Fu Jieyang, Liu Yiting, Yoshioka Takuya, Igai Katsura, Mabuchi Takako, Kihara Kumiko, Murakami Takumi, Lo Nathan, Ohkuma Moriya, Hongoh Yuichi
School of Life Science and Technology, Institute of Science Tokyo, 2-12-1 Ookayama, Meguro-ku, Tokyo 152-8550, Japan.
School of Life and Environmental Sciences, University of Sydney, Corner of Parramatta and City roads, Sydney, NSW 2006, Australia.
ISME J. 2025 Jan 2;19(1). doi: 10.1093/ismejo/wraf178.
Mixotricha paradoxa is a large cellulolytic flagellate present in the hindgut of the termite Mastotermes darwiniensis. This parabasalid flagellate is unique in its reliance on ectosymbiotic spirochetes for motility. We analyzed the transcriptome of M. paradoxa and the genomes of the ectosymbiotic spirochete Propulsinema mixotrichae ("Treponematales"), the rod-shaped ectosymbiont Synergitannerella mixotrichae (Bacteroidales), and the endosymbiont Endomicrobiellum mixotrichae (Endomicrobiales), all of which are obligately associated with M. paradoxa and were taxonomically described in this study. Mixotricha paradoxa highly expressed genes for diverse glycoside hydrolases (GHs) and likely ferments sugars to H2, CO2, acetate, ethanol, and glycerol. Similar to the case for parasitic parabasalids such as Trichomonas vaginalis, transcripts for biosynthesis of nucleotides and many amino acids were not detected in our analyses of M. paradoxa. Propulsinema mixotrichae possesses genes encoding proteins for the assembly of flagella and for those in pathways associated with chemotaxis and dinitrogen fixation. Such genes are absent in S. mixotrichae, which instead possesses numerous genes encoding glycoside hydrolase enzymes, which are largely complementary to the glycoside hydrolase repertoire of M. paradoxa. Endomicrobiellum mixotrichae appears to provide nucleotides and nine amino acids to its host, which in turn likely supplies three amino acids, including tryptophan, to E. mixotrichae. Because bacterial cells, in addition to wood particles, were observed in food vacuoles of M. paradoxa, these ecto- and endosymbionts may be digested by the flagellate host. Overall, the distinct roles of each symbiont highlight the efficient functional division of labor that has evolved in this holobiont.
奇异混毛虫是一种存在于达尔文澳白蚁后肠中的大型纤维素分解鞭毛虫。这种副基体鞭毛虫在依赖外共生螺旋体进行运动方面独具特色。我们分析了奇异混毛虫的转录组以及外共生螺旋体推进混毛虫(“密螺旋体目”)、杆状外共生体混合协同菌(拟杆菌目)和内共生体内微菌(内微菌目)的基因组,所有这些共生体都与奇异混毛虫有 obligately 关联,并且在本研究中进行了分类描述。奇异混毛虫高度表达多种糖苷水解酶(GHs)的基因,并可能将糖类发酵为氢气、二氧化碳、乙酸、乙醇和甘油。与诸如阴道毛滴虫等寄生性副基体的情况类似,在我们对奇异混毛虫的分析中未检测到核苷酸和许多氨基酸生物合成的转录本。推进混毛虫拥有编码鞭毛组装蛋白以及与趋化性和固氮相关途径中蛋白的基因。混合协同菌中不存在此类基因,相反,它拥有众多编码糖苷水解酶的基因,这些基因在很大程度上与奇异混毛虫的糖苷水解酶库互补。内微菌似乎为其宿主提供核苷酸和九种氨基酸,反过来宿主可能向内微菌提供三种氨基酸,包括色氨酸。因为在奇异混毛虫的食物泡中除了木颗粒外还观察到细菌细胞,这些外共生体和内共生体可能会被鞭毛虫宿主消化。总体而言,每个共生体的独特作用突出了在这个共生体中进化出的高效功能分工。