Genetic variability in beta-defensins is not associated with susceptibility to Staphylococcus aureus bacteremia.
Human beta-defensins are key components of human innate immunity to a variety of pathogens, including Staphylococcus aureus. The aim of the present study was to investigate a potential association between gene variations in DEFB1 and DEFB103/DEFB4 and the development of S. aureus bacteremia (SAB) em...
Main Authors: | , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2012-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC3285211?pdf=render |
id |
doaj-7e607d0edf0b4d2fbdb1f7846723f612 |
---|---|
record_format |
Article |
spelling |
doaj-7e607d0edf0b4d2fbdb1f7846723f6122020-11-25T01:53:30ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0172e3231510.1371/journal.pone.0032315Genetic variability in beta-defensins is not associated with susceptibility to Staphylococcus aureus bacteremia.Peder FodeAnders Rhod LarsenBjarke FeenstraCathrine JespersgaardRobert Leo SkovMarc SteggerVance G FowlerDanish SAB Study Group ConsortiumPaal Skytt AndersenHuman beta-defensins are key components of human innate immunity to a variety of pathogens, including Staphylococcus aureus. The aim of the present study was to investigate a potential association between gene variations in DEFB1 and DEFB103/DEFB4 and the development of S. aureus bacteremia (SAB) employing a case-control design.Cases were unique patients with documented SAB, identified with the National S. aureus Bacteremia Register, a comprehensive dataset of all episodes of community associated-SABs (CA-SAB) occurring in children (≤20 yrs) in Denmark from 1990 to 2006. Controls were age-matched healthy individuals with no history of SAB. DNA obtained from cases and controls using the Danish Newborn Screening Biobank were genotyped for functional polymorphisms of DEFB1 by Sanger sequencing and copy number variation of the DEFB103 and DEFB4 genes using Pyrosequencing-based Paralogue Ratio Test (P-PRT).193 ethnic Danish SAB cases with 382 age-matched controls were used for this study. S. aureus isolates represented a variety of bacterial (i.e., different spa types) types similar to SAB isolates in general. DEFB1 minor allele frequencies of rs11362 (cases vs. controls 0.47/0.44), rs1800972 (0.21/0.24), and rs1799946 (0.32/0.33) were not significantly different in cases compared with controls. Also, DEFB4/DEFB103 gene copy numbers (means 4.83/4.92) were not significantly different in cases compared with controls.Using a large, unique cohort of pediatric CA-SAB, we found no significant association between DEFB1 genetic variation or DEFB4/DEFB103 gene copy number and susceptibility for SAB.http://europepmc.org/articles/PMC3285211?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Peder Fode Anders Rhod Larsen Bjarke Feenstra Cathrine Jespersgaard Robert Leo Skov Marc Stegger Vance G Fowler Danish SAB Study Group Consortium Paal Skytt Andersen |
spellingShingle |
Peder Fode Anders Rhod Larsen Bjarke Feenstra Cathrine Jespersgaard Robert Leo Skov Marc Stegger Vance G Fowler Danish SAB Study Group Consortium Paal Skytt Andersen Genetic variability in beta-defensins is not associated with susceptibility to Staphylococcus aureus bacteremia. PLoS ONE |
author_facet |
Peder Fode Anders Rhod Larsen Bjarke Feenstra Cathrine Jespersgaard Robert Leo Skov Marc Stegger Vance G Fowler Danish SAB Study Group Consortium Paal Skytt Andersen |
author_sort |
Peder Fode |
title |
Genetic variability in beta-defensins is not associated with susceptibility to Staphylococcus aureus bacteremia. |
title_short |
Genetic variability in beta-defensins is not associated with susceptibility to Staphylococcus aureus bacteremia. |
title_full |
Genetic variability in beta-defensins is not associated with susceptibility to Staphylococcus aureus bacteremia. |
title_fullStr |
Genetic variability in beta-defensins is not associated with susceptibility to Staphylococcus aureus bacteremia. |
title_full_unstemmed |
Genetic variability in beta-defensins is not associated with susceptibility to Staphylococcus aureus bacteremia. |
title_sort |
genetic variability in beta-defensins is not associated with susceptibility to staphylococcus aureus bacteremia. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2012-01-01 |
description |
Human beta-defensins are key components of human innate immunity to a variety of pathogens, including Staphylococcus aureus. The aim of the present study was to investigate a potential association between gene variations in DEFB1 and DEFB103/DEFB4 and the development of S. aureus bacteremia (SAB) employing a case-control design.Cases were unique patients with documented SAB, identified with the National S. aureus Bacteremia Register, a comprehensive dataset of all episodes of community associated-SABs (CA-SAB) occurring in children (≤20 yrs) in Denmark from 1990 to 2006. Controls were age-matched healthy individuals with no history of SAB. DNA obtained from cases and controls using the Danish Newborn Screening Biobank were genotyped for functional polymorphisms of DEFB1 by Sanger sequencing and copy number variation of the DEFB103 and DEFB4 genes using Pyrosequencing-based Paralogue Ratio Test (P-PRT).193 ethnic Danish SAB cases with 382 age-matched controls were used for this study. S. aureus isolates represented a variety of bacterial (i.e., different spa types) types similar to SAB isolates in general. DEFB1 minor allele frequencies of rs11362 (cases vs. controls 0.47/0.44), rs1800972 (0.21/0.24), and rs1799946 (0.32/0.33) were not significantly different in cases compared with controls. Also, DEFB4/DEFB103 gene copy numbers (means 4.83/4.92) were not significantly different in cases compared with controls.Using a large, unique cohort of pediatric CA-SAB, we found no significant association between DEFB1 genetic variation or DEFB4/DEFB103 gene copy number and susceptibility for SAB. |
url |
http://europepmc.org/articles/PMC3285211?pdf=render |
work_keys_str_mv |
AT pederfode geneticvariabilityinbetadefensinsisnotassociatedwithsusceptibilitytostaphylococcusaureusbacteremia AT andersrhodlarsen geneticvariabilityinbetadefensinsisnotassociatedwithsusceptibilitytostaphylococcusaureusbacteremia AT bjarkefeenstra geneticvariabilityinbetadefensinsisnotassociatedwithsusceptibilitytostaphylococcusaureusbacteremia AT cathrinejespersgaard geneticvariabilityinbetadefensinsisnotassociatedwithsusceptibilitytostaphylococcusaureusbacteremia AT robertleoskov geneticvariabilityinbetadefensinsisnotassociatedwithsusceptibilitytostaphylococcusaureusbacteremia AT marcstegger geneticvariabilityinbetadefensinsisnotassociatedwithsusceptibilitytostaphylococcusaureusbacteremia AT vancegfowler geneticvariabilityinbetadefensinsisnotassociatedwithsusceptibilitytostaphylococcusaureusbacteremia AT danishsabstudygroupconsortium geneticvariabilityinbetadefensinsisnotassociatedwithsusceptibilitytostaphylococcusaureusbacteremia AT paalskyttandersen geneticvariabilityinbetadefensinsisnotassociatedwithsusceptibilitytostaphylococcusaureusbacteremia |
_version_ |
1724990599618101248 |