scholarly journals Updates to the zoonotic niche map of Ebola virus disease in Africa

eLife ◽  
2016 ◽  
Vol 5 ◽  
Author(s):  
David M Pigott ◽  
Anoushka I Millear ◽  
Lucas Earl ◽  
Chloe Morozoff ◽  
Barbara A Han ◽  
...  

As the outbreak of Ebola virus disease (EVD) in West Africa is now contained, attention is turning from control to future outbreak prediction and prevention. Building on a previously published zoonotic niche map (<xref ref-type="bibr" rid="bib27">Pigott et al., 2014</xref>), this study incorporates new human and animal occurrence data and expands upon the way in which potential bat EVD reservoir species are incorporated. This update demonstrates the potential for incorporating and updating data used to generate the predicted suitability map. A new data portal for sharing such maps is discussed. This output represents the most up-to-date estimate of the extent of EVD zoonotic risk in Africa. These maps can assist in strengthening surveillance and response capacity to contain viral haemorrhagic fevers.

2018 ◽  
Vol 6 (1) ◽  
pp. 1-18
Author(s):  
Brian S.Singer ◽  
Stefan K Blinov

Ebola was first reported in 1976 in Sudan and Congo and named after the river where it was identified. They cause fulminating disease characterized by acute fever followed by generalized hemorrhagic syndrome that is associated with 90% mortality in the most severe forms. It was later reported in Gabon, Central Africa and between 2 and 4 August 2014, a total of 108 new cases of Ebola virus disease (EVD) (laboratory-confirmed, probable, and suspect cases) as well as 45 deaths were reported from Guinea, Liberia, Nigeria, and Sierra Leone. Surveillance and response represent the final crucial steps in achieving effective control of Ebola virus disease, it should be followed by an effective public health response – delivered as integrated packages – with the purpose to interrupt transmission in well defined areas. In addition, intensive efficacy and pharmacovigilance assessment of these interventions including diagnostics, drugs and vaccines against Ebola and other emerging infectious diseases including NTDs must be carefully re-evaluated, and the cut-offs determined and monitored over time, in addition to enhance cross-border collaboration and strengthen effective coordination across African government and populations. Control interventions were very successful in containing the epidemic of EVD.


2019 ◽  
Vol 19 (1) ◽  
Author(s):  
Charles Njuguna ◽  
Amara Jambai ◽  
Alexander Chimbaru ◽  
Anders Nordstrom ◽  
Roland Conteh ◽  
...  

2019 ◽  
Vol 33 ◽  
Author(s):  
Thomas Nagbe ◽  
Jeremias Domingos Naiene ◽  
Julius Monday Rude ◽  
Nuha Mahmoud ◽  
Mohammed Kromah ◽  
...  

2021 ◽  
Vol 15 (8) ◽  
pp. e0009566
Author(s):  
Anna Bratcher ◽  
Nicole A. Hoff ◽  
Reena H. Doshi ◽  
Adva Gadoth ◽  
Megan Halbrook ◽  
...  

Background Ebola virus (EBOV) is a zoonotic filovirus spread through exposure to infected bodily fluids of a human or animal. Though EBOV is capable of causing severe disease, referred to as Ebola Virus Disease (EVD), individuals who have never been diagnosed with confirmed, probable or suspected EVD can have detectable EBOV antigen-specific antibodies in their blood. This study aims to identify risk factors associated with detectable antibody levels in the absence of an EVD diagnosis. Methodology Data was collected from September 2015 to August 2017 from 1,366 consenting individuals across four study sites in the DRC (Boende, Kabondo-Dianda, Kikwit, and Yambuku). Seroreactivity was determined to EBOV GP IgG using Zaire Ebola Virus Glycoprotein (EBOV GP antigen) ELISA kits (Alpha Diagnostic International, Inc.) in Kinshasa, DRC; any result above 4.7 units/mL was considered seroreactive. Among the respondents, 113 (8.3%) were considered seroreactive. Several zoonotic exposures were associated with EBOV seroreactivity after controlling for age, sex, healthcare worker status, location, and history of contact with an EVD case, namely: ever having contact with bats, ever having contact with rodents, and ever eating non-human primate meat. Contact with monkeys or non-human primates was not associated with seroreactivity. Conclusions This analysis suggests that some zoonotic exposures that have been linked to EVD outbreaks can also be associated with EBOV GP seroreactivity in the absence of diagnosed EVD. Future investigations should seek to clarify the relationships between zoonotic exposures, seroreactivity, asymptomatic infection, and EVD.


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