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Development of a Multiplex Real-Time PCR Assay for the Simultaneous Detection of Two Fungal Pathogens Causing Pneumonia.
Lim, Ho-Jae; Ahn, Seojin; No, Jee-Hyun; Park, Min-Young; Kim, Min-Jin; Sohn, Yong-Hak; Shin, Kwang-Soo; Park, Jung-Eun; Yang, Yong-Jin.
Affiliation
  • Lim HJ; Department of Molecular Diagnostics, Seegene Medical Foundation, Seoul 04805, Republic of Korea.
  • Ahn S; Department of Molecular Diagnostics, Seegene Medical Foundation, Seoul 04805, Republic of Korea.
  • No JH; Department of Molecular Diagnostics, Seegene Medical Foundation, Seoul 04805, Republic of Korea.
  • Park MY; Department of Molecular Diagnostics, Seegene Medical Foundation, Seoul 04805, Republic of Korea.
  • Kim MJ; Department of Molecular Diagnostics, Seegene Medical Foundation, Seoul 04805, Republic of Korea.
  • Sohn YH; Department of Molecular Diagnostics, Seegene Medical Foundation, Seoul 04805, Republic of Korea.
  • Shin KS; Department of Microbiology, Graduate School, Daejeon University, Daejeon 34520, Republic of Korea.
  • Park JE; Department of Integrative Biological Sciences & BK21 FOUR Educational Research Group for Age-Associated Disorder Control Technology, Chosun University, Gwangju 61452, Republic of Korea.
  • Yang YJ; Department of Molecular Diagnostics, Seegene Medical Foundation, Seoul 04805, Republic of Korea.
J Fungi (Basel) ; 10(9)2024 Aug 29.
Article in En | MEDLINE | ID: mdl-39330379
ABSTRACT
Infectious diseases caused by fungal sources are of great interest owing to their increasing prevalence. Invasive fungal infections, including invasive pulmonary aspergillosis caused by Aspergillus fumigatus, and Pneumocystis pneumonia caused by Pneumocystis jirovecii, are significant causes of morbidity and mortality among immunocompromised patients. The accurate and timely detection of these pathogens in this high-risk population is crucial for effective patient management. We developed a multiplex real-time polymerase chain reaction (PCR) assay, RF2 mRT-PCR, specifically designed to detect two respiratory fungi, P. jirovecii and A. fumigatus, and evaluated its performance in specimens of patients with lower respiratory tract infection. The performance was evaluated using 731 clinical samples, 55 reference species, and one synthetic DNA. The reproducibility test yielded a probit curve with a lower limit of detection of 19.82 copies/reaction for P. jirovecii and 64.20 copies/reaction for A. fumigatus. The RF2 mRT-PCR assay did not cross-react with non-A. fumigatus Aspergillus species or other common bacterial and viral species, and showed 100% in vitro sensitivity and specificity with reference assays. Additionally, it simultaneously detected A. fumigatus and P. jirovecii in co-infected samples. Therefore, the RF2 mRT-PCR assay is an efficient and reliable tool for in vitro diagnosis of A. fumigatus and P. jirovecii pulmonary infections.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Fungi (Basel) Year: 2024 Document type: Article Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Fungi (Basel) Year: 2024 Document type: Article Country of publication: Switzerland