Host transcriptional signatures associated with disease tolerance and environmental persistence in a mosquito–microsporidian system
- 1Department of Zoology, University of British Columbia, Vancouver, BC, Canada. [email protected]
- 2Institute of Biology, University of Neuchâtel, Neuchâtel, Switzerland. [email protected]
Abstract
Despite strong theory linking parasite life history to virulence and transmission, how parasite strategies affect host responses remains poorly understood. Here, experimental evolution and RNA-sequencing were combined in the mosquito-microsporidian system Anopheles gambiae-Vavraia culicis to test whether parasite lineages selected for early or late transmission differ in the host responses they elicit. Early lineages were selected from hosts that died early in infection, whereas late lineages were selected from hosts that died later, generating parasite populations that differ in growth, virulence and environmental persistence. Mosquitoes were infected with evolved parasite lineages and sampled at a common sporulating stage. A reference infection response was defined relative to uninfected controls. Early- and late-selected parasites showed consistent, yet partly distinct, changes in host gene expression. Co-expression network analysis identified gene modules whose activity covaried with parasite traits, including virulence and environmental persistence. One module enriched for tissue maintenance and metabolic functions was negatively associated with virulence, consistent with reduced damage. Another module enriched for membrane and signalling functions was positively associated with environmental persistence, suggesting that host state at transmission may influence the environment in which transmission stages develop. Together, these results identify distinct host states linked to parasite life-history variation.
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BibTeX
@article{silva2026host,
title = {{Host transcriptional signatures associated with disease tolerance and environmental persistence in a mosquito–microsporidian system}},
author = {Luís M. Silva},
journal = {Communications Biology},
year = {2026},
month = jul,
doi = {10.1038/s42003-026-10633-x},
url = {https://doi.org/10.1038/s42003-026-10633-x},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Host transcriptional signatures associated with disease tolerance and environmental persistence in a mosquito–microsporidian system
AU - Luís M. Silva
PY - 2026
DA - 2026/07/04
JO - Communications Biology
DO - 10.1038/s42003-026-10633-x
UR - https://doi.org/10.1038/s42003-026-10633-x
AB - Despite strong theory linking parasite life history to virulence and transmission, how parasite strategies affect host responses remains poorly understood. Here, experimental evolution and RNA-sequencing were combined in the mosquito-microsporidian system Anopheles gambiae-Vavraia culicis to test whether parasite lineages selected for early or late transmission differ in the host responses they elicit. Early lineages were selected from hosts that died early in infection, whereas late lineages were selected from hosts that died later, generating parasite populations that differ in growth, virulence and environmental persistence. Mosquitoes were infected with evolved parasite lineages and sampled at a common sporulating stage. A reference infection response was defined relative to uninfected controls. Early- and late-selected parasites showed consistent, yet partly distinct, changes in host gene expression. Co-expression network analysis identified gene modules whose activity covaried with parasite traits, including virulence and environmental persistence. One module enriched for tissue maintenance and metabolic functions was negatively associated with virulence, consistent with reduced damage. Another module enriched for membrane and signalling functions was positively associated with environmental persistence, suggesting that host state at transmission may influence the environment in which transmission stages develop. Together, these results identify distinct host states linked to parasite life-history variation.
SN - 2399-3642
ER -