INTRODUCTION
EVD is a severe contagious disease affecting humans and non-human primates. It can be transmitted to humans through direct contact with blood, tissue, body fluids and secretions from an infected animal or human.
• Zaire ebolavirus (ZEBOV);
• Sudan ebolavirus (SEBOV);
• Bundibugyo ebolavirus (BEBOV);
• Reston ebolavirus (REBOV) and
• Tai Forest ebolavirus (TEBOV).
Their genomes can
differ by 30-40%.
All but REBOV have been detected only in Africa. REBOV was
isolated in 1989-90 in Reston (USA) from macaques imported from the
Philippines. In 2008, pigs from pig farms close to Manilla (Philippines) also
tested positive for REBOV. The related Marburg virus, genus Marburgvirus, is
morphologically indistinguishable and induces symptoms similar to Ebolavirus.
The latter occurred in a village near the Ebola River, from which the disease takes its name. The 2014–2016 outbreak in West Africa was the largest Ebola outbreak since the virus was first discovered in 1976.
The outbreak
started in Guinea and then moved across land borders to Sierra Leone and
Liberia. The current 2018-2019 outbreak in eastern DRC is highly complex, with
insecurity adversely affecting public health response activities.
The latest epidemic of Ebola Virus Disease (EVD) in Congo
has rapidly evolved into a largest outbreak in history. Deployed in an
operational environment characterized by ongoing volatility, EVD prevention,
treatment and containment efforts have faced multiple difficulties.
Mistrust of EVD responders by local communities, coupled with targeted attacks on healthcare workers and facilities, have proved to be serious operational challenges.
Despite aggressive efforts to stamp out the disease across three provinces, the
virus has continued to spread and is responsible for the deaths of 3,303 people
to date (as of 24th November 2019) with an overall fatality rate of 67%.