MALDI-TOF MS performance compared to direct examination, culture, and 16S rDNA PCR for the rapid diagnosis of bone and joint infections

被引:13
|
作者
Lallemand, E. [1 ]
Coiffier, G. [2 ,3 ,4 ]
Arvieux, C. [3 ,5 ]
Brillet, E. [3 ,6 ]
Guggenbuhl, P. [2 ,3 ,4 ,7 ]
Jolivet-Gougeon, A. [1 ,2 ,7 ,8 ]
机构
[1] Rennes Univ Hosp, Pole Biol, Rue Henri Le Guilloux, F-35043 Rennes, France
[2] INSERM UMR U991, Rennes, France
[3] Ctr Reference Infect Osteo Articulaires Complexes, Rennes, France
[4] Rennes Univ Hosp, Serv Rhumatol, Rue Henri Le Guilloux, F-35043 Rennes, France
[5] Rennes Univ Hosp, Serv Malad Infect, Rue Henri Le Guilloux, F-35043 Rennes, France
[6] Rennes Univ Hosp, Imagerie Osteo Articulaire, Rue Henri Le Guilloux, F-35043 Rennes, France
[7] Univ Rennes 1, F-35043 Rennes, France
[8] Univ Rennes 1, EA 1254, Equipe Microbiol, 2 Ave Prof Leon Bernard, F-35043 Rennes, France
关键词
DESORPTION IONIZATION-TIME; FLIGHT MASS-SPECTROMETRY; RIBOSOMAL-RNA GENE; DIRECT IDENTIFICATION; SEPTIC ARTHRITIS; URINE SAMPLES; BACTERIA; MICROORGANISMS; AMPLIFICATION; PATHOGENS;
D O I
10.1007/s10096-016-2608-x
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The rapid identification of bacterial species involved in bone and joint infections (BJI) is an important element to optimize the diagnosis and care of patients. The aim of this study was to evaluate the usefulness of matrix-assisted laser desorption ionization mass spectrometry (MALDI-TOF MS) for the rapid diagnosis of bone infections, directly on synovial fluid (SF) or on crushed osteoarticular samples (CS). From January to October 2013, we prospectively analyzed 111 osteoarticular samples (bone and joint samples, BJS) from 78 patients in care at the University Hospital of Rennes, France. The diagnosis procedure leading to the sample collection was linked to a suspicion of infection, inflammatory disease, arthritis, or for any bone or joint abnormalities. Standard bacteriological diagnosis and molecular biology analysis [16S rRNA polymerase chain reaction (PCR) and sequencing] were conducted. In addition, analysis by MALDI-TOF MS was performed directly on the osteoarticular samples, as soon as the amount allowed. Culture, which remains the gold standard for the diagnosis of BJI, has the highest sensitivity (85.9 %) and remains necessary to test antimicrobial susceptibility. The 16S rDNA PCR results were positive in the group with positive BJI (28.6 %) and negative in the group without infection. Direct examination remains insensitive (31.7 %) but more effective than MALDI-TOF MS directly on the sample (6.3 %). The specificity was 100 % in all cases, except for culture (74.5 %). Bacterial culture remains the gold standard, especially enrichment in blood bottles. Direct analysis of bone samples with MALDI-TOF MS is not useful, possibly due to the low inoculum of BJS.
引用
收藏
页码:857 / 866
页数:10
相关论文
共 50 条
  • [1] MALDI-TOF MS performance compared to direct examination, culture, and 16S rDNA PCR for the rapid diagnosis of bone and joint infections
    E. Lallemand
    G. Coiffier
    C. Arvieux
    E. Brillet
    P. Guggenbuhl
    A. Jolivet-Gougeon
    European Journal of Clinical Microbiology & Infectious Diseases, 2016, 35 : 857 - 866
  • [2] Rapid direct detection of pathogens for diagnosis of joint infections by MALDI-TOF MS after liquid enrichment in the BacT/Alert blood culture system
    Noll, Christine
    Nasruddin-Yekta, Azadda
    Sternisek, Pia
    Weig, Michael
    Gross, Uwe
    Schilling, Arndt F.
    Beil, Frank Timo
    Bader, Oliver
    PLOS ONE, 2020, 15 (12):
  • [3] Rapid species-level identification of vaginal and oral lactobacilli using MALDI-TOF MS analysis and 16S rDNA sequencing
    Anderson, Annette Carola
    Sanunu, Mohamed
    Schneider, Christian
    Clad, Andreas
    Karygianni, Lamprini
    Hellwig, Elmar
    Al-Ahmad, Ali
    BMC MICROBIOLOGY, 2014, 14
  • [4] Rapid species-level identification of vaginal and oral lactobacilli using MALDI-TOF MS analysis and 16S rDNA sequencing
    Annette Carola Anderson
    Mohamed Sanunu
    Christian Schneider
    Andreas Clad
    Lamprini Karygianni
    Elmar Hellwig
    Ali Al-Ahmad
    BMC Microbiology, 14
  • [5] Identification of airborne bacteria by 16S rDNA sequencing, MALDI-TOF MS and the MIDI microbial identification system
    Fykse, Else Marie
    Tjarnhage, Torbjorn
    Humppi, Tarmo
    Eggen, Vilde Sorvik
    Ingebretsen, Andre
    Skogan, Gunnar
    Olofsson, Goran
    Wasterby, Par
    Gradmark, Per-Ake
    Larsson, Anders
    Dybwad, Marius
    Blatny, Janet Martha
    AEROBIOLOGIA, 2015, 31 (03) : 271 - 281
  • [6] Identification of airborne bacteria by 16S rDNA sequencing, MALDI-TOF MS and the MIDI microbial identification system
    Else Marie Fykse
    Torbjörn Tjärnhage
    Tarmo Humppi
    Vilde Sørvik Eggen
    Andre Ingebretsen
    Gunnar Skogan
    Göran Olofsson
    Pär Wästerby
    Per-Åke Gradmark
    Anders Larsson
    Marius Dybwad
    Janet Martha Blatny
    Aerobiologia, 2015, 31 : 271 - 281
  • [7] Comparison of MALDI-TOF MS Biotyper and 16S rDNA sequencing for the identification of Pseudomonas species isolated from fish
    Kacaniova, Miroslava
    Kluga, Alina
    Kantor, Attila
    Medo, Juraj
    Ziarovska, Jana
    Puchalski, Czeslaw
    Terentjeva, Margarita
    MICROBIAL PATHOGENESIS, 2019, 132 : 313 - 318
  • [8] MALDI-TOF MS与16S rDNA方法对乳酸菌鉴定分析比较
    宋丹靓敏
    陈晴
    周梦瑶
    张佳欣
    程莎莎
    方如雪
    姜毓君
    满朝新
    中国乳品工业, 2021, 49 (10) : 4 - 7+53
  • [9] MALDI-TOF for species identification of nonfermenting bacteria: Evaluation and comparison to 16S rDNA sequencing
    Mellmann, A.
    Cloud, J.
    Maier, T.
    Keckevoet, U.
    Rarnminger, I.
    Iwen, P.
    Dunn, J.
    Hall, G.
    Wilson, D.
    LaSala, P. R.
    Kostrzewa, M.
    Harmsen, D.
    INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY, 2007, 297 : 16 - 17
  • [10] Comparison of VITEK2, MALDI-TOF MS, and 16S rDNA sequencing for identification of Myroides odoratus and Myroides odoratimimus
    Schroettner, Percy
    Rudolph, Wolfram W.
    Eing, Bodo R.
    Bertram, Sebastian
    Gunzer, Florian
    DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2014, 79 (02) : 155 - 159