Point-of-care molecular diagnosis of Mycoplasma pneumoniae including macrolide sensitivity using quenching probe polymerase chain reaction

被引:12
作者
Ishiguro, Nobuhisa [1 ]
Sato, Rikako [1 ]
Mori, Toshihiko [2 ]
Tanaka, Hiroshi [3 ]
Narita, Mitsuo [4 ]
Nagano, Takashi [5 ]
Owaku, Masato [5 ]
Miyajima, Kensuke [5 ]
Manabe, Atsushi [1 ]
机构
[1] Hokkaido Univ, Dept Pediat, Grad Sch Med, Sapporo, Hokkaido, Japan
[2] NTT East Sapporo Hosp, Dept Pediat, Sapporo, Hokkaido, Japan
[3] Sapporo Cough Asthma & Allergy Ctr, Sapporo, Hokkaido, Japan
[4] Sapporo Tokushukai Hosp, Dept Pediat, Sapporo, Hokkaido, Japan
[5] MIZUHO MEDY Co Ltd, Tosu, Saga, Japan
来源
PLOS ONE | 2021年 / 16卷 / 10期
关键词
REAL-TIME PCR; AMPLIFICATION ASSAY; CLINICAL-EVALUATION; RESISTANT STRAINS; RIBOSOMAL-RNA; INFECTIONS; OUTBREAK; MINOCYCLINE; MUTATIONS; ADULTS;
D O I
10.1371/journal.pone.0258694
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objectives Macrolides are generally considered to be the drugs of choice for treatment of patients with Mycoplasma pneumoniae infection. However, macrolide-resistant M. pneumoniae has been emerging since about 2000. The Smart Gene system (MIZUHO MEDY Co., Ltd., Tosu, Japan) is a novel fully automated system for detection of pathogens using the method of quantitative polymerase chain reaction (qPCR) with QProbe (QProbe PCR). The entire procedure is completed within 50 min and the size of the instrument is small (15 x 34 x 30 cm). The purpose of this study was to evaluate the usefulness of the Smart Gene system for detection of M. pneumoniae and detection of a point mutation at domain V of the 23S rRNA gene of M. pneumoniae. Materials Pharyngeal swab samples were collected from 154 patients who were suspected of having respiratory tract infections associated with M. pneumoniae. Results Compared with the results of qPCR, the sensitivity and specificity of the Smart Gene system were 98.7% (78/79) and 100.0% (75/75), respectively. A point mutation at domain V of the 23S rRNA gene was detected from 7 (9.0%) of 78 M. pneumoniae-positive samples by the Smart Gene system and these results were confirmed by direct sequencing. The minimum inhibitory concentrations of clarithromycin among the 5 isolates of M. pneumoniae with a point mutation at domain V of the 23S rRNA gene were >64 mu g/ml and those among the 33 isolates without a mutation in the 23S rRNA gene were Conclusion The Smart Gene system is a rapid and accurate assay for detection of the existence of M. pneumoniae and a point mutation at domain V of the 23S rRNA gene of M. pneumoniae at the same time. The Smart Gene system is suitable for point-of-care testing in both hospital and outpatient settings.
引用
收藏
页数:19
相关论文
共 61 条
  • [1] Averbuch D, 2011, EMERG INFECT DIS, V17, P1079, DOI [10.3201/eid1706.101558, 10.3201/eid/1706.101558]
  • [2] Multicenter Evaluation of the ePlex Respiratory Pathogen Panel for the Detection of Viral and Bacterial Respiratory Tract Pathogens in Nasopharyngeal Swabs
    Babady, N. Esther
    England, Matthew R.
    Smith, Kristen L. Jurcic
    He, Taojun
    Wijetunge, Dona Saumya
    Tang, Yi-Wei
    Chamberland, Robin R.
    Menegus, Marilyn
    Swierkosz, Ella M.
    Jerris, Robert C.
    Greene, Wallace
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2018, 56 (02)
  • [3] Panels and Syndromic Testing in Clinical Microbiology
    Bard, Jennifer Dien
    McElvania, Erin
    [J]. CLINICS IN LABORATORY MEDICINE, 2020, 40 (04) : 393 - 420
  • [4] A controlled intervention study to improve antibiotic use in a Russian paediatric hospital
    Berild, Dag
    Abrahamsen, Tore G.
    Andresen, Stein
    Bjorlow, Egil
    Haug, Ola
    Kossenko, Irina M.
    Kubar, Olga I.
    Lelek, Michaela
    Mintchenko, Svetlana I.
    Pyasetskaya, Maria F.
    Ringertz, Signe H.
    Sysenko, Galina A.
    [J]. INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2008, 31 (05) : 478 - 483
  • [5] RAPID AND SIMPLE METHOD FOR PURIFICATION OF NUCLEIC-ACIDS
    BOOM, R
    SOL, CJA
    SALIMANS, MMM
    JANSEN, CL
    WERTHEIMVANDILLEN, PME
    VANDERNOORDAA, J
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (03) : 495 - 503
  • [6] Center TNS, 2020, STAT MED CAR ACT PUB
  • [7] Comparison of Pyrosequencing, Sanger Sequencing, and Melting Curve Analysis for Detection of Low-Frequency Macrolide-Resistant Mycoplasma pneumoniae Quasispecies in Respiratory Specimens
    Chan, Kwok-Hung
    To, Kelvin K. W.
    Chan, Betsy W. K.
    Li, Clara P. Y.
    Chiu, Susan S.
    Yuen, Kwok-Yung
    Ho, Pak-Leung
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2013, 51 (08) : 2592 - 2598
  • [8] Clinical Evaluation of the New High-Throughput Luminex NxTAG Respiratory Pathogen Panel Assay for Multiplex Respiratory Pathogen Detection
    Chen, Jonathan H. K.
    Lam, Ho-Yin
    Yip, Cyril C. Y.
    Wong, Sally C. Y.
    Chan, Jasper F. W.
    Ma, Edmond S. K.
    Cheng, Vincent C. C.
    Tang, Bone S. F.
    Yuen, Kwok-Yung
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2016, 54 (07) : 1820 - 1825
  • [9] Emergence of macrolide-resistant strains during an outbreak of Mycoplasma pneumoniae infections in children
    Chironna, M.
    Sallustio, A.
    Esposito, S.
    Perulli, M.
    Chinellato, I.
    Di Bari, C.
    Quarto, M.
    Cardinale, F.
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2011, 66 (04) : 734 - 737
  • [10] The Evolution of Advanced Molecular Diagnostics for the Detection and Characterization of Mycoplasma pneumoniae
    Diaz, Maureen H.
    Winchell, Jonas M.
    [J]. FRONTIERS IN MICROBIOLOGY, 2016, 7