[HTML][HTML] Delayed disease progression in cynomolgus macaques infected with Ebola virus Makona strain

A Marzi, F Feldmann, PW Hanley, DP Scott… - Emerging infectious …, 2015 - ncbi.nlm.nih.gov
A Marzi, F Feldmann, PW Hanley, DP Scott, S Günther, H Feldmann
Emerging infectious diseases, 2015ncbi.nlm.nih.gov
In late 2013, the largest documented outbreak of Ebola hemorrhagic fever started in Guinea
and has since spread to neighboring countries, resulting in almost 27,000 cases and>
11,000 deaths in humans. In March 2014, Ebola virus (EBOV) was identified as the
causative agent. This study compares the pathogenesis of a new EBOV strain, Makona,
which was isolated in Guinea in 2014 with the prototype strain from the 1976 EBOV outbreak
in the former Zaire. Both strains cause lethal disease in cynomolgus macaques with similar …
Abstract
In late 2013, the largest documented outbreak of Ebola hemorrhagic fever started in Guinea and has since spread to neighboring countries, resulting in almost 27,000 cases and> 11,000 deaths in humans. In March 2014, Ebola virus (EBOV) was identified as the causative agent. This study compares the pathogenesis of a new EBOV strain, Makona, which was isolated in Guinea in 2014 with the prototype strain from the 1976 EBOV outbreak in the former Zaire. Both strains cause lethal disease in cynomolgus macaques with similar pathologic changes and hallmark features of Ebola hemorrhagic fever. However, disease progression was delayed in EBOV-Makona–infected animals, suggesting decreased rather than increased virulence of this most recent EBOV strain.
ncbi.nlm.nih.gov