High-throughput single-cell isolation of Bifidobacterium strains from the gut microbiome

preprint OA: closed CC-BY-NC-ND-4.0
📄 Open PDF Full text JSON View at publisher

Abstract

ABSTRACT While metagenomic studies can highlight strain-level diversity within microbial communities, the diversity obtained is often incomplete. Moreover, their utility for phenotypic characterizations remains hampered without the subjacent, systematic isolation procedures required with traditional culturomics. In this work, we examined the capabilities of a commercially available high-throughput single-cell dispensing solution to selectively target and isolate diverse strains of a genus of interest, Bifidobacterium , from fecal samples. The general performance of the single-cell dispenser was first assessed, revealing a low doublet frequency of 11.5% and an ability to preserve global genus diversity when a mixed culture of Bifidobacterium was dispensed. Culturing-related factors including the use of an effective selection medium, such as the Bifidus Selective Medium supplemented with mupirocin (BSM-MUP), and the length of incubation were found to be critical in determining isolation success. Leveraging these results, we obtained a total of 622 viable isolates from five Singaporean fecal samples, among which ∼98.7% were bifidobacteria. Whole-genome sequencing of 96 isolates revealed six different Bifidobacterium species with both inter- and intra-subject lineage diversity, and the majority of the assemblies were not previously captured using metagenomic sequencing. Our findings validate the ability of high-throughput culturomics to recover diverse, novel bacterial strains and open up the possibility to robustly interrogate their functional characteristics, advancing our understanding of important microbiomes. IMPORTANCE The field of microbial culturomics is still in its early stages. Enhancing our ability to isolate and phenotypically test bacterial strains from their multicellular environment is crucial for advancing microbiome research and healthcare development. Given the time- and cost-inefficiencies of traditional culturing methods, a more efficient, high-throughput approach to obtain isolates is needed. In the present study, we assessed a single-cell dispensing platform and developed a workflow to isolate diverse Bifidobacterium strains from fecal samples. We demonstrated here the capability of this novel technology to efficiently obtain hundreds of isolates of a targeted organism, covering both species and strain diversities. This generalizable and scalable method allows for the high-throughput recovery of microbes with little optimization needed for novel targets, providing a fundamental step in improving the culturomic framework to complement metagenomic approaches and enable isolate-level functional studies of important microbiomes.
Full text 2,768 characters · extracted from oa-html · click to expand
ABSTRACT While metagenomic studies can highlight strain-level diversity within microbial communities, the diversity obtained is often incomplete. Moreover, their utility for phenotypic characterizations remains hampered without the subjacent, systematic isolation procedures required with traditional culturomics. In this work, we examined the capabilities of a commercially available high-throughput single-cell dispensing solution to selectively target and isolate diverse strains of a genus of interest, Bifidobacterium, from fecal samples. The general performance of the single-cell dispenser was first assessed, revealing a low doublet frequency of 11.5% and an ability to preserve global genus diversity when a mixed culture of Bifidobacterium was dispensed. Culturing-related factors including the use of an effective selection medium, such as the Bifidus Selective Medium supplemented with mupirocin (BSM-MUP), and the length of incubation were found to be critical in determining isolation success. Leveraging these results, we obtained a total of 622 viable isolates from five Singaporean fecal samples, among which ∼98.7% were bifidobacteria. Whole-genome sequencing of 96 isolates revealed six different Bifidobacterium species with both inter- and intra-subject lineage diversity, and the majority of the assemblies were not previously captured using metagenomic sequencing. Our findings validate the ability of high-throughput culturomics to recover diverse, novel bacterial strains and open up the possibility to robustly interrogate their functional characteristics, advancing our understanding of important microbiomes. IMPORTANCE The field of microbial culturomics is still in its early stages. Enhancing our ability to isolate and phenotypically test bacterial strains from their multicellular environment is crucial for advancing microbiome research and healthcare development. Given the time- and cost-inefficiencies of traditional culturing methods, a more efficient, high-throughput approach to obtain isolates is needed. In the present study, we assessed a single-cell dispensing platform and developed a workflow to isolate diverse Bifidobacterium strains from fecal samples. We demonstrated here the capability of this novel technology to efficiently obtain hundreds of isolates of a targeted organism, covering both species and strain diversities. This generalizable and scalable method allows for the high-throughput recovery of microbes with little optimization needed for novel targets, providing a fundamental step in improving the culturomic framework to complement metagenomic approaches and enable isolate-level functional studies of important microbiomes. Competing Interest Statement The authors have declared no competing interest.

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-html

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. This is a recent paper (2025) — citers typically take a year or two to land, and the OpenAlex reference graph may still be filling in.

Source provenance

europepmc
last seen: 2026-05-20T01:45:00.602351+00:00
unpaywall
last seen: 2026-05-24T02:00:01.246996+00:00
License: CC-BY-NC-ND-4.0