# Comparison of Two DNA Labeling Dyes Commonly Used to Detect Metabolically Active Bacteria

**Authors:** Leena Malayil, Suhana Chattopadhyay, Neha Sripathi, Emmanuel F. Mongodin, Amy R. Sapkota

PMC · DOI: 10.3390/microorganisms13051015 · Microorganisms · 2025-04-28

## TL;DR

This study compares two DNA labeling dyes, BrdU and PMA, to detect active bacteria in environmental and product samples using sequencing.

## Contribution

The study provides a direct comparison of BrdU and PMA labeling methods for identifying metabolically active bacteria in diverse sample types.

## Key findings

- BrdU-labeled samples showed lower alpha diversity compared to PMA-treated and non-treated samples.
- Pseudomonas was more abundant in BrdU-treated samples, while Acinetobacter was more abundant in non-treated samples.
- PMA-treated samples overestimated the fraction of metabolically active bacteria compared to BrdU-treated samples.

## Abstract

Bacteria are ubiquitous in the environment and critical to human health and disease, yet only a small fraction can be identified through standard culture methods. Advances in next-generation sequencing techniques have improved bacterial identification, but these DNA-based methods cannot distinguish live bacteria from relic DNA. Recently, DNA-labeling dyes (e.g., 5-bromo-2′-deoxyuridine [BrdU] and propidium monoazide [PMA]) have been used to detect metabolically active bacteria in different sample types. Here, we compare BrdU and PMA in combination with 16SrRNA gene sequencing to characterize metabolically active bacteria in two different sample types: (1) manufactured products (n = 78; cigarettes, hookah, and little cigar) and (2) natural samples (n = 186; rainwater, soil, and produce). Metabolically active bacterial communities identified in BrdU-labeled samples had lower alpha diversity than that of PMA-treated and non-treated samples. Pseudomonas, Sphingomonas, Enterobacter, and Acinetobacter were observed in all the samples tested. Irrespective of sample type, Pseudomonas was predominant in BrdU-treated samples, while Acinetobacter was more abundant in non-treated samples compared to PMA-treated samples. We also observed that PMA-treated samples tend to overestimate the metabolically active bacterial fraction compared to BrdU-treated samples. Overall, our study highlights how different labeling techniques influence bacterial community analysis findings, underscoring the need for careful selection of labeling approaches when assessing environmental samples.

## Linked entities

- **Chemicals:** BrdU (PubChem CID 6035), PMA (PubChem CID 171116383)
- **Species:** Pseudomonas (taxon 286), Sphingomonas (taxon 13687), Enterobacter (taxon 547), Acinetobacter (taxon 469)

## Full-text entities

- **Chemicals:** propidium monoazide (MESH:C533957), 5-bromo-2'-deoxyuridine (MESH:D001973), PMA (-)
- **Species:** Acinetobacter (genus) [taxon 469], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Enterobacter (genus) [taxon 547], Homo sapiens (human, species) [taxon 9606], Sphingomonas (genus) [taxon 13687], Pseudomonas (RNA similarity group I, genus) [taxon 286]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12114394/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12114394/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12114394/full.md

---
Source: https://tomesphere.com/paper/PMC12114394