Evidence map›Paper›PMID 39480870›Full record

ArticlePLoS neglected tropical diseases2024

Insights into trypanosomiasis transmission: Age, infection rates, and bloodmeal analysis of Glossina fuscipes fuscipes in N.W. Uganda.

Lucas J Cunningham, Johan Esterhuizen, John W Hargrove, Mike Lehane, Jennifer Lord, Jessica Lingley, T N Clement Mangwiro, Mercy Opiyo, Iñaki Tirados, Steve J Torr

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Article
  2. 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

10 authors.

Lucas J CunninghamDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.ORCID 0000-0002-3017-4074
Johan EsterhuizenDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
John W HargroveDSI-NRF Centre for Epidemiological Modelling and Analysis, University of Stellenbosch, Stellenbosch, South Africa.
Mike LehaneDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Jennifer LordDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Jessica LingleyDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
T N Clement MangwiroBindura University of Science Education, Bindura, Zimbabwe.
Mercy OpiyoMalaria Elimination Initiative, Institute of Global Health Sciences, University of California San Francisco, San Francisco, California, United States of America.
Iñaki TiradosDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Steve J TorrDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.ORCID 0000-0001-9550-4030

Funding

Bill and Melinda GatesTrypa-NO! study
6 · The paper itself

Abstract

backgroundTsetse flies (Glossina) transmit species of Trypanosoma which cause human African trypanosomiasis (HAT) and animal African trypanosomiasis (AAT). Understanding the epidemiology of this disease and controlling the vector rationally requires analysis of the abundance, age structure, infection rates and feeding patterns of tsetse populations.

methodsWe analysed a population of G. fuscipes fuscipes in the Koboko district of Uganda. Seasonal variation in the abundance of tsetse was assessed from the numbers of tsetse caught in pyramidal traps. The age structure of the population was assessed by dissecting female tsetse to estimate their ovarian categories. Classical and PCR-based methods were utilised to determine the presence of the three major pathogenic species of salivarian trypanosomes: T. vivax, T. congolense and T. brucei in a subset (n = 2369) of flies. Further, bloodmeal analysis was carried out using PCR to amplify and sequence a portion of the vertebrate cytb gene.

resultsThe abundance and age structure of tsetse populations were relatively stable and a slight seasonal four-fold variation in abundance appeared to be correlated with rainfall. Analyses of age structure suggests a low natural daily mortality of 1.75% (1.62-1.88). Infection rates estimated were significantly greater (1.9-9.3 times) using the PCR-based method compared to the classical dissection-based method. Positive rates for T. brucei sl, T. congolense and T. vivax were 1.6% (1.32-2.24), 2.4% (1.83-3.11and 2.0% (1.46-2.63), respectively by PCR. The majority of bloodmeals were identified as cattle (39%, 30.5-47.8) and human (37%, 28.4-45.6).

conclusionThe seasonally stable abundance, low mortality rate and high proportion of bloodmeals from humans may explain, in part, why this district has historically been a focus of sleeping sickness. Additionally, the high rates of cattle feeding indicate insecticide treated cattle may prove to be a useful vector control strategy in the area.

Indexed as

SeasonsTsetse FliesAge FactorsAnimalsBloodCattleFeeding BehaviorFemaleHumansInsect VectorsMalePolymerase Chain ReactionTrypanosomaTrypanosomiasis, AfricanUganda

Identifiers

PMID39480870
PMCPMC11556741

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.