Evidence map›Paper›PMID 24968100›Full record

ArticlePLoS computational biology2014

Optimal sampling strategies for detecting zoonotic disease epidemics.

Jake M Ferguson, Jessica B Langebrake, Vincent L Cannataro, Andres J Garcia, Elizabeth A Hamman, Maia Martcheva, Craig W Osenberg

Abstract read
In one paragraph

Article in PLoS computational biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. A Bayesian Modeling Approach to Optimize Longitudinal Biomarker Sampling Schedules Using Hormonal Data.American journal of human biology : the official journal of the Human Biology Council · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. A Practitioner-Driven Research Agenda for Syndromic Surveillance.Public health reports (Washington, D.C. : 1974)
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Jake M FergusonDepartment of Biology, University of Florida, Gainesville, Florida, United States of America.
Jessica B LangebrakeDepartment of Mathematics, University of Florida, Gainesville, Florida, United States of America.
Vincent L CannataroDepartment of Biology, University of Florida, Gainesville, Florida, United States of America.
Andres J GarciaEmerging Pathogens Institute, University of Florida, Gainesville, Florida, United States of America; Department of Geography, University of Florida, Gainesville, Florida, United States of America.
Elizabeth A HammanDepartment of Biology, University of Florida, Gainesville, Florida, United States of America.
Maia MartchevaDepartment of Mathematics, University of Florida, Gainesville, Florida, United States of America.
Craig W OsenbergDepartment of Biology, University of Florida, Gainesville, Florida, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The early detection of disease epidemics reduces the chance of successful introductions into new locales, minimizes the number of infections, and reduces the financial impact. We develop a framework to determine the optimal sampling strategy for disease detection in zoonotic host-vector epidemiological systems when a disease goes from below detectable levels to an epidemic. We find that if the time of disease introduction is known then the optimal sampling strategy can switch abruptly between sampling only from the vector population to sampling only from the host population. We also construct time-independent optimal sampling strategies when conducting periodic sampling that can involve sampling both the host and the vector populations simultaneously. Both time-dependent and -independent solutions can be useful for sampling design, depending on whether the time of introduction of the disease is known or not. We illustrate the approach with West Nile virus, a globally-spreading zoonotic arbovirus. Though our analytical results are based on a linearization of the dynamical systems, the sampling rules appear robust over a wide range of parameter space when compared to nonlinear simulation models. Our results suggest some simple rules that can be used by practitioners when developing surveillance programs. These rules require knowledge of transition rates between epidemiological compartments, which population was initially infected, and of the cost per sample for serological tests.

Indexed as

EpidemicsModels, BiologicalPopulation SurveillanceAnimalsComputational BiologyDisease VectorsHumansModels, StatisticalWest Nile FeverWest Nile virusZoonoses

Identifiers

PMID24968100
PMCPMC4072525

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.