Cutibacterium is recognized as the most common organism recovered from failed shoulder joint replacements. Shoulder arthroplasty wounds are often inoculated by Cutibacterium released from the dermal pilocebaceous units when the skin is incised. When these planktonic (free floating) bacteria come in contact with prosthetic joint surfaces, they can form a biofilm that protects them from antibiotics and host defenses. Efforts to minimize the risk of periprosthetic infections focus on minimizing the size of the inoculum and on killing the introduced organisms before they have an opportunity to form a durable biofilm.
Here are a few relevant articles
Biofilm formation by Propionibacterium acnes is a characteristic of invasive isolates
Propionibacterium acnes (Cutibacterium) has been shown to form biofilm both in vitro and
in vivo. These authors analyzed biofilm formation by 93 P. acnes isolates, either from invasive infections (n = 45) or from the skin of healthy people (n = 48). The majority of isolates from deep infections produced biofilm in a microtitre model of biofilm formation, whereas the skin isolates were poor biofilm producers (p <0.001 for a difference). They concluded that there was a role for biofilm formation in P. acnes virulence. The type distribution, as determined by sequencing of recA, was similar among isolates isolated from skin and from deep infections, demonstrating that P. acnes isolates with different genetic backgrounds have pathogenic potential. The biofilm formed on plastic and on bone cement was analysed by scanning electron microscopy (EM) and by transmission EM. The biofilm was seen as a 10-lm-thick layer covering the bacteria and was composed of filamentous as well as more amorphous structures. Interestingly, the presence of human plasma in solution or at the plastic surface inhibits biofilm formation, which could explain why P. acnes primarily infect plasma-poor environments
of, for example, joint prostheses and cerebrospinal shunts. This work underlines the importance of biofilm formation in P. acnes pathogenesis, and shows that biofilm formation should be considered in the diagnosis and treatment of invasive P. acnes infections.
Delayed Propionibacterium acnes surgical site infections occur only in the presence of an implant
Cutibacterium acnes Biofilm Study during Bone Cells Interaction
These authors point out that Cutibacterium acnes can exist internally with osteoblast-like cells. For commensal strains, less than 1% of the bacteria were internalized. C. acnes infection seems to have no cytotoxic effect on the bone cells. Commensal C. acnes showed a significant increase in biofilm formation after osteoblast-like internalization for 50% of the strains (2.8-fold increase). This phenomenon is exacerbated on a titanium, the material commonly used for shoulder implants.
For the strains associated with bone and prosthesis infections, they observed a similar internalization rate, but did not notice any increase in biofilm formation. Fluorescent staining revealed more live bacteria within the biofilm after osteoblast-like cell interaction for all strains. They did not find any link between clinical origin and phylotype.
Comparative analyses of biofilm formation among different Cutibacterium acnes isolates
These authors point out that Cutibacterium isolates exhibit marked heterogeneity and can be divided into at least 6 phylotypes by multilocus sequence typing and that biofilm formation may well be a relevant factor for Cutibacterium virulence. They performed a first comparative analysis of 58 diverse skin- or implant-isolates covering all six C. acnes phylotypes to investigate biofilm formation dynamics, biofilm morphology and attachment properties to abiotic surfaces.
Their results suggest that biofilm formation correlates with the phylotype, rather than the anatomical isolation site. IA1 isolates, particularly SLST sub-types A1 and A2, showed highest biofilm amounts in the microtiter plate assays, followed by isolates of the IC, IA2 and II phylotypes.
Microscopic evaluation revealed well-structured three-dimensional biofilms and relatively high adhesive properties to abiotic surfaces for phylotypes IA1, IA2 and IC.
Representatives of phylotype III formed biofilms with comparable biomass, but with less defined structures, whereas IB as well as II isolates showed the least complex three-dimensional morphology.
Proteinase K- and DNase I-treatment reduced attachment rates of all phylotypes, therefore, indicating that extracellular DNA and proteins are critical for adhesion to abiotic surfaces. Moreover, proteins seem to be pivotal structural biofilm components as mature biofilms of all phylotypes were proteinase
K-sensitive, whereas the sensitivity to DNase I-treatment varied depending on the phylotype.
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