Genomic and induction evidence for bacteriophage contributions to sargassum-bacteria symbioses.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY Microbiome Pub Date : 2024-08-01 DOI:10.1186/s40168-024-01860-7
Alexandra K Stiffler, Poppy J Hesketh-Best, Natascha S Varona, Ashley Zagame, Bailey A Wallace, Brian E Lapointe, Cynthia B Silveira
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Abstract

Background: Symbioses between primary producers and bacteria are crucial for nutrient exchange that fosters host growth and niche adaptation. Yet, how viruses that infect bacteria (phages) influence these bacteria-eukaryote interactions is still largely unknown. Here, we investigate the role of viruses on the genomic diversity and functional adaptations of bacteria associated with pelagic sargassum. This brown alga has dramatically increased its distribution range in the Atlantic in the past decade and is predicted to continue expanding, imposing severe impacts on coastal ecosystems, economies, and human health.

Results: We reconstructed 73 bacterial and 3963 viral metagenome-assembled genomes (bMAGs and vMAGs, respectively) from coastal Sargassum natans VIII and surrounding seawater. S. natans VIII bMAGs were enriched in prophages compared to seawater (28% and 0.02%, respectively). Rhodobacterales and Synechococcus bMAGs, abundant members of the S. natans VIII microbiome, were shared between the algae and seawater but were associated with distinct phages in each environment. Genes related to biofilm formation and quorum sensing were enriched in S. natans VIII phages, indicating their potential to influence algal association in their bacterial hosts. In-vitro assays with a bacterial community harvested from sargassum surface biofilms and depleted of free viruses demonstrated that these bacteria are protected from lytic infection by seawater viruses but contain intact and inducible prophages. These bacteria form thicker biofilms when growing on sargassum-supplemented seawater compared to seawater controls, and phage induction using mitomycin C was associated with a significant decrease in biofilm formation. The induced metagenomes were enriched in genomic sequences classified as temperate viruses compared to uninduced controls.

Conclusions: Our data shows that prophages contribute to the flexible genomes of S. natans VIII-associated bacteria. These prophages encode genes with symbiotic functions, and their induction decreases biofilm formation, an essential capacity for flexible symbioses between bacteria and the alga. These results indicate that prophage acquisition and induction contribute to genomic and functional diversification during sargassum-bacteria symbioses, with potential implications for algae growth. Video Abstract.

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噬菌体对马尾藻-细菌共生作用的基因组和诱导证据。
背景:初级生产者与细菌之间的共生关系对于促进宿主生长和生态位适应的营养交换至关重要。然而,感染细菌的病毒(噬菌体)如何影响这些细菌-真核生物之间的相互作用在很大程度上仍是未知数。在这里,我们研究了病毒对浮游马尾藻相关细菌的基因组多样性和功能适应性的作用。在过去十年中,这种褐色藻类在大西洋的分布范围急剧扩大,预计还将继续扩大,对沿海生态系统、经济和人类健康造成严重影响:结果:我们从沿海马尾藻八号和周围海水中重建了 73 个细菌元基因组和 3963 个病毒元基因组(分别为 bMAGs 和 vMAGs)。与海水相比,S. natans VIII bMAGs富含原生噬菌体(分别为 28% 和 0.02%)。在 S. natans VIII 微生物组中含量丰富的 Rhodobacterales 和 Synechococcus bMAGs 在藻类和海水中是共有的,但在每种环境中都与不同的噬菌体有关。S. natans VIII噬菌体中富含与生物膜形成和法定量感应相关的基因,这表明它们有可能影响细菌宿主与藻类的结合。用从马尾藻表面生物膜中提取的、去除了游离病毒的细菌群落进行体外试验表明,这些细菌受到海水病毒的溶解性感染保护,但含有完整的、可诱导的噬菌体。与海水对照组相比,这些细菌在添加了马尾藻的海水中生长时会形成更厚的生物膜,而使用丝裂霉素 C 诱导噬菌体会显著减少生物膜的形成。与未诱导的对照组相比,诱导的元基因组富含被归类为温带病毒的基因组序列:我们的数据表明,噬菌体为纳坦氏菌 VIII 相关细菌的灵活基因组做出了贡献。这些噬菌体编码具有共生功能的基因,它们的诱导会减少生物膜的形成,而生物膜的形成是细菌与藻类灵活共生的基本能力。这些结果表明,在马尾藻与细菌共生过程中,噬菌体的获得和诱导有助于基因组和功能的多样化,对藻类的生长具有潜在的影响。视频摘要。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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