Evidence map›Paper›PMID 25015890›Full record

ArticleApplied and environmental microbiology2014

Factors limiting the spread of the protective symbiont Hamiltonella defensa in Aphis craccivora Aphids.

Hannah R Dykstra, Stephanie R Weldon, Adam J Martinez, Jennifer A White, Keith R Hopper, George E Heimpel, Mark K Asplen, Kerry M Oliver

Abstract read
In one paragraph

Article in Applied and environmental microbiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Article
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  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Local adaptation to hosts and parasitoids shapeProceedings. Biological sciences · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Plant-Mediated Horizontal Transmission ofFrontiers in microbiology · 2020
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

8 authors.

Hannah R DykstraDepartment of Entomology, University of Georgia, Athens, Georgia, USA.
Stephanie R WeldonDepartment of Entomology, University of Georgia, Athens, Georgia, USA.
Adam J MartinezDepartment of Entomology, University of Georgia, Athens, Georgia, USA.
Jennifer A WhiteDepartment of Entomology, University of Kentucky, Lexington, Kentucky, USA.
Keith R HopperUSDA, ARS, Newark, Delaware, USA.
George E HeimpelDepartment of Entomology, University of Minnesota, St. Paul, Minnesota, USA.
Mark K AsplenDepartment of Entomology, University of Minnesota, St. Paul, Minnesota, USA.
Kerry M OliverDepartment of Entomology, University of Georgia, Athens, Georgia, USA kmoliver@uga.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many insects are associated with heritable symbionts that mediate ecological interactions, including host protection against natural enemies. The cowpea aphid, Aphis craccivora, is a polyphagous pest that harbors Hamiltonella defensa, which defends against parasitic wasps. Despite this protective benefit, this symbiont occurs only at intermediate frequencies in field populations. To identify factors constraining H. defensa invasion in Ap. craccivora, we estimated symbiont transmission rates, performed fitness assays, and measured infection dynamics in population cages to evaluate effects of infection. Similar to results with the pea aphid, Acyrthosiphon pisum, we found no consistent costs to infection using component fitness assays, but we did identify clear costs to infection in population cages when no enemies were present. Maternal transmission rates of H. defensa in Ap. craccivora were high (ca. 99%) but not perfect. Transmission failures and infection costs likely limit the spread of protective H. defensa in Ap. craccivora. We also characterized several parameters of H. defensa infection potentially relevant to the protective phenotype. We confirmed the presence of H. defensa in aphid hemolymph, where it potentially interacts with endoparasites, and performed real-time quantitative PCR (qPCR) to estimate symbiont and phage abundance during aphid development. We also examined strain variation of H. defensa and its bacteriophage at multiple loci, and despite our lines being collected in different regions of North America, they were infected with a nearly identical strains of H. defensa and APSE4 phage. The limited strain diversity observed for these defensive elements may result in relatively static protection profile for this defensive symbiosis.

Indexed as

SymbiosisAnimalsAphidsBacteriophagesDNA, ViralEnterobacteriaceaeMolecular Sequence DataNorth AmericaSequence Analysis, DNADNA, Viral

Identifiers

PMID25015890
PMCPMC4178609

What OpenQuestion holds

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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.