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Polymorphisms in the retinoic acid-1 like-receptor family of genes and their association with clinical outcome of dengue virus infection

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Abstract

Polymorphisms in the DDX58 and IFIH1 genes, which code for the retinoic acid inducible gene-1 protein and myeloid differentiation factor (MDA) 5, were investigated in 120 dengue (DEN) cases (88 dengue fever [DF] cases and 32 dengue hemorrhagic fever [DHF] cases) and 109 healthy controls (HCs) to investigate their association with dengue. The results revealed a lower carrier frequency of the DDX58 rs3205166 G allele in DEN than in HCs and a higher frequency of the DDX58 rs669260 T/C genotype in DHF than in DF cases (P = 0.043, OR with 95 % CI 3.358 [1.038-10.861]). This suggests that polymorphisms in DDX58 gene influence the clinical outcome of DENV infection.

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References

  1. Shepard DS, Halasa YA, Tyagi BK, Adhish SV, Nandan D, Karthiga KS, Chellaswamy V, Gaba M, Arora NK, the INCLEN Study Group (2014) Economic and disease burden of dengue illness in India. Am J Trop Med Hyg 91:1235–1242

    Article  PubMed Central  PubMed  Google Scholar 

  2. Bhatt S, Gething PW, Brady OJ, Messina JP, Farlow AW, Moyes CL, Drake JM, Brownstein JS, Hoen AG, Sankoh O, Myers MF, George DB, Jaenisch T, Wint GR, Simmons CP, Scott TW, Farrar JJ, Hay SI (2013) The global distribution and burden of dengue. Nature 496:504–507. doi:10.1038/nature12060

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  3. Herrero LJ, Zakhary A, Gahan ME, Nelson MA, Herring BL, Hapel AJ, Keller PA, Obeysekera M, Chen W, Sheng KC, Taylor A, Wolf S, Bettadapura J, Broor S, Dar L, Mahalingam S (2013) Dengue virus therapeutic intervention strategies based on viral, vector and host factors involved in disease pathogenesis. Pharmacol Ther 137:266–282

    Article  CAS  PubMed  Google Scholar 

  4. Kawai T, Akira S (2009) The roles of TLRs, RLRs and NLRs in pathogen recognition. Int Immunol 21(4):317–337. doi:10.1093/intimm/dxp017

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  5. Loo YM, Fornek J, Crochet N, Bajwa G, Perwitasari O, Martinez-Sobrido L, Akira S, Gill MA, García-Sastre A, Katze MG, Gale M Jr (2008) Distinct RIG-I and MDA5 signaling by RNA viruses in innate immunity. J Virol 82:335–345

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  6. Nasirudeen AM, Wong HH, Thien P, Xu S, Lam KP, Liu DX (2011) RIG-I, MDA5 and TLR3 synergistically play an important role in restriction of dengue virus infection. PLoS Negl Trop 5:e926. doi:10.1371/journal.pntd.0000926

    Article  CAS  Google Scholar 

  7. Brown MG, McAlpine SM, Huang YY, Haidl ID, Al-Afif A, Marshall JS, Anderson R (2012) RNA sensors enable human mast cell anti-viral chemokine production and IFN-mediated protection in response to antibody-enhanced dengue virus infection. PLoS ONE 7(3):e34055. doi:10.1371/journal.pone.0034055

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  8. Olagnier D, Scholte FE, Chiang C, Albulescu IC, Nichols C, He Z, Lin R, Snijder EJ, van Hemert MJ, Hiscott J (2014) Inhibition of dengue and chikungunya virus infections by RIG-I-mediated type I interferon-independent stimulation of the innate antiviral response. J Virol 88:4180–4194. doi:10.1128/JVI.03114-13

    Article  PubMed Central  PubMed  Google Scholar 

  9. Hu J, Nistal-Villán E, Voho A, Ganee A, Kumar M, Ding Y, García-Sastre A, Wetmur JG (2010) A common polymorphism in the caspase recruitment domain of RIG-I modifies the innate immune response of human dendritic cells. J Immunol 185(1):424–432. doi:10.4049/jimmunol.0903291

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  10. Liu S, Wang H, Jin Y, Podolsky R, Reddy MV, Pedersen J, Bode B, Reed J, Steed D, Anderson S, Yang P, Muir A, Steed L, Hopkins D, Huang Y, Purohit S, Wang CY, Steck AK, Montemari A, Eisenbarth G, Rewers M, She JX (2009) IFIH1 polymorphisms are significantly associated with type 1 diabetes and IFIH1 gene expression in peripheral blood mononuclear cells. Hum Mol Genet 18:358–365. doi:10.1093/hmg/ddn342

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  11. Kennedy RB, Ovsyannikova IG, Haralambieva IH, O’Byrne MM, Jacobson RM, Pankratz VS, Poland GA (2012) Multigenic control of measles vaccine immunity mediated by polymorphisms in measles receptor, innate pathway, and cytokine genes. Vaccine 30(12):2159–2167. doi:10.1016/j.vaccine.2012.01.025

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  12. Haralambieva IH, Ovsyannikova IG, Umlauf BJ, Vierkant RA, Shane Pankratz V, Jacobson RM, Poland GA (2011) Genetic polymorphisms in host antiviral genes: associations with humoral and cellular immunity to measles vaccine. Vaccine 29:8988–8997. doi:10.1016/j.vaccine.2011.09.043

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  13. Hoffmann F, Schmidt A, Dittmann Chevillotte M, Wisskirchen C, Hellmuth JC, Willms S, Gilmore RH, Glas J, Folwaczny M, Müller T, Berg T, Spengler U, Fitzmaurice K, Kelleher D, Reisch N, Rice CM, Endres S, Rothenfusser S (2014) Polymorphisms in MDA-5 link protein function to clearance of hepatitis C virus. Hepatology 61:460–470. doi:10.1002/hep.27344

    Article  Google Scholar 

  14. Cen H, Wang W, Leng RX, Wang TY, Pan HF, Fan YG, Wang B, Ye DQ (2013) Association of IFIH1 rs1990760 polymorphism with susceptibility to autoimmune diseases: a meta-analysis. Autoimmunity 46:455–462. doi:10.3109/08916934.2013.796937

    Article  CAS  PubMed  Google Scholar 

  15. Witsø E, Tapia G, Cinek O, Pociot FM, Stene LC, Rønningen KS (2011) Polymorphisms in the innate immune IFIH1 gene, frequency of enterovirus in monthly fecal samples during infancy, and islet autoimmunity. PLoS ONE 6:e27781. doi:10.1371/journal.pone.0027781

    Article  PubMed Central  PubMed  Google Scholar 

  16. Pang L, Gong X, Liu N, Xie G, Gao W, Kong G, Li X, Zhang J, Jin Y, Duan ZA (2014) Polymorphism in melanoma differentiation-associated gene 5 may be a risk factor for enterovirus 71 infection. Clin Microbiol Infect. 20:O711–O717. doi:10.1111/1469-0691.12618

    Article  CAS  PubMed  Google Scholar 

  17. Alagarasu K, Bachal RV, Memane RS, Shah PS, Cecilia D (2015) Polymorphisms in the RNA sensing toll like receptor genes and its association with clinical outcomes of dengue virus infection. Immunobiology 220:164–168. doi:10.1016/j.imbio.2014.09.020

    Article  CAS  PubMed  Google Scholar 

  18. World Health Organisation (1999) Prevention and control of Dengue and Dengue haemorrhagic fever: comprehensive guidelines. WHO Regional Publication, SEARO 29:12–23

    Google Scholar 

  19. Sole X, Guino E, Valls J, Iniesta R, Moreno V (2006) SNPStats: a web tool for the analysis of association studies. Bioinformatics 22:1928–1929

    Article  CAS  PubMed  Google Scholar 

  20. Ovsyannikova IG, Dhiman N, Haralambieva IH, Vierkant RA, O’Byrne MM, Jacobson RM, Poland GA (2010) Rubella vaccine-induced cellular immunity: evidence of associations with polymorphisms in the Toll-like, vitamin A and D receptors, and innate immune response genes. Hum Genet 127:207–221. doi:10.1007/s00439-009-0763-1

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  21. The International HapMap Consortium (2003) The International HapMap Project. Nature 426:789–796

    Article  Google Scholar 

  22. Priyadarshini D, Gadia RR, Tripathy A, Gurukumar KR, Bhagat A, Patwardhan S, Mokashi N, Vaidya D, Shah PS, Cecilia D (2010) Clinical findings and pro-inflammatory cytokines in dengue patients in western india: a facility-based study. PLoS ONE 5:e8709

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  23. Villar L, Dayan GH, Arredondo-García JL, Rivera DM, Cunha R, Deseda C, Reynales H, Costa MS, Morales-Ramírez JO, Carrasquilla G, Rey LC, Dietze R, Luz K, Rivas E, Montoya MC, Supelano MC, Zambrano B, Langevin E, Boaz M, Tornieporth N, Saville M, Noriega F (2014) Efficacy of a tetravalent dengue vaccine in children in Latin America. N Engl J Med 372:113–123

    Article  PubMed  Google Scholar 

  24. Capeding MR, Tran NH, Hadinegoro SR, Ismail HI, Chotpitayasunondh T, Chua MN, Luong CQ, Rusmil K, Wirawan DN, Nallusamy R, Pitisuttithum P, Thisyakorn U, Yoon IK, van der Vliet D, Langevin E, Laot T, Hutagalung Y, Frago C, Boaz M, Wartel TA, Tornieporth NG, Saville M, Bouckenooghe A, CYD14 Study Group (2014) Clinical efficacy and safety of a novel tetravalent dengue vaccine in healthy children in Asia: a phase 3, randomised, observer-masked, placebo-controlled trial. Lancet 384(9951):1358–1365. doi:10.1016/S0140-6736(14)61060-6

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

The authors thank all the study subjects for their participation in the study. The authors acknowledge Mr. Anand Singh, Mrs. Bachal RV, Mr. Kakade MB and Mrs. Asha Bhagat for their help in collection and testing of the samples for dengue.

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Correspondence to K. Alagarasu.

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Alagarasu, K., Memane, R.S. & Shah, P.S. Polymorphisms in the retinoic acid-1 like-receptor family of genes and their association with clinical outcome of dengue virus infection. Arch Virol 160, 1555–1560 (2015). https://doi.org/10.1007/s00705-015-2417-z

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  • DOI: https://doi.org/10.1007/s00705-015-2417-z

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