Host genotype and infection status interact to shape microbiomes in Daphnia magna.

IF 2.1 3区 医学 Q2 PARASITOLOGY Parasitology Pub Date : 2024-11-15 DOI:10.1017/S0031182024000787
Amruta Rajarajan, Ellen Decaestecker, Lore Bulteel, Jean-Claude Walser, Piet Spaak, Justyna Wolinska
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Abstract

Host–bacterial communities (microbiomes) are influenced by a wide range of factors including host genotype and parasite exposure. However, few studies disentangle temporal and host-genotype-specific variation in microbiome response to infection across several host tissues. We experimentally exposed the freshwater crustacean Daphnia magna to its fungal parasite Metschnikowia bicuspidata and characterized changes in host–bacterial communities associated with the parasite's development within the host. We used 16S rRNA gene sequencing to assess bacterial communities of the host (a) 24 h (‘initial parasite exposure’) and (b) 10 days (‘successful infection’) after exposure to a standard dose of M. bicuspidata spores, in host guts, body tissue (excluding guts) and whole individuals. We also investigated whether bacterial community responses to parasite exposure varied by host genotype.Parasite exposure did not immediately alter host gut bacterial communities, but drove host-genotype-specific changes in the bacterial community composition of whole individuals. We validated that these changes were not driven by shifts in bacterial communities of the culturing medium, due to the addition of the parasite spore solution. Successful infection (i.e. the proliferation of M. bicuspidata spores in the host body) reduced alpha diversity and shifted abundance of dominant bacterial orders in the gut. Moreover, it induced a host-genotype-specific changes in body bacterial community composition. Overall, bacterial community responses to parasite exposure and subsequent infection are complex: they occur in a host-genotype-dependent manner, differentially at distinct timepoints after parasite exposure, and in specific host tissue.

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宿主基因型和感染状态相互作用,形成大型蚤体内的微生物群。
宿主-细菌群落(微生物组)受宿主基因型和寄生虫暴露等多种因素的影响。然而,很少有研究能区分微生物组对多种宿主组织感染的反应在时间和宿主基因型上的特异性差异。我们通过实验将淡水甲壳动物大型蚤暴露于真菌寄生虫 Metschnikowia bicuspidata,并描述了寄生虫在宿主体内发育过程中宿主细菌群落的变化。我们使用 16S rRNA 基因测序法评估了宿主(a)暴露于标准剂量的 M. bicuspidata 孢子 24 小时后("初始寄生虫暴露")和(b)10 天后("成功感染")宿主内脏、身体组织(不包括内脏)和整个个体中的细菌群落。寄生虫暴露并不会立即改变宿主肠道细菌群落,但会促使宿主基因型特异性地改变整个个体的细菌群落组成。我们验证了这些变化不是由于加入寄生虫孢子溶液导致培养基中细菌群落发生变化而引起的。成功的感染(即双孢蘑菇孢子在宿主体内的增殖)降低了肠道中优势菌目的α多样性和丰度。此外,它还诱导宿主基因型特异性地改变体内细菌群落组成。总之,细菌群落对寄生虫暴露和随后感染的反应是复杂的:它们以依赖于宿主基因型的方式发生,在寄生虫暴露后的不同时间点和特定宿主组织中发生不同的反应。
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来源期刊
Parasitology
Parasitology 医学-寄生虫学
CiteScore
4.80
自引率
4.20%
发文量
280
审稿时长
3-8 weeks
期刊介绍: Parasitology is an important specialist journal covering the latest advances in the subject. It publishes original research and review papers on all aspects of parasitology and host-parasite relationships, including the latest discoveries in parasite biochemistry, molecular biology and genetics, ecology and epidemiology in the context of the biological, medical and veterinary sciences. Included in the subscription price are two special issues which contain reviews of current hot topics, one of which is the proceedings of the annual Symposia of the British Society for Parasitology, while the second, covering areas of significant topical interest, is commissioned by the editors and the editorial board.
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