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Chicken Embryo as an In Vivo Model to Revive Viable but Non-Culturable Pathogens
Published on: May 30, 2025
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'Viable but non-culturable cells' are dead.
1Department of Animal Science, Jeonbuk National University, Jeonju-si, Jeollabuk-do, 54896, South Korea.
Environmental Microbiology
|March 16, 2021
Summary
Bacteria can enter a dormant state to survive stress, like antibiotics. However, research shows that only viable persister cells, not dead cell shells, can revive and reconstitute infections.
Area of Science:
- Microbiology
- Bacterial Physiology
- Stress Response
Background:
- Bacteria can enter dormant states to survive environmental stress, including antibiotics.
- Persister cells, a subpopulation of bacteria, inactivate ribosomes to become dormant.
- Stress can also lead to the formation of dead, hollow cell shells.
Purpose of the Study:
- To differentiate between viable persister cells and non-viable cell shells.
- To clarify the mechanisms of bacterial resuscitation after stress.
- To address the misclassification of dead cell shells as viable in microbiology.
Main Methods:
- Analysis of bacterial dormancy and resuscitation pathways.
- Distinguishing between persister cells and cell shells based on viability markers.
- Experimental data interpretation to assess resuscitation potential.
Main Results:
- Persister cells possess an elegantly regulated pathway for dormancy and resuscitation.
- Dead cell shells, despite intact membranes, lack the cellular content for revival.
- Resuscitation observed in stressed bacterial populations is attributed to viable persister cells.
Conclusions:
- Bacterial resuscitation after stress is mediated by viable persister cells, not dead cell shells.
- The concept of 'viable but non-culturable cells' (VBNCs) may have historically misidentified dead cell shells as viable.
- Accurate identification of dormant bacterial states is crucial for understanding infection persistence and treatment failure.
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