济州岛熔岩管Manjanggul洞原核微生物群落结构及其生态潜力

IF 2.3 3区 生物学 Q3 MICROBIOLOGY
Minji Kim, So-Jeong Kim, In-Tae Cha, Soo-Je Park
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引用次数: 0

摘要

本研究调查了韩国济州岛被联合国教科文组织列为世界遗产的熔岩管Manjanggul洞穴的原核微生物群——包括古细菌和细菌。尽管具有重要的地质意义,但济州岛不同洞穴系统中的古细菌和细菌群落结构在很大程度上仍未被探索,主要是由于进入限制。本研究利用古细菌和细菌16S rRNA基因的高通量测序,以及生物统计学方法来阐明Manjanggul洞穴内这些群落的结构和多样性。结果表明,细菌群落以变形菌门(Proteobacteria)为主,古细菌门以绿原菌门(Crenarchaeota)为主。值得注意的是,氨氧化古细菌亚硝基藻属含量非常丰富,而氨氧化细菌(亚硝基球菌属和亚硝基单胞菌属)含量极低。亚硝酸盐氧化细菌属Nitrospira在所有样品中都持续丰富,这表明Nitrososphaera/Nitrospira可能在洞穴生态系统中有氧硝化作用中起关键作用。有趣的是,还观察到高比例的盐古菌,这可能归因于济州岛独特的地质特征,表明Manjanggul洞穴内存在独特的微生物生态系统。综上所述,本研究为当地洞穴相关原核生物群落与外部微生物种群的混合提供了分子证据,表明在Manjanggul洞穴中这两个群落的组成可能发生了变化。这些发现强调了研究人类活动对洞穴微生物生态系统影响的重要性,以及保护这些独特环境的保护策略的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Revealing the Prokaryotic Microbial Community Structures and their Ecological Potentials in Manjanggul Cave, a Lava Tube on Jeju Island.

This study investigated the prokaryotic microbiota-comprising both archaea and bacteria-of Manjanggul Cave, a UNESCO World Heritage lava tube on Jeju Island, South Korea. Despite their geological significance, the archaeal and bacterial community structures within Jeju Island's diverse cave systems have remained largely unexplored, primarily due to access restrictions. Here, we used high-throughput sequencing of archaeal and bacterial 16S rRNA genes, as well as biostatistics, to elucidate the structure and diversity of these communities within Manjanggul Cave. The findings revealed that the bacterial community was dominated by Proteobacteria, while Crenarchaeota (classified by silva) was the predominant archaeal phylum. Notably, the ammonia-oxidizing archaeal genus Nitrososphaera was highly abundant, whereas ammonia-oxidizing bacteria (genera Nitrosococcus and Nitrosomonas) were detected at extremely low levels. The nitrite-oxidizing bacterial genus Nitrospira was consistently abundant across all samples, suggesting that Nitrososphaera/Nitrospira may play crucial roles in aerobic nitrification within the cave ecosystem. Intriguingly, a high proportion of haloarchaea was also observed, which may be attributed to the unique geological characteristics of Jeju Island, indicating a distinct microbial ecosystem within Manjanggul Cave. In conclusion, this study provides molecular evidence for the mixing of indigenous cave-associated prokaryotic communities with external microbial populations, suggesting potential alterations in the composition of both communities within Manjanggul Cave. These findings underscore the importance of research to understand the impact of human activities on cave microbial ecosystems, and the need for conservation strategies to preserve these unique environments.

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来源期刊
Current Microbiology
Current Microbiology 生物-微生物学
CiteScore
4.80
自引率
3.80%
发文量
380
审稿时长
2.5 months
期刊介绍: Current Microbiology is a well-established journal that publishes articles in all aspects of microbial cells and the interactions between the microorganisms, their hosts and the environment. Current Microbiology publishes original research articles, short communications, reviews and letters to the editor, spanning the following areas: physiology, biochemistry, genetics, genomics, biotechnology, ecology, evolution, morphology, taxonomy, diagnostic methods, medical and clinical microbiology and immunology as applied to microorganisms.
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