海洋菌群作为中上层鱼类感染寄生虫的潜在关键生命周期途径。

IF 3.7 2区 医学 Q1 PARASITOLOGY International journal for parasitology Pub Date : 2024-05-01 DOI:10.1016/j.ijpara.2023.11.001
Clarisse Louvard , Russell Q.-Y. Yong , Scott C. Cutmore , Thomas H. Cribb
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摘要

浮游生物是中上层生态系统的重要组成部分,有助于形成中上层营养链,并支持海洋栖息地之间的连通性。本研究系统地分析了澳大利亚昆士兰州近海的冻疮软体动物和刺胞动物所携带的吸虫群落。在昆士兰北斯特拉德布鲁克岛的海滩上采集了四种软体动物和三种刺胞动物。两种软体动物和所有三种刺胞动物都含有大量的半类囊蚴(水螅目:半类总科)。通过分子序列分析,鉴定出4个半足科8个类群(棘足科、棘足科、半足科和棘足科)。其中4个分类群被鉴定为种。除一种双虫外,所有吸虫类群均为两个或多个寄主共有;腹足动物和刺胞动物均有5种。据推测,这些半尿样细胞的生命周期具有高度可塑性,涉及到囊蚴传播到最终宿主的多种机会性途径。半水生生物对浮游生物的传播和利用可能随着海洋表面的利用和顶端捕食者的个体发育营养变化而变化。在衣原体中发现的吸虫种类很少,这与显著的生态特异性是一致的,并且推断其他远洋吸虫使用不涉及衣原体生物的替代传播途径。这种途径可能只涉及i)远洋寄主;Ii)底栖或底栖寄主,在潜水时被顶端捕食者吃掉;或iii)依赖于猎物垂直迁移的传播链中的底栖和远洋宿主。开放海洋生态系统连通性对寄生虫传播的影响被确定为迫切需要研究的领域。
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The oceanic pleuston community as a potentially crucial life-cycle pathway for pelagic fish-infecting parasitic worms

Pleustonic organisms form an important part of pelagic ecosystems by contributing to pelagic trophic chains and supporting connectivity between oceanic habitats. This study systematically analysed the trematode community harboured by pleustonic molluscs and cnidarians from offshore Queensland, Australia. Four mollusc and three cnidarian species were collected from beaches of North Stradbroke Island, Queensland. Two mollusc species and all three cnidarians harboured large numbers of hemiuroid metacercariae (Trematoda: Hemiuroidea). Eight taxa from four hemiuroid families (Accacoeliidae, Didymozoidae, Hemiuridae and Sclerodistomidae) were distinguished via molecular sequencing. Four of those taxa were identified to species. All trematode taxa except one didymozoid were shared by two or more host species; five species occurred in both gastropods and cnidarians. It is hypothesised that the life-cycles of these hemiuroids are highly plastic, involving multiple opportunistic pathways of metacercarial transmission to the definitive hosts. Transmission and the use of pleuston by hemiuroids likely varies with sea surface use and ontogenetic trophic shifts of apex predators. The small number of trematode species found in pleuston is consistent with significant ecological specificity, and the inference that other pelagic trematodes use alternative pathways of transmission that do not involve pleustonic organisms. Such pathways may involve i) pelagic hosts exclusively; ii) benthic or demersal hosts exclusively, consumed by apex predators during their dives; or iii) both benthic and pelagic hosts in transmission chains dependent on vertical migrations of prey. The influence of the connectivity of open-ocean ecosystems on parasite transmission is identified as an area in critical need of research.

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来源期刊
CiteScore
8.40
自引率
2.50%
发文量
76
审稿时长
23 days
期刊介绍: International Journal for Parasitology offers authors the option to sponsor nonsubscriber access to their articles on Elsevier electronic publishing platforms. For more information please view our Sponsored Articles page. The International Journal for Parasitology publishes the results of original research in all aspects of basic and applied parasitology, including all the fields covered by its Specialist Editors, and ranging from parasites and host-parasite relationships of intrinsic biological interest to those of social and economic importance in human and veterinary medicine and agriculture.
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