Propionibacterium acnes: Disease-Causing Agent or Common Contaminant? Detection in Diverse Patient Samples by Next-Generation Sequencing

被引:72
|
作者
Mollerup, Sarah [1 ]
Friis-Nielsen, Jens [2 ]
Vinner, Lasse [1 ]
Hansen, Thomas Arn [1 ]
Richter, Stine Raith [1 ]
Fridholm, Helena [1 ]
Herrera, Jose Alejandro Romero [2 ]
Lund, Ole [2 ]
Brunak, Soren [2 ,3 ]
Izarzugaza, Jose M. G. [2 ]
Mourier, Tobias [1 ]
Nielsen, Lars Peter [4 ,5 ]
Hansen, Anders Johannes [1 ]
机构
[1] Univ Copenhagen, Nat Hist Museum Denmark, Ctr GeoGenet, Copenhagen, Denmark
[2] Tech Univ Denmark, Dept Syst Biol, Ctr Biol Sequence Anal, DK-2800 Lyngby, Denmark
[3] Univ Copenhagen, Panum Inst, Dis Syst Biol Program, DK-2200 Copenhagen, Denmark
[4] Statens Serum Inst, Dept Autoimmunol & Biomarkers, Copenhagen S, Denmark
[5] Aalborg Univ, Hlth Sci, Aalborg, Denmark
基金
新加坡国家研究基金会;
关键词
HUMAN SKIN MICROBIOME; LYMPH-NODES; SURGERY; DNA; IDENTIFICATION; SARCOIDOSIS; INFECTIONS; DISCOVERY; PATHOGEN; IMPACT;
D O I
10.1128/JCM.02723-15
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Propionibacterium acnes is the most abundant bacterium on human skin, particularly in sebaceous areas. P. acnes is suggested to be an opportunistic pathogen involved in the development of diverse medical conditions but is also a proven contaminant of human clinical samples and surgical wounds. Its significance as a pathogen is consequently a matter of debate. In the present study, we investigated the presence of P. acnes DNA in 250 next-generation sequencing data sets generated from 180 samples of 20 different sample types, mostly of cancerous origin. The samples were subjected to either microbial enrichment, involving nuclease treatment to reduce the amount of host nucleic acids, or shotgun sequencing. We detected high proportions of P. acnes DNA in enriched samples, particularly skin tissue-derived and other tissue samples, with the levels being higher in enriched samples than in shotgun-sequenced samples. P. acnes reads were detected in most samples analyzed, though the proportions in most shotgun-sequenced samples were low. Our results show that P. acnes can be detected in practically all sample types when molecular methods, such as next-generation sequencing, are employed. The possibility of contamination from the patient or other sources, including laboratory reagents or environment, should therefore always be considered carefully when P. acnes is detected in clinical samples. We advocate that detection of P. acnes always be accompanied by experiments validating the association between this bacterium and any clinical condition.
引用
收藏
页码:980 / 987
页数:8
相关论文
共 50 条
  • [21] Next-generation sequencing-based assay for detection of human papillomavirus in clinical samples
    Yeom, E.
    Park, M. R.
    Lee, S.
    Choi, Z.
    Shin, S.
    Lee, S-t.
    Choi, J. R.
    ANNALS OF ONCOLOGY, 2024, 35
  • [22] Comparative Analysis of Metagenomic Next-Generation Sequencing, Sanger Sequencing, and Conventional Culture for Detecting Common Pathogens Causing Lower Respiratory Tract Infections in Clinical Samples
    Yi, Qiaolian
    Zhang, Ge
    Wang, Tong
    Li, Jin
    Kang, Wei
    Zhang, Jingjia
    Liu, Yali
    Xu, Yingchun
    MICROORGANISMS, 2025, 13 (03)
  • [23] Next-generation Sequencing Results Require Higher Inoculum for Cutibacterium acnes Detection Than Conventional Anaerobic Culture
    Fernandez-Rodriguez, Diana
    Cho, Jeongeun
    Parvizi, Niosha
    Khan, Adam Z.
    Parvizi, Javad
    Namdari, Surena
    CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 2023, 481 (12) : 2484 - 2491
  • [24] Identification and characterization of disease-causing genes in non-5q-SMA by next-generation sequencing technology: Lessons learned from NeurOmics study
    Karakaya, M.
    Storbeck, M.
    Strathmann, E.
    Delle Vedove, A.
    Hoelker, I.
    Altmueller, J.
    Motameny, S.
    Alawbathani, S.
    Thiele, H.
    Polat, I.
    Wunderlich, G.
    Ardicli, D.
    Topaloglu, H.
    Kirschner, J.
    Schrank, B.
    Maroofian, R.
    Magnusson, O.
    Yis, U.
    Nuernberg, P.
    Heller, R.
    Wirth, B.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 1483 - 1484
  • [25] Optimum Designs for Next-Generation Sequencing to Discover Rare Variants for Common Complex Disease
    Shi, Gang
    Rao, D. C.
    GENETIC EPIDEMIOLOGY, 2011, 35 (06) : 572 - 579
  • [26] Next-generation sequencing for measurable residual disease detection in acute myeloid leukaemia
    Ghannam, Jack
    Dillon, Laura W.
    Hourigan, Christopher S.
    BRITISH JOURNAL OF HAEMATOLOGY, 2020, 188 (01) : 77 - 85
  • [27] Next-Generation Sequencing: An Advanced Diagnostic Tool for Detection of Pancreatic Disease/Disorder
    Biswas, Suvro
    Afrose, Shamima
    Mita, Mohasana Akter
    Hasan, Md. Robiul
    Shimu, Mst. Sharmin Sultana
    Zaman, Shahriar
    Saleh, Md. Abu
    JGH OPEN, 2024, 8 (11):
  • [28] Standardized Minimal Residual Disease Detection by Next-Generation Sequencing in Multiple Myeloma
    Yao, Qiumei
    Bai, Yinlei
    Orfao, Alberto
    Chim, Chor Sang
    FRONTIERS IN ONCOLOGY, 2019, 9
  • [29] The detection of mosaic mutationsin hereditary aortic disease through next-generation sequencing
    Yan, Z. G.
    Yang, H.
    Zhang, Y. H.
    Zhou, Z.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 277 - 278
  • [30] Rare APOE p.Gly4Glu: A putative disease-causing variant for early-onset Alzheimer's disease identified by next-generation sequencing
    Wu, Chu-Ting
    Hu, Liang-Hsuan
    Weng, Hui-Ying
    Liu, Yen-Ming
    Lin, Yung-Feng
    Tsai, Shih-Feng
    Lo, Raymond Y.
    Ching, Yung-Hao
    TZU CHI MEDICAL JOURNAL, 2025, 37 (02):