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Publication Detail
Identification of bacteria and potential sources in neonates at risk of infection delivered by Caesarean and vaginal birth
  • Publication Type:
    Journal article
  • Publication Sub Type:
    Journal Article
  • Authors:
    Gonzales-Marin C, Spratt DA, Millar MR, Simmonds M, Kempley ST, Allaker RP
  • Publication date:
  • Pagination:
    31, 41
  • Journal:
    Journal of Medical Microbiology
  • Volume:
  • Issue:
  • Status:
  • Print ISSN:
Neonatal gastric aspirates (NGA) are routinely screened in UK hospitals to investigate fetal/ neonatal infections associated with cases of adverse pregnancy outcome (APO). he aim of this study was to describe and compare the microbiology of NGA from Caesarean nd vaginal deliveries using molecular methods, and to evaluate other possible clinical and non-clinical variables that may have determined the presence of the bacteria in the amples. The value of using NGA and molecular methods to investigate potential athogens associated with the risk of early infection was also evaluated. Bacteria were identified by a combined molecular approach on the basis of the 16S rRNA gene using both clone analysis and denaturing gradient gel electrophoresis. A total of 43 and 34 different species were identified in the vaginal (n5121) and Caesarean (n5119) deliveries, respectively; 26 of the species observed (51%) were comm. on to both modalities, although usually less prevalent in the Caesarean cases. Multivariate analysis confirmed an association between infection and prolonged rupture of membranes in vaginal deliveries (odds ratio55.7, 95% confidence interval51.1-29.0). Various associations between infection and given variables were also shown, including labour, intrapartum antibiotic prophylaxis, and time and place of sample collection. The molecular methods allowed identification of a range of bacteria and potential sources not previously observed in NGA, including possible genito-urinary, gastrointestinal and oral pathogens. NGA represents a valuable sample for investigating potential pathogens associated with APO and the risk of early infection in neonates using molecular methods. © 2012 SGM Printed in Great Britain.
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