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      Long-read MinION™ sequencing of 16S and 16S-ITS-23S rRNA genes provides species-level resolution of Lactobacillaceae in mixed communities

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          Abstract

          The Lactobacillaceae are lactic acid bacteria harnessed to deliver important outcomes across numerous industries, and their unambiguous, species-level identification from mixed community environments is an important endeavor. Amplicon-based metataxonomics using short-read sequencing of partial 16S rRNA gene regions is widely used to support this, however, the high genetic similarity among Lactobacillaceae species restricts our ability to confidently describe these communities even at genus level. Long-read sequencing (LRS) of the whole 16S rRNA gene or the near complete rRNA operon (16S-ITS-23S) has the potential to improve this. We explored species ambiguity amongst Lactobacillaceae using in-silico tool RibDif2, which identified allele overlap when various partial and complete 16S rRNA gene and 16S-ITS-23S rRNA regions were amplified. We subsequently implemented LRS by MinION™ to compare the capacity of V3–V4, 16S and 16S-ITS-23S rRNA amplicons to accurately describe the diversity of a 20-species Lactobacillaceae mock community in practice. In-silico analysis identified more instances of allele/species overlap with V3–V4 amplicons ( n = 43) compared to the 16S rRNA gene ( n = 11) and partial ( n = up to 15) or complete ( n = 0) 16S-ITS-23S rRNA amplicons. With subsequent LRS of a DNA mock community, 80% of target species were identified using V3–V4 amplicons whilst the 16S rRNA gene and 16S-ITS-23S rRNA region amplicons resulted in 95 and 100% of target species being identified. A considerable reduction in false-positive identifications was also seen with 16S rRNA gene ( n = 3) and 16S-ITS-23S rRNA region ( n = 9) amplicons compared with V3–V4 amplicons ( n = 43). Whilst the target species affected by allele overlap in V3–V4 and 16S rRNA gene sequenced mock communities were predicted by RibDif2, unpredicted species ambiguity was observed in 16S-ITS-23S rRNA sequenced communities. Considering the average nucleotide identity (ANI) between ambiguous species (~97%) and the basecall accuracy of our MinION™ sequencing protocol (96.4%), the misassignment of reads between closely related taxa is to be expected. With basecall accuracy exceeding 99% for recent MinION™ releases, the increased species-level differentiating power promised by longer amplicons like the 16S-ITS-23S rRNA region, may soon be fully realized.

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          A taxonomic note on the genus Lactobacillus: Description of 23 novel genera, emended description of the genus Lactobacillus Beijerinck 1901, and union of Lactobacillaceae and Leuconostocaceae

          The genus Lactobacillus comprises 261 species (at March 2020) that are extremely diverse at phenotypic, ecological and genotypic levels. This study evaluated the taxonomy of Lactobacillaceae and Leuconostocaceae on the basis of whole genome sequences. Parameters that were evaluated included core genome phylogeny, (conserved) pairwise average amino acid identity, clade-specific signature genes, physiological criteria and the ecology of the organisms. Based on this polyphasic approach, we propose reclassification of the genus Lactobacillus into 25 genera including the emended genus Lactobacillus, which includes host-adapted organisms that have been referred to as the Lactobacillus delbrueckii group, Paralactobacillus and 23 novel genera for which the names Holzapfelia, Amylolactobacillus, Bombilactobacillus, Companilactobacillus, Lapidilactobacillus, Agrilactobacillus, Schleiferilactobacillus, Loigolactobacilus, Lacticaseibacillus, Latilactobacillus, Dellaglioa, Liquorilactobacillus, Ligilactobacillus, Lactiplantibacillus, Furfurilactobacillus, Paucilactobacillus, Limosilactobacillus, Fructilactobacillus, Acetilactobacillus, Apilactobacillus, Levilactobacillus, Secundilactobacillus and Lentilactobacillus are proposed. We also propose to emend the description of the family Lactobacillaceae to include all genera that were previously included in families Lactobacillaceae and Leuconostocaceae. The generic term 'lactobacilli' will remain useful to designate all organisms that were classified as Lactobacillaceae until 2020. This reclassification reflects the phylogenetic position of the micro-organisms, and groups lactobacilli into robust clades with shared ecological and metabolic properties, as exemplified for the emended genus Lactobacillus encompassing species adapted to vertebrates (such as Lactobacillus delbrueckii, Lactobacillus iners, Lactobacillus crispatus, Lactobacillus jensensii, Lactobacillus johnsonii and Lactobacillus acidophilus) or invertebrates (such as Lactobacillus apis and Lactobacillus bombicola).
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            List of Prokaryotic names with Standing in Nomenclature (LPSN) moves to the DSMZ

            The List of Prokaryotic names with Standing in Nomenclature (LPSN) was acquired in November 2019 by the DSMZ and was relaunched using an entirely new production system in February 2020. This article describes in detail the structure of the new site, navigation, page layout, search facilities and new features.
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              Sequencing and beyond: integrating molecular 'omics' for microbial community profiling.

              High-throughput DNA sequencing has proven invaluable for investigating diverse environmental and host-associated microbial communities. In this Review, we discuss emerging strategies for microbial community analysis that complement and expand traditional metagenomic profiling. These include novel DNA sequencing strategies for identifying strain-level microbial variation and community temporal dynamics; measuring multiple 'omic' data types that better capture community functional activity, such as transcriptomics, proteomics and metabolomics; and combining multiple forms of omic data in an integrated framework. We highlight studies in which the 'multi-omics' approach has led to improved mechanistic models of microbial community structure and function.
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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/2431746/overviewRole: Role: Role: Role: Role: Role: Role:
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                URI : https://loop.frontiersin.org/people/404325/overviewRole: Role:
                URI : https://loop.frontiersin.org/people/2220736/overviewRole: Role:
                URI : https://loop.frontiersin.org/people/154120/overviewRole: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/247403/overviewRole: Role: Role: Role:
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                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                07 December 2023
                2023
                : 14
                : 1290756
                Affiliations
                [1] 1Tasmanian Institute of Agriculture, University of Tasmania , Hobart, TAS, Australia
                [2] 2Quantal Bioscience Pty Ltd. , Sydney, NSW, Australia
                [3] 3Department of Biotechnology and Biomedicine, Technical University of Denmark , Lyngby, Denmark
                [4] 4Department of Biology, Section for Ecology and Evolution, University of Copenhagen , Copenhagen, Denmark
                Author notes

                Edited by: Sarah O'Flaherty, North Carolina State University, United States

                Reviewed by: Athanasios Zervas, Aarhus University, Denmark; Dieter Maurice Tourlousse, National Institute of Advanced Industrial Science and Technology (AIST), Japan

                *Correspondence: Sandra A. Olivier, sandra.olivier@ 123456quantalbioscience.com
                Article
                10.3389/fmicb.2023.1290756
                10740194
                38143859
                713c2438-5ba3-48a6-9266-fea054d178e6
                Copyright © 2023 Olivier, Bull, Strube, Murphy, Ross, Bowman and Chapman.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 08 September 2023
                : 15 November 2023
                Page count
                Figures: 0, Tables: 6, Equations: 1, References: 46, Pages: 15, Words: 10604
                Funding
                The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was funded by Quantal Bioscience Pty Ltd., and the Tasmanian Institute of Agriculture, University of Tasmania. MS was supported by the Danish National Research Foundation (DNRF137) and RM was supported by the Department of Biology at the University of Copenhagen and a European Research Council Consolidator grant (ERC-CoG-771349). The funders were not involved in the study design, analysis, interpretation of data, the writing of this article or the decision to submit it for publication.
                Categories
                Microbiology
                Original Research
                Custom metadata
                Evolutionary and Genomic Microbiology

                Microbiology & Virology
                lactobacillaceae,amplicon sequencing,nanopore,long read sequencing,metataxonomics,microbiome,rrna

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