临床囊性纤维化金黄色葡萄球菌分离株的关键基因型和表型特征。

IF 2.4 4区 医学 Q3 MICROBIOLOGY
Micaela Mossop, Luca Robinson, Jhih-Hang Jiang, Anton Y Peleg, Luke V Blakeway, Nenad Macesic, Audrey Perry, Stephen Bourke, Fatima R Ulhuq, Tracy Palmer
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引用次数: 0

摘要

介绍。在英国,三分之一的CF患者同时感染了金黄色葡萄球菌和铜绿假单胞菌。CF慢性细菌感染导致肺组织逐渐破坏,最终导致本组患者呼吸衰竭。差距的声明。在铜绿假单胞菌存在或不存在的情况下,金黄色葡萄球菌对囊性纤维化(CF)肺功能下降的作用尚不清楚。确定一系列金黄色葡萄球菌临床分离株的分子和表型特征将有助于进一步了解其致病能力。我们的目的是使用分子和表型工具来表征25个临床金黄色葡萄球菌分离株,这些分离株来自泰恩河畔纽卡斯尔皇家维多利亚医院CF患者的单感染和合并感染铜绿假单胞菌。提取基因组DNA并测序。用多位点序列分型方法构建7个管家基因的系统发育。使用Roary计算全基因组,并使用eggNOG-mapper分配同源群,用于确定核心,辅助和独特基因组之间的差异。利用PubMLST、eBURST、agrate和spaTyper分别对序列型、克隆复合体、agr和spa型进行鉴定。采用Kirby-Bauer圆盘扩散试验测定抗生素耐药性。用羊红细胞琼脂板进行溶血表型检测,用刚果红琼脂显示黏液表型。临床菌株根据agr型、序列型和克隆复合体紧密聚集。COG分析显示,核心、附属和独特泛基因组群之间的COG家族富集具有统计学意义。独特的基因组在复制、重组和修复以及防御机制方面显著丰富。已知的毒力基因和毒素在该组中含量很高,在11株菌株中鉴定出独特的基因。从同一患者分离的菌株均超过平均核苷酸识别阈值,但在表型性状上存在差异。合并感染组对大环内酯类药物的耐药性明显增高。金黄色葡萄球菌菌株的遗传和表型能力存在巨大差异。进一步研究这些与CF肺中其他物种的差异可能有助于了解物种间的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterisation of key genotypic and phenotypic traits of clinical cystic fibrosis Staphylococcus aureus isolates.

Introduction. One third of people with CF in the UK are co-infected by both Staphylococcus aureus and Pseudomonas aeruginosa. Chronic bacterial infection in CF contributes to the gradual destruction of lung tissue, and eventually respiratory failure in this group.Gap Statement. The contribution of S. aureus to cystic fibrosis (CF) lung decline in the presence or absence of P. aeruginosa is unclear. Defining the molecular and phenotypic characteristics of a range of S. aureus clinical isolates will help further understand its pathogenic capabilities.Aim. Our objective was to use molecular and phenotypic tools to characterise twenty-five clinical S. aureus isolates collected from mono- and coinfection with P. aeruginosa from people with CF at the Royal Victoria Infirmary, Newcastle upon Tyne.Methodology. Genomic DNA was extracted and sequenced. Multilocus sequence typing was used to construct phylogeny from the seven housekeeping genes. A pangenome was calculated using Roary, and cluster of Orthologous groups were assigned using eggNOG-mapper which were used to determine differences within core, accessory, and unique genomes. Characterisation of sequence type, clonal complex, agr and spa types was carried out using PubMLST, eBURST, AgrVATE and spaTyper, respectively. Antibiotic resistance was determined using Kirby-Bauer disc diffusion tests. Phenotypic testing of haemolysis was carried out using ovine red blood cell agar plates and mucoid phenotypes visualised using Congo red agar.Results. Clinical strains clustered closely based on agr type, sequence type and clonal complex. COG analysis revealed statistically significant enrichment of COG families between core, accessory and unique pangenome groups. The unique genome was significantly enriched for replication, recombination and repair, and defence mechanisms. The presence of known virulence genes and toxins were high within this group, and unique genes were identified in 11 strains. Strains which were isolated from the same patient all surpassed average nucleotide identity thresholds, however, differed in phenotypic traits. Antimicrobial resistance to macrolides was significantly higher in the coinfection group.Conclusion. There is huge variation in genetic and phenotypic capabilities of S. aureus strains. Further studies on how these may differ in relation to other species in the CF lung may give insight into inter-species interactions.

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来源期刊
Journal of medical microbiology
Journal of medical microbiology 医学-微生物学
CiteScore
5.50
自引率
3.30%
发文量
143
审稿时长
4.5 months
期刊介绍: Journal of Medical Microbiology provides comprehensive coverage of medical, dental and veterinary microbiology, and infectious diseases. We welcome everything from laboratory research to clinical trials, including bacteriology, virology, mycology and parasitology. We publish articles under the following subject categories: Antimicrobial resistance; Clinical microbiology; Disease, diagnosis and diagnostics; Medical mycology; Molecular and microbial epidemiology; Microbiome and microbial ecology in health; One Health; Pathogenesis, virulence and host response; Prevention, therapy and therapeutics
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