从干眼症患者眼表分离出的金黄色葡萄球菌和粪肠球菌的基因组学。

IF 3 2区 医学 Q1 OPHTHALMOLOGY Experimental eye research Pub Date : 2024-09-05 DOI:10.1016/j.exer.2024.110071
Ahmed M. Amer , Maria Naqvi , Colin Charnock
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引用次数: 0

摘要

干眼症等眼表炎症性疾病正变得越来越普遍。针对有害细菌开发新的治疗策略可带来显著的治疗效果。本研究的目的是分析从挪威干眼症患者眼表面分离出的常见眼部病原体金黄色葡萄球菌和较罕见的眼底炎相关菌种粪肠球菌的特征。这 7 个分离物(5 个金黄色葡萄球菌和 2 个粪肠球菌)构成了我们之前对 61 名干眼症患者的眼部微生物组进行研究时分离到的每个物种的全套成员。我们的目的是研究这些分离物与眼表健康有关的致病潜力。为此,我们使用了全基因组测序、针对毒力基因的多重 PCR 和抗生素敏感性测试,其中包括临床相关的制剂。粪肠球菌分离物仅对庆大霉素有抗药性。金黄色葡萄球菌分离物对大多数测试过的抗生素都有敏感性,只有两个分离物对三甲氧苄青霉素/磺胺甲噁唑有抗药性,三个分离物对氨苄西林有抗药性。敏感性包括对治疗这些物种眼部感染的几种一线抗生素的敏感性。因此,如果需要,可以选择治疗方法。不过,一些金黄色葡萄球菌对庆大霉素和利福平产生了自发耐药性,这可能会引起关注。分离物的全基因组测序显示,金黄色葡萄球菌的基因组大小为 2.74 - 2.83 Mbp,粪肠球菌的基因组大小为 2.86 Mbp,这是这些物种的典型基因组大小。多位点序列分型和与以前发表的基因组的系统进化比较结果表明,这两个物种都不存在眼睛特异性集群。基因组分析表明,研究中的所有分离物都有很高的致病性。耐药性基因组分析表明,所有金黄色葡萄球菌分离物中都含有 beta-内酰胺酶 blaZ 基因,其中两个分离物中含有 dfrG 基因;而粪肠杆菌分离物中则含有 lsa(A) 基因,该基因使粪肠杆菌对林可霉素类和链霉亲和素 A 具有内在耐药性。毒力因子筛选显示,金黄色葡萄球菌和粪大肠杆菌分离物中都存在各种致病性相关基因。这些基因包括编码产生毒素的基因和与逃避宿主免疫系统有关的因子。一些已发现的基因(tst、hylA 和 hylB)被认为与干眼症的病理生理学有关。最后,通过多重 PCR 分析证实了金黄色葡萄球菌特定毒力基因的存在。
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Genomics of Staphylococcus aureus and Enterococcus faecalis isolated from the ocular surface of dry eye disease sufferers

Ocular surface inflammatory disorders, such as dry eye, are becoming increasingly prevalent. Developing new treatment strategies targeting harmful bacteria could provide significant therapeutic benefits. The purpose of this study was to characterize the common ocular pathogen Staphylococcus aureus and the rarer endophthalmitis-associated species Enterococcus faecalis isolated from the ocular surface of dry eye disease patients in Norway. Together the 7 isolates (5 S. aureus and 2 E. faecalis) comprise the complete set of members of each species isolated in our previous study of the ocular microbiome of 61 dry eye sufferers. We aimed to investigate the pathogenic potential of these isolates in relation to ocular surface health. To this end, we used whole genome sequencing, multiplex PCR directed at virulence genes and antibiotic susceptibility tests encompassing clinically relevant agents. The E. faecalis isolates showed resistance to only gentamicin. S. aureus isolates displayed susceptibility to most of the tested antibiotics, except for two isolates which showed resistance to trimethoprim/sulfamethoxazole and three isolates which were resistant to ampicillin. Susceptibilities included sensitivity to several first-line antibiotics for treatment of ocular infections by these species. Thus, treatment options would be available if required. However, spontaneous resistance development to gentamicin and rifampicin occurred in some S. aureus which could be a cause for concern. Whole genome sequencing of the isolates showed genome sizes ranging from 2.74 to 2.83 Mbp for S. aureus and 2.86 Mbp for E. faecalis, which is typical for these species. Multilocus sequence typing and phylogenetic comparisons with previously published genomes, did not suggest the presence of eye-specific clusters for either species. Genomic analysis indicated a high probability of pathogenicity among all isolates included in the study. Resistome analysis revealed the presence of the beta-lactamase blaZ gene in all S. aureus isolates and the dfrG gene in two of them; while E. faecalis isolates carried the lsa(A) gene which confers intrinsic resistance to lincosamides and streptogramin A in this species. Screening for virulence factors revealed the presence of various pathogenicity associated genes in both S. aureus and E. faecalis isolates. These included genes coding for toxin production and factors associated with evading the host immune system. Some of the identified genes (tst, hylA & hylB) are suggested to be linked to the pathophysiology of dry eye disease. Lastly, the presence of specific S. aureus virulence genes was confirmed through multiplex PCR analysis.

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来源期刊
Experimental eye research
Experimental eye research 医学-眼科学
CiteScore
6.80
自引率
5.90%
发文量
323
审稿时长
66 days
期刊介绍: The primary goal of Experimental Eye Research is to publish original research papers on all aspects of experimental biology of the eye and ocular tissues that seek to define the mechanisms of normal function and/or disease. Studies of ocular tissues that encompass the disciplines of cell biology, developmental biology, genetics, molecular biology, physiology, biochemistry, biophysics, immunology or microbiology are most welcomed. Manuscripts that are purely clinical or in a surgical area of ophthalmology are not appropriate for submission to Experimental Eye Research and if received will be returned without review.
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