Population variation in NAIP functional copy number confers increased cell death upon Legionella pneumophila infection

被引:21
作者
Boniotto, Michele [1 ,2 ]
Tailleux, Ludovic [3 ]
Lomma, Mariella [4 ]
Gicquel, Brigitte [3 ]
Buchrieser, Carmen [4 ]
Garcia, Sylvie [5 ]
Quintana-Murci, Lluis [1 ,2 ]
机构
[1] Inst Pasteur, Unit Human Evolutionary Genet, F-75015 Paris, France
[2] Inst Pasteur, CNRS, URA3012, F-75015 Paris, France
[3] Inst Pasteur, Unit Mycobacterial Genet, F-75015 Paris, France
[4] CNRS, URA 2171, F-75015 Paris, France
[5] CNRS, URA 1961, F-75015 Paris, France
关键词
NAIP; Legionella; Infection; Copy number variation; SPINAL MUSCULAR-ATROPHY; NOD-LIKE RECEPTORS; GENE; RECOGNITION; INFLAMMATION; APOPTOSIS; INSIGHTS; IMMUNITY; PROTEIN;
D O I
10.1016/j.humimm.2011.10.014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The NAIP gene encodes an intracellular innate immunity receptor that senses flagellin. The genomic region containing NAIP presents a complex genomic organization and includes various NAIP paralogs. Here, we assessed the degree of copy number variation of the complete NAIP gene (NAIPFull) in various human populations and studied the functional impact of such variation on host cell fate using Legionella pneumophila as an infection model. We determined that African populations have a NAIPFull duplication at a higher frequency than Europeans and Asians, with an increased transcription of the gene. In addition, we demonstrated that a higher amount of the NAIPFull protein dramatically increases cell death upon infection by L. pneumophila, a mechanism that may account for increased host resistance to infection. We postulate that the NAIPFull gene duplication might have been evolutionary maintained, or even selected for, because it may confer an advantage to the host against flagellated bacteria. (C) 2012 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:196 / 200
页数:5
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