Evidence map›Paper›PMID 26485147›Full record

ArticlePloS one2015

Flea-Associated Bacterial Communities across an Environmental Transect in a Plague-Endemic Region of Uganda.

Ryan Thomas Jones, Jeff Borchert, Rebecca Eisen, Katherine MacMillan, Karen Boegler, Kenneth L Gage

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Trial
  2. Article
  3. Emergence, global dispersal, and local adaptations ofApplied and environmental microbiology · 2026
    Review
  4. Review
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  6. Article
  7. The facultative intracellular symbiontFrontiers in microbiology · 2025
    Article
  8. Article
  9. Article
  10. Molecular detection ofFrontiers in veterinary science · 2023
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. 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

6 authors at 3 institutions in 2 countries.

Ryan Thomas JonesDepartment of Microbiology and Immunology, Montana State University, Bozeman, Montana, United States of America; Montana Institute on Ecosystems, Montana State University, Bozeman, Montana, United States of America.
Jeff BorchertDivision of Vector-Borne Disease; Centers for Disease Control and Prevention, Fort Collins, Colorado, United States of America.
Rebecca EisenDivision of Vector-Borne Disease; Centers for Disease Control and Prevention, Fort Collins, Colorado, United States of America.
Katherine MacMillanDivision of Vector-Borne Disease; Centers for Disease Control and Prevention, Fort Collins, Colorado, United States of America.
Karen BoeglerDivision of Vector-Borne Disease; Centers for Disease Control and Prevention, Fort Collins, Colorado, United States of America.
Kenneth L GageDivision of Vector-Borne Disease; Centers for Disease Control and Prevention, Fort Collins, Colorado, United States of America.
Centers for Disease Control and Prevention · USMontana State University · USVector & Vector-Borne Diseases Research Institute · TZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The vast majority of human plague cases currently occur in sub-Saharan Africa. The primary route of transmission of Yersinia pestis, the causative agent of plague, is via flea bites. Non-pathogenic flea-associated bacteria may interact with Y. pestis within fleas and it is important to understand what factors govern flea-associated bacterial assemblages. Six species of fleas were collected from nine rodent species from ten Ugandan villages between October 2010 and March 2011. A total of 660,345 16S rRNA gene DNA sequences were used to characterize bacterial communities of 332 individual fleas. The DNA sequences were binned into 421 Operational Taxonomic Units (OTUs) based on 97% sequence similarity. We used beta diversity metrics to assess the effects of flea species, flea sex, rodent host species, site (i.e. village), collection date, elevation, mean annual precipitation, average monthly precipitation, and average monthly temperature on bacterial community structure. Flea species had the greatest effect on bacterial community structure with each flea species harboring unique bacterial lineages. The site (i.e. village), rodent host, flea sex, elevation, precipitation, and temperature also significantly affected bacterial community composition. Some bacterial lineages were widespread among flea species (e.g. Bartonella spp. and Wolbachia spp.), but each flea species also harbored unique bacterial lineages. Some of these lineages are not closely related to known bacterial diversity and likely represent newly discovered lineages of insect symbionts. Our finding that flea species has the greatest effect on bacterial community composition may help future investigations between Yersinia pestis and non-pathogenic flea-associated bacteria. Characterizing bacterial communities of fleas during a plague epizootic event in the future would be helpful.

Indexed as

ActinobacteriaAnimalsBacillotaBacteroidetesBase SequenceDNA, BacterialHumansInsect VectorsMicrobial ConsortiaPlagueProteobacteriaRNA, Ribosomal, 16SRodentiaSequence Analysis, DNASiphonapteraUgandaDNA, BacterialRNA, Ribosomal, 16S

Identifiers

PMID26485147
PMCPMC4617453
OpenAlexW2099550759

What OpenQuestion holds

Textmetadata
LicenceCC0
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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.