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A Mouse Model to Assess Innate Immune Response to Staphylococcus aureus Infection
Published on: February 28, 2019
Intracellular Staphylococcus aureus. A mechanism for the indolence of osteomyelitis
J K Ellington1, M Harris, L Webb
1Department of Orthopaedic Surgery,Wake Forest University School of Medicine, Winston Salem, North Carolina 27103, USA.
Abstract:
Staphylococcus aureus is the bacterial pathogen which is responsible for approximately 80% of all cases of human osteomyelitis. It can invade and remain within osteoblasts. The fate of intracellular Staph. aureus after the death of the osteoblast has not been documented. We exposed human osteoblasts to Staph. aureus. After infection, the osteoblasts were either lysed with Triton X-100 or trypsinised. The bacteria released from both the trypsinised and lysed osteoblasts were cultured and counted. Colonies of the recovered bacteria were then introduced to additional cultures of human osteoblasts. The number of intracellular Staph. aureus recovered from the two techniques was equivalent. Staph. aureus recovered from time zero and 24 hours after infection, followed by lysis/trypsinisation, were capable of invading a second culture of human osteoblasts. Our findings indicate that dead or dying osteoblasts are capable of releasing viable Staph. aureus and that Staph. aureus released from dying or dead osteoblasts is capable of reinfecting human osteoblasts in culture.
Insights
Viable Staphylococcus aureus (Staph. aureus) can be released from dead osteoblasts, the bone-forming cells. These released bacteria can then successfully reinfect new osteoblasts, contributing to osteomyelitis.
Area of Science:
- Microbiology
- Cell Biology
- Orthopedics
Background:
- Staphylococcus aureus is a primary cause of human osteomyelitis.
- This bacterium invades and persists within osteoblasts.
- The fate of intracellular bacteria after host cell death is unknown.
Purpose of the Study:
- To investigate the viability and infectivity of Staphylococcus aureus released from dead or dying osteoblasts.
- To understand the intracellular survival and release mechanism of Staph. aureus in osteomyelitis.
Main Methods:
- Human osteoblasts were infected with Staph. aureus.
- Osteoblasts were subsequently lysed or trypsinized to release intracellular bacteria.
- Released bacteria were cultured, quantified, and used to infect new osteoblast cultures.
Main Results:
- Equivalent numbers of Staph. aureus were recovered using both lysis and trypsinization methods.
- Staph. aureus recovered from infected osteoblasts (at time zero and 24 hours) could successfully invade a second osteoblast culture.
- These findings demonstrate the viability and reinfectivity of bacteria released from dead osteoblasts.
Conclusions:
- Dead or dying osteoblasts release viable Staphylococcus aureus.
- Staph. aureus released from compromised osteoblasts can re-initiate infection in new host cells.
- This mechanism may play a significant role in the persistence and recurrence of osteomyelitis.
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