Phagocytosis by macrophages decreases the radiance of bioluminescent Staphylococcus aureus

Abstract Background In vivo evaluations of the antimicrobial efficacy of biomaterials often use bioluminescent imaging modalities based on bioluminescent bacteria to allow follow-up in single animals. Bioluminescence production by bacteria is dependent on their metabolic activity. It is well known t...

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Main Authors: Elles C. Boonstra, Liliana Agresti, Henny C. van der Mei, Paul C. Jutte, Jelmer Sjollema
Format: Article
Language:English
Published: BMC 2025-01-01
Series:BMC Microbiology
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Online Access:https://doi.org/10.1186/s12866-024-03674-x
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author Elles C. Boonstra
Liliana Agresti
Henny C. van der Mei
Paul C. Jutte
Jelmer Sjollema
author_facet Elles C. Boonstra
Liliana Agresti
Henny C. van der Mei
Paul C. Jutte
Jelmer Sjollema
author_sort Elles C. Boonstra
collection DOAJ
description Abstract Background In vivo evaluations of the antimicrobial efficacy of biomaterials often use bioluminescent imaging modalities based on bioluminescent bacteria to allow follow-up in single animals. Bioluminescence production by bacteria is dependent on their metabolic activity. It is well known that several factors can influence the metabolism of bacteria, such as the use of antimicrobials and changes in bacterial growth phase. However, little is known about the influence of intracellular residence of bacteria on bioluminescence. For example, Staphylococcus aureus can survive in the peri-implant tissue and is known to survive intracellularly in macrophages. Results In this study, we evaluated the bioluminescent radiance of S. aureus upon phagocytosis by macrophages. We showed that S. aureus reduced its bioluminescence upon phagocytosis by macrophages compared to S. aureus in a single culture. Simultaneously, bacterial numbers as measured by colony-forming units remained constant over time. S. aureus was released extracellularly as a result of macrophage cell death. Following this release, the bacteria increased their bioluminescence again. Replenishment of fresh macrophages showed an immediate increase in bioluminescence. Moreover, the addition of fresh macrophages showed a diminished decrease in bioluminescence at 24 h of coculture, but this effect did not last. Conclusion Together, this study demonstrates that phagocytosis by macrophages decreases bioluminescence of S. aureus, which is an important factor to consider when using bioluminescent imaging to study the infection process in an in vivo model.
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spelling doaj-art-c1e6dcad5ef64bbe988e0fd679ea26102025-01-12T12:10:13ZengBMCBMC Microbiology1471-21802025-01-0125111010.1186/s12866-024-03674-xPhagocytosis by macrophages decreases the radiance of bioluminescent Staphylococcus aureusElles C. Boonstra0Liliana Agresti1Henny C. van der Mei2Paul C. Jutte3Jelmer Sjollema4Department of Orthopedics, University Medical Center GroningenDepartment of Biomaterials and Biomedical Technology, University Medical Center GroningenDepartment of Biomaterials and Biomedical Technology, University Medical Center GroningenDepartment of Orthopedics, University Medical Center GroningenDepartment of Biomaterials and Biomedical Technology, University Medical Center GroningenAbstract Background In vivo evaluations of the antimicrobial efficacy of biomaterials often use bioluminescent imaging modalities based on bioluminescent bacteria to allow follow-up in single animals. Bioluminescence production by bacteria is dependent on their metabolic activity. It is well known that several factors can influence the metabolism of bacteria, such as the use of antimicrobials and changes in bacterial growth phase. However, little is known about the influence of intracellular residence of bacteria on bioluminescence. For example, Staphylococcus aureus can survive in the peri-implant tissue and is known to survive intracellularly in macrophages. Results In this study, we evaluated the bioluminescent radiance of S. aureus upon phagocytosis by macrophages. We showed that S. aureus reduced its bioluminescence upon phagocytosis by macrophages compared to S. aureus in a single culture. Simultaneously, bacterial numbers as measured by colony-forming units remained constant over time. S. aureus was released extracellularly as a result of macrophage cell death. Following this release, the bacteria increased their bioluminescence again. Replenishment of fresh macrophages showed an immediate increase in bioluminescence. Moreover, the addition of fresh macrophages showed a diminished decrease in bioluminescence at 24 h of coculture, but this effect did not last. Conclusion Together, this study demonstrates that phagocytosis by macrophages decreases bioluminescence of S. aureus, which is an important factor to consider when using bioluminescent imaging to study the infection process in an in vivo model.https://doi.org/10.1186/s12866-024-03674-xHost-Pathogen interactionIntracellular survivalInfectionsIn vivo imagingCoculture of bacteria and mammalian cellsImmune evasion
spellingShingle Elles C. Boonstra
Liliana Agresti
Henny C. van der Mei
Paul C. Jutte
Jelmer Sjollema
Phagocytosis by macrophages decreases the radiance of bioluminescent Staphylococcus aureus
BMC Microbiology
Host-Pathogen interaction
Intracellular survival
Infections
In vivo imaging
Coculture of bacteria and mammalian cells
Immune evasion
title Phagocytosis by macrophages decreases the radiance of bioluminescent Staphylococcus aureus
title_full Phagocytosis by macrophages decreases the radiance of bioluminescent Staphylococcus aureus
title_fullStr Phagocytosis by macrophages decreases the radiance of bioluminescent Staphylococcus aureus
title_full_unstemmed Phagocytosis by macrophages decreases the radiance of bioluminescent Staphylococcus aureus
title_short Phagocytosis by macrophages decreases the radiance of bioluminescent Staphylococcus aureus
title_sort phagocytosis by macrophages decreases the radiance of bioluminescent staphylococcus aureus
topic Host-Pathogen interaction
Intracellular survival
Infections
In vivo imaging
Coculture of bacteria and mammalian cells
Immune evasion
url https://doi.org/10.1186/s12866-024-03674-x
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