象血酵母菌的专性共生体,具有强烈减少的基因组,类似于吸虱的共生细菌。

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jana Martin Říhová, Roman Vodička, Václav Hypša
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引用次数: 0

摘要

血螨单属小目舌虱是一种系统发育位置不明确的小群体外寄生虫,与吸吮虱和咀嚼虱有亲缘关系。先前基于16S rRNA基因的筛选表明,血酵母菌含有一种共生细菌,其DNA在昆虫中专性共生共生体的核苷酸组成中表现出强烈的变化。在Phthiraptera中,已知最小的基因组存在于与吸吮虱相关的共生体中,吸吮虱只以哺乳动物的血液为食,而与以皮肤衍生物为食的咀嚼虱共生的共生体的基因组普遍较大。在这项研究中,我们研究了与大象血霉菌相关的共生体的基因组特征。我们对象人元基因组进行了测序和组装,并提取了其共生细菌的基因组草图,结果表明,该共生体的基因组明显减少,基因组长度为0.39 Mbp,是已知的Phthiraptera共生体中最小的基因组。多基因系统发育分析将共生体归入由其他昆虫的长分枝共生体组成的三个集群之一。更具体地说,它与其他几种吸虱的共生体以及舌蝇的专性共生体Wigglesworthia舌蝇聚集在一起。与基因组的急剧减少相一致,象人共生体失去了许多代谢能力。然而,它保留了四种B族维生素的功能途径,这是吸血昆虫共生体的典型特征。考虑到基因组、代谢和系统发育特征,这种新的共生体与几种已知的吸虱而不是咀嚼虱非常相似。重要意义舌虱是一种独特的永久性体外寄生虫,与吸吮虱和咀嚼虱密切相关。这两类虱子在形态、生态和捕食策略上都有所不同。由于它们的饮食来源不同,即哺乳动物的血液与脊椎动物的皮肤衍生物,它们也与专性细菌共生体表现出不同的共生模式。虽然Rhynchophthirina与吸吮和咀嚼虱子有某些共同特征,但其专一共生细菌的性质及其代谢作用尚不清楚。在这项研究中,我们组装了来自象血菌(Rhynchophthirina)的共生细菌的基因组,证明了它与吸虱的几种共生体的密切相似性和系统发育接近性。基因组高度减少(代表虱子相关共生体中最小的基因组),并表现出代谢途径的显著丧失。然而,与其他吸虱共生体类似,它保留了合成几种B族维生素的必要途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An obligate symbiont of Haematomyzus elephantis with a strongly reduced genome resembles symbiotic bacteria in sucking lice.

The parvorder Rhynchophthirina with a single genus Haematomyzus is a small group of ectoparasites of unclear phylogenetic position, related to sucking and chewing lice. Previous screening based on the 16S rRNA gene indicated that Haematomyzus harbors a symbiotic bacterium whose DNA exhibits a strong shift in nucleotide composition typical of obligate mutualistic symbionts in insects. Within Phthiraptera, the smallest known genomes are found in the symbionts associated with sucking lice, which feed exclusively on mammal blood, compared to the generally larger genomes of the symbionts inhabiting chewing lice, which feed on skin derivatives. In this study, we investigate the genome characteristics of the symbiont associated with Haematomyzus elephantis. We sequenced and assembled the H. elephantis metagenome, extracted a genome draft of its symbiotic bacterium, and showed that the symbiont has a significantly reduced genome, which is with 0.39 Mbp the smallest genome among the symbionts known from Phthiraptera. Multigenic phylogenetic analysis places the symbiont into one of three clusters composed of long-branched symbionts from other insects. More specifically, it clusters together with symbionts from several other sucking lice and also with Wigglesworthia glossinidia, an obligate symbiont of tsetse flies. Consistent with the dramatic reduction of its genome, the H. elephantis symbiont lost many metabolic capacities. However, it retained functional pathways for four B vitamins, a trait typical for symbionts in blood-feeding insects. Considering genomic, metabolic, and phylogenetic characteristics, the new symbiont closely resembles those known from several sucking lice rather than chewing lice.IMPORTANCERhynchophthirina is a unique small group of permanent ectoparasites that is closely related to both sucking and chewing lice. These two groups of lice differ in their morphology, ecology, and feeding strategies. As a consequence of their different dietary sources, i.e., mammals' blood vs vertebrate skin derivatives, they also exhibit distinct patterns of symbiosis with obligate bacterial symbionts. While Rhynchophthirina shares certain traits with sucking and chewing lice, the nature of its obligate symbiotic bacterium and its metabolic role is not known. In this study, we assemble the genome of symbiotic bacterium from Haematomyzus elephantis (Rhynchophthirina), demonstrating its close similarity and phylogenetic proximity to several symbionts of sucking lice. The genome is highly reduced (representing the smallest genome among louse-associated symbionts) and exhibits a significant loss of metabolic pathways. However, similar to other sucking louse symbionts, it retains essential pathways for the synthesis of several B vitamins.

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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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