PKPD modeling of the inoculum effect of combined ceftazidime/avibactam and colistin against KPC-3 <i>Klebsiella pneumoniae</i> isolate

The inoculum effect (IE) characterizes a decrease in the antimicrobial effect of antibiotics with increasing inoculum. To face antimicrobial resistance, antibiotic combinations are progressively used. In this context, the effect of combination may be affected by IE, especially drugs for which an IE has been described. The objective was to characterize the IE of a carbapenemase (KPC-3) <i>Klebsiella pneumoniae</i> isolate on the combination of ceftazidime/avibactam (CZA) and colistin (CST). <i>In vitro</i> time-kill curves with single and combined drugs were performed at four different inocula. The IE of each drug was described using pharmacokinetic/pharmacodynamic modeling, and interactions on IE were investigated with the general pharmacodynamic interaction model when drugs were combined. The IE was assessed by evaluating the significance of the parameters associated with the IE model compared to the no IE model and by comparing the CFU counts over time predicted with the IE model vs the no IE model. Rapid bacterial killing was observed at 10<sup>4</sup> CFU/mL. For both 5·10<sup>5</sup> and 10<sup>7</sup> CFU/mL inocula, initial decays followed by re-growth were observed with drugs alone, while the combination prevented the emergence of resistance. Eradication was never achieved at 10<sup>8</sup> CFU/mL. The IE was best modeled as a reduction of CZA maximum bactericidal effect and as an increase in CST EC<sub>50</sub> with increasing inoculum. However, no interaction between IEs was significant, meaning that CST did not modify the IE of CZA and inversely. IE may be important at least as demonstrated by <i>in vitro</i> antibiotic combination studies.

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Journal
Antimicrobial Agents and Chemotherapy
Published
2025-04-14
DOI
https://doi.org/10.1128/aac.01797-24
Primary Topic
Antibiotic Resistance in Bacteria
Type
article
Field-Weighted Citation Impact
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article

PKPD modeling of the inoculum effect of combined ceftazidime/avibactam and colistin against KPC-3 Klebsiella pneumoniae isolate

Jean‐Winoc Decousser, Romain Aubry, Julien M. Buyck, Patrice Nordmann et al.
Antimicrobial Agents and Chemotherapy
Antibiotic Resistance in Bacteria
article

PKPD modeling of the inoculum effect of combined ceftazidime/avibactam and colistin against KPC-3 Klebsiella pneumoniae isolate

Jean‐Winoc Decousser, Romain Aubry, Julien M. Buyck, Patrice Nordmann, Nicolas Grégoire, Laure Prouvensier, Alexia Chauzy, Sandrine Marchand, Sebastian G. Wicha
article en

Abstract

The inoculum effect (IE) characterizes a decrease in the antimicrobial effect of antibiotics with increasing inoculum. To face antimicrobial resistance, antibiotic combinations are progressively used. In this context, the effect of combination may be affected by IE, especially drugs for which an IE has been described. The objective was to characterize the IE of a carbapenemase (KPC-3) <i>Klebsiella pneumoniae</i> isolate on the combination of ceftazidime/avibactam (CZA) and colistin (CST). <i>In vitro</i> time-kill curves with single and combined drugs were performed at four different inocula. The IE of each drug was described using pharmacokinetic/pharmacodynamic modeling, and interactions on IE were investigated with the general pharmacodynamic interaction model when drugs were combined. The IE was assessed by evaluating the significance of the parameters associated with the IE model compared to the no IE model and by comparing the CFU counts over time predicted with the IE model vs the no IE model. Rapid bacterial killing was observed at 10<sup>4</sup> CFU/mL. For both 5·10<sup>5</sup> and 10<sup>7</sup> CFU/mL inocula, initial decays followed by re-growth were observed with drugs alone, while the combination prevented the emergence of resistance. Eradication was never achieved at 10<sup>8</sup> CFU/mL. The IE was best modeled as a reduction of CZA maximum bactericidal effect and as an increase in CST EC<sub>50</sub> with increasing inoculum. However, no interaction between IEs was significant, meaning that CST did not modify the IE of CZA and inversely. IE may be important at least as demonstrated by <i>in vitro</i> antibiotic combination studies.

Antimicrobial Agents and ChemotherapyVol. 69(5)
University of Fribourg (CH), Inserm (FR), Universität Hamburg (DE), École Nationale Vétérinaire d'Alfort (FR), Université Paris-Est Créteil (FR), Université de Poitiers (FR), Assistance Publique – Hôpitaux de Paris (FR), University of Lausanne (CH)
Agence Nationale de la Recherche, Institut National de la Santé et de la Recherche Médicale, Université de Poitiers
Good health and well-being
Openalex Percentile: Top 94%
Antibiotic Resistance in Bacteria
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