New Parameters to Quantitatively Express the Invasiveness of Bacterial Strains from Implant-Related Orthopaedic Infections into Osteoblast Cells.
Davide CampocciaLucio MontanaroStefano RavaioliIlaria CanginiFrancesca TestoniLivia VisaiCarla Renata ArciolaPublished in: Materials (Basel, Switzerland) (2018)
Complete eradication of bacterial infections is often a challenging task, especially in presence of prosthetic devices. Invasion of non-phagocytic host cells appears to be a critical mechanism of microbial persistence in host tissues. Hidden within host cells, bacteria elude host defences and antibiotic treatments that are intracellularly inactive. The intracellular invasiveness of bacteria is generally measured by conventional gentamicin protection assays. The efficiency of invasion, however, markedly differs across bacterial species and adjustments to the titre of the microbial inocula used in the assays are often needed to enumerate intracellular bacteria. Such changes affect the standardisation of the method and hamper a direct comparison of bacteria on a same scale. This study aims at investigating the precise relation between inoculum, in terms of multiplicity of infection (MOI), and internalised bacteria. The investigation included nine Staphylococcus aureus, seven Staphylococcus epidermidis, five Staphylococcus lugdunensis and two Enterococcus faecalis clinical strains, which are co-cultured with MG63 human osteoblasts. Unprecedented insights are offered on the relations existing between MOI, number of internalised bacteria and per cent of internalised bacteria. New parameters are identified that are of potential use for qualifying the efficiency of internalization and compare the behaviour of bacterial strains.
Keyphrases
- staphylococcus aureus
- induced apoptosis
- escherichia coli
- cell cycle arrest
- biofilm formation
- microbial community
- endoplasmic reticulum stress
- high throughput
- pseudomonas aeruginosa
- risk assessment
- cystic fibrosis
- helicobacter pylori infection
- cell proliferation
- climate change
- reactive oxygen species
- candida albicans