Department of Ophthalmology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Department of Ophthalmology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan
BMJ Open Ophthalmol. 2023 Sep;8(1). doi: 10.1136/bmjophth-2023-001342.
To evaluate the usefulness of metagenomic analysis in the search for causative organisms of bacterial endophthalmitis.
Twenty-one consecutive treatment-naïve patients (13 men and 8 women; mean age, 60.8±19.8 years) with suspected endophthalmitis were recruited. Vitrectomy was performed to diagnose and treat endophthalmitis. Bacterial culture and metagenomic analysis of the vitreous body were performed. Extracted DNA was analysed using 16S rRNA sequences, and libraries were sequenced on an Illumina MiSeq sequencer. To compare the bacterial composition in each case, α and β diversities were determined.
Patients were categorised into three groups: endophthalmitis cases with matching predominant organisms according to metagenomic analysis and bacterial culture, those with negative results for bacterial culture and those with negative results in both cases. In 7 of 15 culture-negative cases, results from metagenomic analysis could detect pathogens. The diversity of bacterial populations was significantly lower in the group with positive results for predominant bacteria according to culture and metagenomic analysis. All patients with uveitis were included in the group for which the causative pathogen could not be determined by culture or metagenomic analysis. The structures of bacterial populations significantly differed between the positive and negative groups by culture and metagenomic analysis.
Metagenomic analysis could be useful for prompt detection of causative pathogens, for precise diagnosis of infection, and as a marker of inflammation processes such as uveitis.
评估宏基因组分析在寻找细菌性眼内炎病原体中的作用。
连续招募了 21 例未经治疗的疑似眼内炎患者(13 名男性和 8 名女性;平均年龄 60.8±19.8 岁)。对患者进行玻璃体切除术以诊断和治疗眼内炎。对玻璃体进行细菌培养和宏基因组分析。提取 DNA 后,采用 16S rRNA 序列进行分析,并在 Illumina MiSeq 测序仪上对文库进行测序。为了比较每个病例中的细菌组成,确定了 α 和 β 多样性。
患者分为三组:根据宏基因组分析和细菌培养结果确定主要病原体的眼内炎病例、细菌培养阴性病例和两种方法均阴性病例。在 15 例培养阴性病例中,有 7 例可通过宏基因组分析检测到病原体。根据培养和宏基因组分析确定主要细菌的病例组的细菌种群多样性显著降低。所有患有葡萄膜炎的患者均被纳入无法通过培养或宏基因组分析确定病原体的组。通过培养和宏基因组分析,阳性和阴性组的细菌种群结构存在显著差异。
宏基因组分析可用于快速检测病原体,准确诊断感染,并作为葡萄膜炎等炎症过程的标志物。