본문 바로가기
KERD
논문KCI 등재

Comparison of 16S Ribosomal RNA Targeted Sequencing and Culture for Bacterial Identification in Normally Sterile Body Fluid Samples: Report of a 10-Year Clinical Laboratory Review

2

조회

0

다운로드

0

인용

0

참고문헌

키워드

주제분류병리학

초록

As 16S ribosomal RNA (rRNA)-targeted sequencing can detect DNA from non-viable bacteria, it can be used to identify pathogens from clinical samples even in patients pretreated with antibiotics. We compared the results of 16S rRNA-targeted sequencing and culture for identifying bacterial species in normally sterile body fluid (NSBF): cerebrospinal, pericardial, peritoneal and pleural fluids. Over a 10-year period, a total of 312 NSBF samples were evaluated simultaneously using 16S rRNA-targeted sequencing and culture. Results were concordant in 287/312 (92.0%) samples, including 277 (88.8%) negative and 10 (3.2%) positive samples. Of the 16 sequencing-positive, culture-negative samples, eight showed clinically relevant isolates that included Fusobacterium nucleatum subsp. nucleatum, Streptococcus pneumoniae, and Staphylococcus spp. All these samples were obtained from the patients pretreated with antibiotics. The diagnostic yield of 16S rRNA-targeted sequencing combined with culture was 11.2%, while that of culture alone was 6.1%. 16S rRNA-targeted sequencing in conjunction with culture could be useful for identifying bacteria in NSBF samples, especially when patients have been pretreated with antibiotics and when anaerobic infection is suspected.

Abstract

As 16S ribosomal RNA (rRNA)-targeted sequencing can detect DNA from non-viable bacteria, it can be used to identify pathogens from clinical samples even in patients pretreated with antibiotics. We compared the results of 16S rRNA-targeted sequencing and culture for identifying bacterial species in normally sterile body fluid (NSBF): cerebrospinal, pericardial, peritoneal and pleural fluids. Over a 10-year period, a total of 312 NSBF samples were evaluated simultaneously using 16S rRNA-targeted sequencing and culture. Results were concordant in 287/312 (92.0%) samples, including 277 (88.8%) negative and 10 (3.2%) positive samples. Of the 16 sequencing-positive, culture-negative samples, eight showed clinically relevant isolates that included Fusobacterium nucleatum subsp. nucleatum, Streptococcus pneumoniae, and Staphylococcus spp. All these samples were obtained from the patients pretreated with antibiotics. The diagnostic yield of 16S rRNA-targeted sequencing combined with culture was 11.2%, while that of culture alone was 6.1%. 16S rRNA-targeted sequencing in conjunction with culture could be useful for identifying bacteria in NSBF samples, especially when patients have been pretreated with antibiotics and when anaerobic infection is suspected.

참고문헌 (20)

  1. Altun O, "Rapid identification of microorganisms from sterile body fluids by use of FilmArray", J Clin Microbiol, 53, pp.710~712 (2015)
  2. Grif K, "Improvement of detection of bacterial pathogens in normally sterile body sites with a focus on orthopedic samples by use of a commercial 16S rRNA broad-range PCR and sequence analysis", J Clin Microbiol, 50, pp.2250~2254 (2012)
  3. Rampini SK, "Broad-range 16S rRNA gene polymerase chain reaction for diagnosis of culture-negative bacterial infections", Clin Infect Dis, 53, pp.1245~1251 (2011)
  4. Sontakke S, "Use of broad range 16S rDNA PCR in clinical microbiology", J Microbiol Methods, 76, pp.217~225 (2009)
  5. Leber AL, "Clinical microbiology procedures handbook", pp.3.5~3.7 (2016), ASM Press
  6. CLSI, "Interpretive criteria for identification of bacteria and fungi by targeted DNA sequencing" (2018), Clinical and Laboratory Standards Institute
  7. Li X, "Use of tuf as a target for sequence-based identification of Gram-positive cocci of the genus Enterococcus, Streptococcus, coagulase-negative Staphylococcus, and Lactococcus", Ann Clin Microbiol Antimicrob, 11, pp.31~ (2012)
  8. Dauga C, "Evolution of the gyrB gene and the molecular phylogeny of Enterobacteriaceae: a model molecule for molecular systematic studies", Int J Syst Evol Microbiol, 52, pp.531~547 (2002)
  9. Basein T, "Microbial identification using DNA target amplification and sequencing: clinical utility and impact on patient management", Open Forum Infect Dis, 5, pp.ofy257~ (2018)
  10. Varani S, "Diagnosis of bloodstream infections in immunocompromised patients by real-time PCR", J Infect, 58, pp.346~351 (2009)
  11. Welinder-Olsson C, "Comparison of broad-range bacterial PCR and culture of cerebrospinal fluid for diagnosis of community-acquired bacterial meningitis", Clin Microbiol Infect, 13, pp.879~886 (2007)
  12. Fiore AE, "Clinical outcomes of meningitis caused by Streptococcus pneumoniae in the era of antibiotic resistance", Clin Infect Dis, 30, pp.71~77 (2000)
  13. Kanegaye JT, "Lumbar puncture in pediatric bacterial meningitis: defining the time interval for recovery of cerebrospinal fluid pathogens after parenteral antibiotic pretreatment", Pediatrics, 108, pp.1169~1174 (2001)
  14. Yang CC, "Characteristics and outcomes of Fusobacterium nucleatum bacteremia–a 6-year experience at a tertiary care hospital in northern Taiwan", Diagn Microbiol Infect Dis, 70, pp.167~174 (2011)
  15. de Vries JJ, "Campylobacter species isolated from extra-oro-intestinal abscesses: a report of four cases and literature review", Eur J Clin Microbiol Infect Dis, 27, pp.1119~1123 (2008)
  16. Jenkins C, "Detection and identification of bacteria in clinical samples by 16S rRNA gene sequencing: comparison of two different approaches in clinical practice", J Med Microbiol, 61, pp.483~488 (2012)
  17. Velásquez-Mejía EP, "Impact of DNA extraction, sample dilution, and reagent contamination on 16S rRNA gene sequencing of human feces", Appl Microbiol Biotechnol, 102, pp.403~411 (2018)
  18. Salter SJ, "Reagent and laboratory contamination can critically impact sequence-based microbiome analyses", BMC Biol, 12, pp.87~ (2014)
  19. Kolbert CP, "Ribosomal DNA sequencing as a tool for identification of bacterial pathogens", Curr Opin Microbiol, 2, pp.299~305 (1999)
  20. Bourbeau P, "Use of the BacT", Alert blood culture system for culture of sterile body fluids other than blood, 1998, pp.36, 3273~3277

관련 논문AI추천

Utility of a Direct 16S rDNA PCR and Sequencing for Etiological Diagnosis of Infective Endocarditis김미나, 김민선, 성흥섭, 이재원, 장정현, 정성호, 최상호대한진단검사의학회 · Annals of Laboratory Medicine2017 · 제37권 제6호Utility of Conventional Culture and MALDI-TOF MS for Identification of Microbial Communities in Bronchoalveolar Lavage Fluid in Comparison with the GS Junior Next Generation Sequencing System박무석, 성지연, 신미화, 용동은, 이경원, 이상훈, 황윤지대한진단검사의학회 · Annals of Laboratory Medicine2018 · 제38권 제2호혈액 배양 액체배지에서 세균성 병원균 검출을 위한 16S rDNA PCR의평가박건, 김영숙, 김진희, 문대수, 박영진, 비두루, 신종희, 장숙진대한임상미생물학회 · Annals of Clinical Microbiology2006 · 제9권 제1호Detection of Listeria monocytogenes in CSF from Three Patients with Meningoencephalitis by Next-Generation SequencingAo Shen, Haitao Ren, Honglong Wu, Hongzhi Guan, Jiali Zhou, Liying Cui, Ming Yao, Ruixue Sun, Xia Lv, Yicheng Zhu, Yinxin Zhang대한신경과학회 · Journal of Clinical Neurology2016 · 제12권 제4호Evaluation of the Seeplex® Meningitis ACE Detection Kit for the Detection of 12 Common Bacterial and Viral Pathogens of Acute Meningitis구선회, 권계철, 김지명, 박종우, 신소연, 신소영대한진단검사의학회 · Annals of Laboratory Medicine2012 · 제32권 제1호Factors Associated with the Performance of Direct PCR Detection of Mycobacteria in Clinical Specimens: Retrospective Real-world Data박창훈대한진단검사의학회 · Laboratory Medicine Online2023 · 제13권 제3호

이 간행물의 다른 논문 (16건)