Evaluation of 16S rRNA broad range PCR assay for microbial detection in serum specimens in sepsis patients

被引:18
作者
Mishra, Deepanshi [1 ]
Satpathy, Gita [1 ,2 ]
Wig, Naveet [3 ]
Fazal, Farhan [3 ]
Ahmed, Nishat Hussain [1 ]
Panda, Subrat Kumar [4 ]
机构
[1] All India Inst Med Sci, Ocular Microbiol, Dr RP Ctr Ophthalm Sci, New Delhi, India
[2] All India Inst Med Sci, Dept Microbiol, New Delhi, India
[3] All India Inst Med Sci, Dept Med, New Delhi, India
[4] All India Inst Med Sci, Dept Pathol, New Delhi, India
关键词
Broad range PCR assay; Automated culture; Nucleotide sequencing; NCBI BLAST analysis; Sepsis; Blood stream infection; BLOOD-STREAM INFECTIONS; MOLECULAR DIAGNOSIS; MORTALITY; RDNA;
D O I
10.1016/j.jiph.2020.01.007
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Early and accurate laboratory diagnosis and appropriate management of infection improves the survival rate in sepsis. In this study we evaluated broad range 16S rRNA and 16 S-23 S intergenic spacer region (ISR) PCR assays followed by nucleotide sequencing directly from patients' serum and automated blood culture for laboratory diagnosis in admitted sepsis patients. Methods: A broad range 16S rRNA PCR and 16 S-23 S ISR PCR assay followed by nucleotide sequencing was used directly from patients' serum in hospital admitted patients in 62 sepsis and 16 suspected blood stream infection (sBSI) patients. Automated blood culture was also used in the same patients. Nucleotide sequences were analyzed against NCBI Genbank database and organisms were identified using CLSI MM18A guidelines. Results: Bacterial culture were positive in 10/62 (16.12%) sepsis and 3/16 (18.75%) suspected BSI patients along with 3 detected fungi (2 in sepsis and 1 in suspected BSI group). PCR assay was positive in 36/62 (58.06%) sepsis and 6/16 (37.5%) suspected BSI patients respectively. All but 2 bacteria (both from culture negative patients) detected by PCR assay could be identified from nucleotide sequencing. Survival in sepsis patients was 77%. PCR assay could detect bacteria in 9/14 (64.28%) of sepsis patients with death. Conclusion: Broad range PCR assay was far superior for early diagnosis of infection. The bacteria which could not be detected by culture and were not commonly reported from this centre, were detected by the broad range PCR assays. Detection of these rare bacteria/fungi had significant clinical correlation with patient's underlying clinical conditions, immune status and prognosis. The tests could provide definitive diagnosis of infection in >58% of sepsis patients, which helped in patient management and better survival. (C) 2020 The Author(s). Published by Elsevier Ltd on behalf of King Saud Bin Abdulaziz University for Health Sciences. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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页码:998 / 1002
页数:5
相关论文
共 22 条
[1]  
[Anonymous], 2010, PERFORMANCE STANDARD
[2]   Clinicomicrobiological profile of the Indian elderly with sepsis [J].
Arland, Arvind Kumar ;
Kumar, Nilesh ;
Gambhir, Indrajeet Singh .
ANNALS OF TROPICAL MEDICINE AND PUBLIC HEALTH, 2016, 9 (05) :316-320
[3]  
BAUER AW, 1966, AM J CLIN PATHOL, V45, P493
[4]   A Comparative Study to Assess the Determinants and Outcomes of Sepsis Treated in Medical Wards and ICU in an Indian Teaching Hospital [J].
Bhattacharya, Prasanta Kumar ;
Gautom, Debdutta ;
Nath, Neena ;
Saikia, Hiranya .
JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 2016, 10 (06) :OC1-OC6
[5]   Molecular diagnosis of bloodstream infections with a new dual-priming oligonucleotide-based multiplex PCR assay [J].
Carrara, Lucrecia ;
Navarro, Ferran ;
Turbau, Miguel ;
Seres, Montse ;
Moran, Indalecio ;
Quintana, Isabel ;
Martino, Rodrigo ;
Gonzalez, Yesica ;
Brell, Albert ;
Cordon, Oscar ;
Diestra, Karol ;
Mata, Caterina ;
Mirelis, Beatriz ;
Coll, Pere .
JOURNAL OF MEDICAL MICROBIOLOGY, 2013, 62 :1673-1679
[6]   Assessment of Global Incidence and Mortality of Hospital-treated Sepsis [J].
Fleischmann, Carolin ;
Scherag, Andre ;
Adhikari, Neill K. J. ;
Hartog, Christiane S. ;
Tsaganos, Thomas ;
Schlattmann, Peter ;
Angus, Derek C. ;
Reinhart, Konrad .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2016, 193 (03) :259-272
[7]   Evaluation of broad-range 16S rRNA PCR for the diagnosis of bloodstream infections: two years of experience [J].
Hassan, Reem M. ;
El Enany, Mervat G. ;
Rizk, Hussien H. .
JOURNAL OF INFECTION IN DEVELOPING COUNTRIES, 2014, 8 (10) :1252-1258
[8]   Comparative Analysis of Two Broad-Range PCR Assays for Pathogen Detection in Positive-Blood-Culture Bottles: PCR-High-Resolution Melting Analysis versus PCR-Mass Spectrometry [J].
Jeng, Kevin ;
Gaydos, Charlotte A. ;
Blyn, Lawrence B. ;
Yang, Samuel ;
Won, Helen ;
Matthews, Heather ;
Toleno, Donna ;
Hsieh, Yu-Hsiang ;
Carroll, Karen C. ;
Hardick, Justin ;
Masek, Billy ;
Kecojevic, Alexander ;
Sampath, Rangarajan ;
Peterson, Stephen ;
Rothman, Richard E. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2012, 50 (10) :3287-3292
[9]   Comparison of 16S rRNA gene PCR and BACTEC 9240 for detection of neonatal bacteremia [J].
Jordan, JA ;
Durso, MB .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (07) :2574-2578
[10]   Improving the Diagnosis of Bloodstream Infections: PCR Coupled with Mass Spectrometry [J].
Jordana-Lluch, Elena ;
Gimenez, Montserrat ;
Quesada, M. Dolores ;
Ausina, Vicente ;
Martro, Elisa .
BIOMED RESEARCH INTERNATIONAL, 2014, 2014