No association between the SARS-CoV-2 variants and mortality rates in the Eastern Mediterranean Region

dc.contributor.authorOmais, Saad
dc.contributor.authorKharroubi, Samer A.
dc.contributor.authorZaraket, Hassan
dc.contributor.departmentDepartment of Biology
dc.contributor.departmentDepartment of Nutrition and Food Sciences
dc.contributor.departmentExperimental Pathology, Microbiology, and Immunology
dc.contributor.facultyFaculty of Arts and Sciences (FAS)
dc.contributor.facultyFaculty of Agricultural and Food Sciences (FAFS)
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:21:08Z
dc.date.available2025-01-24T11:21:08Z
dc.date.issued2021
dc.description.abstractAs the novel coronavirus SARS-CoV-2 continues to spread in all countries, there is a growing interest in monitoring and understanding the impact of emerging strains on virus transmission and disease severity. Here, we analyzed SARS-CoV-2 genomic sequences reported in the Eastern Mediterranean Region (EMR) countries, as of 1 January 2021. The majority (~75%) of these sequences originated from three out of 22 EMR countries, and 65.8% of all sequences belonged to GISAID clades GR, GH, G and GV. A delay ranging between 30 and 150 days from sample collection to sequence submission was observed across all countries, limiting the utility of such data in informing public health policies. We identified ten common non-synonymous mutations represented among SARS-CoV-2 in the EMR and several country-specific ones. Two substitutions, spike_D614G and NSP12_P323L, were predominantly concurrent in most countries. While the single incidence of NSP12_P323L was positively correlated with higher case fatality rates in EMR, no such association was established for the double (spike_D614G and NSP12_P323L) concurrent variant across the region. Our study identified critical data gaps in EMR highlighting the importance of enhancing surveillance and sequencing capacities in the region. © 2021 Elsevier B.V.
dc.identifier.doihttps://doi.org/10.1016/j.gene.2021.145843
dc.identifier.eid2-s2.0-85111024017
dc.identifier.pmid34274478
dc.identifier.urihttp://hdl.handle.net/10938/25213
dc.language.isoen
dc.publisherElsevier B.V.
dc.relation.ispartofGene
dc.sourceScopus
dc.subjectCase fatality rate
dc.subjectEast mediterranean region
dc.subjectSars-cov-2
dc.subjectVariants
dc.subjectWhole genome
dc.subjectAdolescent
dc.subjectAdult
dc.subjectChild
dc.subjectChild, preschool
dc.subjectCovid-19
dc.subjectFemale
dc.subjectGenome, viral
dc.subjectHumans
dc.subjectInfant
dc.subjectInfant, newborn
dc.subjectMale
dc.subjectMediterranean region
dc.subjectMiddle aged
dc.subjectMutation
dc.subjectYoung adult
dc.subjectAspartic acid
dc.subjectCoronavirus spike glycoprotein
dc.subjectGlycine
dc.subjectLeucine
dc.subjectProline
dc.subjectArticle
dc.subjectCladistics
dc.subjectControlled study
dc.subjectCoronavirus disease 2019
dc.subjectHuman
dc.subjectMortality rate
dc.subjectNewborn
dc.subjectNonhuman
dc.subjectPublic health
dc.subjectPublic policy
dc.subjectSevere acute respiratory syndrome coronavirus 2
dc.subjectSouthern europe
dc.subjectViral genomics
dc.subjectVirus genome
dc.subjectVirus mutation
dc.subjectVirus strain
dc.subjectWhole genome sequencing
dc.subjectEpidemiology
dc.subjectGenetics
dc.subjectMortality
dc.subjectPreschool child
dc.subjectVirology
dc.titleNo association between the SARS-CoV-2 variants and mortality rates in the Eastern Mediterranean Region
dc.typeArticle

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