{"title":"Divergent Genetic Pathways Underlying Convergent Parasitic Behaviours in Blowflies","authors":"Gisele Antoniazzi Cardoso, Pedro Mariano-Martins, Gustavo Amaral Faria, Inoka Karunaratne, Patricia Jacqueline Thyssen, Tatiana Teixeira Torres","doi":"10.1111/mec.17785","DOIUrl":null,"url":null,"abstract":"<p>Blowfly (Diptera: Calliphoridae) exhibit diverse feeding strategies, with most species developing on decomposing organic matter. However, parasitism has evolved within the family, and some species convergently gained the ability to explore the tissues of living vertebrate hosts, which imposes critical veterinary, medical, and agricultural issues worldwide. It is yet unknown how this phenotype has evolved and whether it is determined by the same genetic architecture in different species or not. To address these questions, we evaluated key behavioural phenotypes in species with contrasting feeding habits, focusing on female oviposition preferences and larval survival on distinct diets, both critical aspects of their life cycles. These assays allowed us to propose hypotheses of how oviposition and larval behaviours contribute to feeding habits displayed in nature for parasitic and saprophagous species. Additionally, a transcriptome-wide analysis revealed genes and functional pathways potentially linked to parasitic behaviour by comparing gene expression profiles and coding sequence evolution. In the genetic analysis, we identified genes with important functions related to the measured behaviours, revealing that distinct genes may underlie each independent case of parasitism evolution, suggesting a non-parallel evolutionary pathway for this convergent trait.</p>","PeriodicalId":210,"journal":{"name":"Molecular Ecology","volume":"34 11","pages":""},"PeriodicalIF":4.5000,"publicationDate":"2025-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/mec.17785","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Ecology","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/mec.17785","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Blowfly (Diptera: Calliphoridae) exhibit diverse feeding strategies, with most species developing on decomposing organic matter. However, parasitism has evolved within the family, and some species convergently gained the ability to explore the tissues of living vertebrate hosts, which imposes critical veterinary, medical, and agricultural issues worldwide. It is yet unknown how this phenotype has evolved and whether it is determined by the same genetic architecture in different species or not. To address these questions, we evaluated key behavioural phenotypes in species with contrasting feeding habits, focusing on female oviposition preferences and larval survival on distinct diets, both critical aspects of their life cycles. These assays allowed us to propose hypotheses of how oviposition and larval behaviours contribute to feeding habits displayed in nature for parasitic and saprophagous species. Additionally, a transcriptome-wide analysis revealed genes and functional pathways potentially linked to parasitic behaviour by comparing gene expression profiles and coding sequence evolution. In the genetic analysis, we identified genes with important functions related to the measured behaviours, revealing that distinct genes may underlie each independent case of parasitism evolution, suggesting a non-parallel evolutionary pathway for this convergent trait.
期刊介绍:
Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include:
* population structure and phylogeography
* reproductive strategies
* relatedness and kin selection
* sex allocation
* population genetic theory
* analytical methods development
* conservation genetics
* speciation genetics
* microbial biodiversity
* evolutionary dynamics of QTLs
* ecological interactions
* molecular adaptation and environmental genomics
* impact of genetically modified organisms