirus 2en_US
dc.subjectsingle nucleotide polymorphismen_US
dc.subjectvery elderlyen_US
dc.subjectvirus detectionen_US
dc.subjectvirus genomeen_US
dc.subjectvirus isolationen_US
dc.subjectvirus loaden_US
dc.subjectwhole genome sequencingen_US
dc.subjectyoung adulten_US
dc.subjectgeneticsen_US
dc.subjectisolation and purificationen_US
dc.subjectmutationen_US
dc.subjectvirologyen_US
dc.subjectwhole genome sequencingen_US
dc.subjectCOVID-19en_US
dc.subjectGenome, Viralen_US
dc.subjectHumansen_US
dc.subjectMutationen_US
dc.subjectPhylogenyen_US
dc.subjectSARS-CoV-2en_US
dc.subjectWhole Genome Sequencingen_US
dc.titleWhole Genome Sequencing and Phylogenetic Analysis of SARS CoV 2 strains in Turkeyen_US
dc.typeArticleen_US
dc.identifier.volume15en_US
dc.identifier.issue4en_US
dc.identifier.startpage470en_US
dc.identifier.endpage477en_US
dc.identifier.doi10.3855/JIDC.14560-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid36961438000-
dc.authorscopusid56727931300-
dc.authorscopusid57188698668-
dc.authorscopusid57194019069-
dc.authorscopusid6602146139-
dc.identifier.pmid33956645en_US
dc.identifier.scopus2-s2.0-85105517346en_US
dc.identifier.wosWOS:000651611500004en_US
dc.identifier.scopusqualityQ3-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.grantfulltextopen-
item.openairetypeArticle-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.03. Basic Medical Sciences-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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