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Erin Mordecai

Publications and source records attributed to Erin Mordecai.

3 recordsLinked to original sources

Phenomenological forecasting of disease incidence using heteroskedastic Gaussian processes: a dengue case study

In 2015 the US federal government sponsored a dengue forecasting competition using historical case data from Iquitos, Peru and San Juan, Puerto Rico. Competitors were evaluated on several aspects of out-of-sample forecasts including the targets of peak week, peak incidence during that week and total season incidence across each of several seasons. Our team was one of the top performers of that competition, outperforming all other teams in multiple targets/locals. In this paper we report on our methodology, a large component of which, surprisingly, ignores the known biology of epidemics at large---in particular relationships between dengue transmission and environmental factors---and instead relies on flexible nonparametric nonlinear Gaussian process (GP) regression fits that "memorize" the trajectories of past seasons, and then "match" the dynamics of the unfolding season to past ones in real-time. Our phenomenological approach has advantages in situations where disease dynamics are less well understood, e.g., at sites with shorter histories of disease (such as Iquitos), or where measurements and forecasts of ancillary covariates like precipitation are unavailable and/or where the strength of association with cases are as yet unknown. In particular, we show that the GP approach generally outperforms a more classical generalized linear (autoregressive) model (GLM) that we developed to utilize abundant covariate information. We illustrate variations of our method(s) on the two benchmark locales alongside a full summary of results submitted by other contest competitors.

stat.AP

Mapping physiological suitability limits of malaria in Africa under climate change

We mapped current and future temperature suitability for malaria transmission in Africa using a published model that incorporates nonlinear physiological responses to temperature of the mosquito vector Anopheles gambiae and the malaria parasite Plasmodium falciparum. We found that a larger area of Africa currently experiences the ideal temperature for transmission than previously supposed. Under future climate projections, we predicted a modest increase in the overall area suitable for malaria transmission, but a net decrease in the most suitable area. Combined with population density projections, our maps suggest that areas with temperatures suitable for year-round, highest risk transmission will shift from coastal West Africa to the Albertine Rift between Democratic Republic of Congo and Uganda, while areas with seasonal transmission suitability will shift toward sub-Saharan coastal areas. Mapping temperature suitability places important bounds on malaria transmissibility and, along with local level demographic, socioeconomic, and ecological factors, can indicate where resources may be best spent on malaria control.

q-bio.QM

Understanding uncertainty in temperature effects on vector-borne disease: A Bayesian approach

Extrinsic environmental factors influence the distribution and population dynamics of many organisms, including insects that are of concern for human health and agriculture. This is particularly true for vector-borne infectious diseases, like malaria, which is a major source of morbidity and mortality in humans. Understanding the mechanistic links between environment and population processes for these diseases is key to predicting the consequences of climate change on transmission and for developing effective interventions. An important measure of the intensity of disease transmission is the reproductive number $R_0$. However, understanding the mechanisms linking $R_0$ and temperature, an environmental factor driving disease risk, can be challenging because the data available for parameterization are often poor. To address this we show how a Bayesian approach can help identify critical uncertainties in components of $R_0$ and how this uncertainty is propagated into the estimate of $R_0$. Most notably, we find that different parameters dominate the uncertainty at different temperature regimes: bite rate from 15-25$^\circ$ C; fecundity across all temperatures, but especially $\sim$25-32$^\circ$ C; mortality from 20-30$^\circ$ C; parasite development rate at $\sim$15-16$^\circ$C and again at $\sim$33-35$^\circ$C. Focusing empirical studies on these parameters and corresponding temperature ranges would be the most efficient way to improve estimates of $R_0$. While we focus on malaria, our methods apply to improving process-based models more generally, including epidemiological, physiological niche, and species distribution models.

q-bio.QM