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

dc.contributor.coauthorBowdish, Dawn M. E.
dc.contributor.coauthorSakamoto, Kaori
dc.contributor.coauthorHill, Philip C.
dc.contributor.coauthorSirugo, Giorgio
dc.contributor.coauthorNewport, Melanie J.
dc.contributor.coauthorGordon, Siamon
dc.contributor.coauthorHill, Adrian V. S.
dc.contributor.coauthorVannberg, Fredrick O.
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorLack, Nathan Alan
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T11:39:38Z
dc.date.issued2013
dc.description.abstractBackground: 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 ?2 = 6.5, p = 0.001, rs12998782, Mantel-Haenszel 2x2 ?2 = 6.59, p = 0.001, rs13389814 Mantel-Haenszel 2x2 ?2 = 6.9, p = 0.0009) were associated with susceptibility to tuberculosis and one (rs7559955, Mantel-Haenszel 2x2 ?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.
dc.description.fulltextYES
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipWellcome Trust
dc.description.sponsorshipNIH
dc.description.sponsorshipMcMaster Immunology Research Centre
dc.description.sponsorshipM. G. DeGroote Institute for Infectious Disease Research
dc.description.versionPublisher version
dc.description.volume14
dc.identifier.eissn1471-2350
dc.identifier.embargoNO
dc.identifier.filenameinventorynoIR00077
dc.identifier.issn1471-2350
dc.identifier.quartileQ4
dc.identifier.scopus2-s2.0-84876725812
dc.identifier.urihttps://hdl.handle.net/20.500.14288/130
dc.identifier.wos318862300001
dc.keywordsScavenger receptors
dc.keywordsMycobacterium tuberculosis
dc.keywordsSingle nucleotide polymorphisms
dc.keywordsCase control study
dc.keywordsMARCO
dc.language.isoeng
dc.publisherBioMed Central
dc.relation.grantno1 R15 AI094436-01A1
dc.relation.ispartofBMC Medical Genetics
dc.relation.urihttp://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/1109
dc.subjectGenetics
dc.subjectHeredity
dc.titleGenetic variants of MARCO are associated with susceptibility to pulmonary tuberculosis in a Gambian population
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorLack, Nathan Alan
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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