Application

Single-Cell Microbial Genomics Unveil the microbial universe with unprecedented precision and scale

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Microbial communities influence critical biological and ecological processes, yet much of their diversity and function remain poorly understood. Methods like 16S rRNA sequencing and shotgun metagenomics provide broad overviews but lack the resolution to characterize individual microbes. High-throughput single-cell microbial genomics bridges this gap, enabling detailed analysis of tens of thousands of cells to uncover their diversity, functions, and evolutionary dynamics.

High-throughput SINGLE-CELL genomics
  • Taxonomic resolution: strain-level
  • Functional profiling: yes
  • Linkage with additional DNA: yes
  • De novo assembly: yes (SAGs)
  • Absolute quantification: yes
16S rRNA
sequencing
  • Taxonomic resolution: genus-level
  • Functional profiling: no
  • Linkage with additional DNA: no
  • De novo assembly: no
  • Absolute quantification: no
Shotgun
metagenomics
  • Taxonomic resolution: species-level
  • Functional profiling: yes
  • Linkage with additional DNA: no
  • De novo assembly: limited (MAGs)
  • Absolute quantification: no

OBTAIN HIGH-QUALITY SINGLE AMPLIFIED GENOMES (SAGs) AT SCALE WITH SPCs

ENCAPSULATION
Isolate individual cells into Semi-Permeable Capsules.
LYSIS AND DNA PURIFICATION
Lyse cells under harsh chemical & enzymatic conditions to access DNA.
GENOME AMPLIFICATION
Amplify whole genomes with MDA optimized for even coverage.
SINGLE CELL BARCODING
Attach barcodes to single amplified genomes (SAGs) by iterative rounds of ligation.
LIBRARY PREPARATION AND SEQUENCING
Process labeled DNA using commercial short-read or long-read library preparation kits.
DATA ANALYSIS
Obtain demultiplexed single amplified genomes (SAGs).

Our single-cell microbial genomics solution is library prep agnostic, allowing you to choose your preferred sequencing provider for either short-read or long-read sequencing

SHORT-READ SEQUENCING

Profile microbial diversity and assemble genomes efficiently.

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LONG-READ SEQUENCING

Characterize complex genomic regions and repetitive sequences.

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PROOF OF CONCEPT

First, we processed well-characterized E. coli and B. subtilis bacteria. Upon sequencing of ~3,000 single-amplified genomes (SAGs), key technical metrics, such as cross-contamination and genome recovery, were measured to evaluate workflow performance. Next, we analyzed an oral microbiome sample, comparing the results of SAG sequencing to in silico-constructed metagenomes.

- Excellent genome retention in semi-permeable capsules.

- >90% genome recovery per SAG at sequencing depths below 10x.

- Co-occurrence of AMR and virulence genes preserved and linked to the host in SAG data.

- SAG assemblies produced longer contigs than corresponding in silico MAGs.

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BENCHMARKING

We sequenced ~10,000 SAGs prepared from a commercially available microbial community standard consisting of bacterial cells with varying characteristics, such as Gram stain, GC content, and genome size. The single-cell approach was benchmarked against shotgun metagenomics.

ENVIRONMENTAL SAMPLES

We compared the results of sequencing ~1,500 SAGs prepared from soil and aquatic samples to matched bulk metagenomic datasets. To account for differences arising from the cell lysis method, metagenomic libraries were prepared using both standard bead beating and chemical lysis methods.

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Applications

MICROBIOME PROFILING

Identify microbial strains within complex communities at high throughput for accurate insights into microbiome composition and functions.

MICROBIAL DARK MATTER DISCOVERY

Uncover hidden microbial diversity and functional potential by assembling genomes of uncultivated microbes de novo.

VIRULENCE & RESISTANCE

Identify microbial strains within complex communities at high throughput for accurate insights into microbiome composition and functions.

VIROLOGY

Perform de novo viral genome assembly in environmental samples and link viruses to hosts to uncover ecological dynamics and interactions.

EXTRACHROMOSOMAL DNA LINKAGE

SPC technology captures both chromosomal and extrachromosomal DNA by tagging them with the same barcode during the barcoding process.

Linking mobile genetic elements identifies horizontal gene transfer events, while associations with viruses reveal viral-host interactions. Additionally, linking genomes of co-occurring microorganisms offer valuable insights into microbial community dynamics.

Link gDNA to viruses infecting cells
Link gDNA of two co-occurring microorganisms
Link gDNA to plasmids

MINI-METAGENOMICS

When detailed strain-level insights are not required, SPCs can be used for mini-metagenomics by encapsulating multiple cells within a single capsule. This cost-effective approach allows for the analysis of microbial community composition and interactions, shedding light on ecological roles and functional relationships within diverse environments.

Targeted Sequencing

Single-cell whole-genome sequencing offers comprehensive insights, but many biological questions can be effectively addressed by analyzing specific genes. Targeted sequencing provides a cost-effective approach to uncover gene co-occurrence, interactions, and functional linkages. This method is particularly useful for linking traits, such as antimicrobial resistance, to taxonomic information (via phylogenetic marker genes).

Barcoded

Barcode amplified genes of interest to analyze co-occurrence quantitatively

  • 100s of targets possible
  • Digital analysis
  • Moderate cost
  • Link genes to microbes at genus/species level
Concatenated

Skip barcoding and analyze gene co-occurrence qualitatively

  • Up to 10 targets
  • Qualitative
  • Cost efficient
  • Link genes to microbes at genus/species level
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Hybridization capture

Capture genes of interest and link them to single-cell genomes for comprehensive insights

  • 100s of targets possible
  • Digital analysis
  • Higher cost
  • Link genes to individual microbes (strain-level)
Read Application Note
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