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Article: The phylogeography of MERS-CoV in hospital outbreak-associated cases compared to sporadic cases in Saudi Arabia

TitleThe phylogeography of MERS-CoV in hospital outbreak-associated cases compared to sporadic cases in Saudi Arabia
Authors
KeywordsEpidemiology
Hospital outbreaks
MERS-CoV
Nosocomial
Phylogenetics
Phylogeography
Issue Date2020
Citation
Viruses, 2020, v. 12, n. 5, article no. v12050540 How to Cite?
AbstractThis study compared the phylogeography of MERS-CoV between hospital outbreak-associated cases and sporadic cases in Saudi Arabia. We collected complete genome sequences from human samples in Saudi Arabia and data on the multiple risk factors of human MERS-CoV in Saudi Arabia reported from 2012 to 2018. By matching each sequence to human cases, we identified isolates as hospital outbreak-associated cases or sporadic cases. We used Bayesian phylogenetic methods including temporal, discrete trait analysis and phylogeography to uncover transmission routes of MERS-CoV isolates between hospital outbreaks and sporadic cases. Of the 120 sequences collected between 19 June 2012 and 23 January 2017, there were 64 isolates from hospital outbreak-associated cases and 56 from sporadic cases. Overall, MERS-CoV is fast evolving at 7.43 × 10-4 substitutions per site per year. Isolates from hospital outbreaks showed unusually fast evolutionary speed in a shorter time-frame than sporadic cases. Multiple introductions of different MERS-CoV strains occurred in three separate hospital outbreaks. MERS-CoV appears to be mutating in humans. The impact of mutations on viruses transmissibility in humans is unknown.
Persistent Identifierhttp://hdl.handle.net/10722/325475
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChen, Xin-
dc.contributor.authorAdam, Dillon Charles-
dc.contributor.authorChughtai, Abrar Ahmad-
dc.contributor.authorStelzer-Braid, Sacha-
dc.contributor.authorScotch, Matthew-
dc.contributor.authorMacIntyre, Chandini Raina-
dc.date.accessioned2023-02-27T07:33:36Z-
dc.date.available2023-02-27T07:33:36Z-
dc.date.issued2020-
dc.identifier.citationViruses, 2020, v. 12, n. 5, article no. v12050540-
dc.identifier.urihttp://hdl.handle.net/10722/325475-
dc.description.abstractThis study compared the phylogeography of MERS-CoV between hospital outbreak-associated cases and sporadic cases in Saudi Arabia. We collected complete genome sequences from human samples in Saudi Arabia and data on the multiple risk factors of human MERS-CoV in Saudi Arabia reported from 2012 to 2018. By matching each sequence to human cases, we identified isolates as hospital outbreak-associated cases or sporadic cases. We used Bayesian phylogenetic methods including temporal, discrete trait analysis and phylogeography to uncover transmission routes of MERS-CoV isolates between hospital outbreaks and sporadic cases. Of the 120 sequences collected between 19 June 2012 and 23 January 2017, there were 64 isolates from hospital outbreak-associated cases and 56 from sporadic cases. Overall, MERS-CoV is fast evolving at 7.43 × 10-4 substitutions per site per year. Isolates from hospital outbreaks showed unusually fast evolutionary speed in a shorter time-frame than sporadic cases. Multiple introductions of different MERS-CoV strains occurred in three separate hospital outbreaks. MERS-CoV appears to be mutating in humans. The impact of mutations on viruses transmissibility in humans is unknown.-
dc.languageeng-
dc.relation.ispartofViruses-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectEpidemiology-
dc.subjectHospital outbreaks-
dc.subjectMERS-CoV-
dc.subjectNosocomial-
dc.subjectPhylogenetics-
dc.subjectPhylogeography-
dc.titleThe phylogeography of MERS-CoV in hospital outbreak-associated cases compared to sporadic cases in Saudi Arabia-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.3390/v12050540-
dc.identifier.pmid32422937-
dc.identifier.pmcidPMC7290704-
dc.identifier.scopuseid_2-s2.0-85084790200-
dc.identifier.volume12-
dc.identifier.issue5-
dc.identifier.spagearticle no. v12050540-
dc.identifier.epagearticle no. v12050540-
dc.identifier.eissn1999-4915-
dc.identifier.isiWOS:000565860200057-

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