Evaluation of a multiplex PCR kit for detection of 17 respiratory pathogens in hospitalized patients

被引:1
|
作者
Zhang, Cuiping [1 ]
Chen, Xiaoyan [1 ]
Wang, Lu [1 ]
Song, Juan [1 ]
Zhou, Chunmei [2 ]
Wang, Xiaohuan [2 ]
Ma, Yan [2 ]
Chen, Cuicui [1 ]
Guo, Wei [2 ]
Song, Yuanlin [1 ,3 ,4 ,5 ,6 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Pulm Med, Shanghai Key Lab Lung Inflammat & Injury, Shanghai, Peoples R China
[2] Fudan Univ, Zhongshan Hosp, Dept Lab Med, Shanghai, Peoples R China
[3] Shanghai Inst Infect Dis & Biosecur, Shanghai, Peoples R China
[4] Shanghai Resp Res Inst, Shanghai, Peoples R China
[5] Fudan Univ, Huashan Hosp, Natl Clin Res Ctr Aging & Med, Shanghai, Peoples R China
[6] Fudan Univ, Jinshan Hosp, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
Multiplex polymerase chain reaction (PCR); pathogen detection; rapid diagnostics; molecular diagnostics; pneumonia; COMMUNITY-ACQUIRED PNEUMONIA; STENOTROPHOMONAS-MALTOPHILIA; STREPTOCOCCUS-PNEUMONIAE; DIAGNOSIS;
D O I
10.21037/jtd-22-544
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Rapid pathogen identification is critical for optimizing diagnosis and treatment of infectious diseases. Multiplex polymerase chain reaction (PCR) is a sensitive, broad-spectrum molecular detection technique that is simple and rapid to perform. It is capable of simultaneously screening for multiple pathogens within a short time range. Here, we designed and evaluated a multiplex PCR kit for the identification of 17 common respiratory pathogens in clinical samples from hospitalized patients. Methods: A total of 452 samples from hospitalized patients, including 242 respiratory and 210 nonrespiratory samples, were analyzed for 13 bacteria and 4 fungi by a multiplex fluorescent PCR kit. The diagnostic performance of the kit was assessed by considering routine microbiology as the reference standard. Results: The overall positivity rate of the multiplex PCR kit was 86.9%, much higher than that noted on routine microbiology (56.9%). Furthermore, the co-infection detection rate was also significantly higher than that noted on routine microbiology (69.5% vs. 15.0%). Compared with routine microbiology, kit sensitivity was >90% for detection of most target bacteria, with a negative predictive value (NPV) of >99%, especially for detection of Pseudomonas aeruginosa, Klebsiella pneumoniae, Acinetobacter baumannii, Stenotrophomonas maltophilia, Enterococcus faecium, Enterococcus faecalis and Escherichia coli. The kit was noted to be particularly superior in identifying Stenotrophomonas maltophilia and Streptococcus pneumoniae as compared to routine microbiology. The multiplex PCR kit was noted to be less sensitive (33.3-59.6%) and more specific (93.9100.0%) for detection of mycobacteria and fungi. Conclusions: Our multiplex PCR kit offers a rapid and sensitive diagnosis of common bacterial pneumonia, although sensitivity for mycobacteria and fungi warrants enhancement. Further optimization includes minimizing false positivity and increasing relevance to clinical application.
引用
收藏
页码:3386 / +
页数:13
相关论文
共 50 条
  • [21] Multiplex PCR system for the detection of mastitiscausing pathogens
    St-Pierre, J. M.
    Thibault, C.
    Bissonnette, N.
    JOURNAL OF ANIMAL SCIENCE, 2007, 85 : 367 - 367
  • [22] Detection of microbial pathogens in shellfish with multiplex PCR
    Brasher, CW
    DePaola, A
    Jones, DD
    Bej, AK
    CURRENT MICROBIOLOGY, 1998, 37 (02) : 101 - 107
  • [23] A Novel Capillary Electrophoresis-Based Multiplex PCR Assay for Detection of Respiratory Pathogens
    Stevenson, Jeffery B.
    Hymas, Weston C.
    Hillyard, David R.
    ANNALS OF CLINICAL AND LABORATORY SCIENCE, 2011, 41 (01): : 33 - 38
  • [24] Validation of a multiplex reverse transcriptase PCR ELISA for the detection of 19 respiratory tract pathogens
    Puppe, W.
    Weigl, J.
    Groendahl, B.
    Knuf, M.
    Rockahr, S.
    von Bismarck, P.
    Aron, G.
    Niesters, H. G. M.
    Osterhaus, A. D. M. E.
    Schmitt, H. -J.
    INFECTION, 2013, 41 (01) : 77 - 91
  • [25] Validation of a multiplex reverse transcriptase PCR ELISA for the detection of 19 respiratory tract pathogens
    W. Puppe
    J. Weigl
    B. Gröndahl
    M. Knuf
    S. Rockahr
    P. von Bismarck
    G. Aron
    H. G. M. Niesters
    A. D. M. E. Osterhaus
    H.-J. Schmitt
    Infection, 2013, 41 : 77 - 91
  • [26] Optimization and evaluation of a multiplex PCR for simultaneous detection of prominent foodborne pathogens of Enterobacteriaceae
    Babu, Litty
    Reddy, Prakash
    Murali, Harishchandra Sripathy
    Batra, Harsh Vardhan
    ANNALS OF MICROBIOLOGY, 2013, 63 (04) : 1591 - 1599
  • [27] Performance Evaluation of Multiplex PCR for Detection of Bacterial Pathogens Associated with Infectious Colitis
    Shin, S.
    Park, M. -J.
    Song, W.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2019, 21 (03): : S42 - S42
  • [28] Optimization and evaluation of a multiplex PCR for simultaneous detection of prominent foodborne pathogens of Enterobacteriaceae
    Litty Babu
    Prakash Reddy
    Harishchandra Sripathy Murali
    Harsh Vardhan Batra
    Annals of Microbiology, 2013, 63 : 1591 - 1599
  • [29] Evaluation of a multiplex ligation-dependent probe amplification assay for the detection of respiratory pathogens in oncological patients
    Berning, Lucia
    Aberle, Stephan W.
    Simon, Benedikt
    Luger, Christoph
    Apfalter, Petra
    Machherndl-Spandl, Sigrid
    Kerschner, Heidrun
    JOURNAL OF CLINICAL VIROLOGY, 2014, 60 (02) : 141 - 146
  • [30] Simultaneous Detection of 13 Key Bacterial Respiratory Pathogens by Combination of Multiplex PCR and Capillary Electrophoresis
    JIANG Lu Xi
    REN Hong Yu
    ZHOU Hai Jian
    ZHAO Si Hong
    HOU Bo Yan
    YAN Jian Ping
    QIN Tian
    CHEN Yu
    Biomedical and Environmental Sciences, 2017, 30 (08) : 549 - 561