Direct 16S/18S rRNA Gene PCR Followed by Sanger Sequencing as a Clinical Diagnostic Tool for Detection of Bacterial and Fungal Infections: a Systematic Review and Meta-Analysis

被引:10
|
作者
Drevinek, Pavel [1 ,2 ]
Hollweck, Regina [3 ]
Lorenz, Michael G. [4 ]
Lustig, Michael [4 ]
Bjarnsholt, Thomas [5 ,6 ]
机构
[1] Charles Univ Prague, Fac Med 2, Dept Med Microbiol, Prague, Czech Republic
[2] Motol Univ Hosp, Prague, Czech Republic
[3] Novustat GmbH, Wollerau, Switzerland
[4] Molzym GmbH & Co KG, Bremen, Germany
[5] Rigshosp, Ctr Diagnost, Dept Clin Microbiol, Copenhagen, Denmark
[6] Univ Copenhagen, Costerton Biofilm Ctr, Copenhagen, Denmark
关键词
agnostic molecular diagnosis; added value of sequencing; bacterial meningitis; change of antibiotic treatment; culture-negative infections; fastidious and rare pathogens; infectious endocarditis; joint infections; nongrowing pathogens; sepsis; POLYMERASE-CHAIN-REACTION; BROAD-RANGE PCR; MOLECULAR DIAGNOSIS; BLOOD-SAMPLES; IDENTIFICATION; PATHOGENS; ACCURACY; BACTEREMIA; SEPTIFAST; CHILDREN;
D O I
10.1128/jcm.00338-23
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
rRNA gene Sanger sequencing is being used for the identification of cultured pathogens. A new diagnostic approach is sequencing of uncultured samples by using the commercial DNA extraction and sequencing platform SepsiTest (ST). rRNA gene Sanger sequencing is being used for the identification of cultured pathogens. A new diagnostic approach is sequencing of uncultured samples by using the commercial DNA extraction and sequencing platform SepsiTest (ST). The goal was to analyze the clinical performance of ST with a focus on nongrowing pathogens and the impact on antibiotic therapy. A literature search used PubMed/Medline, Cochrane, Science Direct, and Google Scholar. Eligibility followed PRISMA-P criteria. Quality and risk of bias were assessed drawing on QUADAS-2 (quality assessment of diagnostic accuracy studies, revised) criteria. Meta-analyses were performed regarding accuracy metrics compared to standard references and the added value of ST in terms of extra found pathogens. We identified 25 studies on sepsis, infectious endocarditis, bacterial meningitis, joint infections, pyomyositis, and various diseases from routine diagnosis. Patients with suspected infections of purportedly sterile body sites originated from various hospital wards. The overall sensitivity (79%; 95% confidence interval [CI], 73 to 84%) and specificity (83%; 95% CI, 72 to 90%) were accompanied by large effect sizes. ST-related positivity was 32% (95% CI, 30 to 34%), which was significantly higher than the culture positivity (20%; 95% CI, 18 to 22%). The overall added value of ST was 14% (95% CI, 10 to 20%) for all samples. With 130 relevant taxa, ST uncovered high microbial richness. Four studies demonstrated changes of antibiotic treatment at 12% (95% CI, 9 to 15%) of all patients upon availability of ST results. ST appears to be an approach for the diagnosis of nongrowing pathogens. The potential clinical role of this agnostic molecular diagnostic tool is discussed regarding changes of antibiotic treatment in cases where culture stays negative.
引用
收藏
页数:18
相关论文
共 13 条
  • [1] Microbiological culture versus 16S/18S rRNA gene PCR-sanger sequencing for infectious keratitis: a three-arm, diagnostic cross-sectional study
    Hammoudeh, Yasmeen
    Suresh, Lakshmi
    Ong, Zun Zheng
    Lister, Michelle M.
    Mohammed, Imran
    Thomas, D. John I.
    Cottell, Jennifer L.
    Holden, Jennifer M.
    Said, Dalia G.
    Dua, Harminder S.
    Ting, Darren Shu Jeng
    FRONTIERS IN MEDICINE, 2024, 11
  • [2] Use of Universal 16S rRNA Gene PCR as a Diagnostic Tool for Venous Access Port-Related Bloodstream Infections
    Guembe, M.
    Marin, M.
    Martin-Rabadan, P.
    Echenagusia, A.
    Camunez, F.
    Rodriguez-Rosales, G.
    Simo, G.
    Echenagusia, M.
    Bouza, E.
    JOURNAL OF CLINICAL MICROBIOLOGY, 2013, 51 (03) : 799 - 804
  • [3] Evaluation of direct 16S rRNA PCR from clinical samples for bacterial detection in normally sterile body sites
    Satilmis, Serife
    Toprak, Nurver Ulger
    Ilgin, Can
    Soyletir, Guner
    JOURNAL OF INFECTION IN DEVELOPING COUNTRIES, 2019, 13 (11): : 978 - 983
  • [4] Comparative analysis of the leprosy detection rate regarding its clinical spectrum through PCR using the 16S rRNA gene: a scientometrics and meta-analysis
    Silva, Marcos Jesse Abrahao
    Brasil, Thiago Pinto
    Silva, Caroliny Soares
    Frota, Cristiane Cunha
    Sardinha, Daniele Melo
    Figueira, Luiza Raquel Tapajos
    Neves, Keitty Anne Silva
    dos Santos, Everaldina Cordeiro
    Lima, Karla Valeria Batista
    Ghisi, Nedia de Castilhos
    Lima, Luana Nepomuceno Gondim Costa
    FRONTIERS IN MICROBIOLOGY, 2024, 15
  • [5] 16S Ribosomal Ribonucleic Acid Gene Polymerase Chain Reaction in the Diagnosis of Bloodstream Infections: A Systematic Review and Meta-Analysis
    Su, Guoming
    Fu, Zhuqing
    Hu, Liren
    Wang, Yueying
    Zhao, Zuguo
    Yang, Weiqing
    PLOS ONE, 2015, 10 (05):
  • [6] Validation and Retrospective Clinical Evaluation of a Quantitative 16S rRNA Gene Metagenomic Sequencing Assay for Bacterial Pathogen Detection in Body Fluids
    Culbreath, Karissa
    Melanson, Suzanne
    Gale, James
    Baker, Justin
    Li, Fan
    Saebo, Oystein
    Kommedal, Oyvind
    Contreras, Deisy
    Garner, Omai B.
    Yang, Shangxin
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2019, 21 (05) : 913 - 923
  • [7] Direct 16S/ITS rRNA Gene PCR Followed by Sanger Sequencing for Detection of Mycetoma Causative Agents in Dakar, Senegal: A Pilot Study Among Patients with Mycetoma Attending Aristide Le Dantec University Hospital
    Diongue, Khadim
    Dione, Jean-Noel
    Diop, Abdoulaye
    Kabtani, Jihane
    Diallo, Mamadou Alpha
    L'Ollivier, Coralie
    Seck, Mame Cheikh
    Ndiaye, Mouhamadou
    Badiane, Aida Sadikh
    Ndiaye, Daouda
    Ranque, Stephane
    MYCOPATHOLOGIA, 2024, 189 (05)
  • [8] A detailed analysis of 16S rRNA gene sequencing and conventional PCR-based testing for the diagnosis of bacterial pathogens and discovery of novel bacteria
    Li, Mei-Na
    Wang, Ting
    Wang, Nan
    Han, Qiang
    You, Xue-Ming
    Zhang, Shuai
    Zhang, Cui-Cui
    Shi, Yong-Qiang
    Qiao, Pei-Zhuang
    Man, Cheng-Lian
    Feng, Teng
    Li, Yue-Yue
    Zhu, Zhuang
    Quan, Ke-Ji
    Xu, Teng-Lin
    Zhang, George Fei
    ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY, 2024, 117 (01):
  • [9] Broad-range PCR, cloning and sequencing of the full 16S rRNA gene for detection of bacterial DNA in synovial fluid samples of Tunisian patients with reactive and undifferentiated arthritis
    Siala, Mariam
    Gdoura, Radhouane
    Fourati, Hela
    Rihl, Markus
    Jaulhac, Benoit
    Younes, Mohamed
    Sibilia, Jean
    Baklouti, Sofien
    Bargaoui, Naceur
    Sellami, Slaheddine
    Sghir, Abdelghani
    Hammami, Adnane
    ARTHRITIS RESEARCH & THERAPY, 2009, 11 (04)
  • [10] Comparative Analysis of Airborne Bacterial and Fungal Communities in South-Eastern Italy and in Albania Using the Compositional Analysis of 16S and ITS rRNA Gene Sequencing Datasets
    Romano, Salvatore
    Pepkolaj, Leke
    Fragola, Mattia
    Peccarrisi, Dalila
    Dhimitri, Jostina
    Buccolieri, Alessandro
    Tala, Adelfia
    Alifano, Pietro
    Quarta, Gianluca
    Calcagnile, Lucio
    ATMOSPHERE, 2024, 15 (10)