Literature DB >> 34879216

Interactions between the foreign body reaction and Staphylococcus aureus biomaterial-associated infection. Winning strategies in the derby on biomaterial implant surfaces.

Colin W K Rosman1, Jan Maarten van Dijl2, Jelmer Sjollema1.   

Abstract

Biomaterial-associated infections (BAIs) are an increasing problem where antibiotic therapies are often ineffective. The design of novel strategies to prevent or combat infection requires a better understanding of how an implanted foreign body prevents the immune system from eradicating surface-colonizing pathogens. The objective of this review is to chart factors resulting in sub-optimal clearance of Staphylococcus aureus bacteria involved in BAIs. To this end, we first describe three categories of bacterial mechanisms to counter the host immune system around foreign bodies: direct interaction with host cells, modulation of intercellular communication, and evasion of the immune system. These mechanisms take place in a time frame that differentiates sterile foreign body reactions, BAIs, and soft tissue infections. In addition, we identify experimental interventions in S. aureus BAI that may impact infectious mechanisms. Most experimental treatments modulate the host response to infection or alter the course of BAI through implant surface modulation. In conclusion, the first week after implantation and infection is crucial for the establishment of an S. aureus biofilm that resists the local immune reaction and antibiotic treatment. Although established and chronic S. aureus BAI is still treatable and manageable, the focus of interventions should lie on this first period.

Entities:  

Keywords:  Staphylococcus aureus; biofilm; biomaterial-associated infection; foreign body reaction

Mesh:

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Year:  2021        PMID: 34879216     DOI: 10.1080/1040841X.2021.2011132

Source DB:  PubMed          Journal:  Crit Rev Microbiol        ISSN: 1040-841X            Impact factor:   7.391


  2 in total

1.  Outer membrane vesicles of the oral pathogen Porphyromonas gingivalis promote aggregation and phagocytosis of Staphylococcus aureus.

Authors:  Marines du Teil Espina; Anna Haider Rubio; Yanyan Fu; Marina López-Álvarez; Giorgio Gabarrini; Jan Maarten van Dijl
Journal:  Front Oral Health       Date:  2022-07-22

2.  Synthesis of the cyanobacterial halometabolite Chlorosphaerolactylate B and demonstration of its antimicrobial effect in vitro and in vivo.

Authors:  Nikoline Jensen; Henrik Elvang Jensen; Bent Aalbaek; Sophie Amalie Blirup-Plum; Sara M Soto; Virginio Cepas; Yuly López; Yaiza Gabasa; Ignacio Gutiérrez-Del-Río; Claudio J Villar; Felipe Lombó; María José Iglesias; Raquel Soengas; Fernando López Ortiz; Louise Kruse Jensen
Journal:  Front Microbiol       Date:  2022-09-29       Impact factor: 6.064

  2 in total

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