与沉积物和水相比,蜗牛胃肠道细菌群落具有不同的生物地理模式。

IF 3.9 3区 生物学 Q2 MICROBIOLOGY MicrobiologyOpen Pub Date : 2024-06-02 DOI:10.1002/mbo3.1413
Daniel P. R. Herlemann, Helen Tammert, Carmen Kivistik, Kairi Käiro, Veljo Kisand
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引用次数: 0

摘要

影响细菌群落组成分布的因素尚不十分清楚。地理模式的作用表明细菌的扩散受到限制,但这仍然是一个争论不休的话题。与宿主相关的细菌面临着独特的扩散挑战,因为它们通常依赖于宿主,而宿主为其共生体提供了特定的环境。在这项研究中,我们考察了生物地理距离对巴氏栉水母(Ampullaceana balthica)胃肠道细菌多样性和细菌群落组成的影响。我们比较了宿主相关细菌群落与水和沉积物中细菌群落的影响。这种比较是通过 16S 核糖体 RNA 基因测序进行的。我们发现,我们在爱沙尼亚、丹麦和德国北部采样的细菌群落在水、沉积物和胃肠道中各不相同。在每种基质中,不同国家的细菌群落也各不相同。这表明,基质类型是决定细菌群落组成的主要因素。我们分别分析了水体、沉积物和胃肠道细菌群落在地理距离增加时的更替率。我们发现,与水体细菌群落相比,胃肠道细菌群落的更替率较低。这意味着胃肠道细菌群落的组成在不同距离上保持相对稳定,而水体细菌群落则表现出更大的变异性。不过,胃肠道的国家特异性扩增子序列变异比例最低,这表明细菌定植于当地细菌群落。由于水和胃肠道之间的重叠率最高,因此胃肠道细菌群落似乎是由水细菌群落定殖的。我们的研究证实,宿主相关群落的生物地理模式与水和沉积物细菌群落不同。这些宿主相关群落由来自水体细菌群落的大量兼性共生体组成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Distinct biogeographical patterns in snail gastrointestinal tract bacterial communities compared with sediment and water

The factors that influence the distribution of bacterial community composition are not well understood. The role of geographical patterns, which suggest limited dispersal, is still a topic of debate. Bacteria associated with hosts face unique dispersal challenges as they often rely on their hosts, which provide specific environments for their symbionts. In this study, we examined the effect of biogeographic distances on the bacterial diversity and composition of bacterial communities in the gastrointestinal tract of Ampullaceana balthica. We compared the effects on the host-associated bacterial community to those on bacterial communities in water and sediment. This comparison was made using 16S ribosomal RNA gene sequencing. We found that the bacterial communities we sampled in Estonia, Denmark, and Northern Germany varied between water, sediment, and the gastrointestinal tract. They also varied between countries within each substrate. This indicates that the type of substrate is a dominant factor in determining bacterial community composition. We separately analyzed the turnover rates of water, sediment, and gastrointestinal bacterial communities over increasing geographic distances. We observed that the turnover rate was lower for gastrointestinal bacterial communities compared to water bacterial communities. This implies that the composition of gastrointestinal bacteria remains relatively stable over distances, while water bacterial communities exhibit greater variability. However, the gastrointestinal tract had the lowest percentage of country-specific amplicon sequence variants, suggesting bacterial colonization from local bacterial communities. Since the overlap between the water and gastrointestinal tract was highest, it appears that the gastrointestinal bacterial community is colonized by the water bacterial community. Our study confirmed that biogeographical patterns in host-associated communities differ from those in water and sediment bacterial communities. These host-associated communities consist of numerous facultative symbionts derived from the water bacterial community.

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来源期刊
MicrobiologyOpen
MicrobiologyOpen MICROBIOLOGY-
CiteScore
8.00
自引率
0.00%
发文量
78
审稿时长
20 weeks
期刊介绍: MicrobiologyOpen is a peer reviewed, fully open access, broad-scope, and interdisciplinary journal delivering rapid decisions and fast publication of microbial science, a field which is undergoing a profound and exciting evolution in this post-genomic era. The journal aims to serve the research community by providing a vehicle for authors wishing to publish quality research in both fundamental and applied microbiology. Our goal is to publish articles that stimulate discussion and debate, as well as add to our knowledge base and further the understanding of microbial interactions and microbial processes. MicrobiologyOpen gives prompt and equal consideration to articles reporting theoretical, experimental, applied, and descriptive work in all aspects of bacteriology, virology, mycology and protistology, including, but not limited to: - agriculture - antimicrobial resistance - astrobiology - biochemistry - biotechnology - cell and molecular biology - clinical microbiology - computational, systems, and synthetic microbiology - environmental science - evolutionary biology, ecology, and systematics - food science and technology - genetics and genomics - geobiology and earth science - host-microbe interactions - infectious diseases - natural products discovery - pharmaceutical and medicinal chemistry - physiology - plant pathology - veterinary microbiology We will consider submissions across unicellular and cell-cluster organisms: prokaryotes (bacteria, archaea) and eukaryotes (fungi, protists, microalgae, lichens), as well as viruses and prions infecting or interacting with microorganisms, plants and animals, including genetic, biochemical, biophysical, bioinformatic and structural analyses. The journal features Original Articles (including full Research articles, Method articles, and Short Communications), Commentaries, Reviews, and Editorials. Original papers must report well-conducted research with conclusions supported by the data presented in the article. We also support confirmatory research and aim to work with authors to meet reviewer expectations. MicrobiologyOpen publishes articles submitted directly to the journal and those referred from other Wiley journals.
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