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使用咽拭子诊断和基因分型肺孢子菌。

Use of Oropharyngeal Washes to Diagnose and Genotype Pneumocystis jirovecii.

机构信息

Division of Infectious Diseases ; Curriculum in Genetics and Molecular Biology , University of North Carolina School of Medicine ; Department of Epidemiology , Gillings School of Global Public Health, University of North Carolina , Chapel Hill.

Division of Infectious Diseases.

出版信息

Open Forum Infect Dis. 2015 Jun 3;2(3):ofv080. doi: 10.1093/ofid/ofv080. eCollection 2015 Sep.

Abstract

Pneumocystis jirovecii is a symbiotic respiratory fungus that presents in 2 clinical forms: pneumonia in immunocompromised patients or colonization, defined by the presence of the organism without associated clinical symptoms. Currently, diagnosis requires invasive bronchoscopy, which may not be available in some settings and is inappropriate for detecting colonization in healthy individuals. Noninvasive diagnostic techniques and molecular strain typing tools that can be used on these samples are critical for conducting studies to better understand transmission. We evaluated 2 real-time polymerase chain reaction (PCR) assays targeting dihydropteroate synthase and the major surface glycoprotein for detection in 77 oropharyngeal washes (OPWs) from 43 symptomatic human immunodeficiency virus-infected patients who underwent bronchoscopy. We also evaluated the ability of a new microsatellite (MS) genotyping panel to strain type infections from these samples. Each PCR used individually provided a high sensitivity (>80%) for detection of pneumonia but a modest specificity (<70%). When used in combination, specificity was increased to 100% with a drop in sensitivity (74%). Concentration of organisms by PCR in the OPW tended to be lower in colonized individuals compared with those with pneumonia, but differences in concentration could not clearly define colonization in symptomatic individuals. Oropharyngeal wash samples were genotyped using 6 MSs with ≥4 alleles successfully genotyped in the majority of colonized patients and ≥5 alleles in patients with pneumonia. The MS profile was consistent over time within patients with serial OPWs analyzed. Microsatellite genotyping on noninvasive samples may aid in studying the molecular epidemiology of this pathogen without requiring invasive diagnostic techniques.

摘要

卡氏肺孢子虫是一种共生呼吸真菌,有 2 种临床形式:免疫功能低下患者的肺炎或定植,表现为存在该生物体而无相关临床症状。目前,诊断需要进行有创性支气管镜检查,但在某些情况下可能无法进行,并且不适合检测健康个体的定植。能够用于这些样本的非侵入性诊断技术和分子菌株分型工具对于开展研究以更好地了解传播至关重要。我们评估了针对二氢叶酸合成酶和主要表面糖蛋白的 2 种实时聚合酶链反应(PCR)检测方法,用于检测 43 名接受支气管镜检查的有症状人类免疫缺陷病毒感染患者的 77 份咽拭子(OPW)。我们还评估了一种新的微卫星(MS)基因分型面板对这些样本中感染株进行分型的能力。单独使用每个 PCR 对肺炎的检测敏感性均很高(>80%),但特异性较低(<70%)。当联合使用时,特异性提高到 100%,但敏感性下降(74%)。与肺炎患者相比,OPW 中 PCR 检测到的生物体浓度在定植个体中往往较低,但在有症状个体中,浓度差异无法明确定义定植。使用 6 个 MS 对咽拭子样本进行基因分型,成功对大多数定植患者的 4 个以上等位基因和肺炎患者的 5 个以上等位基因进行了基因分型。在分析的连续 OPW 中,患者内的 MS 图谱随时间保持一致。非侵入性样本的 MS 基因分型可能有助于在无需有创性诊断技术的情况下研究该病原体的分子流行病学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6932/4498285/098fc4ad8f3a/ofv08001.jpg

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