# Performance of time-lapsed turbidimetry and agar plating as bacterial quantification methods

**Authors:** Angelika Dewicki, Matthew Henkel, Norie Sugitani, Alexander Applegate, Brian T. Campfield

PMC · DOI: 10.1128/spectrum.01807-25 · Microbiology Spectrum · 2025-12-26

## TL;DR

This study compares two bacterial quantification methods and finds that liquid broth turbidimetry is more precise and sensitive than agar plating, especially at low bacterial densities.

## Contribution

The study provides a systematic comparison of agar plating and turbidimetry for quantifying diverse clinically relevant pathogens.

## Key findings

- Both methods showed strong correlation across a wide range of bacterial concentrations.
- Turbidimetry was more sensitive and precise at low bacterial densities.
- Turbidimetry better distinguished bacterial burdens in an in vivo mouse infection model.

## Abstract

Accurate bacterial quantification is crucial for studying microbial pathogenesis, host-pathogen interactions, and therapeutic interventions. Two widely used methods include agar plating with colony-forming unit (CFU) enumeration and time-lapsed turbidimetry in liquid broth culture. While agar plating remains the gold standard in both in vitro and in vivo infection models, liquid broth turbidimetry is commonly used to assess growth kinetics, microbial fitness, antibiotic susceptibility, and bacterial genetics. While strain-specific CFU and turbidimetry (OD) calibration studies exist, a comprehensive and systematic comparison of these methods for quantifying a broad array of clinically relevant pathogens remains largely unexplored. Here, we conducted a head-to-head comparison of agar plating and liquid broth turbidimetry to quantify the growth of Klebsiella pneumoniae, Pseudomonas aeruginosa, and Staphylococcus aureus in vitro and evaluated their performance in vivo using a murine model of K. pneumoniae pulmonary infection. Across all pathogens tested, both methods exhibited strong correlation over a broad dynamic range (6–7 log10 dilutions). Liquid broth turbidimetry demonstrated enhanced sensitivity at low bacterial densities, as well as greater precision. In the in vivo murine pneumonia model, this method more accurately distinguished bacterial burdens at the site of infection (lung) and dissemination (spleen) between wild-type and Toll-like receptor 4 knockout mice. Overall, liquid broth turbidimetry is a reliable alternative to agar plating with a high degree of correlation for bacterial quantification and improved precision, highlighting its potential utility in studies of bacteriology and infectious diseases.

Accurate bacterial quantification is fundamental to microbiology research and clinical diagnostics. While agar plating is a widely used method, our study demonstrates that liquid broth turbidimetry provides accurate bacterial quantification, which is fundamental to microbiology research and clinical diagnostics. While agar plating is a widely used method, our study demonstrates that liquid broth turbidimetry provides a highly correlative and more precise approach for quantifying diverse, clinically relevant bacterial pathogens, including when dealing with low bacterial density. The enhanced sensitivity and precision may be valuable for early infection detection, monitoring treatment efficacy, and understanding microbial dynamics in research settings where accurate quantification of even low-density organisms is essential. The findings support considering liquid broth turbidimetry as a complementary or alternative method for bacterial growth quantification.

## Linked entities

- **Species:** Klebsiella pneumoniae (taxon 573), Pseudomonas aeruginosa (taxon 287), Staphylococcus aureus (taxon 1280), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Tlr4 (toll-like receptor 4) [NCBI Gene 21898] {aka Lps, Ly87, Ran/M1, Rasl2-8}
- **Diseases:** bacterial (MESH:D001424), infectious diseases (MESH:D003141), K. pneumoniae pulmonary infection (MESH:D011014), infection (MESH:D007239)
- **Chemicals:** agar (MESH:D000362)
- **Species:** Pseudomonas aeruginosa (species) [taxon 287], Staphylococcus aureus (species) [taxon 1280], Mus musculus (house mouse, species) [taxon 10090], Klebsiella pneumoniae (species) [taxon 573]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12889079/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12889079/full.md

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Source: https://tomesphere.com/paper/PMC12889079