# Effects of Comparative Killing by Pradofloxacin and Seven Other Antimicrobials Against Varying Bacterial Densities of Swine Isolates of Pasteurella multocida

**Authors:** Joseph M. Blondeau, Shantelle D. Fitch

PMC · DOI: 10.3390/microorganisms13020221 · Microorganisms · 2025-01-21

## TL;DR

This study compares how well pradofloxacin and other antibiotics kill bacteria in pigs, showing pradofloxacin is highly effective.

## Contribution

The study demonstrates pradofloxacin's rapid and effective killing of Pasteurella multocida across various bacterial densities and drug concentrations.

## Key findings

- Pradofloxacin killed 92–96.9% of cells at mutant prevention concentration within 2–24 hours.
- Pradofloxacin achieved 99.9–100% kill at maximum serum concentration after 12–24 hours.
- Pradofloxacin was rapidly bactericidal at maximum tissue concentration against high bacterial densities.

## Abstract

Bacterial killing is important for recovering from infection. Pasteurella multocida is a key bacterial pathogen causing swine respiratory disease and is associated with substantial mortality. Antimicrobial therapy remains an important therapeutic intervention for treating infected animals. Pradofloxacin (fluoroquinolone) is the most recently approved antimicrobial agent for treating pigs with swine respiratory disease. We compared in vitro killing of swine P. multocida strains by pradofloxacin in comparison to ceftiofur, enrofloxacin, florfenicol, marbofloxacin, tildipirosin, tilmicosin, and tulathromycin over a range of bacterial densities and four clinically relevant drug concentrations. Pradofloxacin killed 92–96.9% of cells across 106–108 cfu/mL densities at the mutant prevention drug concentration following 2–24 h of drug exposure, 96.9–98.9% of cells across 106–109 cfu/mL at the maximum serum drug concentration following 30 min of drug exposure, increasing to 99.9–100% kill following 12–24 h of drug exposure. At the maximum tissue drug concentration and against bacterial densities of 106–109 cfu/mL, pradofloxacin killed 91.3–99.8% of cells following 2 h of drug exposure, which increased to 99.9–100% kill following 12–24 h of drug exposure. Pradofloxacin was rapidly bactericidal across a range of bacterial densities and at clinically relevant drug concentrations. Pradofloxacin will be an important antibiotic for treating pigs with swine respiratory disease and where clinically indicated.

## Linked entities

- **Chemicals:** Pradofloxacin (PubChem CID 9802884), ceftiofur (PubChem CID 6328657), enrofloxacin (PubChem CID 71188), florfenicol (PubChem CID 114811), marbofloxacin (PubChem CID 60651), tildipirosin (PubChem CID 24860548), tilmicosin (PubChem CID 5282521), tulathromycin (PubChem CID 9832301)
- **Species:** Pasteurella multocida (taxon 747)

## Full-text entities

- **Diseases:** infected (MESH:D007239), respiratory disease (MESH:D012140)
- **Chemicals:** enrofloxacin (MESH:D000077422), marbofloxacin (MESH:C080260), fluoroquinolone (MESH:D024841), tulathromycin (MESH:C485204), tilmicosin (MESH:C052319), ceftiofur (MESH:C053503), tildipirosin (MESH:C576258), Pradofloxacin (MESH:C507250), florfenicol (MESH:C035534)
- **Species:** Pasteurella multocida (species) [taxon 747], Sus scrofa (pig, species) [taxon 9823]

## Full text

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## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC11857592/full.md

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Source: https://tomesphere.com/paper/PMC11857592