Evidence map›Paper›PMID 32790670›Full record

ReviewPLoS neglected tropical diseases2020

Ecological processes underlying the emergence of novel enzootic cycles: Arboviruses in the neotropics as a case study.

Sarah Guth, Kathryn A Hanley, Benjamin M Althouse, Mike Boots

Open access · goldAbstract readReview
In one paragraph

Review in PLoS neglected tropical diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 6% of its field
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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
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  11. African ZIKV lineage fails to sustain infectivity in an in vitro mimetic urban cycle.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2023
    Article
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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

4 authors at 2 institutions in 1 country.

Sarah GuthDepartment of Integrative Biology, University of California, Berkeley, California, United States of America.ORCID 0000-0001-5533-9456
Kathryn A HanleyDepartment of Biology, New Mexico State University, Las Cruces, New Mexico, United States of America.
Benjamin M AlthouseDepartment of Biology, New Mexico State University, Las Cruces, New Mexico, United States of America.
Mike BootsDepartment of Integrative Biology, University of California, Berkeley, California, United States of America.
New Mexico State University · USUniversity of California, Berkeley · US

Funding

Mechanisms and Public Health Impact of Sylvatic Dengue Virus Emergence in BorneoU01AI115577 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI VASILAKIS, NIKOS · 2016 to 2019
$2.4M
Ecology and evolution of multiple transmission modes: anther-smut diseaseR01GM122061 · NIGMS · UNIVERSITY OF VIRGINIA · PI ANTONOVICS, JANIS · 2016 to 2019
$1.6M
Biotechnology and Biological Sciences Research Council BB/L010879/1NIAID NIH HHS U01 AI115577NIGMS NIH HHS R01 GM122061
6 · The paper itself

Abstract

Pathogens originating from wildlife (zoonoses) pose a significant public health burden, comprising the majority of emerging infectious diseases. Efforts to control and prevent zoonotic disease have traditionally focused on animal-to-human transmission, or "spillover." However, in the modern era, increasing international mobility and commerce facilitate the spread of infected humans, nonhuman animals (hereafter animals), and their products worldwide, thereby increasing the risk that zoonoses will be introduced to new geographic areas. Imported zoonoses can potentially "spill back" to infect local wildlife-a danger magnified by urbanization and other anthropogenic pressures that increase contacts between human and wildlife populations. In this way, humans can function as vectors, dispersing zoonoses from their ancestral enzootic systems to establish reservoirs elsewhere in novel animal host populations. Once established, these enzootic cycles are largely unassailable by standard control measures and have the potential to feed human epidemics. Understanding when and why translocated zoonoses establish novel enzootic cycles requires disentangling ecologically complex and stochastic interactions between the zoonosis, the human population, and the natural ecosystem. In this Review, we address this challenge by delineating potential ecological mechanisms affecting each stage of enzootic establishment-wildlife exposure, enzootic infection, and persistence-applying existing ecological concepts from epidemiology, invasion biology, and population ecology. We ground our discussion in the neotropics, where four arthropod-borne viruses (arboviruses) of zoonotic origin-yellow fever, dengue, chikungunya, and Zika viruses-have separately been introduced into the human population. This paper is a step towards developing a framework for predicting and preventing novel enzootic cycles in the face of zoonotic translocations.

Indexed as

ArbovirusesAmericasAnimalsAnimals, WildArbovirus InfectionsCommunicable Diseases, EmergingEcosystemHumansMosquito VectorsTropical ClimateZoonoses

Identifiers

PMID32790670
PMCPMC7425862
OpenAlexW3049085485

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.