{"title":"济州岛熔岩管Manjanggul洞原核微生物群落结构及其生态潜力","authors":"Minji Kim, So-Jeong Kim, In-Tae Cha, Soo-Je Park","doi":"10.1007/s00284-025-04318-7","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":11360,"journal":{"name":"Current Microbiology","volume":"82 8","pages":"331"},"PeriodicalIF":2.3000,"publicationDate":"2025-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Revealing the Prokaryotic Microbial Community Structures and their Ecological Potentials in Manjanggul Cave, a Lava Tube on Jeju Island.\",\"authors\":\"Minji Kim, So-Jeong Kim, In-Tae Cha, Soo-Je Park\",\"doi\":\"10.1007/s00284-025-04318-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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.</p>\",\"PeriodicalId\":11360,\"journal\":{\"name\":\"Current Microbiology\",\"volume\":\"82 8\",\"pages\":\"331\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-06-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s00284-025-04318-7\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s00284-025-04318-7","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
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.
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.