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In the past decade the Zaire strain of Ebola virus (ZEBOV) has emerged repeatedly into human populations in central Africa and caused massive die-offs of gorillas and chimpanzees. We tested the view that emergence events are independent and caused by ZEBOV variants that have been long resident at each locality. Phylogenetic analyses place the earliest known outbreak at Yambuku, Democratic Republic of Congo, very near to the root of the ZEBOV tree, suggesting that viruses causing all other known outbreaks evolved from a Yambuku-like virus after 1976. The tendency for earlier outbreaks to be directly ancestral to later outbreaks suggests that outbreaks are epidemiologically linked and may have occurred at the front of an advancing wave. While the ladder-like phylogenetic structure could also bear the signature of positive selection, our statistical power is too weak to reach a conclusion in this regard. Distances among outbreaks indicate a spread rate of about 50 km per year that remains consistent across spatial scales. Viral evolution is clocklike, and sequences show a high level of small-scale spatial structure. Genetic similarity decays with distance at roughly the same rate at all spatial scales. Our analyses suggest that ZEBOV has recently spread across the region rather than being long persistent at each outbreak locality. Controlling the impact of Ebola on wild apes and human populations may be more feasible than previously recognized. Genetic, spatial, and temporal data reveal that the Zaire strain of Ebola virus has spread recently across the region rather than being a long-term resident in the locations where the outbreaks have occurred. [ABSTRACT FROM AUTHOR]

The authors explore the intraspecific history of Ebola virus Zaire (EBOVZ), and conveys that the virus association with the fruit bats in the sampled area can only be traced back a few years. They argue that the phylogenetic analysis of the viral polymerase (L) gene derived from three species of fruit bats caught near affected villages may constitute a long-missing wildlife reservoir for EBOVZ, and the amplified virus is the product of mutations that have accumulated within the last 30 years.