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Three-Dimensional In Vitro Staphylococcus aureus Abscess Communities Display Antibiotic Tolerance and Protection from Neutrophil Clearance.
Hofstee, Marloes I; Riool, Martijn; Terjajevs, Igors; Thompson, Keith; Stoddart, Martin J; Richards, R Geoff; Zaat, Sebastian A J; Moriarty, T Fintan.
Afiliación
  • Hofstee MI; AO Research Institute Davos, Davos, Switzerland.
  • Riool M; Amsterdam UMC, University of Amsterdam, Department of Medical Microbiology and Infection Prevention, Amsterdam Institute for Infection and Immunity, Amsterdam, The Netherlands.
  • Terjajevs I; Amsterdam UMC, University of Amsterdam, Department of Medical Microbiology and Infection Prevention, Amsterdam Institute for Infection and Immunity, Amsterdam, The Netherlands.
  • Thompson K; AO Research Institute Davos, Davos, Switzerland.
  • Stoddart MJ; AO Research Institute Davos, Davos, Switzerland.
  • Richards RG; AO Research Institute Davos, Davos, Switzerland.
  • Zaat SAJ; AO Research Institute Davos, Davos, Switzerland.
  • Moriarty TF; Amsterdam UMC, University of Amsterdam, Department of Medical Microbiology and Infection Prevention, Amsterdam Institute for Infection and Immunity, Amsterdam, The Netherlands.
Infect Immun ; 88(11)2020 10 19.
Article en En | MEDLINE | ID: mdl-32817328
ABSTRACT
Staphylococcus aureus is a prominent human pathogen in bone and soft-tissue infections. Pathophysiology involves abscess formation, which consists of central staphylococcal abscess communities (SACs), surrounded by a fibrin pseudocapsule and infiltrating immune cells. Protection against the ingress of immune cells such as neutrophils, or tolerance to antibiotics, remains largely unknown for SACs and is limited by the lack of availability of in vitro models. We describe a three-dimensional in vitro model of SACs grown in a human plasma-supplemented collagen gel. The in vitro SACs reached their maximum size by 24 h and elaborated a fibrin pseudocapsule, as confirmed by electron and immunofluorescence microscopy. The in vitro SACs tolerated 100× the MIC of gentamicin alone and in combination with rifampin, while planktonic controls and mechanically dispersed SACs were efficiently killed. To simulate a host response, SACs were exposed to differentiated PLB-985 neutrophil-like (dPLB) cells and to primary human neutrophils at an early stage of SAC formation or after maturation at 24 h. Both cell types were unable to clear mature in vitro SACs, but dPLB cells prevented SAC growth upon early exposure before pseudocapsule maturation. Neutrophil exposure after plasmin pretreatment of the SACs resulted in a significant decrease in the number of bacteria within the SACs. The in vitro SAC model mimics key in vivo features, offers a new tool to study host-pathogen interactions and drug efficacy assessment, and has revealed the functionality of the S. aureus pseudocapsule in protecting the bacteria from host phagocytic responses and antibiotics.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones Estafilocócicas / Farmacorresistencia Microbiana / Absceso Límite: Humans Idioma: En Revista: Infect Immun Año: 2020 Tipo del documento: Article País de afiliación: Suiza

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones Estafilocócicas / Farmacorresistencia Microbiana / Absceso Límite: Humans Idioma: En Revista: Infect Immun Año: 2020 Tipo del documento: Article País de afiliación: Suiza