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Shotgun metagenomic analysis reveals new insights into bacterial community profiles in tempeh

OBJECTIVE: Amplicon sequencing targeting 16S ribosomal RNA (rRNA) has been widely used to profile the microbial community from fermented food samples. However, polymerase chain reaction (PCR) steps on amplicon sequencing analysis and intragenomic heterogeneity within 16S rRNA are believed to contrib...

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Autores principales: Yulandi, Adi, Suwanto, Antonius, Waturangi, Diana Elizabeth, Wahyudi, Aris Tri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7731626/
https://www.ncbi.nlm.nih.gov/pubmed/33308279
http://dx.doi.org/10.1186/s13104-020-05406-6
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author Yulandi, Adi
Suwanto, Antonius
Waturangi, Diana Elizabeth
Wahyudi, Aris Tri
author_facet Yulandi, Adi
Suwanto, Antonius
Waturangi, Diana Elizabeth
Wahyudi, Aris Tri
author_sort Yulandi, Adi
collection PubMed
description OBJECTIVE: Amplicon sequencing targeting 16S ribosomal RNA (rRNA) has been widely used to profile the microbial community from fermented food samples. However, polymerase chain reaction (PCR) steps on amplicon sequencing analysis and intragenomic heterogeneity within 16S rRNA are believed to contribute to bias in estimating microbial community composition. As potential paraprobiotics sources, a comprehensive profiling study of tempeh microbial ecology could contribute to tempeh product development. This study employed a shotgun metagenomic approach, where metagenome fragments from tempeh samples were sequenced directly for taxonomic and functional profiling analysis. RESULTS: Taxonomic profiling showed that Proteobacteria, Firmicutes, and Bacteroidetes were the dominant phyla from the shotgun metagenomic analysis in all tempeh samples. In terms of composition, this shotgun metagenomic study revealed that Proteobacteria was the most abundant phylum. Functional profiling showed that iron complex outer-membrane recepter protein (KEGG ID: K02014) was the most transcribed gene based on this metagenomic analysis. The metagenome-assembled genomes (MAGs) results from the binning pipeline could reveal almost complete whole genome sequence of Lactobacillus fermentum, Enterococcus cecorum, Escherichia coli, Klebsiella pneumoniae, and Acinetobacter baumannii.
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spelling pubmed-77316262020-12-15 Shotgun metagenomic analysis reveals new insights into bacterial community profiles in tempeh Yulandi, Adi Suwanto, Antonius Waturangi, Diana Elizabeth Wahyudi, Aris Tri BMC Res Notes Research Note OBJECTIVE: Amplicon sequencing targeting 16S ribosomal RNA (rRNA) has been widely used to profile the microbial community from fermented food samples. However, polymerase chain reaction (PCR) steps on amplicon sequencing analysis and intragenomic heterogeneity within 16S rRNA are believed to contribute to bias in estimating microbial community composition. As potential paraprobiotics sources, a comprehensive profiling study of tempeh microbial ecology could contribute to tempeh product development. This study employed a shotgun metagenomic approach, where metagenome fragments from tempeh samples were sequenced directly for taxonomic and functional profiling analysis. RESULTS: Taxonomic profiling showed that Proteobacteria, Firmicutes, and Bacteroidetes were the dominant phyla from the shotgun metagenomic analysis in all tempeh samples. In terms of composition, this shotgun metagenomic study revealed that Proteobacteria was the most abundant phylum. Functional profiling showed that iron complex outer-membrane recepter protein (KEGG ID: K02014) was the most transcribed gene based on this metagenomic analysis. The metagenome-assembled genomes (MAGs) results from the binning pipeline could reveal almost complete whole genome sequence of Lactobacillus fermentum, Enterococcus cecorum, Escherichia coli, Klebsiella pneumoniae, and Acinetobacter baumannii. BioMed Central 2020-12-11 /pmc/articles/PMC7731626/ /pubmed/33308279 http://dx.doi.org/10.1186/s13104-020-05406-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Note
Yulandi, Adi
Suwanto, Antonius
Waturangi, Diana Elizabeth
Wahyudi, Aris Tri
Shotgun metagenomic analysis reveals new insights into bacterial community profiles in tempeh
title Shotgun metagenomic analysis reveals new insights into bacterial community profiles in tempeh
title_full Shotgun metagenomic analysis reveals new insights into bacterial community profiles in tempeh
title_fullStr Shotgun metagenomic analysis reveals new insights into bacterial community profiles in tempeh
title_full_unstemmed Shotgun metagenomic analysis reveals new insights into bacterial community profiles in tempeh
title_short Shotgun metagenomic analysis reveals new insights into bacterial community profiles in tempeh
title_sort shotgun metagenomic analysis reveals new insights into bacterial community profiles in tempeh
topic Research Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7731626/
https://www.ncbi.nlm.nih.gov/pubmed/33308279
http://dx.doi.org/10.1186/s13104-020-05406-6
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