Timing matters: exploring emergence patterns of two species of trematode furcocercariae from their snail hosts.

IF 1.5 4区 医学 Q3 PARASITOLOGY
Petra Kundid, Camila Pantoja, Miroslava Soldanova
{"title":"Timing matters: exploring emergence patterns of two species of trematode furcocercariae from their snail hosts.","authors":"Petra Kundid, Camila Pantoja, Miroslava Soldanova","doi":"10.14411/fp.2025.008","DOIUrl":null,"url":null,"abstract":"<p><p>Cercariae are motile infectious larval stages of digenetic trematodes that emerge from their molluscan first intermediate host to seek the next host in their life cycle. A crucial transmission strategy of trematodes involves releasing the maximum number of cercariae at times that coincide with the presence and activity of the next hosts, thereby increasing the likelihood of successful infection and continuation of the parasite's life cycle. We investigated the cercarial emergence of two furcocercous (with forked tail) trematodes Tylodelphys clavata (von Nordmann, 1832) and unidentified species of Sanguinicola Plehn, 1905 from naturally infected Ampullaceana balthica (Linnaeus) and Radix auricularia (Linnaeus) snails under natural light and constant temperature conditions. Both trematodes, which are important fish pathogens, showed distinct daily emergence rhythms influenced by light intensity, with emergence peaking at sunset and night for T. clavata and at night for Sanguinicola sp. The daily emergence rhythms of T. clavata cercariae were consistent in both summer and autumn, indicating adaptability to natural changes in seasonal photoperiods. The interspecific differences in emergence patterns are likely related to the behavioural patterns of upstream, i.e., next in the life cycle, fish hosts. Cercarial output also varied between trematode species and seasons, likely due to combined effects of snail size, intensity of trematode infection in snails and size of cercariae rather than seasonal temperatures. The trematodes were molecularly characterised using mitochondrial (cox1) and nuclear (28S rDNA and ITS1-5.8S-ITS2) regions to confirm their identity and facilitate future studies. This study highlights the importance of light-regulated and host-synchronised cercarial emergence rhythms for increased trematode transmission success and reveals significant variation in cercarial output influenced by environmental and biological factors, contributing to a deeper understanding of trematode ecology and disease management.</p>","PeriodicalId":55154,"journal":{"name":"Folia Parasitologica","volume":"72 ","pages":""},"PeriodicalIF":1.5000,"publicationDate":"2025-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Folia Parasitologica","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.14411/fp.2025.008","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PARASITOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Cercariae are motile infectious larval stages of digenetic trematodes that emerge from their molluscan first intermediate host to seek the next host in their life cycle. A crucial transmission strategy of trematodes involves releasing the maximum number of cercariae at times that coincide with the presence and activity of the next hosts, thereby increasing the likelihood of successful infection and continuation of the parasite's life cycle. We investigated the cercarial emergence of two furcocercous (with forked tail) trematodes Tylodelphys clavata (von Nordmann, 1832) and unidentified species of Sanguinicola Plehn, 1905 from naturally infected Ampullaceana balthica (Linnaeus) and Radix auricularia (Linnaeus) snails under natural light and constant temperature conditions. Both trematodes, which are important fish pathogens, showed distinct daily emergence rhythms influenced by light intensity, with emergence peaking at sunset and night for T. clavata and at night for Sanguinicola sp. The daily emergence rhythms of T. clavata cercariae were consistent in both summer and autumn, indicating adaptability to natural changes in seasonal photoperiods. The interspecific differences in emergence patterns are likely related to the behavioural patterns of upstream, i.e., next in the life cycle, fish hosts. Cercarial output also varied between trematode species and seasons, likely due to combined effects of snail size, intensity of trematode infection in snails and size of cercariae rather than seasonal temperatures. The trematodes were molecularly characterised using mitochondrial (cox1) and nuclear (28S rDNA and ITS1-5.8S-ITS2) regions to confirm their identity and facilitate future studies. This study highlights the importance of light-regulated and host-synchronised cercarial emergence rhythms for increased trematode transmission success and reveals significant variation in cercarial output influenced by environmental and biological factors, contributing to a deeper understanding of trematode ecology and disease management.

时间问题:探索两种吸虫糠尾蚴从它们的蜗牛宿主中出现的模式。
尾蚴是遗传吸虫的活动感染性幼虫阶段,它们从软体动物的第一个中间宿主中出现,在其生命周期中寻找下一个宿主。吸虫的一个关键传播策略是在与下一个宿主的存在和活动相吻合的时间释放最大数量的尾蚴,从而增加成功感染的可能性和寄生虫生命周期的延续。在自然光和恒温条件下,研究了自然感染的Ampullaceana balthica (Linnaeus)和Radix auricularia (Linnaeus)钉螺中两种丝状(带叉尾)吸虫Tylodelphys clavata (von Nordmann, 1832)和未识别种Sanguinicola Plehn, 1905的尾蚴出现情况。两种吸虫都是重要的鱼类病原体,受光照强度的影响,其日羽化节律明显不同,clavata的羽化高峰在日落和夜间,Sanguinicola sp的羽化高峰在夜间。clavata尾蚴的日羽化节律在夏秋两季一致,表明其对季节光周期自然变化的适应性。出现模式的种间差异可能与上游的行为模式有关,即生命周期的下一个阶段,鱼类宿主。尾蚴产量也因吸虫种类和季节而异,可能是由于蜗牛大小、蜗牛体内吸虫感染强度和尾蚴大小的综合影响,而不是季节温度。利用线粒体(cox1)和细胞核(28S rDNA和ITS1-5.8S-ITS2)区对吸虫进行分子表征,以确定其身份,为今后的研究奠定基础。这项研究强调了光调节和宿主同步的尾蚴出苗节律对增加吸虫传播成功率的重要性,并揭示了受环境和生物因素影响的尾蚴产量的显著变化,有助于更深入地了解吸虫生态学和疾病管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Folia Parasitologica
Folia Parasitologica 医学-寄生虫学
CiteScore
2.70
自引率
0.00%
发文量
25
审稿时长
>12 weeks
期刊介绍: FOLIA PARASITOLOGICA, issued in online versions, is an international journal that covers the whole field of general, systematic, ecological and experimental parasitology. It publishes original research papers, research notes and review articles. Contributions from all branches of animal parasitology, such as morphology, taxonomy, biology, biochemistry, physiology, immunology, molecular biology and evolution of parasites, and host-parasite relationships, are eligible. Novelty and importance in the international (not local or regional) context are required. New geographical records of parasites, records of new hosts, regional parasite and/or host surveys (if they constitute the principal substance of manuscript), local/regional prevalence surveys of diseases, local/regional studies on epidemiology of well known diseases and of parasite impact on human/animal health, case reports, routine clinical studies and testing of established diagnostic or treatment procedures, will not be considered. One species description will also not be considered unless they include more general information, such as new diagnostic characters, host-parasite associations, phylogenetic implications, etc. Manuscripts found suitable on submission will be reviewed by at least two reviewers.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信