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GWAS Study

Human Genetic Susceptibility to Native Valve Staphylococcus aureus Endocarditis in Patients With S. aureus Bacteremia: Genome-Wide Association Study.

Moreau K, Clemenceau A, Le Moing V et al.

29670602 PubMed ID
GWAS Study Type
319 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

MK
Moreau K
CA
Clemenceau A
LM
Le Moing V
MD
Messika-Zeitoun D
AP
Andersen PS
BN
Bruun NE
SR
Skov RL
CF
Couzon F
BC
Bouchiat C
EM
Erpelding ML
VB
van Belkum A
BY
Bossé Y
DX
Duval X
VF
Vandenesch F
Chapter II

Abstract

Summary of the research findings

Staphylococcus aureus infective endocarditis (SaIE) is a severe complication of S. aureus bacteremia (SAB) occurring in up to 22% of patients. Bacterial genetic factors and host conditions for SaIE have been intensely studied before; however, to date no study has focused on predisposing host genetic factors to SaIE. The present study aimed to identify genetic polymorphisms associated with SaIE by a Genome-Wide Association Study (GWAS) of 67 patients with definite native valve SaIE (cases) and 72 matched native valve patients with SAB but without IE (controls). All patients were enrolled in the VIRSTA cohort (Le Moing et al., 2015) study. Four single nucleotide polymorphisms (SNPs) located on chromosome 3 were associated with SaIE (P < 1 × 10-5) without reaching conventional genome-wide significance. For all, the frequency of the minor allele was lower in cases than in controls, suggesting a protective effect of the minor allele against SaIE. The same association was observed using an independent Danish verification cohort of SAB with (n = 57) and without (n = 123) IE. Ex vivo analysis of aortic valve tissues revealed that SaIE associated SNPs mentioned above were associated with significantly higher mRNA expression levels of SLC7A14, a predicted cationic amino acid transporter protein. Taken together, our results suggest an IE-protective effect of SNPs on chromosome 3 during the course of SAB. The effects of protective minor alleles may be mediated by increasing expression levels of SLC7A14 in valve tissues. We conclude that occurrence of SaIE may be the combination of a well-adapted bacterial genotype to a susceptible host.

67 European ancestry cases, 72 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

319
Total Participants
GWAS
Study Type
Yes
Replicated
57 Danish ancestry cases, 123 Danish ancestry controls
Replication Participants
European
Ancestry
France, Denmark
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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