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Updated: May 3, 2026

High Throughput, Real-time, Dual-readout Testing of Intracellular Antimicrobial Activity and Eukaryotic Cell Cytotoxicity
Published on: November 16, 2016
Interaction of intraleukocytic bacteria and antibiotics
Abstract:
Bacteria that survive inside polymorphonuclear neutrophils (PMN) following phagocytosis are protected from the bactericidal action of most antibiotics. Two possible explanations are altered metabolism by intraleukocytic bacteria or failure of antibiotics to enter the phagosome. The oxygen consumption of intraleukocytic and extraleukocytic bacteria was measured as an index of bacterial metabolism. PMN respiration and bactericidal activity were suppressed with large doses of hydrocortisone and extraleukocytic bacterial oxygen consumption was abolished by the addition of lysostaphin. Intraleukocytic bacterial continued to consume oxygen suggesting that surviving ingested micro-organisms are metabolically active. Neither penicillin (which cannot kill intraleukocytic bacteria) nor rifampin (which can kill intraleukocytic bacteria) was bactericidal for staphylococci at 5 degrees C. Thus, rifampin is not uniquely able to kill "resting" bacteria.Intraleukocytic or extraleukocytic Staphylococcus aurens were incubated with [benzyl-(14)C]penicillin for 2 h at 37 degrees C. Live intraleukocytic bacteria bound only 13% as much penicillin as live bacteria incubated with killed PMN. To measure the penetration of antibiotics into PMN, [(14)C]rifampin and [(14)C]penicillin were measured in leukocyte pellets and in the supernatant fluid. The total water space in the pellets was quantitated using tritium water and the extracellular water space was measured using Na(235)SO(4). All penicillin associated with the cell pellet could be accounted for in extracellular water. Thus penicillin was completely excluded from the leukocytes. Rifampin was concentrated in the cell pellet 2.2 times when compared with the supernatant concentration. These studies suggest that a likely explanation for the survival of phagocytized bacteria in the presence of high concentrations of most antibiotics is the inability of the antibiotic to enter the phagocyte. Rifampin, which is highly lipid soluble, can enter leukocytes and kill intracellular bacteria.
Insights
Bacteria surviving inside immune cells are protected from antibiotics because drugs cannot enter these cells. Rifampin, unlike penicillin, can penetrate phagocytes to kill intracellular bacteria, explaining its effectiveness against resistant microbes.
Area of Science:
- Microbiology and Immunology
- Pharmacology and Drug Discovery
Background:
- Bacteria phagocytized by polymorphonuclear neutrophils (PMN) exhibit resistance to common antibiotics.
- Survival mechanisms for intracellular bacteria include altered metabolism or antibiotic exclusion from the phagosome.
Purpose of the Study:
- To investigate the reasons behind antibiotic ineffectiveness against intracellular bacteria.
- To determine if antibiotics can penetrate phagocytic cells to reach ingested bacteria.
- To compare the intracellular efficacy of penicillin and rifampin.
Main Methods:
- Measured oxygen consumption of intracellular and extracellular bacteria to assess metabolic activity.
- Used radiolabeled penicillin and rifampin to quantify antibiotic penetration into PMN.
- Quantified intracellular and extracellular water spaces within PMN pellets.
Main Results:
- Intracellular bacteria remained metabolically active, consuming oxygen.
- Penicillin was completely excluded from PMN, with no intracellular accumulation detected.
- Rifampin demonstrated significant penetration into PMN, concentrating 2.2-fold within the cell pellet.
Conclusions:
- The primary reason for intracellular bacterial survival is the inability of most antibiotics to enter phagocytic cells.
- Rifampin's lipophilicity allows it to penetrate PMN, enabling it to kill intracellular bacteria.
- Antibiotic entry into phagocytes is critical for eradicating intracellular bacterial infections.
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