Beyond the consensus: defining the significance of foot and mouth disease viral sequence diversity
Foot-and mouth disease is caused by a small virus (FMDV) which has an RNA genome. In common with most other RNA viruses, the replication machinery of FMDV makes errors when it copies the genome during replication. As a consequence, the virus evolves very rapidly and can quickly adapt to different environmental pressures. During the 2001 and 2007 outbreaks in the UK, we exploited these properties to finger-print FMDVs recovered from field samples to show how viruses collected on different farms were related to each other. These data provide valuable information to assist in epidemiological tracing and were used in real-time in 2007 to support Defra's control and eradication policy. It is likely that this type of analysis will be widely used to support any future incursions of FMD in the UK (or elsewhere in Europe).
However, our current interpretation of these data is limited by our understanding of the fine-scale processes that underpin the genetic changes that are observed during transmission of the virus at the herd-to-herd (or animal-to-animal) level. The aim of this project is to use a "next-generation" sequencing technology to reveal, for the first time, the complex mixture of viruses that are present within samples and are the starting material for fine-scale evolution of FMDV. We have conducted preliminary experiments to optimise and evaluate this method using a samples collected from a single cow that had been experimentally inoculated with FMDV. These data demonstrate that we are able to measure the frequency of even very rare genetic variants that exist in feet lesions from an infected animal. Many of these variants represent genetic intermediates that were previously undetected using conventional methods.
We therefore, conclude that this new sequencing methodology is well-suited to revealing the fine substructure of complex viral populations and will be a valuable tool to quantify the high-resolution evolutionary dynamics of FMDV. During this project, we aim to extend this approach to generate data from a wider range of samples that have already been collected (and archived) from previous field outbreaks of FMD, and from controlled experimental transmission studies and develop models that quantify the effects of transmission on genetic diversity.
In addition to improving our understanding of the way that FMDV evolves, we anticipate that the findings from this project will have broad application to the transmission biology of other acutely acting viral infections including viruses of human and veterinary importance such as classical swine fever, swine vesicular disease virus, rabies virus, influenza and corona-like (SARS) viruses.