# PMA-qPCA: Accelerating the market release of high-quality Bradyrhizobium diazoefficiens inoculant

**Authors:** Mariana Cap, Camila Frydman, Antonella Galiñanes, Camila Aranguiz, Irina Faraco, Luisina Andriolo, Viviana Parreño, Marina Mozgovoj, Mohammad H. Ghazimoradi, Mohammad H. Ghazimoradi, Mohammad H. Ghazimoradi

PMC · DOI: 10.1371/journal.pone.0325878 · PLOS One · 2025-10-21

## TL;DR

This paper introduces a fast and accurate method to count viable Bradyrhizobium diazoefficiens in inoculants, reducing testing time from 120 to 5 hours.

## Contribution

The first validated PMA-qPCR assay for quantifying Bradyrhizobium diazoefficiens in commercial inoculants.

## Key findings

- The PMA-qPCR assay showed high efficiency (90–105%) and a detection range from 8.74 to 3.14 log CFU/mL.
- The method achieved strong correlation (R² of 0.82) with traditional plate counting while drastically reducing processing time.
- It successfully distinguished viable bacteria from non-viable cells in serial dilutions.

## Abstract

Traditional culture-based quantification of Bradyrhizobium diazoefficiens in inoculants presents significant limitations due to its labor-intensive and time-consuming nature. To address this limitation, we aimed to validate a propidium monoazide quantitative PCR (PMA-qPCR) assay as a rapid and reliable alternative for estimating Bradyrhizobium diazoefficiens counts in commercial inoculants. Key experiments optimized PMA concentration (50, 75 and 100 µM) to selectively inhibit DNA amplification from non-viable cells without interfering with viable cell signal. Assay´s efficiency, limit of detection and quantification, intra-assay repeatability and inter-assay reproducibility were determined. The assay demonstrated high efficiency (90–105%), a limit of detection (LOD) of 3.14 log CFU/mL, and a dynamic range from 8.74 to 3.14 log CFU/mL. Robust intra-assay repeatability (SD < 0.3) and inter-assay reproducibility (CV < 10%) were confirmed. The method successfully distinguished quarter-strength and 10-fold serial dilutions of viable bacteria, even in the presence of non-viable cells. Final validation against standard plate counting showed a strong linear correlation with an R² of 0.82. Crucially, this PMA-qPCR assay reduced processing time from 120 hours to just 5 hours, offering a significant improvement in turnaround time while maintaining strong agreement with the reference method. This study marks the first application of PMA-qPCR for Bradyrhizobium diazoefficiens quantification in inoculants, highlighting its potential as a high-throughput tool to enhance efficiency and precision for industrial batch-to-batch quality control.

## Linked entities

- **Species:** Bradyrhizobium diazoefficiens (taxon 1355477)

## Full-text entities

- **Chemicals:** propidium monoazide (MESH:C533957), PMA (-)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Bradyrhizobium diazoefficiens (species) [taxon 1355477]

## Full text

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## Figures

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## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12539688/full.md

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Source: https://tomesphere.com/paper/PMC12539688