Rapid Diagnosis of Pneumocystis jirovecii Pneumonia and Respiratory Tract Colonization by Next-Generation Sequencing.

IF 3.6 3区 生物学 Q2 MYCOLOGY Mycopathologia Pub Date : 2024-05-05 DOI:10.1007/s11046-024-00849-y
Fanfan Xing, Chaowen Deng, Zhendong Luo, Shan Zou, Min Liu, Haiyan Ye, Linlin Sun, Chi-Ching Tsang, Simon K F Lo, Susanna K P Lau, Patrick C Y Woo
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Abstract

Objectives: To describe the epidemiology of Pneumocystis jirovecii pneumonia and colonization diagnosed by next-generation sequencing (NGS) and explore the usefulness of the number of P. jirovecii sequence reads for the diagnosis of P. jirovecii pneumonia.

Methods: We examined the NGS results for P. jirovecii in respiratory samples collected from patients and analysed their clinical, radiological and microbiological characteristics.

Results: Among 285 respiratory samples collected over a 12-month period (January to December 2022), P. jirovecii sequences were detected in 56 samples from 53 patients. Fifty (94.3%) of the 53 patients were HIV-negative. Following our case definitions, 37 (69.8%) and 16 (30.2%) of the 53 patients had P. jirovecii infection and colonization respectively. P. jirovecii infection was associated with presence of underlying disease with immunosuppression (94.6% vs 18.8%, P < 0.05), positive serum 1,3-β-D-glucan (41.2% vs 0%, P < 0.01) and higher number of P. jirovecii sequence reads (P < 0.005). In contrast, P. jirovecii colonization was associated with the male sex (93.8% vs 54.1%, P < 0.01), another definitive infectious disease diagnosis of the respiratory tract (43.8% vs 2.7%, P < 0.001) and higher survival (100% vs 67.6%, P < 0.01). Although P. jirovecii pneumonia was associated with higher number of P. jirovecii reads in respiratory samples, only a sensitivity of 82.14% and a specificity of 68.75% could be achieved.

Conclusion: Detection of P. jirovecii sequences in respiratory samples has to be interpreted discreetly. A combination of clinical, radiological and laboratory findings is still the most crucial in determining whether a particular case is genuine P. jirovecii pneumonia.

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利用新一代测序技术快速诊断肺孢子虫肺炎和呼吸道定植。
目的描述通过下一代测序(NGS)诊断的肺孢子虫肺炎和定植的流行病学,并探讨肺孢子虫肺炎诊断中肺孢子虫序列读数的有用性:方法:我们检测了患者呼吸道样本中的 P. jirovecii 的 NGS 结果,并分析了其临床、放射学和微生物学特征:结果:在为期 12 个月(2022 年 1 月至 12 月)收集的 285 份呼吸道样本中,53 名患者的 56 份样本检测到了 P. jirovecii 序列。53 名患者中有 50 人(94.3%)HIV 阴性。根据我们的病例定义,53 名患者中分别有 37 人(69.8%)和 16 人(30.2%)感染了 P. jirovecii 并已定植。琼脂癣菌感染与存在免疫抑制的基础疾病有关(94.6% 对 18.8%,P 结论:琼脂癣菌感染与免疫抑制有关:在呼吸道样本中检测到 P. jirovecii 序列必须谨慎解读。综合临床、放射学和实验室结果仍是确定某一病例是否为真正的 P. jirovecii 肺炎的关键。
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来源期刊
Mycopathologia
Mycopathologia 生物-真菌学
CiteScore
6.80
自引率
3.60%
发文量
76
审稿时长
3 months
期刊介绍: Mycopathologia is an official journal of the International Union of Microbiological Societies (IUMS). Mycopathologia was founded in 1938 with the mission to ‘diffuse the understanding of fungal diseases in man and animals among mycologists’. Many of the milestones discoveries in the field of medical mycology have been communicated through the pages of this journal. Mycopathologia covers a diverse, interdisciplinary range of topics that is unique in breadth and depth. The journal publishes peer-reviewed, original articles highlighting important developments concerning medically important fungi and fungal diseases. The journal highlights important developments in fungal systematics and taxonomy, laboratory diagnosis of fungal infections, antifungal drugs, clinical presentation and treatment, and epidemiology of fungal diseases globally. Timely opinion articles, mini-reviews, and other communications are usually invited at the discretion of the editorial board. Unique case reports highlighting unprecedented progress in the diagnosis and treatment of fungal infections, are published in every issue of the journal. MycopathologiaIMAGE is another regular feature for a brief clinical report of potential interest to a mixed audience of physicians and laboratory scientists. MycopathologiaGENOME is designed for the rapid publication of new genomes of human and animal pathogenic fungi using a checklist-based, standardized format.
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