{"title":"LIFE CYCLE VARIATION AND HOST-PARASITE INTERACTIONS OF FOUR CONGENERIC SPECIES OF TURTLE ACANTHOCEPHALANS.","authors":"Ryan W Koch, Yetkin Ipek, Matthew G Bolek","doi":"10.1645/24-34","DOIUrl":null,"url":null,"abstract":"<p><p>Turtle acanthocephalans in the genus Neoechinorhynchus have complex life cycles and are thought to involve an ostracod intermediate host and a turtle definitive host. For Neoechinorhynchus emydis, an additional snail paratenic host is part of its life cycle. However, how snails become infected and whether other species of Neoechinorhynchus can be found in snails remains unclear. This study was conducted to understand the survival, development, and host use of 4 species of turtle acanthocephalans (Neoechinorhynchus chrysemydis, N. emydis, Neoechinorhynchus emyditoides, and Neoechinorhynchus pseudemydis) in their intermediate, paratenic, and definitive hosts. Using eggs recovered from adult acanthocephalans from naturally infected turtle hosts in Oklahoma, experimental infections were conducted in 2 species of ostracods and 1 species of freshwater snail. Ionomes also were generated for these acanthocephalans and their turtle definitive hosts to better understand resource competition. Upon ingestion by ostracods, eggs of all 4 species of acanthocephalans hatched in both ostracod species. However, no further acanthocephalan development occurred in Cypridopsis sp. ostracods, whereas all 4 acanthocephalan species grew and developed into infective juveniles over 28-32 days in Physocypria sp. ostracods. Of the 4 species of acanthocephalans, N. emydis grew faster early in ostracods and was the only species to survive and establish in snail hosts. This finding was supported by the observation of proboscis remnants in the feces of snails that ingested ostracods infected with N. chrysemydis, N. emyditoides, and N. pseudemydis. In contrast, when snails were exposed to eggs of all 4 acanthocephalan species, eggs were passed in the feces, resulting in no infections. The overall ionomic composition of adult acanthocephalans and their turtle hosts suggested that the hosts and parasites share host resources. However, specific elemental differences indicated that turtle acanthocephalans can accumulate heavy metals at concentrations higher than those in their hosts. Results of this study support previous field observations and hypotheses that (1) Physocypria sp. ostracods serve as intermediate hosts for N. chrysemydis, N. emydis, N. emyditoides, and N. pseudemydis; (2) N. emydis uses snail paratenic hosts, but snails are a non-viable route of transmission to turtles for N. chrysemydis, N. emyditoides, and N. pseudemydis; and (3) as adults, these 4 acanthocephalan species utilize their turtle definitive hosts similarly in terms of ionomic composition. This work challenges the traditional view of the acanthocephalan life cycle and sets the stage for future hypotheses.</p>","PeriodicalId":16659,"journal":{"name":"Journal of Parasitology","volume":null,"pages":null},"PeriodicalIF":1.0000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Parasitology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1645/24-34","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PARASITOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Turtle acanthocephalans in the genus Neoechinorhynchus have complex life cycles and are thought to involve an ostracod intermediate host and a turtle definitive host. For Neoechinorhynchus emydis, an additional snail paratenic host is part of its life cycle. However, how snails become infected and whether other species of Neoechinorhynchus can be found in snails remains unclear. This study was conducted to understand the survival, development, and host use of 4 species of turtle acanthocephalans (Neoechinorhynchus chrysemydis, N. emydis, Neoechinorhynchus emyditoides, and Neoechinorhynchus pseudemydis) in their intermediate, paratenic, and definitive hosts. Using eggs recovered from adult acanthocephalans from naturally infected turtle hosts in Oklahoma, experimental infections were conducted in 2 species of ostracods and 1 species of freshwater snail. Ionomes also were generated for these acanthocephalans and their turtle definitive hosts to better understand resource competition. Upon ingestion by ostracods, eggs of all 4 species of acanthocephalans hatched in both ostracod species. However, no further acanthocephalan development occurred in Cypridopsis sp. ostracods, whereas all 4 acanthocephalan species grew and developed into infective juveniles over 28-32 days in Physocypria sp. ostracods. Of the 4 species of acanthocephalans, N. emydis grew faster early in ostracods and was the only species to survive and establish in snail hosts. This finding was supported by the observation of proboscis remnants in the feces of snails that ingested ostracods infected with N. chrysemydis, N. emyditoides, and N. pseudemydis. In contrast, when snails were exposed to eggs of all 4 acanthocephalan species, eggs were passed in the feces, resulting in no infections. The overall ionomic composition of adult acanthocephalans and their turtle hosts suggested that the hosts and parasites share host resources. However, specific elemental differences indicated that turtle acanthocephalans can accumulate heavy metals at concentrations higher than those in their hosts. Results of this study support previous field observations and hypotheses that (1) Physocypria sp. ostracods serve as intermediate hosts for N. chrysemydis, N. emydis, N. emyditoides, and N. pseudemydis; (2) N. emydis uses snail paratenic hosts, but snails are a non-viable route of transmission to turtles for N. chrysemydis, N. emyditoides, and N. pseudemydis; and (3) as adults, these 4 acanthocephalan species utilize their turtle definitive hosts similarly in terms of ionomic composition. This work challenges the traditional view of the acanthocephalan life cycle and sets the stage for future hypotheses.
期刊介绍:
The Journal of Parasitology is the official peer-reviewed journal of the American Society of Parasitologists (ASP). The journal publishes original research covering helminths, protozoa, and other parasitic organisms and serves scientific professionals in microbiology, immunology, veterinary science, pathology, and public health. Journal content includes original research articles, brief research notes, announcements of the Society, and book reviews. Articles are subdivided by topic for ease of reference and range from behavior and pathogenesis to systematics and epidemiology. The journal is published continuously online with one full volume printed at the end of each year.