Fluorescent antibody-based detection and ultrastructural analysis of Streptococcus pneumoniae in human sputum.

IF 6.2 Q1 RESPIRATORY SYSTEM Pneumonia Pub Date : 2025-03-05 DOI:10.1186/s41479-025-00157-z
Ana G Jop Vidal, Meg Francis, Maneesha Chitanvis, Kenichi Takeshita, Ithiel J Frame, Poonam Sharma, Patricio Vidal, Claudio F Lanata, Carlos Grijalva, William Daley, Jorge E Vidal
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Abstract

Background: Pneumococcal pneumonia continues to be a significant global health burden, affecting both children and adults. Traditional diagnostic methods for sputum analysis remain challenging. The objective of this study was twofold: to develop a rapid and easy-to-perform assay for the identification of Streptococcus pneumoniae (Spn) directly in sputum specimens using fluorescence microscopy, and to characterize with high-resolution confocal microscopy the ultrastructure of pneumococci residing in human sputum.

Methods: We fluorescently labeled antibodies against the pneumococcal capsule (Spn-FLUO). The specificity and sensitivity of Spn-FLUO for detecting Spn was evaluated in vitro and in vivo using mouse models of carriage and disease, human nasopharyngeal specimens, and sputum from patients with pneumococcal pneumonia. Spn was confirmed in the specimens using culture and a species-specific qPCR assay. Spn strains were serotyped by Quellung. Confocal microscopy and Imaris software analysis were utilized to resolve the ultrastructure of pneumococci in human sputum.

Results: Compared with cultures and qPCR, Spn-FLUO demonstrated high sensitivity (78-96%) in nasopharyngeal samples from mice and humans. The limit of detection (LOD) in nasopharyngeal samples was ≥ 1.6 × 10⁴ GenEq/ml. The specificity in human nasopharyngeal specimens was 100%. In lung specimens from mice infected with pneumococci, Spn-FLUO reached 100% sensitivity with a LOD of ≥ 1.39 × 10⁴ GenEq/ml. In human sputum, the sensitivity for detecting Spn was 92.7% with a LOD of 3.6 × 10³ GenEq/ml. Ultrastructural studies revealed that pneumococci are expectorated as large aggregates with a median size of 1336 μm².

Conclusions: Spn-FLUO is a rapid and sensitive assay for detecting Spn in human sputum within 30 min, encompassing a range of both vaccine and non-vaccine serotypes associated with pneumococcal pneumonia. The study highlights that most pneumococci form aggregates in human sputum.

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人痰中肺炎链球菌荧光抗体检测及超微结构分析。
背景:肺炎球菌肺炎仍然是一个重大的全球卫生负担,影响儿童和成人。传统的痰液分析诊断方法仍然具有挑战性。本研究的目的有两个:利用荧光显微镜建立一种快速且易于操作的方法,用于直接鉴定痰标本中的肺炎链球菌(Spn),并利用高分辨率共聚焦显微镜表征人类痰中肺炎球菌的超微结构。方法:荧光标记抗肺炎球菌荚膜抗体(Spn-FLUO)。Spn- fluo检测Spn的特异性和敏感性在体外和体内通过小鼠携带和疾病模型、人鼻咽标本和肺炎球菌肺炎患者的痰液进行评估。Spn通过培养和种特异性qPCR检测在标本中得到证实。Spn菌株用Quellung分型。利用共聚焦显微镜和Imaris软件分析分析人痰中肺炎球菌的超微结构。结果:与培养和qPCR相比,Spn-FLUO在小鼠和人鼻咽样品中显示出高灵敏度(78-96%)。鼻咽标本的检出限(LOD)≥1.6 × 10⁴GenEq/ml。在人鼻咽标本中的特异性为100%。在感染肺炎球菌的小鼠肺标本中,Spn-FLUO达到100%的灵敏度,LOD≥1.39 × 10⁴GenEq/ml。在人痰中,检测Spn的灵敏度为92.7%,LOD为3.6 × 10³GenEq/ml。超微结构研究显示,肺炎球菌咳痰为大聚集体,中位大小为1336 μm²。结论:Spn- fluo是一种快速、灵敏的检测方法,可在30分钟内检测人痰中的Spn,包括一系列与肺炎球菌肺炎相关的疫苗和非疫苗血清型。该研究强调,大多数肺炎球菌在人类痰中形成聚集体。
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Pneumonia
Pneumonia RESPIRATORY SYSTEM-
自引率
1.50%
发文量
7
审稿时长
11 weeks
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