{"title":"Species-Specific Prey Preference and Behavioral Responses to Tetraselmis Chloroplast Donors in the Euglenoid Rapaza viridis","authors":"Yuri Yanagihara, Yuichiro Kashiyama, Masami Nakazawa","doi":"10.1111/jeu.70077","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Plastids originated through endosymbiosis and enabled the emergence of photosynthetic eukaryotes. However, in several eukaryotic lineages, plastids are not permanently integrated but are instead acquired transiently through predation, a phenomenon known as kleptoplasty. Although kleptoplasty has been documented across diverse eukaryotic groups, the extent to which prey identity constrains plastid acquisition and subsequent maintenance remains poorly defined. In particular, it is unclear whether kleptoplastic organisms exploit plastid donors broadly or depend on highly selective host–prey interactions. Here, we investigated prey responses and feeding behavior in the kleptoplastic euglenoid <i>Rapaza viridis</i> using a phylogenetically diverse set of <i>Tetraselmis</i> species. Through comparative analysis of ingestion behavior, behavioral interactions, and postingestion chloroplast fate among candidate chloroplast donors, we show that <i>R. viridis</i> exhibits strong prey specificity at the species level. Although <i>R. viridis</i> has been shown to depend on <i>Tetraselmis</i> as a source of kleptoplasts, our results demonstrate that ingestion, functional retention, and growth support are restricted to species belonging to the subgenus <i>Tetraselmis</i>. These findings indicate that chloroplast acquisition in <i>R. viridis</i> is constrained by fine-scale host–prey compatibility, rather than by prey availability alone, and highlight the importance of selective prey recognition and post-ingestion processing in regulating kleptoplasty.</p>\n </div>","PeriodicalId":15672,"journal":{"name":"Journal of Eukaryotic Microbiology","volume":"73 2","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2026-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Eukaryotic Microbiology","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jeu.70077","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Plastids originated through endosymbiosis and enabled the emergence of photosynthetic eukaryotes. However, in several eukaryotic lineages, plastids are not permanently integrated but are instead acquired transiently through predation, a phenomenon known as kleptoplasty. Although kleptoplasty has been documented across diverse eukaryotic groups, the extent to which prey identity constrains plastid acquisition and subsequent maintenance remains poorly defined. In particular, it is unclear whether kleptoplastic organisms exploit plastid donors broadly or depend on highly selective host–prey interactions. Here, we investigated prey responses and feeding behavior in the kleptoplastic euglenoid Rapaza viridis using a phylogenetically diverse set of Tetraselmis species. Through comparative analysis of ingestion behavior, behavioral interactions, and postingestion chloroplast fate among candidate chloroplast donors, we show that R. viridis exhibits strong prey specificity at the species level. Although R. viridis has been shown to depend on Tetraselmis as a source of kleptoplasts, our results demonstrate that ingestion, functional retention, and growth support are restricted to species belonging to the subgenus Tetraselmis. These findings indicate that chloroplast acquisition in R. viridis is constrained by fine-scale host–prey compatibility, rather than by prey availability alone, and highlight the importance of selective prey recognition and post-ingestion processing in regulating kleptoplasty.
期刊介绍:
The Journal of Eukaryotic Microbiology publishes original research on protists, including lower algae and fungi. Articles are published covering all aspects of these organisms, including their behavior, biochemistry, cell biology, chemotherapy, development, ecology, evolution, genetics, molecular biology, morphogenetics, parasitology, systematics, and ultrastructure.