Evidence map›Paper›PMID 26673937›Full record

ArticleBiology letters2015

Symbiont transmission entails the risk of parasite infection.

Hassan Salem, Thomas O Onchuru, Eugen Bauer, Martin Kaltenpoth

Abstract read
In one paragraph

Article in Biology letters, 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
–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

16 citing papers in PubMed.

  1. Article
  2. Fidelity in co-diversified symbiosis.Nature communications · 2026
    Article
  3. The role of animal hosts in shaping gut microbiome variation.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Compartmentalization drives the evolution of symbiotic cooperation.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Review
  12. Links between metamorphosis and symbiosis in holometabolous insects.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
    Review
  13. Article
  14. Article
  15. Symbiont switching and alternative resource acquisition strategies drive mutualism breakdown.Proceedings of the National Academy of Sciences of the United States of America · 2018
    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

4 authors.

Hassan SalemInsect Symbiosis Research Group, Max Planck Institute for Chemical Ecology, 07745 Jena, Germany hsalem@ice.mpg.de.
Thomas O OnchuruInsect Symbiosis Research Group, Max Planck Institute for Chemical Ecology, 07745 Jena, Germany.
Eugen BauerInsect Symbiosis Research Group, Max Planck Institute for Chemical Ecology, 07745 Jena, Germany Luxembourg Centre for Systems Biomedicine, University of Luxembourg, L-4362 Esch-sur-Alzette, Luxembourg.
Martin KaltenpothInsect Symbiosis Research Group, Max Planck Institute for Chemical Ecology, 07745 Jena, Germany Department of Evolutionary Ecology, Johannes Gutenberg University, 55128 Mainz, Germany mkaltenpoth@uni-mainz.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Like many animals, firebugs (Hemiptera, Pyrrhocoridae) rely on behavioural adaptations to successfully endow their offspring with microbial mutualists. To transmit the nutritionally beneficial Coriobacteriaceae symbionts, female firebugs smear egg surfaces with symbiont-containing faecal droplets that are subsequently ingested by newly hatched nymphs through active probing to initiate infection. Alternatively, the symbionts can be acquired horizontally through contact with faeces of infected conspecifics. Here, we report that these adaptations ensuring successful transmission of bacterial symbionts among firebugs are exploited by the specialized trypanosomatid parasite Leptomonas pyrrhocoris. Using comparative transcriptomics, fluorescence in situ hybridization (FISH) and controlled bioassays, we demonstrate that the transmission cycle of L. pyrrhocoris mirrors that of the bacterial mutualists, with high efficiency for both vertical and horizontal transmission. This indicates that the parasite capitalizes on pre-existing behavioural adaptations (egg smearing and probing) to facilitate its own transfer within host populations, adaptations that likely evolved to initiate and maintain an association with beneficial gut symbionts. Thus, the transmission of mutualistic microbes across host generations can entail a significant risk of co-transmitting pathogens or parasites, thereby exerting selective pressures on the host to evolve more specific mechanisms of transfer.

Indexed as

ActinobacteriaAnimalsBehavior, AnimalFecesFemaleHeteropteraSymbiosisTranscriptomeTrypanosomatinahost–parasite interactionmutualismsymbiontvertical and horizontal transmission

Identifiers

PMID26673937
PMCPMC4707701

What OpenQuestion holds

Textmetadata
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.