Association of SARS susceptibility with single nucleic acid polymorphisms of OAS1 and MxA genes: a case-control study

被引:86
作者
He, Jing
Feng, Dan
de Vlas, Sake J.
Wang, Hongwei
Fontanet, Arnaud
Zhang, Panhe
Plancoulaine, Sabine
Tang, Fang
Zhan, Lin
Yang, Hong
Wang, Tianbao
Richardus, Jan H.
Habbema, J. Dik F.
Cao, Wuchun [1 ]
机构
[1] Beijing Inst Microbiol & Epidemiol, State Key Lab Pathogen & Biosecur, Beijing, Peoples R China
[2] Univ Med Ctr, Erasmus MC, Dept Publ Hlth, Rotterdam, Netherlands
[3] Inst Pasteur, Emerging Dis Epidemiol Unit, Paris, France
[4] Univ Paris 05, INSERM, U550, Fac Med Necker, Paris, France
[5] Beijing Gen Hosp Armed Police, Beijing, Peoples R China
关键词
D O I
10.1186/1471-2334-6-106
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Host genetic factors may play a role in susceptibility and resistance to SARS associated coronavirus (SARS-CoV) infection. The study was carried out to investigate the association between the genetic polymorphisms of 2',5'-oligoadenylate synthetase 1 (OAS1) gene as well as myxovirus resistance 1 (MxA) gene and susceptibility to SARS in Chinese Han population. Methods: A hospital-based case-control study was conducted. A collective of 66 SARS cases and 64 close contact uninfected controls were enrolled in this study. End point real time polymerase chain reaction (PCR) and PCR-based Restriction Fragment Length Polymorphism (RFLP) analysis were used to detect the single nucleic polymorphisms (SNPs) in OAS1 and MxA genes. Information on other factors associated with SARS infection was collected using a pre-tested questionnaire. Univariate and multivariate logistic analyses were conducted. Results: One polymorphism in the 3'-untranslated region (3'-UTR) of the OAS1 gene was associated with SARS infection. Compared to AA genotype, AG and GG genotypes were found associated with a protective effect on SARS infection with ORs (95% CI) of 0.42 (0.20 similar to 0.89) and 0.30 (0.09 similar to 0.97), respectively. Also, a GT genotype at position 88 in the MxA gene promoter was associated with increased susceptibility to SARS infection compared to a GG genotype (OR=3.06, 95% CI: 1.25 similar to 7.50). The associations of AG genotype in OAS1 and GT genotype in MxA remained significant in multivariate analyses after adjusting for SARS protective measures (OR=0.38, 95% CI: 0.14 similar to 0.98 and OR=3.22, 95% CI: 1.13 similar to 9.18, respectively). Conclusion: SNPs in the OAS1 3'-UTR and MxA promoter region appear associated with host susceptibility to SARS in Chinese Han population.
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页数:7
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共 29 条
[1]   The cleavage/polyadenylation activity triggered by a U-rich motif sequence is differently required depending on the poly(A) site location at either the first or last 3′-terminal exon of the 2′-5′ oligo(A) synthetase gene [J].
Aissouni, Y ;
Perez, C ;
Calmels, B ;
Benech, PD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (39) :35808-35814
[2]   WHO declares Beijing to be free of SARS [J].
Ashraf, H .
LANCET, 2003, 361 (9376) :2212-2212
[3]   STRUCTURE OF 2 FORMS OF THE INTERFERON-INDUCED (2-'-5-') OLIGO-A SYNTHETASE OF HUMAN-CELLS BASED ON CDNAS AND GENE-SEQUENCES [J].
BENECH, P ;
MORY, Y ;
REVEL, M ;
CHEBATH, J .
EMBO JOURNAL, 1985, 4 (09) :2249-2256
[4]   Treatment of SARS with human interferons [J].
Cinatl, J ;
Morgenstern, B ;
Bauer, G ;
Chandra, P ;
Rabenau, H ;
Doerr, HW .
LANCET, 2003, 362 (9380) :293-294
[5]  
Enserink M, 2004, SCIENCE, V303, P1273
[6]   Differential transcriptional expresion of the polymorphic myxovirus resistance protein A in response to interferonalpha treatment [J].
Fernández-Arcás, N ;
Blanco, A ;
Gaitán, J ;
Nyqvist, M ;
Alonso, A ;
Reyes-Engel, A .
PHARMACOGENETICS, 2004, 14 (03) :189-193
[7]   Polymorphisms of interferon-inducible genes OAS-1 and MxA associated with SARS in the Vietnamese population [J].
Hamano, E ;
Hijikata, M ;
Itoyama, S ;
Quy, T ;
Phi, NC ;
Long, HT ;
Ha, L ;
Van Ban, V ;
Matsushita, I ;
Yanai, H ;
Kirikae, F ;
Kirikae, T ;
Kuratsuji, T ;
Sasazuki, T ;
Keicho, N .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 329 (04) :1234-1239
[8]   Human MxA protein protects mice lacking a functional alpha beta interferon system against La Crosse virus and other lethal viral infections [J].
Hefti, HP ;
Frese, M ;
Landis, H ;
Di Paolo, C ;
Aguzzi, A ;
Haller, O ;
Pavlovic, J .
JOURNAL OF VIROLOGY, 1999, 73 (08) :6984-6991
[9]   Genetic polymorphism of the MxA gene promoter and interferon responsiveness of hepatitis C patients:: Revisited by analyzing two SNP sites (-123 and-88) in vivo and in vitro [J].
Hijikata, M ;
Mishiro, S ;
Miyamoto, C ;
Furuichi, Y ;
Hashimoto, M ;
Ohta, Y .
INTERVIROLOGY, 2001, 44 (06) :379-382
[10]   ACE1 polymorphism and progression of SARS [J].
Itoyama, S ;
Keicho, N ;
Quy, T ;
Phi, NC ;
Long, HT ;
Ha, LD ;
Van Ban, V ;
Ohashi, J ;
Hijikata, M ;
Matsushita, I ;
Kawana, A ;
Yanai, H ;
Kirikae, T ;
Kuratsuji, T ;
Sasazuki, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 323 (03) :1124-1129