| Literature DB >> 34823222 |
C Jessica E Metcalf1, Soa Fy Andriamandimby2, Rachel E Baker3, Emma E Glennon4, Katie Hampson5, T Deirdre Hollingsworth6, Petra Klepac7, Amy Wesolowski8.
Abstract
When a novel pathogen emerges there may be opportunities to eliminate transmission - locally or globally - whilst case numbers are low. However, the effort required to push a disease to elimination may come at a vast cost at a time when uncertainty is high. Models currently inform policy discussions on this question, but there are a number of open challenges, particularly given unknown aspects of the pathogen biology, the effectiveness and feasibility of interventions, and the intersecting political, economic, sociological and behavioural complexities for a novel pathogen. In this overview, we detail how models might identify directions for better leveraging or expanding the scope of data available on the pathogen trajectory, for bounding the theoretical context of emergence relative to prospects for elimination, and for framing the larger economic, behavioural and social context that will influence policy decisions and the pathogen's outcome.Entities:
Keywords: Elimination; Emergence; Endemic; Epidemic; Mathematical model
Mesh:
Year: 2021 PMID: 34823222 PMCID: PMC7612525 DOI: 10.1016/j.epidem.2021.100507
Source DB: PubMed Journal: Epidemics ISSN: 1878-0067 Impact factor: 4.396
Fig. 1Schematic of endemicity vs.
elimination for an emerging pathogen, focusing on a definition of elimination corresponding to absence of transmission, and illustrating the importance of temporal and spatial scale. The top three panels illustrate the spatial pattern of reported cases of an emerging pathogen at three points in time, where filled points indicate the x,y coordinates of each reported case, and color-filled areas indicate different administrative boundaries, such as regions. The bottom panel shows the corresponding numbers of reported cases (y axis) over time (x axis), with the black line showing cumulative cases across all regions, and colored lines showing case totals for each region (y axis), with colors as on the upper panel. In some regions, the pathogen may stochastically fade-out (brown area contains no points after the first panel, and brown line goes to zero on the lower panel) corresponding to elimination (assuming that no infections are missed by case reporting). Alternatively, in some regions, the pathogen might establish continuous circulation (blue and green areas always contain points in the top panels, blue and green lines are always above zero on the lower panel); in others, the pathogen might never arrive, or might rapidly go extinct, but then be reintroduced (purple areas and lines). Thus, the spatial and temporal scales of analysis will define conclusions as to whether the pathogen is endemic or has been eliminated. For example, focusing within the brown area, one might conclude a status of persistent elimination had been achieved. However, if the full spatial extent is considered, pathogen circulation is ongoing at the end of the time-series (black line indicating cumulative cases is above zero at the end of the time-series). (For interpretation of the references to color in this figure legend, the reader is referred to the web version of this article.)
Examples of data-sources, their uses and integration into models, and associated core challenges. That many of the listed data-sources are open-access has been critical to their utility in responding to infectious disease outbreaks.
| Type of data | Uses | Integration into models | Challenges |
|---|---|---|---|
| Routine surveillance for cases laboratory confirmed suspected syndromic | Estimate parameters (Rt, generation time); effectiveness of interventions; evidence of circulation | Fit both biological parameters and estimates of the impact of interventions (e. g., trajectory matching); verification of elimination | Collation, harmonization, Sensitivity and specificity (especially for syndromic surveillance) |
| Genetic sequence data | Infer transmission pathways, pathogen relatedness, distinguish cryptic transmission versus incursions; inferring dynamical/immunological differences between variants | Timing and number of introductions; using variant frequencies/distribution to infer pathogen characteristics/fitness | Speed of pathogen evolution (limits inference of who infected whom e. g. in nosocomial transmission ( |
| Serology | Estimate attack rate/force of infection; susceptibility | Landscape of immunity, i.e. retrospective or prospective pathogen spread | Difficult to collect, variance among assays, waning at initially unknown rates (Takahashi et al., 2021), uncertain (and often hard to resolve) relationship between serology and protection; |
| Animal reservoir sequencing (or serology) | Spillover (and spillback) risk; | Model frequency of spillover/introductions | Hard to sample a wide area |
| Census based population density, structure by age, etc | Case fatality, morbidity in different settings | Burden, costeffectiveness, spread | Unavailable in some resource poor settings |
| Timing, location and scope of interventions | Rt, and impact of interventions | Cost-effectiveness | Disentangling specific effects of interventions when deployed in combination in different populations/intensities |
| Remote sensing/satellite imagery | Populations at risk, suitable habitat, seasonality of transmission and global range | Climate role may be limited for emerging pathogens | |
| Mobile phone data, social media data | Mobility | Modulation of Rt, responses to policy information | Not necessarily clear that it captures transmission relevant movement; may not be available for critical populations |
| Social media related information providing a window onto sentiment dynamics | Evolution of social norms, spread of misinformation | Behaviour feedbacks on transmission | Mapping from social media to behaviour not always straightforward |