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Association between mannose-binding lectin gene polymorphisms and susceptibility to severe acute respiratory syndrome coronavirus infection

Identifieur interne : 000415 ( PascalFrancis/Curation ); précédent : 000414; suivant : 000416

Association between mannose-binding lectin gene polymorphisms and susceptibility to severe acute respiratory syndrome coronavirus infection

Auteurs : HONGXING ZHANG [République populaire de Chine] ; GANGQIAO ZHOU [République populaire de Chine] ; LIANTENG ZHI [République populaire de Chine] ; HAO YANG [République populaire de Chine] ; YUN ZHAI [République populaire de Chine] ; XIAOJIA DONG [République populaire de Chine] ; XIUMEI ZHANG [République populaire de Chine] ; XUE GAO [République populaire de Chine] ; YUNPING ZHU [République populaire de Chine] ; FUCHU HE [République populaire de Chine]

Source :

RBID : Pascal:05-0492671

Descripteurs français

English descriptors

Abstract

Background. Genetic determinants of susceptibility to severe acute respiratory syndrome coronavirus (SARS-CoV) infection remain unknown. We assessed whether mannose-binding lectin (MBL) gene polymorphisms were associated with susceptibility to SARS-CoV infection or disease severity in an ethnically homogeneous population born in northern China. Methods. The frequencies of 1 mutation in codon 54 and 3 promoter polymorphisms at nt -550, -221, and 4 were ascertained in 352 patients with SARS and 392 control subjects, by means of polymerase chain reaction direct sequencing. Results. Of 352 patients with SARS and 392 control subjects, 120 (34.4%) and 91 (23.2%) were carriers of the codon 54 variant, respectively (odds ratio [OR], 1.73 [95% confidence interval {CI}, 1.25-2.39]; P = .00086). A total of 123 (36.0%) of 352 patients with SARS and 100 (25.5%) of 392 control subjects had haplotype pairs associated with medium or low expression of MBL (OR, 1.67 [95% CI, 1.21-2.29]; P = .00187). The population-attributable fraction of patients with SARS that was associated with having the codon 54 variant was 20.1% (95% CI, 7.9%-32.3%). Conclusions. MBL gene polymorphisms were significantly associated with susceptibility to SARS-CoV infection; this might be explained by the reduced expression of functional MBL secondary to having the codon 54 variant.
pA  
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A02 01      @0 JIDIAQ
A03   1    @0 J. infect. dis.
A05       @2 192
A06       @2 8
A08 01  1  ENG  @1 Association between mannose-binding lectin gene polymorphisms and susceptibility to severe acute respiratory syndrome coronavirus infection
A11 01  1    @1 HONGXING ZHANG
A11 02  1    @1 GANGQIAO ZHOU
A11 03  1    @1 LIANTENG ZHI
A11 04  1    @1 HAO YANG
A11 05  1    @1 YUN ZHAI
A11 06  1    @1 XIAOJIA DONG
A11 07  1    @1 XIUMEI ZHANG
A11 08  1    @1 XUE GAO
A11 09  1    @1 YUNPING ZHU
A11 10  1    @1 FUCHU HE
A14 01      @1 Department of Genomics and Proteomics, Beijing Institute of Radiation Medicine @2 Beijing @3 CHN @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut. @Z 5 aut. @Z 8 aut. @Z 9 aut. @Z 10 aut.
A14 02      @1 Chinese National Human Genome Center at Beijing @2 Beijing @3 CHN @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut. @Z 5 aut. @Z 6 aut. @Z 7 aut. @Z 10 aut.
A14 03      @1 Institute of Biophysics, Chinese Academy of Science @2 Beijing @3 CHN @Z 1 aut.
A14 04      @1 Institute of Biomedical Sciences, Fudan University @2 Shanghai @3 CHN @Z 10 aut.
A20       @1 1355-1361
A21       @1 2005
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A47 01  1    @0 05-0492671
A60       @1 P
A61       @0 A
A64 01  1    @0 The Journal of infectious diseases
A66 01      @0 USA
C01 01    ENG  @0 Background. Genetic determinants of susceptibility to severe acute respiratory syndrome coronavirus (SARS-CoV) infection remain unknown. We assessed whether mannose-binding lectin (MBL) gene polymorphisms were associated with susceptibility to SARS-CoV infection or disease severity in an ethnically homogeneous population born in northern China. Methods. The frequencies of 1 mutation in codon 54 and 3 promoter polymorphisms at nt -550, -221, and 4 were ascertained in 352 patients with SARS and 392 control subjects, by means of polymerase chain reaction direct sequencing. Results. Of 352 patients with SARS and 392 control subjects, 120 (34.4%) and 91 (23.2%) were carriers of the codon 54 variant, respectively (odds ratio [OR], 1.73 [95% confidence interval {CI}, 1.25-2.39]; P = .00086). A total of 123 (36.0%) of 352 patients with SARS and 100 (25.5%) of 392 control subjects had haplotype pairs associated with medium or low expression of MBL (OR, 1.67 [95% CI, 1.21-2.29]; P = .00187). The population-attributable fraction of patients with SARS that was associated with having the codon 54 variant was 20.1% (95% CI, 7.9%-32.3%). Conclusions. MBL gene polymorphisms were significantly associated with susceptibility to SARS-CoV infection; this might be explained by the reduced expression of functional MBL secondary to having the codon 54 variant.
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C03 01  X  FRE  @0 Coronavirus @2 NW @5 01
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C03 01  X  SPA  @0 Coronavirus @2 NW @5 01
C03 02  X  FRE  @0 Mannose @2 NK @5 05
C03 02  X  ENG  @0 Mannose @2 NK @5 05
C03 02  X  SPA  @0 Manosa @2 NK @5 05
C03 03  X  FRE  @0 Lectine @5 06
C03 03  X  ENG  @0 Lectin @5 06
C03 03  X  SPA  @0 Lectina @5 06
C03 04  X  FRE  @0 Polymorphisme @5 07
C03 04  X  ENG  @0 Polymorphism @5 07
C03 04  X  SPA  @0 Polimorfismo @5 07
C03 05  X  FRE  @0 Microbiologie @5 08
C03 05  X  ENG  @0 Microbiology @5 08
C03 05  X  SPA  @0 Microbiología @5 08
C03 06  X  FRE  @0 Infection @5 09
C03 06  X  ENG  @0 Infection @5 09
C03 06  X  SPA  @0 Infección @5 09
C03 07  X  FRE  @0 Syndrome respiratoire aigu sévère @2 NM @5 14
C03 07  X  ENG  @0 Severe acute respiratory syndrome @2 NM @5 14
C03 07  X  SPA  @0 Síndrome respiratorio agudo severo @2 NM @5 14
C03 08  X  FRE  @0 Association genetique @4 INC @5 79
C07 01  X  FRE  @0 Coronaviridae @2 NW
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C07 02  X  FRE  @0 Nidovirales @2 NW
C07 02  X  ENG  @0 Nidovirales @2 NW
C07 02  X  SPA  @0 Nidovirales @2 NW
C07 03  X  FRE  @0 Virus @2 NW
C07 03  X  ENG  @0 Virus @2 NW
C07 03  X  SPA  @0 Virus @2 NW
C07 04  X  FRE  @0 Appareil respiratoire pathologie @5 13
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C07 04  X  SPA  @0 Aparato respiratorio patología @5 13
C07 05  X  FRE  @0 Virose
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C07 06  X  FRE  @0 Poumon pathologie @5 16
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C07 06  X  SPA  @0 Pulmón patología @5 16
N21       @1 346
N44 01      @1 OTO
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Pascal:05-0492671

Le document en format XML

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<s1>Department of Genomics and Proteomics, Beijing Institute of Radiation Medicine</s1>
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<series>
<title level="j" type="main">The Journal of infectious diseases</title>
<title level="j" type="abbreviated">J. infect. dis.</title>
<idno type="ISSN">0022-1899</idno>
<imprint>
<date when="2005">2005</date>
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<title level="j" type="main">The Journal of infectious diseases</title>
<title level="j" type="abbreviated">J. infect. dis.</title>
<idno type="ISSN">0022-1899</idno>
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<term>Coronavirus</term>
<term>Infection</term>
<term>Lectin</term>
<term>Mannose</term>
<term>Microbiology</term>
<term>Polymorphism</term>
<term>Severe acute respiratory syndrome</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Coronavirus</term>
<term>Mannose</term>
<term>Lectine</term>
<term>Polymorphisme</term>
<term>Microbiologie</term>
<term>Infection</term>
<term>Syndrome respiratoire aigu sévère</term>
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<div type="abstract" xml:lang="en">Background. Genetic determinants of susceptibility to severe acute respiratory syndrome coronavirus (SARS-CoV) infection remain unknown. We assessed whether mannose-binding lectin (MBL) gene polymorphisms were associated with susceptibility to SARS-CoV infection or disease severity in an ethnically homogeneous population born in northern China. Methods. The frequencies of 1 mutation in codon 54 and 3 promoter polymorphisms at nt -550, -221, and 4 were ascertained in 352 patients with SARS and 392 control subjects, by means of polymerase chain reaction direct sequencing. Results. Of 352 patients with SARS and 392 control subjects, 120 (34.4%) and 91 (23.2%) were carriers of the codon 54 variant, respectively (odds ratio [OR], 1.73 [95% confidence interval {CI}, 1.25-2.39]; P = .00086). A total of 123 (36.0%) of 352 patients with SARS and 100 (25.5%) of 392 control subjects had haplotype pairs associated with medium or low expression of MBL (OR, 1.67 [95% CI, 1.21-2.29]; P = .00187). The population-attributable fraction of patients with SARS that was associated with having the codon 54 variant was 20.1% (95% CI, 7.9%-32.3%). Conclusions. MBL gene polymorphisms were significantly associated with susceptibility to SARS-CoV infection; this might be explained by the reduced expression of functional MBL secondary to having the codon 54 variant.</div>
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