Browsing by Author "Wright, David M."
Now showing 1 - 2 of 2
Results Per Page
Sort Options
Item A new phylodynamic model of Mycobacterium bovis transmission in a multi-host system uncovers the role of the unobserved reservoir(Public Library of Science, 2021-06-25) O'Hare, Anthony; Balaz, Daniel; Wright, David M.; McCormick, Carl; McDowell, Stanley W.J.; Trewby, Hannah; Skuce, Robin A.; Kao, Rowland r.For single host pathogens, pathogen genetic data have been transformative for understanding the transmission and control of many diseases, particuarly rapidly evolving RNA viruses. However garnering similar insights where pathogens are multi-host is more challenging, particularly when the evolution of the pathogen is slower and pathogen sampling often heavily biased. This is the case for Mycobacterium bovis, the causative agent of bovine Tuberculosis (bTB) and for which the Eurasian badger plays an as yet poorly understood role in transmission and spread. Here we have developed a computational model that incorporates M. bovis genetic data from cattle only with a highly abstracted model of an unobserved reservoir. Our research shows that a model in which the reservoir does not contribute to pathogen diversity, but is a source of infection in spatially localised areas around each farm, better describes the patterns of outbreaks observed in a population-level sample of a single M. bovis genotype in Northern Ireland over a period of 15 years, compared to models in which either the reservoir has no role, disease spread is spatially extensive, or where they generate considerable diversity on their own. While this reservoir model is not explicitly a model of badgers, its characteristics are consistent with other data that would suggest a reservoir consisting of infected badgers that contribute substantially to cattle infection, but could not maintain disease on their own.Item Relative abundance of Mycobacterium bovis molecular types in cattle: a simulation study of potential epidemiological drivers(BMC, 2017-08-22) Trewby, Hannah; Wright, David M.; Skuce, Robin A.; McCormick, Carl; Mallon, Thomas R.; Presho, Eleanor L.; Kao, Rowland R.; Haydon, Daniel T.; Biek, RomanBackground: The patterns of relative species abundance are commonly studied in ecology and epidemiology to provide insights into underlying dynamical processes. Molecular types (MVLA-types) of Mycobacterium bovis, the causal agent of bovine tuberculosis, are now routinely recorded in culture-confirmed bovine tuberculosis cases in Northern Ireland. In this study, we use ecological approaches and simulation modelling to investigate the distribution of relative abundances of MVLA-types and its potential drivers. We explore four biologically plausible hypotheses regarding the processes driving molecular type relative abundances: sampling and speciation; structuring of the pathogen population; historical changes in population size; and transmission heterogeneity (superspreading). Results: Northern Irish herd-level MVLA-type surveillance shows a right-skewed distribution of MVLA-types, with a small number of types present at very high frequencies and the majority of types very rare. We demonstrate that this skew is too extreme to be accounted for by simple neutral ecological processes. Simulation results indicate that the process of MVLA-type speciation and the manner in which the MVLA-typing loci were chosen in Northern Ireland cannot account for the observed skew. Similarly, we find that pathogen population structure, assuming for example a reservoir of infection in a separate host, would drive the relative abundance distribution in the opposite direction to that observed, generating more even abundances of molecular types. However, we find that historical increases in bovine tuberculosis prevalence and/or transmission heterogeneity (superspreading) are both capable of generating the skewed MVLA-type distribution, consistent with findings of previous work examining the distribution of molecular types in human tuberculosis. Conclusion: Although the distribution of MVLA-type abundances does not fit classical neutral predictions, our simulations show that increases in pathogen population size and/or superspreading are consistent with the pattern observed, even in the absence of selective pressures acting on the system.