Clinical Evaluation of the Immunochromatographic System Using Silver Amplification for the Rapid Detection of Mycoplasma pneumoniae

• Published in: Scientific reports Vol. 8; no. 1; pp. 1430 - 7
• Main Authors: Namkoong, Ho, Yamazaki, Masahiko, Ishizaki, Masami, Endo, Ikumi, Harada, Noriaki, Aramaki, Megumi, Tanaka, Yuko, Kaburagi, Sachiko, Ichikawa, Masataka, Ohata, Takanori, Sakaguchi, Shinji, Saito, Fumitake, Nakao, Ayumi, Yuki, Hideki, Mitamura, Keiko
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 23-01-2018; Nature Publishing Group
• Subjects: 13/56; 631/326/2521; 692/699/255/1318; 82/1; Age groups; Antibodies; Antigens; Children; Genetic screening; Humanities and Social Sciences; Infections; Laboratories; Medicine; multidisciplinary; Mycoplasma pneumoniae; Pneumonia; Polymerase chain reaction; Pulmonology; Reagents; Science; Science (multidisciplinary)
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-018-19734-y

Mycoplasma pneumoniae
infection is conventionally diagnosed using serum antibody testing, microbial culture, and genetic testing. Recently, immunochromatography-based rapid mycoplasma antigen test kits have been developed and commercialised for rapid diagnosis of
M
.
pneumoniae
infection. However, as these kits do not provide sufficient sensitivity and specificity, a rapid test kit with improved accuracy is desired. The present prospective study evaluated a rapid
M
.
pneumoniae
diagnostic system utilizing a newly developed silver amplification immunochromatography (SAI) system. We performed dilution sensitivity test and the prospective clinical study evaluating the SAI system. The subjects of the clinical study included both children and adults. All patients suspected to have mycoplasma pneumonia (169 patients) were sequentially enrolled. Twelve patients did not agree to participate and 157 patients were enrolled in the study. The results demonstrate excellent performance of this system with 90.4% sensitivity and 100.0% specificity compared with real-time polymerase chain reaction. When compared with loop-mediated isothermal amplification (LAMP) methods, the results also demonstrate a high performance of this system with 93.0% sensitivity and 100.0% specificity. The SAI system uses a dedicated device for automatic analysis and reading, making it highly objective, and requires less human power, supporting its usefulness in clinical settings.