揭示木质纤维素分解潜力:白蚁肠道内细菌谱系的基因组学探索。

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
João Felipe M Salgado, Vincent Hervé, Manuel A G Vera, Gaku Tokuda, Andreas Brune
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引用次数: 0

摘要

背景:不同白蚁科白蚁肠道内的微生物情况各不相同。低等白蚁(LT)的肠道微生物群以纤维素溶解鞭毛虫为主,这些鞭毛虫会将木质颗粒封存在消化泡中;而在无鞭毛虫的高等白蚁(HT)中,纤维素溶解活动则被归因于纤维相关细菌。然而,人们对各个菌系在纤维消化中的作用知之甚少,尤其是在低等白蚁中:我们研究了从 51 种白蚁肠道元基因组中回收的 2223 个元基因组(MAGs)的木质纤维素分解潜力。在依赖鞭毛虫的LT中,纤维素溶解酶仅限于类杆菌科(Dysgonomonadaceae、Tannerellaceae、Bacteroidaceae、Azobacteroidaceae)和螺旋藻科(Breznakiellaceae)的MAGs,并反映出对纤维糊精的专一性,而它们的半纤维素溶解酶库的特点是对木聚糖和各种杂聚物有活性。相比之下,从无鞭毛虫的 HT 中提取的 MAGs 则拥有与白蚁肠道鞭毛虫相似的外切和内切葡聚糖酶的综合酶库,这突出表明纤维细菌群和螺旋藻群占据了纤维素溶解位点,而这一位点在鞭毛虫消失后空缺。此外,我们还在假单胞菌(Burkholderiales, Pseudomonadales)和放线菌(Actinomycetota, Actinomycetales, Mycobacteriales)的MAGs中直接或间接地检测到了氧化纤维素或改变木质素的依赖氧的酶,它们代表了位于后肠壁的菌系:本研究结果完善了我们对白蚁肠道中木质纤维素共生消化的概念,强调了特定细菌群在依赖鞭毛和不依赖鞭毛的纤维素和半纤维素分解过程中的不同作用,以及在白蚁肠道通过过程中,氧气在微氧外围植物纤维和木质素解聚过程中的作用,这些作用迄今尚未得到重视。视频摘要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unveiling lignocellulolytic potential: a genomic exploration of bacterial lineages within the termite gut.

Background: The microbial landscape within termite guts varies across termite families. The gut microbiota of lower termites (LT) is dominated by cellulolytic flagellates that sequester wood particles in their digestive vacuoles, whereas in the flagellate-free higher termites (HT), cellulolytic activity has been attributed to fiber-associated bacteria. However, little is known about the role of individual lineages in fiber digestion, particularly in LT.

Results: We investigated the lignocellulolytic potential of 2223 metagenome-assembled genomes (MAGs) recovered from the gut metagenomes of 51 termite species. In the flagellate-dependent LT, cellulolytic enzymes are restricted to MAGs of Bacteroidota (Dysgonomonadaceae, Tannerellaceae, Bacteroidaceae, Azobacteroidaceae) and Spirochaetota (Breznakiellaceae) and reflect a specialization on cellodextrins, whereas their hemicellulolytic arsenal features activities on xylans and diverse heteropolymers. By contrast, the MAGs derived from flagellate-free HT possess a comprehensive arsenal of exo- and endoglucanases that resembles that of termite gut flagellates, underlining that Fibrobacterota and Spirochaetota occupy the cellulolytic niche that became vacant after the loss of the flagellates. Furthermore, we detected directly or indirectly oxygen-dependent enzymes that oxidize cellulose or modify lignin in MAGs of Pseudomonadota (Burkholderiales, Pseudomonadales) and Actinomycetota (Actinomycetales, Mycobacteriales), representing lineages located at the hindgut wall.

Conclusions: The results of this study refine our concept of symbiotic digestion of lignocellulose in termite guts, emphasizing the differential roles of specific bacterial lineages in both flagellate-dependent and flagellate-independent breakdown of cellulose and hemicelluloses, as well as a so far unappreciated role of oxygen in the depolymerization of plant fiber and lignin in the microoxic periphery during gut passage in HT. Video Abstract.

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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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