鳗蝇(双翅目,鳗蝇科)的微生物组动态和功能组成:海带蝇营养特化的启示。

IF 3.3 3区 生物学 Q2 ECOLOGY Microbial Ecology Pub Date : 2024-07-03 DOI:10.1007/s00248-024-02403-1
Paul S P Bischof, Theda U P Bartolomaeus, Ulrike Löber, Christoph Bleidorn
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引用次数: 0

摘要

海带蝇科昆虫(双翅目)与海滩海带和其他腐烂海藻有着生态联系。这种独特的营养特化要求苍蝇做出重大适应性调整,以克服藻类食物的局限性。我们的目的是研究苍蝇的微生物组是否可能是这些适应机制之一。我们的分析重点是评估海带蝇成虫和幼虫微生物群的组成和多样性。该物种幼虫的取食习惯一直是众多研究的主题,关于它们是直接食用海带还是主要以相关细菌为食一直存在争议。通过使用 16S rRNA 代谢编码方法,我们发现幼虫微生物群的多样性大大低于成虫,仅有四个可操作的分类单元(OTUs)占主导地位。系统发生学定位发现,幼虫微生物群中最主要的 OTU 是一种未被描述的 Orbaceae 属(Gammaproteobacteria),该 OTU 是所有代谢标码序列读数的一半以上的来源。有趣的是,在成虫微生物组中含量最高的 15 个类群中,几乎找不到这个 OTU,它的元条码序列读数只占不到 2%。在幼虫微生物组中占主导地位的另外三个 OTU 分别是精神杆菌(Gammaproteobacteria)、Wohlfahrtiimonas(Gammaproteobacteria)和 Cetobacterium(Fusobacteriota)。此外,我们还发现幼虫和成虫阶段的功能组成发生了明显的变化,我们的分类分析表明幼虫样本的功能多样性显著下降。我们的研究有助于深入了解褐藻的微生物组动态和功能组成。
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Microbiome Dynamics and Functional Composition in Coelopa frigida (Diptera, Coelopidae): Insights into Trophic Specialization of Kelp Flies.

Coelopidae (Diptera), known as kelp flies, exhibit an ecological association with beached kelp and other rotting seaweeds. This unique trophic specialization necessitates significant adaptations to overcome the limitations of an algal diet. We aimed to investigate whether the flies' microbiome could be one of these adaptive mechanisms. Our analysis focused on assessing composition and diversity of adult and larval microbiota of the kelp fly Coelopa frigida. Feeding habits of the larvae of this species have been subject of numerous studies, with debates whether they directly consume kelp or primarily feed on associated bacteria. By using a 16S rRNA metabarcoding approach, we found that the larval microbiota displayed considerably less diversity than adults, heavily dominated by only four operational taxonomic units (OTUs). Phylogenetic placement recovered the most dominant OTU of the larval microbiome, which is the source of more than half of all metabarcoding sequence reads, as an undescribed genus of Orbaceae (Gammaproteobacteria). Interestingly, this OTU is barely found among the 15 most abundant taxa of the adult microbiome, where it is responsible for less than 2% of the metabarcoding sequence reads. The other three OTUs dominating the larval microbiome have been assigned as Psychrobacter (Gammaproteobacteria), Wohlfahrtiimonas (Gammaproteobacteria), and Cetobacterium (Fusobacteriota). Moreover, we also uncovered a distinct shift in the functional composition between the larval and adult stages, where our taxonomic profiling suggests a significant decrease in functional diversity in larval samples. Our study offers insights into the microbiome dynamics and functional composition of Coelopa frigida.

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来源期刊
Microbial Ecology
Microbial Ecology 生物-海洋与淡水生物学
CiteScore
6.90
自引率
2.80%
发文量
212
审稿时长
3-8 weeks
期刊介绍: The journal Microbial Ecology was founded more than 50 years ago by Dr. Ralph Mitchell, Gordon McKay Professor of Applied Biology at Harvard University in Cambridge, MA. The journal has evolved to become a premier location for the presentation of manuscripts that represent advances in the field of microbial ecology. The journal has become a dedicated international forum for the presentation of high-quality scientific investigations of how microorganisms interact with their environment, with each other and with their hosts. Microbial Ecology offers articles of original research in full paper and note formats, as well as brief reviews and topical position papers.
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