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Phylodynamic Analysis of Ebola Virus Disease Transmission in Sierra Leone

We generated genome sequences from 218 cases of Ebola virus disease (EVD) in Sierra Leone (SLE) during 2014–2015 to complement available datasets, particularly by including cases from a period of low sequence coverage during peak transmission of Ebola virus (EBOV) in the highly-affected Western Area...

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Autores principales: Jansen van Vuren, Petrus, Ladner, Jason T., Grobbelaar, Antoinette A., Wiley, Michael R., Lovett, Sean, Allam, Mushal, Ismail, Arshad, le Roux, Chantel, Weyer, Jacqueline, Moolla, Naazneen, Storm, Nadia, Kgaladi, Joe, Sanchez-Lockhart, Mariano, Conteh, Ousman, Palacios, Gustavo, Paweska, Janusz T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356631/
https://www.ncbi.nlm.nih.gov/pubmed/30654482
http://dx.doi.org/10.3390/v11010071
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author Jansen van Vuren, Petrus
Ladner, Jason T.
Grobbelaar, Antoinette A.
Wiley, Michael R.
Lovett, Sean
Allam, Mushal
Ismail, Arshad
le Roux, Chantel
Weyer, Jacqueline
Moolla, Naazneen
Storm, Nadia
Kgaladi, Joe
Sanchez-Lockhart, Mariano
Conteh, Ousman
Palacios, Gustavo
Paweska, Janusz T.
author_facet Jansen van Vuren, Petrus
Ladner, Jason T.
Grobbelaar, Antoinette A.
Wiley, Michael R.
Lovett, Sean
Allam, Mushal
Ismail, Arshad
le Roux, Chantel
Weyer, Jacqueline
Moolla, Naazneen
Storm, Nadia
Kgaladi, Joe
Sanchez-Lockhart, Mariano
Conteh, Ousman
Palacios, Gustavo
Paweska, Janusz T.
author_sort Jansen van Vuren, Petrus
collection PubMed
description We generated genome sequences from 218 cases of Ebola virus disease (EVD) in Sierra Leone (SLE) during 2014–2015 to complement available datasets, particularly by including cases from a period of low sequence coverage during peak transmission of Ebola virus (EBOV) in the highly-affected Western Area division of SLE. The combined dataset was utilized to produce phylogenetic and phylodynamic inferences, to study sink–source dynamics and virus dispersal from highly-populated transmission hotspots. We identified four districts in SLE where EBOV was introduced and transmission occurred without onward exportation to other districts. We also identified six districts that substantially contributed to the dispersal of the virus and prolonged the EVD outbreak: five of these served as major hubs, with lots of movement in and out, and one acted primarily as a source, exporting the virus to other areas of the country. Positive correlations between case numbers, inter-district transition events, and district population sizes reaffirm that population size was a driver of EBOV transmission dynamics in SLE. The data presented here confirm the role of urban hubs in virus dispersal and of a delayed laboratory response in the expansion and perpetuation of the EVD outbreak in SLE.
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spelling pubmed-63566312019-02-05 Phylodynamic Analysis of Ebola Virus Disease Transmission in Sierra Leone Jansen van Vuren, Petrus Ladner, Jason T. Grobbelaar, Antoinette A. Wiley, Michael R. Lovett, Sean Allam, Mushal Ismail, Arshad le Roux, Chantel Weyer, Jacqueline Moolla, Naazneen Storm, Nadia Kgaladi, Joe Sanchez-Lockhart, Mariano Conteh, Ousman Palacios, Gustavo Paweska, Janusz T. Viruses Article We generated genome sequences from 218 cases of Ebola virus disease (EVD) in Sierra Leone (SLE) during 2014–2015 to complement available datasets, particularly by including cases from a period of low sequence coverage during peak transmission of Ebola virus (EBOV) in the highly-affected Western Area division of SLE. The combined dataset was utilized to produce phylogenetic and phylodynamic inferences, to study sink–source dynamics and virus dispersal from highly-populated transmission hotspots. We identified four districts in SLE where EBOV was introduced and transmission occurred without onward exportation to other districts. We also identified six districts that substantially contributed to the dispersal of the virus and prolonged the EVD outbreak: five of these served as major hubs, with lots of movement in and out, and one acted primarily as a source, exporting the virus to other areas of the country. Positive correlations between case numbers, inter-district transition events, and district population sizes reaffirm that population size was a driver of EBOV transmission dynamics in SLE. The data presented here confirm the role of urban hubs in virus dispersal and of a delayed laboratory response in the expansion and perpetuation of the EVD outbreak in SLE. MDPI 2019-01-16 /pmc/articles/PMC6356631/ /pubmed/30654482 http://dx.doi.org/10.3390/v11010071 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jansen van Vuren, Petrus
Ladner, Jason T.
Grobbelaar, Antoinette A.
Wiley, Michael R.
Lovett, Sean
Allam, Mushal
Ismail, Arshad
le Roux, Chantel
Weyer, Jacqueline
Moolla, Naazneen
Storm, Nadia
Kgaladi, Joe
Sanchez-Lockhart, Mariano
Conteh, Ousman
Palacios, Gustavo
Paweska, Janusz T.
Phylodynamic Analysis of Ebola Virus Disease Transmission in Sierra Leone
title Phylodynamic Analysis of Ebola Virus Disease Transmission in Sierra Leone
title_full Phylodynamic Analysis of Ebola Virus Disease Transmission in Sierra Leone
title_fullStr Phylodynamic Analysis of Ebola Virus Disease Transmission in Sierra Leone
title_full_unstemmed Phylodynamic Analysis of Ebola Virus Disease Transmission in Sierra Leone
title_short Phylodynamic Analysis of Ebola Virus Disease Transmission in Sierra Leone
title_sort phylodynamic analysis of ebola virus disease transmission in sierra leone
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356631/
https://www.ncbi.nlm.nih.gov/pubmed/30654482
http://dx.doi.org/10.3390/v11010071
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