Salem Belkessa, Edoardo Pasolli, Bachir Medrouh, Rebecca P K D Berg, Lee O 'Brien Andersen, Henrik Vedel Nielsen, Christen Rune Stensvold
{"title":"利用16S和18S rRNA基因的下一代测序分析与单细胞肠道原生生物相关的人类肠道微生物群的结构。","authors":"Salem Belkessa, Edoardo Pasolli, Bachir Medrouh, Rebecca P K D Berg, Lee O 'Brien Andersen, Henrik Vedel Nielsen, Christen Rune Stensvold","doi":"10.1016/j.csbj.2025.06.006","DOIUrl":null,"url":null,"abstract":"<p><p>The gut microbiota is a complex microbial ecosystem with a major impact on health and disease. Some gut unicellular eukaryotes (particularly <i>Blastocystis</i>) have been linked to features of intestinal eubiosis. Meanwhile, little is known regarding associations between gut-pathogenic protozoa, such as <i>Giardia</i>, and gut microbiota signatures. We therefore characterized and compared gut microbiota profiles of 60 <i>Giardia</i>-positive and 31 <i>Giardia</i>-negative Algerian individuals using amplicon-based next-generation sequencing of prokaryotic and eukaryotic ribosomal genes and stratifying for co-colonization with other unicellular eukaryotes, such as species of Archamoebae or <i>Blastocystis</i>. Overall, we found that alpha and beta microbiota diversity did not differ significantly between <i>Giardia</i>-positive and <i>Giardia</i>-negative individuals, regardless of the presence or absence of Archamoebae and <i>Entamoeba</i> (<i>p </i>> 0.05). However, significant differences were observed in both alpha and beta diversity between <i>Giardia</i>-positive, <i>Blastocystis</i>-negative and <i>Giardia</i>-positive, <i>Blastocystis</i>-positive individuals (observed richness, <i>p</i> = 0.0016; ANOSIM = 0.001), and similar differences were noticed between <i>Blastocystis</i>-negative and-positive carriers (<i>p</i> < 0.05), regardless of <i>Giardia</i> carrier status. Importantly, these differences in gut microbiota were considered to be independent of factors such as sex, age, and location (<i>p</i> > 0.05). Conclusively, <i>Giardia</i>-positive individuals may exhibit features of eubiosis, but whether this depends on the presence of <i>Blastocystis</i> should be confirmed by future studies. These findings combined might indicate that <i>Blastocystis</i> could be an active driver of gut microbiota diversity.</p>","PeriodicalId":10715,"journal":{"name":"Computational and structural biotechnology journal","volume":"27 ","pages":"2955-2967"},"PeriodicalIF":4.1000,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12273226/pdf/","citationCount":"0","resultStr":"{\"title\":\"Structure analysis of human gut microbiota associated with single-celled gut protists using Next-Generation Sequencing of 16S and 18S rRNA genes.\",\"authors\":\"Salem Belkessa, Edoardo Pasolli, Bachir Medrouh, Rebecca P K D Berg, Lee O 'Brien Andersen, Henrik Vedel Nielsen, Christen Rune Stensvold\",\"doi\":\"10.1016/j.csbj.2025.06.006\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The gut microbiota is a complex microbial ecosystem with a major impact on health and disease. Some gut unicellular eukaryotes (particularly <i>Blastocystis</i>) have been linked to features of intestinal eubiosis. Meanwhile, little is known regarding associations between gut-pathogenic protozoa, such as <i>Giardia</i>, and gut microbiota signatures. We therefore characterized and compared gut microbiota profiles of 60 <i>Giardia</i>-positive and 31 <i>Giardia</i>-negative Algerian individuals using amplicon-based next-generation sequencing of prokaryotic and eukaryotic ribosomal genes and stratifying for co-colonization with other unicellular eukaryotes, such as species of Archamoebae or <i>Blastocystis</i>. Overall, we found that alpha and beta microbiota diversity did not differ significantly between <i>Giardia</i>-positive and <i>Giardia</i>-negative individuals, regardless of the presence or absence of Archamoebae and <i>Entamoeba</i> (<i>p </i>> 0.05). However, significant differences were observed in both alpha and beta diversity between <i>Giardia</i>-positive, <i>Blastocystis</i>-negative and <i>Giardia</i>-positive, <i>Blastocystis</i>-positive individuals (observed richness, <i>p</i> = 0.0016; ANOSIM = 0.001), and similar differences were noticed between <i>Blastocystis</i>-negative and-positive carriers (<i>p</i> < 0.05), regardless of <i>Giardia</i> carrier status. Importantly, these differences in gut microbiota were considered to be independent of factors such as sex, age, and location (<i>p</i> > 0.05). Conclusively, <i>Giardia</i>-positive individuals may exhibit features of eubiosis, but whether this depends on the presence of <i>Blastocystis</i> should be confirmed by future studies. These findings combined might indicate that <i>Blastocystis</i> could be an active driver of gut microbiota diversity.</p>\",\"PeriodicalId\":10715,\"journal\":{\"name\":\"Computational and structural biotechnology journal\",\"volume\":\"27 \",\"pages\":\"2955-2967\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-06-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12273226/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Computational and structural biotechnology journal\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1016/j.csbj.2025.06.006\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Computational and structural biotechnology journal","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.csbj.2025.06.006","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Structure analysis of human gut microbiota associated with single-celled gut protists using Next-Generation Sequencing of 16S and 18S rRNA genes.
The gut microbiota is a complex microbial ecosystem with a major impact on health and disease. Some gut unicellular eukaryotes (particularly Blastocystis) have been linked to features of intestinal eubiosis. Meanwhile, little is known regarding associations between gut-pathogenic protozoa, such as Giardia, and gut microbiota signatures. We therefore characterized and compared gut microbiota profiles of 60 Giardia-positive and 31 Giardia-negative Algerian individuals using amplicon-based next-generation sequencing of prokaryotic and eukaryotic ribosomal genes and stratifying for co-colonization with other unicellular eukaryotes, such as species of Archamoebae or Blastocystis. Overall, we found that alpha and beta microbiota diversity did not differ significantly between Giardia-positive and Giardia-negative individuals, regardless of the presence or absence of Archamoebae and Entamoeba (p > 0.05). However, significant differences were observed in both alpha and beta diversity between Giardia-positive, Blastocystis-negative and Giardia-positive, Blastocystis-positive individuals (observed richness, p = 0.0016; ANOSIM = 0.001), and similar differences were noticed between Blastocystis-negative and-positive carriers (p < 0.05), regardless of Giardia carrier status. Importantly, these differences in gut microbiota were considered to be independent of factors such as sex, age, and location (p > 0.05). Conclusively, Giardia-positive individuals may exhibit features of eubiosis, but whether this depends on the presence of Blastocystis should be confirmed by future studies. These findings combined might indicate that Blastocystis could be an active driver of gut microbiota diversity.
期刊介绍:
Computational and Structural Biotechnology Journal (CSBJ) is an online gold open access journal publishing research articles and reviews after full peer review. All articles are published, without barriers to access, immediately upon acceptance. The journal places a strong emphasis on functional and mechanistic understanding of how molecular components in a biological process work together through the application of computational methods. Structural data may provide such insights, but they are not a pre-requisite for publication in the journal. Specific areas of interest include, but are not limited to:
Structure and function of proteins, nucleic acids and other macromolecules
Structure and function of multi-component complexes
Protein folding, processing and degradation
Enzymology
Computational and structural studies of plant systems
Microbial Informatics
Genomics
Proteomics
Metabolomics
Algorithms and Hypothesis in Bioinformatics
Mathematical and Theoretical Biology
Computational Chemistry and Drug Discovery
Microscopy and Molecular Imaging
Nanotechnology
Systems and Synthetic Biology