A genetic basis of susceptibility to acute pyelonephritis.
(2007) In PLoS ONE 2(9). p.10-825- Abstract
- Background
For unknown reasons, urinary tract infections (UTIs) are clustered in certain individuals. Here we propose a novel, genetically determined cause of susceptibility to acute pyelonephritis, which is the most severe form of UTI. The IL-8 receptor, CXCR1, was identified as a candidate gene when mIL-8Rh mutant mice developed acute pyelonephritis (APN) with severe tissue damage.
Methods and Findings
We have obtained CXCR1 sequences from two, highly selected APN prone patient groups, and detected three unique mutations and two known polymorphisms with a genotype frequency of 23% and 25% compared to 7% in controls (p<0.001 and p<0.0001, respectively). When reflux was excluded, 54% of... (More) - Background
For unknown reasons, urinary tract infections (UTIs) are clustered in certain individuals. Here we propose a novel, genetically determined cause of susceptibility to acute pyelonephritis, which is the most severe form of UTI. The IL-8 receptor, CXCR1, was identified as a candidate gene when mIL-8Rh mutant mice developed acute pyelonephritis (APN) with severe tissue damage.
Methods and Findings
We have obtained CXCR1 sequences from two, highly selected APN prone patient groups, and detected three unique mutations and two known polymorphisms with a genotype frequency of 23% and 25% compared to 7% in controls (p<0.001 and p<0.0001, respectively). When reflux was excluded, 54% of the patients had CXCR1 sequence variants. The UTI prone children expressed less CXCR1 protein than the pediatric controls (p<0.0001) and two sequence variants were shown to impair transcription.
Conclusions
The results identify a genetic innate immune deficiency, with a strong link to APN and renal scarring. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/607964
- author
- organization
- publishing date
- 2007
- type
- Contribution to journal
- publication status
- published
- subject
- in
- PLoS ONE
- volume
- 2
- issue
- 9
- pages
- 10 - 825
- publisher
- Public Library of Science (PLoS)
- external identifiers
-
- wos:000207455500009
- scopus:41049104005
- ISSN
- 1932-6203
- DOI
- 10.1371/journal.pone.0000825
- language
- English
- LU publication?
- yes
- id
- 601a9784-a115-43e1-9a25-51d1b4e1a639 (old id 607964)
- date added to LUP
- 2016-04-01 15:56:24
- date last changed
- 2023-09-04 09:24:17
@article{601a9784-a115-43e1-9a25-51d1b4e1a639, abstract = {{Background<br/><br> <br/><br> For unknown reasons, urinary tract infections (UTIs) are clustered in certain individuals. Here we propose a novel, genetically determined cause of susceptibility to acute pyelonephritis, which is the most severe form of UTI. The IL-8 receptor, CXCR1, was identified as a candidate gene when mIL-8Rh mutant mice developed acute pyelonephritis (APN) with severe tissue damage.<br/><br> Methods and Findings<br/><br> <br/><br> We have obtained CXCR1 sequences from two, highly selected APN prone patient groups, and detected three unique mutations and two known polymorphisms with a genotype frequency of 23% and 25% compared to 7% in controls (p<0.001 and p<0.0001, respectively). When reflux was excluded, 54% of the patients had CXCR1 sequence variants. The UTI prone children expressed less CXCR1 protein than the pediatric controls (p<0.0001) and two sequence variants were shown to impair transcription.<br/><br> Conclusions<br/><br> <br/><br> The results identify a genetic innate immune deficiency, with a strong link to APN and renal scarring.}}, author = {{Lundstedt, Ann-Charlotte and McCarthy, Shane and Gustafsson, Mattias and Godaly, Gabriela and Jodal, Ulf and Karpman, Diana and Leijonhufvud, Irene and Lindén, Carin and Martinell, Jeanette and Ragnarsdottir, Bryndis and Samuelsson, Martin and Truedsson, Lennart and Andersson, Björn and Svanborg, Catharina}}, issn = {{1932-6203}}, language = {{eng}}, number = {{9}}, pages = {{10--825}}, publisher = {{Public Library of Science (PLoS)}}, series = {{PLoS ONE}}, title = {{A genetic basis of susceptibility to acute pyelonephritis.}}, url = {{https://lup.lub.lu.se/search/files/4519610/626138.pdf}}, doi = {{10.1371/journal.pone.0000825}}, volume = {{2}}, year = {{2007}}, }