Abstract
Background and Methodology: The current Ebola virus epidemic in West Africa has been spreading at least since December 2013. The first confirmed case of Ebola virus in Sierra Leone was identified on May 25. Based on viral genetic sequencing data from 72 individuals in Sierra Leone collected between the end of May and mid June, we utilize a range of phylodynamic methods to estimate the basic reproductive number (R0). We additionally estimate the expected lengths of the incubation and infectious periods of the virus. Finally, we use phylogenetic trees to examine the role played by population structure in the epidemic. Results: The median estimates of R0 based on sequencing data alone range between 1.65-2.18, with the most plausible model yielding a median R0 of 2.18 (95% HPD 1.24-3.55). Importantly, our results indicate that, at least until mid June, relief efforts in Sierra Leone were ineffective at lowering the effective reproductive number of the virus. We estimate the expected length of the infectious period to be 2.58 days (median; 95% HPD 1.24-6.98). The dataset appears to be too small in order to estimate the incubation period with high certainty (median expected incubation period 4.92 days; 95% HPD 2.11-23.20). While our estimates of the duration of infection tend to be smaller than previously reported, phylodynamic analyses support a previous estimate that 70% of cases were observed and included in the present dataset. The dataset is too small to show a particular population structure with high significance, however our preliminary analyses suggest that half the population is spreading the virus with an R0 well above 2, while the other half of the population is spreading with an R0 below 1. Conclusions: Overall we show that sequencing data can robustly infer key epidemiological parameters. Such estimates inform public health officials and help to coordinate effective public health efforts. Thus having more sequencing data available for the ongoing Ebola virus epidemic and at the start of new outbreaks will foster a quick understanding of the dynamics of the pathogen.
Highlights
The 2014 West African Ebola virus (EBOV) epidemic is the largest Ebola virus outbreak to date with 7492 cases (4108 confirmed) and 3439 deaths (2078 confirmed) as of 3 October 20141
While our estimates of the duration of infection tend to be smaller than previously reported, phylodynamic analyses support a previous estimate that 70% of cases were observed and included in the present dataset
The dataset is too small to show a particular population structure with high significance, our preliminary analyses suggest that half the population is spreading the virus with an R0 well above 2, while the other half of the population is spreading with an R0 below 1
Summary
The 2014 West African Ebola virus (EBOV) epidemic is the largest Ebola virus outbreak to date with 7492 cases (4108 confirmed) and 3439 deaths (2078 confirmed) as of 3 October 20141. While previous EBOV outbreaks remained localized, the current epidemic has spread across Guinea, Sierra Leone and Liberia with a localized outbreak in Nigeria. Patients exposed to EBOV first undergo an incubation period of 2-21 days before becoming infectious[3,5,6,7]. There is currently no known effective treatment or vaccine for Ebola virus disease and relief efforts focus on bringing down the case fatality rate through supportive care and disease containment[3]. The current Ebola virus epidemic in West Africa has been spreading at least since December 2013. The first confirmed case of Ebola virus in Sierra Leone was identified on May 25. We use phylogenetic trees to examine the role played by population structure in the epidemic
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