Genetic variants of MARCO are associated with susceptibility to pulmonary tuberculosis in a Gambian population

被引:29
作者
Bowdish, Dawn M. E. [1 ]
Sakamoto, Kaori [2 ]
Lack, Nathan A. [3 ]
Hill, Philip C. [4 ,5 ]
Sirugo, Giorgio [4 ,6 ]
Newport, Melanie J. [7 ]
Gordon, Siamon [8 ]
Hill, Adrian V. S. [9 ]
Vannberg, Fredrick O. [10 ]
机构
[1] McMaster Univ, McMaster Immunol Res Ctr, Hamilton, ON L8S 4K1, Canada
[2] Univ Georgia, Coll Vet Med, Dept Pathol, Athens, GA 30605 USA
[3] Koc Univ, Sch Med, TR-34450 Istanbul, Turkey
[4] MRC Labs, Fajara, Gambia
[5] Univ Otago, Sch Med, Dept Prevent & Social Med, Ctr Int Hlth, Dunedin, New Zealand
[6] Osped San Pietro Fatebenefratelli, Rome, Italy
[7] Brighton & Sussex Med Sch, Brighton BN1 9PS, E Sussex, England
[8] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
[9] Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
[10] Georgia Inst Technol, Sch Biol, Atlanta, GA 30332 USA
基金
英国惠康基金;
关键词
Scavenger receptors; Mycobacterium tuberculosis; Single nucleotide polymorphisms; Case control study; MARCO; SCAVENGER RECEPTOR MARCO; MYCOBACTERIUM-TUBERCULOSIS; GENOME-WIDE; COMPLEMENT RECEPTORS; DENDRITIC CELLS; HOST-DEFENSE; LUNG DEFENSE; RISK-FACTORS; SR-AI/II; IN-VIVO;
D O I
10.1186/1471-2350-14-47
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: The two major class A scavenger receptors are scavenger receptor A (SRA), which is constitutively expressed on most macrophage populations, and macrophage receptor with collagenous structure (MARCO), which is constitutively expressed on a more restricted subset of macrophages, (e.g. alveolar macrophages) but whose expression increases on most macrophages during the course of infection. Although the primary role of SRA appears to be clearance of modified host proteins and lipids, mice defective in expression of either MARCO or SRA are immunocompromised in multiple models of infection and in vitro assays, the scavenger receptors have been demonstrated to bind bacteria and to enhance pro-inflammatory signalling to many bacterial lung pathogens; however their importance in Mycobacterium tuberculosis infection, is less clear. Methods: To determine whether polymorphisms in either SRA or MARCO were associated with tuberculosis, a case-control study of was performed. DNA samples from newly-detected, smear-positive, pulmonary tuberculosis cases were collected from The Gambia. Controls for this study consisted of DNA from cord bloods obtained from routine births at local Gambian health clinics. Informed written consent was obtained from patients or their parents or guardians. Ethical approval was provided by the joint The Gambian Government/MRC Joint Ethics Committee. Results: We studied the frequencies of 25 polymorphisms of MSR1 (SRA) and 22 in MARCO in individuals with tuberculosis (n=1284) and matched controls (n=1349). No SNPs within the gene encoding or within 1 kb of the promoter sequence of MSR1 were associated with either susceptibility or resistance to tuberculosis. Three SNPs in MARCO (rs4491733, Mantel-Haenszel 2x2 chi 2 = 6.5, p = 0.001, rs12998782, Mantel-Haenszel 2x2 chi 2 = 6.59, p = 0.001, rs13389814 Mantel-Haenszel 2x2 chi 2 = 6.9, p = 0.0009) were associated with susceptibility to tuberculosis and one (rs7559955, Mantel-Haenszel 2x2 chi 2 = 6.9, p = 0.0009) was associated with resistance to tuberculosis. Conclusions: These findings identify MARCO as a potentially important receptor in the host response to tuberculosis.
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页数:7
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