Functional eubacteria species along with trans-domain gut inhabitants favour dysgenic diversity in oxalate stone disease
| Autor: | Rahul P. Gune, Yogesh S. Shouche, Mangesh V. Suryavanshi, Shrikant S. Bhute |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2018 |
| Předmět: |
0301 basic medicine
Genetics education.field_of_study Multidisciplinary biology Oxalobacter Population lcsh:R Species diversity lcsh:Medicine Gut flora biology.organism_classification medicine.disease Article 03 medical and health sciences 030104 developmental biology Microbial ecology Oxalobacter formigenes Metagenomics medicine lcsh:Q education lcsh:Science Dysbiosis |
| Zdroj: | Scientific Reports Scientific Reports, Vol 8, Iss 1, Pp 1-11 (2018) |
| ISSN: | 2045-2322 |
| Popis: | Analyses across all three domains of life are necessary to advance our understanding of taxonomic dysbiosis in human diseases. In the present study, we assessed gut microbiota (eubacteria, archaea, and eukaryotes) of recurrent oxalate kidney stone suffers to explore the extent of trans-domain and functional species dysbiosis inside the gut. Trans-domain taxonomic composition, active oxalate metabolizer and butyrate-producing diversity were explored by utilizing frc-, but-, and buk- functional gene amplicon analysis. Operational taxonomic units (OTUs) level analyses confound with the observation that dysbiosis in gut microbiota is not just limited to eubacteria species, but also to other domains like archaea and eukaryotes. We found that some of healthy eubacterial population retained together with Oxalobacter formigenes and Lactobacillus plantarum colonization in disease condition (p Oxalobacter non-colonizers; and Prevotella and Ruminococcus species which may contribute to oxalate metabolism and butyrate synthesis as well. Our study underscores fact that microbial dysbiosis is not limited to eubacteria only hence suggest the necessity of the trans-domain surveillance in metabolic diseases for intervention studies. |
| Databáze: | OpenAIRE |
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