# Quantitative metagenomics using a portable protocol

**Authors:** Kaiqin Bian, Andrea Busch, John Norton, Charles Bott, Raul Gonzalez, Kyle Curtis, Dienye Tolofari, Wendell Khunjar, Katherine E. Graham, Ameet J. Pinto

PMC · DOI: 10.1128/aem.02179-25 · Applied and Environmental Microbiology · 2026-02-24

## TL;DR

This paper introduces a portable and rapid workflow for quantitatively analyzing microbial communities in water samples using real-time sequencing.

## Contribution

The novel rD+rQ workflow enables field-deployable, accurate, and rapid microbial quantitation using real-time Nanopore sequencing and multispecies calibration.

## Key findings

- The rD+rQ workflow achieves species-level identification and quantitation comparable to digital PCR.
- BSINC calibration using multispecies spike-ins improves accuracy over single-fragment or single-organism controls.
- Dynamic detection and quantitation limits enhance precision in microbial quantitation.

## Abstract

A field-deployable DNA sequencing approach for quantitative microbial community profiling can enable rapid responses for a range of applications in the water sector—from process control to wastewater surveillance. Current quantitative approaches require complex instrumentation and have long turnaround times for DNA recovery and absolute quantitation. In this study, we report a field-deployable rapid detection and rapid absolute quantitation (rD+rQ) workflow that leverages real-time Nanopore sequencing for quantitative metagenomics. This workflow integrates a high-molecular-weight DNA recovery protocol for diverse environmental matrices of relevance to the water sector, and multiplexed Nanopore sequencing with barcoded spike-in-based calibration (BSINC). BSINC using multispecies genomic spike-in controls exhibits significantly higher calibration accuracy compared to conventional approaches that utilize either a single DNA fragment or single organism spike-in controls. Dynamic detection and quantitation limits were established based on the coverage fraction of sequenced genomes and the coefficient of variation of genome copy numbers across replicates to enhance the accuracy and precision of microbial quantitation. The rD+rQ workflow achieves species-level identification and absolute quantitative results comparable to digital PCR in environmental samples. This portable laboratory and easy-to-use rD+rQ workflow should facilitate rapid decision-making for the water industry.

Rapid and real-time monitoring of microbial communities is critical for a vast array of applications in environmental microbiology and biotechnology. While recent developments in portable sequencing technologies and associated workflows make onsite analysis possible, these approaches do not provide quantitative data on microbial concentrations. In this study, we present a sample and data processing workflow that enables nontargeted and quantitative microbial community profiling and demonstrate its validity on complex environmental samples. This approach for acquiring quantitative data can drive rapid decision-making from bioprocess control to wastewater-based epidemiology.

## Full-text entities

- **Chemicals:** water (MESH:D014867)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12997851/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12997851/full.md

## References

68 references — full list in the complete paper: https://tomesphere.com/paper/PMC12997851/full.md

---
Source: https://tomesphere.com/paper/PMC12997851