Evidence map›Paper›PMID 26205080›Full record

ArticleBMC microbiology2015

Developmental succession of the microbiome of Culex mosquitoes.

Dagne Duguma, Michael W Hall, Paul Rugman-Jones, Richard Stouthamer, Olle Terenius, Josh D Neufeld, William E Walton

Abstract read
In one paragraph

Article in BMC microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing 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

80 citing papers in PubMed.

  1. Article
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  13. FEMS microbes · 2024
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  15. Introducing an environmental microbiome to axenicApplied and environmental microbiology · 2023
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

20 more citing papers are in PubMed but not listed here.

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.

Dagne DugumaDepartment of Entomology, University of California Riverside, Riverside, CA, 92521, USA. duguma@ufl.edu.
Michael W HallDepartment of Biology, University of Waterloo, Waterloo, Ontario, N2L 3G1, Canada. hallm2533@gmail.com.
Paul Rugman-JonesDepartment of Entomology, University of California Riverside, Riverside, CA, 92521, USA. paul.rugman-jones@ucr.edu.
Richard StouthamerDepartment of Entomology, University of California Riverside, Riverside, CA, 92521, USA. richard.stouthamer@ucr.edu.
Olle TereniusDepartment of Ecology, Swedish University of Agricultural Sciences (SLU), Uppsala, Sweden. Olle.Terenius@slu.se.
Josh D NeufeldDepartment of Biology, University of Waterloo, Waterloo, Ontario, N2L 3G1, Canada. jneufeld@uwaterloo.ca.
William E WaltonDepartment of Entomology, University of California Riverside, Riverside, CA, 92521, USA. william.walton@ucr.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe native microflora associated with mosquitoes have important roles in mosquito development and vector competence. Sequencing of bacterial V3 region from 16S rRNA genes across the developmental stages of Culex mosquitoes (early and late larval instars, pupae and adults) was used to test the hypothesis that bacteria found in the larval stage of Culex are transstadially transmitted to the adult stage, and to compare the microbiomes of field-collected versus laboratory-reared mosquitoes.

resultsBeta diversity analysis revealed that bacterial community structure differed among three life stages (larvae, pupae and adults) of Culex tarsalis. Although only ~2% of the total number of bacterial OTUs were found in all stages, sequences from these OTUs accounted for nearly 82% of the total bacterial sequences recovered from all stages. Thorsellia (Gammaproteobacteria) was the most abundant bacterial taxon found across all developmental stages of field-collected Culex mosquitoes, but was rare in mosquitoes from laboratory-reared colonies. The proportion of Thorsellia sequences in the microbiomes of mosquito life stages varied ontogenetically with the greatest proportions recovered from the pupae of C. tarsalis and the lowest from newly emerged adults. The microbiome of field-collected late instar larvae was not influenced significantly by differences in the microbiota of the habitat due to habitat age or biopesticide treatments. The microbiome diversity was the greatest in the early instar larvae and the lowest in laboratory-reared mosquitoes.

conclusionsBacterial communities in early instar C. tarsalis larvae were significantly more diverse when compared to late instar larvae, pupae and newly emerged adults. Some of the bacterial OTUs found in the early instar larvae were also found across developmental stages. Thorsellia dominated the bacterial communities in field-collected immature stages but occurred at much lower relative abundance in adults. Differences in microbiota observed in larval habitats did not influence bacterial community profiles of late instar larvae or adults. However, bacterial communities in laboratory-reared C. tarsalis larvae differed significantly from the field. Determining the role of Thorsellia in mosquitoes and its distribution across different species of mosquitoes warrants further investigation.

Indexed as

MicrobiotaAnimalsBacteriaCluster AnalysisCulexDNA, RibosomalGastrointestinal TractLarvaMolecular Sequence DataPhylogenyPupaRNA, Ribosomal, 16SSequence Analysis, DNADNA, RibosomalRNA, Ribosomal, 16S

Identifiers

PMID26205080
PMCPMC4513620

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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.