囊性纤维化金黄色葡萄球菌分离株超抗原外毒素的流行和产生。

IF 6 2区 医学 Q1 RESPIRATORY SYSTEM
Ying Sun, Buqu Hu, Sahil Chhabra, Jade Tolentino, Nina Suzuki, Jesse Natarajan, Colleen Bianco, Paul Planet, Shardulendra P Sherchand, Rajan Adhikari, Javad Aman, Jon Koff, Govindarajan Rajagopalan
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引用次数: 0

摘要

金黄色葡萄球菌(SA)是最常见的囊性纤维化(CF)肺部病原体,它具有独特的产生超抗原(SAg)外毒素的能力,是公认的最有效的免疫系统激活剂和炎症诱导剂。在此,我们分析了儿童和成人CF临床分离株中sa - sag的分布。然后,我们研究了一些临床分离株产生的具有生物活性的SA-SAg,并测试了CF痰液中SA-SAg的稳定性。研究表明,60- 80%的儿童和成人CF SA分离株携带至少一个SA- sag基因,前者携带强效SA- sag(葡萄球菌肠毒素A和B)的频率更高(30- 60%),这可能解释了为什么SA的存在与儿童CF较差的呼吸结局相关。临床SA分离株的生物膜在人工痰液中容易产生生物活性SA- sag,纯化的SA- sag在体外培养的CF痰液中保持其生物活性。此外,CF SA分离株的免疫刺激潜力取决于其SAg谱。总之,我们的研究证实SA- sag在CF SA分离株中广泛存在。然而,这些分离株的免疫刺激潜力因其SAg谱而异,这可能解释了CF肺病临床表现的异质性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevalence and production of superantigen exotoxins by cystic fibrosis Staphylococcus aureus isolates.

Staphylococcus aureus (SA) is the most common cystic fibrosis (CF) lung pathogen that is uniquely capable of producing superantigen (SAg) exotoxins, which are recognized as the most potent activators of the immune system and inducers of inflammation. Herein, we analyzed the distribution of SA-SAgs among pediatric and adult CF clinical isolates. We then investigated the production of biologically active SA-SAgs by some of these clinical isolates and tested the stability of SA-SAg in CF sputum. We demonstrate that 60-80 % of pediatric and adult CF SA isolates carried at least one SA-SAg gene, with the former harboring potent SA-SAgs (Staphylococcal enterotoxin A and B) more frequently (30-60 %) which may explain why the presence of SA associates with poorer respiratory outcomes in pediatric CF. Biofilms of clinical SA isolates readily produced biologically active SA-SAgs in artificial sputum medium and purified SA-SAgs retained their bioactivity in human CF sputum in vitro. Further, the immunostimulatory potential of the CF SA isolates depended on their SAg profile. Overall, our study confirms that SA-SAgs are widely prevalent in CF SA isolates. However, the immunostimulatory potential of these isolates varied depending on their SAg profile which may explain the heterogeneity in clinical presentation of CF lung disease.

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来源期刊
Journal of Cystic Fibrosis
Journal of Cystic Fibrosis 医学-呼吸系统
CiteScore
10.10
自引率
13.50%
发文量
1361
审稿时长
50 days
期刊介绍: The Journal of Cystic Fibrosis is the official journal of the European Cystic Fibrosis Society. The journal is devoted to promoting the research and treatment of cystic fibrosis. To this end the journal publishes original scientific articles, editorials, case reports, short communications and other information relevant to cystic fibrosis. The journal also publishes news and articles concerning the activities and policies of the ECFS as well as those of other societies related the ECFS.
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