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利用混合映射评估非裔美国人对金黄色葡萄球菌菌血症的遗传易感性。

Evaluating genetic susceptibility to Staphylococcus aureus bacteremia in African Americans using admixture mapping.

作者信息

Cyr D D, Allen A S, Du G-J, Ruffin F, Adams C, Thaden J T, Maskarinec S A, Souli M, Guo S, Dykxhoorn D M, Scott W K, Fowler V G

机构信息

Duke Clinical Research Institute, Duke University Medical Center, Durham, NC, USA.

Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, USA.

出版信息

Genes Immun. 2017 Mar;18(2):95-99. doi: 10.1038/gene.2017.6. Epub 2017 Mar 23.


DOI:10.1038/gene.2017.6
PMID:28332560
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5435963/
Abstract

The incidence of Staphylococcus aureus bacteremia (SAB) is significantly higher in African American (AA) than in European-descended populations. We used admixture mapping (AM) to test the hypothesis that genomic variations with different frequencies in European and African ancestral genomes influence susceptibility to SAB in AAs. A total of 565 adult AAs (390 cases with SAB; 175 age-matched controls) were genotyped for AM analysis. A case-only admixture score and a mixed χ(1df) score (MIX) to jointly evaluate both single-nucleotide polymorphism (SNP) and admixture association (P<5.00e-08) were computed using MIXSCORE. In addition, a permutation scheme was implemented to derive multiplicity adjusted P-values (genome-wide 0.05 significance threshold: P<9.46e-05). After empirical multiplicity adjustment, one region on chromosome 6 (52 SNPs, P=4.56e-05) in the HLA class II region was found to exhibit a genome-wide statistically significant increase in European ancestry. This region encodes genes involved in HLA-mediated immune response and these results provide additional evidence for genetic variation influencing HLA-mediated immunity, modulating susceptibility to SAB.

摘要

非裔美国人(AA)中金黄色葡萄球菌菌血症(SAB)的发病率显著高于欧洲裔人群。我们使用混合映射(AM)来检验这一假设,即在欧洲和非洲祖先基因组中频率不同的基因组变异会影响非裔美国人对SAB的易感性。对总共565名成年非裔美国人(390例SAB患者;175名年龄匹配的对照)进行基因分型以进行AM分析。使用MIXSCORE计算仅病例混合评分和混合χ(1自由度)评分(MIX),以联合评估单核苷酸多态性(SNP)和混合关联(P<5.00e-08)。此外,实施了一种置换方案以得出多重性调整后的P值(全基因组0.05显著性阈值:P<9.46e-05)。经过经验性多重性调整后,发现HLA II类区域中6号染色体上的一个区域(52个SNP,P=4.56e-05)在欧洲血统中呈现出全基因组统计学上的显著增加。该区域编码参与HLA介导的免疫反应的基因,这些结果为影响HLA介导的免疫、调节对SAB易感性的遗传变异提供了额外证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a10c/5435963/aa13a70370ac/gene20176f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a10c/5435963/2136e8b09221/gene20176f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a10c/5435963/aa13a70370ac/gene20176f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a10c/5435963/2136e8b09221/gene20176f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a10c/5435963/aa13a70370ac/gene20176f2.jpg

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[2]
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[3]
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[4]
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[5]
adaptive evolution: Recent insights on how immune evasion, immunometabolic subversion and host genetics impact vaccine development.

Front Cell Infect Microbiol. 2022

[6]
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J Infect. 2023-2

[7]
Human Leukocyte Antigen (HLA) System: Genetics and Association with Bacterial and Viral Infections.

J Immunol Res. 2022

[8]
Admixture Mapping of Sepsis in European Individuals With African Ancestries.

Front Med (Lausanne). 2022-3-8

[9]
Genetic Ancestry Inference and Its Application for the Genetic Mapping of Human Diseases.

Int J Mol Sci. 2021-6-28

[10]
Evasion of Immunological Memory by Infection: Implications for Vaccine Design.

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本文引用的文献

[1]
Familial Clustering of Staphylococcus aureus Bacteremia in First-Degree Relatives: A Danish Nationwide Cohort Study.

Ann Intern Med. 2016-7-5

[2]
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PLoS Pathog. 2016-1-14

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Polymorphisms in HLA Class II Genes Are Associated With Susceptibility to Staphylococcus aureus Infection in a White Population.

J Infect Dis. 2016-3-1

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Trends Microbiol. 2015-6-22

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Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections.

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A genome-wide association study of variants associated with acquisition of Staphylococcus aureus bacteremia in a healthcare setting.

BMC Infect Dis. 2014-2-13

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mBio. 2013-8-20

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J Infect Dis. 2012-8-7

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Haplotype Association Mapping Identifies a Candidate Gene Region in Mice Infected With Staphylococcus aureus.

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