Aerobic anoxygenic phototrophs play important roles in nutrient cycling within cyanobacterial Microcystis bloom microbiomes.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY Microbiome Pub Date : 2024-05-13 DOI:10.1186/s40168-024-01801-4
Haiyuan Cai, Christopher J McLimans, Helong Jiang, Feng Chen, Lee R Krumholz, K David Hambright
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Abstract

Background: During the bloom season, the colonial cyanobacterium Microcystis forms complex aggregates which include a diverse microbiome within an exopolymer matrix. Early research postulated a simple mutualism existing with bacteria benefitting from the rich source of fixed carbon and Microcystis receiving recycled nutrients. Researchers have since hypothesized that Microcystis aggregates represent a community of synergistic and interacting species, an interactome, each with unique metabolic capabilities that are critical to the growth, maintenance, and demise of Microcystis blooms. Research has also shown that aggregate-associated bacteria are taxonomically different from free-living bacteria in the surrounding water. Moreover, research has identified little overlap in functional potential between Microcystis and members of its microbiome, further supporting the interactome concept. However, we still lack verification of general interaction and know little about the taxa and metabolic pathways supporting nutrient and metabolite cycling within Microcystis aggregates.

Results: During a 7-month study of bacterial communities comparing free-living and aggregate-associated bacteria in Lake Taihu, China, we found that aerobic anoxygenic phototrophic (AAP) bacteria were significantly more abundant within Microcystis aggregates than in free-living samples, suggesting a possible functional role for AAP bacteria in overall aggregate community function. We then analyzed gene composition in 102 high-quality metagenome-assembled genomes (MAGs) of bloom-microbiome bacteria from 10 lakes spanning four continents, compared with 12 complete Microcystis genomes which revealed that microbiome bacteria and Microcystis possessed complementary biochemical pathways that could serve in C, N, S, and P cycling. Mapping published transcripts from Microcystis blooms onto a comprehensive AAP and non-AAP bacteria MAG database (226 MAGs) indicated that observed high levels of expression of genes involved in nutrient cycling pathways were in AAP bacteria.

Conclusions: Our results provide strong corroboration of the hypothesized Microcystis interactome and the first evidence that AAP bacteria may play an important role in nutrient cycling within Microcystis aggregate microbiomes. Video Abstract.

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好氧性光营养体在蓝藻微囊藻水华微生物群的营养循环中发挥着重要作用。
背景:在藻华季节,蓝藻微囊藻(Microcystis)会形成复杂的聚集体,其中包括外聚合物基质中的多种微生物群。早期的研究推测这是一种简单的互生关系,细菌从丰富的固定碳源中获益,而微囊藻则接收回收的营养物质。研究人员后来推测,微囊藻聚集体是一个由协同作用和相互作用的物种群落,即相互作用组,每个物种都具有独特的新陈代谢能力,对微囊藻的生长、维持和消亡至关重要。研究还表明,聚集体相关细菌在分类学上不同于周围水体中的自由生活细菌。此外,研究还发现,微囊藻与其微生物组成员之间的功能潜力几乎没有重叠,这进一步支持了相互作用组的概念。然而,我们仍然缺乏对一般相互作用的验证,而且对支持微囊藻聚集体内营养物质和代谢物循环的类群和代谢途径知之甚少:我们对中国太湖中的细菌群落进行了为期 7 个月的研究,对自由生活细菌和聚集体相关细菌进行了比较,结果发现微囊藻聚集体中的需氧无氧光营养细菌(AAP)明显多于自由生活样本,这表明 AAP 细菌可能在整个聚集体群落功能中发挥了作用。然后,我们分析了横跨四大洲 10 个湖泊的 102 个高质量元基因组组装基因组(MAGs)中的开花微生物组细菌基因组成,并与 12 个完整的微囊藻基因组进行了比较,结果发现微生物组细菌和微囊藻拥有互补的生化途径,可在 C、N、S 和 P 循环中发挥作用。将微囊藻藻华中已发表的转录本映射到一个全面的AAP和非AAP细菌MAG数据库(226个MAG)中,结果表明,在AAP细菌中,营养物质循环途径中的基因表达量很高:我们的研究结果有力地证实了假定的微囊藻相互作用组,并首次证明 AAP 细菌可能在微囊藻聚集微生物组的营养循环中发挥重要作用。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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