OSCR

Cestode infection is linked to transcriptional shifts in neuropeptide signalling and caste-specific ageing pathways in a social insect.

Overview

Authors: Giulia Blasi1, Katharina Schwolow1, Hugo Darras2, Susanne Foitzik1
  1. Institute of Organismic and Molecular Evolution (iomE), Johannes Gutenberg University of Mainz,Mainz, 55128 Germany
  2. Centre for Evolutionary and Organismal Biology, School of Medicine, Zhejiang University,Hangzhou, 310058 China
Journal: BMC genomics, volume 27, issue 1, article 547
Dates: received 3 February 2026; accepted 13 May 2026; published online 15 June 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1186/s12864-026-12959-6 · PMID 42298379 · PMCID PMC13267302 · OpenAlex W7164855719
Open access: gold, a free copy (OpenAlex)
Status: data only
Categories: other (organism), other condition (population), cellular / molecular (subfield)
Methods: Statistics
Keywords: Neuropeptides, Ageing, Gene Expression, Parasite Manipulation, Social Insects, Caste
MeSH: Aging*, Ants*, Cestoda*, Neuropeptides*, Signal Transduction*, Animals, Fat Body, Female, Host-Parasite Interactions, Social Behavior (* major topic)
Topic: Neurobiology and Insect Physiology Research (Cellular and Molecular Neuroscience, Neuroscience), according to OpenAlex
Funding: Johannes Gutenberg-Universität Mainz (1030)
Citations: not cited yet (Europe PMC); 89 references in the paper

Abstract

Social insects are key models for phenotypic plasticity, as queens and workers show striking differences in behaviour and lifespan despite sharing the same genome. Neuropeptides are central regulators of behavioural plasticity, and caste-specific ageing is governed by the insulin/insulin-like growth factor 1 signalling–target of rapamycin–juvenile hormone network. Parasites that manipulate host behaviour and lifespan may exploit these regulators by targeting conserved neuropeptides or by altering ageing pathways. Here, we examine a host–parasite system in which the cestode Anomotaenia brevis extends lifespan and alters behaviour in its intermediate host, the ant Temnothorax nylanderi. In the fat body, queens and infected workers showed a higher degree of overlap in gene expression, consistent with a queen-like transcriptional shift in infected workers. This overlap was characterised by genes involved in ageing regulation, indicating that parasites affect components of conserved metabolic and longevity pathways typically associated with the queen phenotype. Parasite-derived peptides did not resemble host neuropeptides, which argues against classical neuropeptide mimicry based on sequence similarity. The parasite may affect host signalling through alternative mechanisms, including indirect modulation of host neuropeptide pathways. Ant neuropeptide and receptor expression varied strongly with caste and infection, with the latter associated with broad downregulation of neuropeptides in the brain, including tachykinin, short neuropeptide-F, allatostatin-A, orcokinin, CAPA, and diuretic hormones. In contrast, caste-related differences were more pronounced in the fat body, where infected workers resembled uninfected queens. This suggests that infection affects neural and peripheral regulatory pathways, reducing worker-like signalling and partially activating queen-like metabolic programmes. Our results reveal that parasites can exploit caste-specific plasticity and identify the molecular pathways used to reprogram host phenotypes.

Supplementary Information: The online version contains supplementary material available at 10.1186/s12864-026-12959-6.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

The paper links to its data, not to its authors' code: see the Data section.

Tracing map

A tracing map links a paper to the code its authors published: this paper has none, so it has no map.

Data

Datasets cited

Data availability

All data supporting the conclusions of this study are included within the article and its Supplementary Materials. Sequencing reads are available in the NCBI database under BioProject accession numbers PRJNA1297301 and PRJNA950591.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 4 authors, 6 keywords, 10 MeSH terms, 1 funder, 88 references.

Cite

This paper

Blasi, G., Schwolow, K., Darras, H., & Foitzik, S. (2026). Cestode infection is linked to transcriptional shifts in neuropeptide signalling and caste-specific ageing pathways in a social insect. BMC genomics, 27(1), 547. https://doi.org/10.1186/s12864-026-12959-6

BibTeX

@article{blasi2026cestode,
author = {Blasi, Giulia and Schwolow, Katharina and Darras, Hugo and Foitzik, Susanne},
title = {{Cestode infection is linked to transcriptional shifts in neuropeptide signalling and caste-specific ageing pathways in a social insect}},
journal = {BMC genomics},
year = {2026},
month = jun,
volume = {27},
number = {1},
pages = {547},
publisher = {BMC},
issn = {1471-2164},
doi = {10.1186/s12864-026-12959-6},
url = {https://doi.org/10.1186/s12864-026-12959-6},
pmid = {42298379},
pmcid = {PMC13267302}
}

RIS

TY - JOUR
AU - Blasi, Giulia
AU - Schwolow, Katharina
AU - Darras, Hugo
AU - Foitzik, Susanne
TI - Cestode infection is linked to transcriptional shifts in neuropeptide signalling and caste-specific ageing pathways in a social insect
T2 - BMC genomics
J2 - BMC Genomics
PY - 2026
DA - 2026/06/15
VL - 27
IS - 1
SP - 547
SN - 1471-2164
PB - BMC
DO - 10.1186/s12864-026-12959-6
UR - https://doi.org/10.1186/s12864-026-12959-6
LA - en
ER -

CSL-JSON

{
"id": "10.1186/s12864-026-12959-6",
"type": "article-journal",
"title": "Cestode infection is linked to transcriptional shifts in neuropeptide signalling and caste-specific ageing pathways in a social insect",
"container-title": "BMC genomics",
"author": [
{
"family": "Blasi",
"given": "Giulia"
},
{
"family": "Schwolow",
"given": "Katharina"
},
{
"family": "Darras",
"given": "Hugo"
},
{
"family": "Foitzik",
"given": "Susanne"
}
],
"container-title-short": "BMC Genomics",
"volume": "27",
"issue": "1",
"page": "547",
"DOI": "10.1186/s12864-026-12959-6",
"PMID": "42298379",
"PMCID": "PMC13267302",
"ISSN": "1471-2164",
"publisher": "BMC",
"URL": "https://doi.org/10.1186/s12864-026-12959-6",
"language": "en",
"issued": {
"date-parts": [
[
2026,
6,
15
]
]
}
}

Similar papers

The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.

[1] doi:10.1038/s41586-026-10747-6 [code]
Ancient feeding-related neuropeptides regulate alloparenting in ants.
Journal: Nature
In common: other, 4 references
[2] doi:10.1111/mec.70360 [code]
Unmated Queens Show Worker-Like Behaviour and Gene Expression in Polygynous Colonies of the Ant Stigmatomma pallipes.
Journal: Molecular ecology
In common: other, cellular / molecular, 4 references
[3] doi:10.1038/s42003-026-10402-w [code]
Temporal orchestration of transcriptional and epigenomic programming underlying maternal embryonic diapause in a cricket model.
Journal: Communications biology
In common: other, 5 references
[4] doi:10.1038/s41586-026-10629-x [code]
Whole-genome duplication shaped cell-type evolution in the vertebrate brain.
Journal: Nature
In common: other, cellular / molecular, 5 references
[5] doi:10.1186/s12864-026-12863-z [code]
Chromosome-level genome assembly of the nematophagous flatworm Luticola nematophagus: revealing molecular adaptations for predation and its biocontrol potential against nematode diseases.
Journal: BMC genomics
In common: other, cellular / molecular, 3 references
[6] doi:10.1093/nar/gkag544 [code]
Single-base resolution atlas reveals moderate conservation and regulatory diversity of m6A modifications across mammals.
Journal: Nucleic acids research
In common: 4 references
[7] doi:10.7554/elife.107393 [code]
Chromosome-scale genome assembly of the European common cuttlefish <i>Sepia officinalis</i>.
Journal: eLife
In common: other, cellular / molecular, 4 references
[8] doi:10.1186/s12864-026-12899-1
Transcriptomic investigation of agonistic behaviors of boxer shrimps (Stenopus species): insights into the potential neural signaling roles of dopamine and acetylcholine.
Journal: BMC genomics
In common: cellular / molecular, 3 references
[9] doi:10.1371/journal.pbio.3003803 [code]
The anti-neural role of BMP signaling is a consequence of its ancestral function in dorsoventral patterning.
Journal: PLoS biology
In common: other, 4 references
[10] doi:10.1038/s41467-026-75225-z [code]
A single-cell atlas of alternative wing development in two hemipteran species.
Journal: Nature communications
In common: other, 3 references

Contribute

The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.

Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.

Request its removal

To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).

Discussion, reproductions, activity

Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.

Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.

Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.