Next generation microbiology and cystic fibrosis diagnostics: are we there yet?

被引:0
|
作者
Moser, Claus [1 ,4 ]
Thomsen, Trine Rolighed [2 ,3 ]
Hoiby, Niels [1 ,4 ]
机构
[1] Copenhagen Univ Hosp, Rigshosp, Dept Clin Microbiol, Henrik Harpestrengsvej 4A, DK-2100 Copenhagen, Denmark
[2] Aalborg Univ, Dept Chem & Biosci, Ctr Microbial Communities, Aalborg, Denmark
[3] Danish Technol Inst, Life Sci, Aarhus, Denmark
[4] Univ Copenhagen, Inst Microbiol & Immunol, Costerton Biofilm Ctr, Copenhagen, Denmark
关键词
clinical diagnostics; lung microbiota; molecular diagnostics; next-generation sequencing; whole-genome sequencing; MYCOBACTERIUM-ABSCESSUS; RESPIRATORY VIRUSES; YOUNG-CHILDREN; INDUCED SPUTUM; INFECTION; INFANTS; 16S; ADULTS; LUNGS;
D O I
10.1097/MCP.0000000000000516
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Purpose of review The major problem for cystic fibrosis patients is the recurrent and chronic infections of the lungs, determining their prognosis. The challenge from biofilm-growing bacteria and emerging viruses urge the microbiological laboratories to develop better and faster diagnostic tools. Of these, molecular diagnostics are rapidly developing. However, beyond detecting many microorganisms, the task is to evaluate their clinical significance. This has always been a problem resulting in Koch's postulates. Then, the task was to distinguish the offending pathogens from the normal flora, as today, however, the normal flora is renamed microbiota. Recent findings This review includes the most recent studies on molecular diagnostics of viral and bacterial infections in cystic fibrosis. Generally, molecular methods have revolutionized virus and bacterial detection, and species-specific and multiplex molecular methods are valuable. However, the large amount of data obtained from new sequencing techniques challenge the interpretation and evaluation of clinical relevance. Summary More research is needed to discriminate offending pathogens from contaminating microbiota and to be able to identify the anatomical origin of the many detected microbes. Furthermore, the sequencing techniques must report all the detected microbes to the species level to allow the clinician to evaluate the properties of the microbes being relevant for the infection.
引用
收藏
页码:599 / 605
页数:7
相关论文
共 50 条
  • [31] DESIGN OF NEXT GENERATION CFTR MRNA THERAPEUTICS FOR THE TREATMENT OF PATIENTS WITH CYSTIC FIBROSIS
    Boeglin, L.
    Dias, A.
    Tran, K.
    Nanduri, P.
    Guenard, C.
    Kaushal, N.
    Abysalh, J.
    Skaleski, J.
    Woo, C.
    Lane, K.
    Morin, R.
    DeRosa, F.
    Androsavich, J.
    Barbier, A.
    Wooster, R.
    PEDIATRIC PULMONOLOGY, 2020, 55 : S239 - S239
  • [32] Towards next generation therapies for cystic fibrosis: Folding, function and pharmacology of CFTR
    Bose, Samuel J.
    Krainer, Georg
    Ng, Demi R. S.
    Schenkel, Mathias
    Shishido, Hideki
    Yoon, Jae Seok
    Haggie, Peter M.
    Schlierf, Michael
    Sheppard, David N.
    Skach, William R.
    JOURNAL OF CYSTIC FIBROSIS, 2020, 19 : S25 - S32
  • [33] The Evaluation of Next Generation Sequencing in Breast Cancer and Cystic Fibrosis Mutation Screening
    Heggarty, Shirley
    Wright, W.
    McCullough, M.
    Beattie, D.
    Graham, C. A.
    JOURNAL OF MEDICAL GENETICS, 2012, 49 : S121 - S121
  • [34] Epidemiology and genetics of cystic fibrosis in Asia: In preparation for the next-generation treatments
    Singh, Meenu
    Rebordosa, Cristina
    Bernholz, Juliane
    Sharma, Neeraj
    RESPIROLOGY, 2015, 20 (08) : 1172 - 1181
  • [35] Next-Generation Sequencing for Molecular Diagnosis of Cystic Fibrosis in a Brazilian Cohort
    Cambraia, Amanda
    Campos Junior, Mario
    Zembrzuski, Veronica Marques
    Junqueira, Ricardo Magrani
    Cabello, Pedro Hernan
    de Cabello, Giselda Maria Kalil
    DISEASE MARKERS, 2021, 2021
  • [36] Next Generation Sequencing to Determine the Cystic Fibrosis Mutation Spectrum in Palestinian Population
    Essawi, O.
    Farraj, M.
    De Leeneer, K.
    Steyaert, W.
    De Pauw, K.
    De Paepe, A.
    Claes, K.
    Essawi, T.
    Coucke, P. J.
    DISEASE MARKERS, 2015, 2015
  • [37] Next generation genetic studies and personalized therapy: the successful model of Cystic Fibrosis
    Lucarelli, Marco
    BIOCHIMICA CLINICA, 2018, 42 (01) : 44 - 50
  • [38] Next generation diagnostics on cardiomyopathy
    Jean-Louis Blouin
    Jeremy Bevillard
    Periklis Makrythanasis
    Michel Guipponi
    Federico Santoni
    Stylianos E Antonarakis
    Siv Fokstuen
    Molecular Cytogenetics, 7 (Suppl 1)
  • [39] Next-Generation Farnesoid X Receptor Agonists in NASH Treatment: Are We There Yet?
    Debosch, Brian J.
    GASTROENTEROLOGY, 2023, 165 (02) : 513 - 514
  • [40] Diagnosis and management of invasive fungal diseases by next-generation sequencing: are we there yet?
    Babady, N. Esther
    Chiu, Charles Y.
    Craney, Arryn
    Gaston, David C.
    Hicklen, Rachel S.
    Hogan, Catherine A.
    John, Teny M.
    Stewart, Adam G.
    EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2024,