دورية أكاديمية
Nuclease activity and protein A release of Staphylococcus aureus clinical isolates determine the virulence in a murine model of acute lung infection
العنوان: | Nuclease activity and protein A release of Staphylococcus aureus clinical isolates determine the virulence in a murine model of acute lung infection |
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المؤلفون: | Ludwig, Nadine, Thörner-van Almsick, Julia, Mersmann, Sina, Bardel, Bernadette, Niemann, Silke, Chasan, Achmet Imam, Schäfers, Michael, Margraf, Andreas, Rossaint, Jan, Kahl, Barbara C., Zarbock, Alexander, Block, Helena |
المصدر: | Frontiers in Immunology ; volume 14 ; ISSN 1664-3224 |
بيانات النشر: | Frontiers Media SA |
سنة النشر: | 2023 |
المجموعة: | Frontiers (Publisher - via CrossRef) |
مصطلحات موضوعية: | Immunology, Immunology and Allergy |
الوصف: | Staphylococcus aureus is a common cause of hospital-acquired pneumonia associated with high mortality. Adequate clinical treatment is impeded by increasing occurrence of antibiotic resistances. Understanding the underlying mechanisms of its virulence during infections is a prerequisite to finding alternative treatments. Here, we demonstrated that an increased nuclease activity of a S. aureus isolate from a person with cystic fibrosis confers a growth advantage in a model of acute lung infection compared to the isogenic strain with low nuclease activity. Comparing these CF-isolates with a common MRSA-USA300 strain with similarly high nuclease activity but significantly elevated levels of Staphylococcal Protein A (SpA) revealed that infection with USA300 resulted in a significantly increased bacterial burden in a model of murine lung infection. Replenishment with the cell wall-bound SpA of S. aureus , which can also be secreted into the environment and binds to tumor necrosis factor receptor -1 (TNFR-1) to the CF-isolates abrogated these differences. In vitro experiments confirmed significant differences in spa -expression between USA300 compared to CF-isolates, thereby influencing TNFR-1 shedding, L-selectin shedding, and production of reactive oxygen species through activation of ADAM17. |
نوع الوثيقة: | article in journal/newspaper |
اللغة: | unknown |
DOI: | 10.3389/fimmu.2023.1259004 |
DOI: | 10.3389/fimmu.2023.1259004/full |
الإتاحة: | https://doi.org/10.3389/fimmu.2023.1259004Test |
حقوق: | https://creativecommons.org/licenses/by/4.0Test/ |
رقم الانضمام: | edsbas.CCD26C6C |
قاعدة البيانات: | BASE |
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