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GWAS Study

Host genome wide association study of infant susceptibility to <i>Shigella</i>-associated diarrhea.

Duchen D, Haque R, Chen L et al.

33649051 PubMed ID
GWAS Study Type
589 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

DD
Duchen D
HR
Haque R
CL
Chen L
WG
Wojcik G
KP
Korpe P
NU
Nayak U
MA
Mentzer AJ
KB
Kirkpatrick B
PW
Petri WA
DP
Duggal P
Chapter II

Abstract

Summary of the research findings

Shigella is a leading cause of moderate-to-severe diarrhea globally and the causative agent of shigellosis and bacillary dysentery. Associated with 80 to 165 million cases of diarrhea and &gt;13% of diarrheal deaths, in many regions, Shigella exposure is ubiquitous while infection is heterogenous. To characterize host-genetic susceptibility to Shigella-associated diarrhea, we performed two independent genome-wide association studies (GWAS) including Bangladeshi infants from the PROVIDE and CBC birth cohorts in Dhaka, Bangladesh. Cases were infants with Shigella-associated diarrhea (n = 143) and controls were infants with no Shigella-associated diarrhea in the first 13 months of life (n = 446). Shigella-associated diarrhea was identified via quantitative PCR (qPCR) threshold cycle (CT ) distributions for the ipaH gene, carried by all four Shigella species and enteroinvasive Escherichia coli Host GWAS were performed under an additive genetic model. A joint analysis identified protective loci on chromosomes 11 (rs582240, within the KRT18P59 pseudogene; P = 6.40 × 10-8; odds ratio [OR], 0.43) and 8 (rs12550437, within the lincRNA RP11-115J16.1; P = 1.49 × 10-7; OR, 0.48). Conditional analyses identified two previously suggestive loci, a protective locus on chromosome 7 (rs10266841, within the 3' untranslated region [UTR] of CYTH3; Pconditional = 1.48 × 10-7; OR, 0.44) and a risk-associated locus on chromosome 10 (rs2801847, an intronic variant within MPP7; Pconditional = 8.37 × 10-8; OR, 5.51). These loci have all been indirectly linked to bacterial type 3 secretion system (T3SS) activity, its components, and bacterial effectors delivered into host cells. Host genetic factors that may affect bacterial T3SS activity and are associated with the host response to Shigella-associated diarrhea may provide insight into vaccine and drug development efforts for Shigella-associated diarrheal disease.

143 Bangladeshi cases, 446 Bangladeshi controls

Chapter III

Study Statistics

Key metrics and study information

589
Total Participants
GWAS
Study Type
No
Replicated
South Asian
Ancestry
Bangladesh
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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