| Literature DB >> 26063222 |
Etienne Simon-Loriere1, Ren-Jye Lin2, Sita Mint Kalayanarooj3, Ampaiwan Chuansumrit4, Isabelle Casademont1, Shyr-Yi Lin2, Han-Pang Yu5, Worachart Lert-Itthiporn6, Wathanee Chaiyaratana7, Nattaya Tangthawornchaikul8, Kanchana Tangnararatchakit4, Sirijitt Vasanawathana9, Bi-Lan Chang5, Prapat Suriyaphol10, Sutee Yoksan11, Prida Malasit12, Philipe Despres13, Richard Paul1, Yi-Ling Lin5, Anavaj Sakuntabhai14.
Abstract
Dengue is a mosquito-borne viral disease that afflicts millions of individuals worldwide every year. Infection by any of the 4 dengue virus (DENV) serotypes can result in a spectrum of disease severity. We investigated the impact of variants of interferon-regulated innate immunity genes with a potent antiviral effect on the outcome of DENV infection. We compared the effect of OAS gene family variants on 2 DENV serotypes in cell culture. While both OAS1-p42 and p46 showed antiviral activity against DENV-2, only OAS1-p42 presented anti-DENV-1 activity. Conversely, whereas both OAS3_S381 and R381 variants were able to block DENV-1 infection, the anti-DENV-2 activity observed for OAS3_S381 was largely lost for the R381 variant. By means of an allelic association study of a cohort of 740 patients with dengue, we found a protective effect of OAS3_R381 against shock (odds ratio [OR], 0.37; P < .001). This effect was due to DENV-2 infections (OR, 0.13; P = .007) but was absent for DENV-1, in accordance with the serotype-dependent OAS3 activity found in the functional study. Severe dengue has long been associated with a cytokine storm of unclear origin. This work identifies an early innate immunity process that could lead to the immune overreaction observed in severe dengue and could be triggered by a specific host genotype-pathogen genotype interaction.Entities:
Keywords: cytokine storm; dengue virus; genetic susceptibility; innate immunity; interferon
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Year: 2015 PMID: 26063222 DOI: 10.1093/infdis/jiv321
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226