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The use of culture-independent tools to characterize bacteria in endo-tracheal aspirates from pre-term infants at risk of bronchopulmonary dysplasia

  • Franziska Stressmann
  • , Gary Connett
  • , Kevin Goss
  • , Tanoj Kollamparambil
  • , Nilesh Patel
  • , Matthew Payne
  • , Victoria Puddy
  • , Julian Legg
  • , Kenneth Bruce
  • , Geraint Rogers

    Research output: Contribution to journalArticlepeer-review

    25 Citations (Scopus)

    Abstract

    Although premature infants are increasingly surviving the neonatal period, up to one-third develop bronchopulmonary dysplasia (BPD). Despite evidence that bacterial colonization of the neonatal respiratory tract by certain bacteria may be a risk factor in BPD development, little is known about the role these bacteria play. The aim of this study was to investigate the use of culture-independent molecular profiling methodologies to identify potential etiological agents in neonatal airway secretions. This study used terminal restriction fragment length polymorphism (T-RFLP) and clone sequence analyses to characterize bacterial species in endo-tracheal (ET) aspirates from eight intubated pre-term infants. A wide range of different bacteria was identified in the samples. Forty- seven T-RF band lengths were resolved in the sample set, with a range of 0-15 separate species in each patient. Clone sequence analyses confirmed the identity of individual species detected by T-RFLP. We speculate that the identification of known opportunistic pathogens including S. aureus, Enterobacter sp., Moraxella catarrhalis, Pseudomonas aeruginosa.

    Original languageEnglish
    Pages (from-to)333-337
    Number of pages5
    JournalJournal of Perinatal Medicine
    Volume38
    Issue number3
    DOIs
    Publication statusPublished - 1 May 2010

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • 16S rDNA
    • Bacterial infections
    • Bronchopulmonary dysplasia
    • Chronic lung disease of prematurity
    • Culture-independent molecular profiling
    • T-RFLP profiling

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