Diagnostic Value of 16S Ribosomal RNA Gene Polymerase Chain Reaction/Sanger Sequencing in Clinical Practice

被引:32
作者
Fida, Madiha [1 ,2 ]
Khalil, Sarwat [1 ,3 ]
Abu Saleh, Omar [1 ]
Challener, Douglas W. [1 ]
Sohail, Muhammad Rizwan [1 ,4 ]
Yang, Joshua N. [2 ]
Pritt, Bobbi S. [2 ]
Schuetz, Audrey N. [2 ]
Patel, Robin [1 ,2 ]
机构
[1] Mayo Clin, Dept Med, Div Infect Dis, Rochester, MN USA
[2] Mayo Clin, Dept Lab Med & Pathol, Div Clin Microbiol, Rochester, MN USA
[3] Univ Minnesota, Dept Med, Div Infect Dis & Int Med, Box 736 UMHC, Minneapolis, MN 55455 USA
[4] Baylor Coll Med, Dept Med, Div Infect Dis, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
molecular diagnostics; 16S rRNA gene PCR; Sanger sequencing; broad range bacterial PCR; bacterial infections; BROAD-RANGE PCR; INFECTIVE ENDOCARDITIS; BACTERIAL IDENTIFICATION; CULTURE; DNA; PATHOGENS; SAMPLES; SEPSIS; IMPACT;
D O I
10.1093/cid/ciab167
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Accurate microbiologic diagnosis is important for appropriate management of infectious diseases. Sequencing-based molecular diagnostics are increasingly used for precision diagnosis of infections. However, their clinical utility is unclear. Methods. We conducted a retrospective analysis of specimens that underwent 16S ribosomal RNA (rRNA) gene polymerase chain reaction (PCR) followed by Sanger sequencing at our institution from April 2017 through March 2019. Results. A total of 566 specimens obtained from 460 patients were studied. Patients were considered clinically infected or noninfected based on final diagnosis and management. In 17% of patients, 16S rRNA PCR/sequencing was positive and in 5% of patients, this test led to an impact on clinical care. In comparison, bacterial cultures were positive in 21% of patients. Specimens with a positive Gram stain had 12 times greater odds of having a positive molecular result than those with a negative Gram stain (95% confidence interval for odds ratio, 5.2-31.4). Overall, PCR positivity was higher in cardiovascular specimens (37%) obtained from clinically infected patients, with bacterial cultures being more likely to be positive for musculoskeletal specimens (P <.001). 16S rRNA PCR/sequencing identified a probable pathogen in 10% culture-negative specimens. Conclusion. 16S rRNA PCR/sequencing can play a role in the diagnostic evaluation of patients with culture-negative infections, especially those with cardiovascular infections.
引用
收藏
页码:961 / 968
页数:8
相关论文
共 41 条
[1]   Utility of 16S rRNA PCR performed on clinical specimens in patient management [J].
Akram, A. ;
Maley, M. ;
Gosbell, I. ;
Nguyen, T. ;
Chavada, R. .
INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2017, 57 :144-149
[2]   Influence of 16S ribosomal RNA gene polymerase chain reaction and sequencing on antibiotic management of bone and joint infections [J].
Alraddadi, B. ;
Al-Azri, S. ;
Forward, K. R. .
CANADIAN JOURNAL OF INFECTIOUS DISEASES & MEDICAL MICROBIOLOGY, 2013, 24 (02) :85-88
[3]   16S rRNA PCR on clinical specimens: Impact on diagnosis and therapeutic management [J].
Bador, J. ;
Nicolas, B. ;
Chapuis, A. ;
Varin, V. ;
Dullier-Taillefumier, N. ;
de Curraize, C. ;
Amoureux, L. ;
Putot, A. ;
Neuwirth, C. .
MEDECINE ET MALADIES INFECTIEUSES, 2020, 50 (01) :63-73
[4]   Microbial Identification Using DNA Target Amplification and Sequencing: Clinical Utility and Impact on Patient Management [J].
Basein, Tinzar ;
Gardiner, Bradley J. ;
Vazquez, Gabriela M. Andujar ;
Chandranesan, Andrew S. Joel ;
Rabson, Arthur R. ;
Doron, Shira ;
Snydman, David R. .
OPEN FORUM INFECTIOUS DISEASES, 2018, 5 (11)
[5]   Evaluation of 16S rRNA Gene PCR Sensitivity and Specificity for Diagnosis of Prosthetic Joint Infection: a Prospective Multicenter Cross-Sectional Study [J].
Bemer, Pascale ;
Plouzeau, Chloe ;
Tande, Didier ;
Leger, Julie ;
Giraudeau, Bruno ;
Valentin, Anne Sophie ;
Jolivet-Gougeon, Anne ;
Vincent, Pascal ;
Corvec, Stephane ;
Gibaud, Sophie ;
Juvin, Marie Emmanuelle ;
Hery-Arnaud, Genevieve ;
Lemarie, Carole ;
Kempf, Marie ;
Bret, Laurent ;
Quentin, Roland ;
Coffre, Carine ;
de Pinieux, Gonzague ;
Bernard, Louis ;
Burucoa, Christophe .
JOURNAL OF CLINICAL MICROBIOLOGY, 2014, 52 (10) :3583-3589
[6]   Comparison of cultures and 16S rRNA sequencing for identification of bacteria in two-stage revision arthroplasties: preliminary report [J].
Bereza, Przemyslaw ;
Ekiel, Alicja ;
Augusciak-Duma, Aleksandra ;
Aptekorz, Malgorzata ;
Wilk, Iwona ;
Kusz, Damian ;
Wojciechowski, Piotr ;
Sieron, Aleksander L. ;
Martirosian, Gayane .
BMC MUSCULOSKELETAL DISORDERS, 2016, 17
[7]   Diagnosis of prosthetic joint infections using UMD-Universal Kit and the automated multiplex-PCR Unyvero i60 ITI® cartridge system: a pilot study [J].
Borde, Johannes P. ;
Haecker, Georg A. ;
Guschl, Sina ;
Serr, Annerose ;
Danner, Tobias ;
Huebner, Johannes ;
Burrack-Lange, Sandra ;
Luedke, Gerd ;
Helwig, Peter ;
Hauschild, Oliver ;
Kern, Winfried V. .
INFECTION, 2015, 43 (05) :551-560
[8]   Etiologic diagnosis of infective endocarditis by broad-range polymerase chain reaction:: A 3-year experience [J].
Bosshard, PP ;
Kronenberg, A ;
Zbinden, R ;
Ruef, C ;
Böttger, EC ;
Altwegg, M .
CLINICAL INFECTIOUS DISEASES, 2003, 37 (02) :167-172
[9]   Streptococcus pneumoniae endocarditis:: Persistence of DNA on heart valve material 7 years after infectious episode [J].
Branger, S ;
Casalta, JP ;
Habib, G ;
Collard, F ;
Raoult, D .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (09) :4435-4437
[10]   Impact of 16S rRNA gene sequence analysis for identification of bacteria on clinical microbiology and infectious diseases [J].
Clarridge, JE .
CLINICAL MICROBIOLOGY REVIEWS, 2004, 17 (04) :840-+