Inference of R0 and Transmission Heterogeneity from the Size Distribution of Stuttering Chains

Abstract
For many infectious disease processes such as emerging zoonoses and vaccine-preventable diseases, and infections occur as self-limited stuttering transmission chains. A mechanistic understanding of transmission is essential for characterizing the risk of emerging diseases and monitoring spatio-temporal dynamics. Thus methods for inferring and the degree of heterogeneity in transmission from stuttering chain data have important applications in disease surveillance and management. Previous researchers have used chain size distributions to infer , but estimation of the degree of individual-level variation in infectiousness (as quantified by the dispersion parameter, ) has typically required contact tracing data. Utilizing branching process theory along with a negative binomial offspring distribution, we demonstrate how maximum likelihood estimation can be applied to chain size data to infer both and the dispersion parameter that characterizes heterogeneity. While the maximum likelihood value for is a simple function of the average chain size, the associated confidence intervals are dependent on the inferred degree of transmission heterogeneity. As demonstrated for monkeypox data from the Democratic Republic of Congo, this impacts when a statistically significant change in is detectable. In addition, by allowing for superspreading events, inference of shifts the threshold above which a transmission chain should be considered anomalously large for a given value of (thus reducing the probability of false alarms about pathogen adaptation). Our analysis of monkeypox also clarifies the various ways that imperfect observation can impact inference of transmission parameters, and highlights the need to quantitatively evaluate whether observation is likely to significantly bias results. This paper focuses on infectious diseases such as monkeypox, Nipah virus and avian influenza that transmit weakly from human to human. These pathogens cannot cause self-sustaining epidemics in the human population, but instead cause limited transmission chains that stutter to extinction. Such pathogens would go extinct if they were confined to humans, but they persist because of continual introduction from an external reservoir (such as animals, for the zoonotic diseases mentioned above). They are important to study because they pose a risk of emerging if they become more transmissible, or conversely to monitor the success of efforts to locally eliminate a pathogen by vaccination. A crucial challenge for these ‘stuttering’ pathogens is to quantify their transmissibility, in terms of the intensity and heterogeneity of disease transmission by infected individuals. In this paper, we use monkeypox as an example to show how these transmission properties can be estimated from commonly available data describing the size of observed stuttering chains. These results make it easier to monitor diseases that pose a risk of emerging (or re-emerging) as self-sustaining human pathogens, or to decide whether a seemingly large chain may signal a worrisome change in transmissibility.