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1
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Zika virus: history, emergence, biology, and prospects for control
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1 Weaver, S.C., Costa, F., Garcia-Blanco, M.A., Ko, A.I., Ribeiro, G.S., Saade, G., Shi, P., Vasilakis, N., Zika virus: history, emergence, biology, and prospects for control. Antiviral Res. 130 (2016), 69–80.
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2
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85005989501
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Zika virus infection in pregnant women in Rio de Janeiro—preliminary report
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2 Brasil, P., Pereira Junior, J.P., Raja Gabaglia, C., Damasceno, L., Wakimoto, M., Ribeiro Nogueira, R.M., Carvalho de Sequeira, P., Machado Siqueira, A., Abreu de Carvalho, L.M., Cotrim da Cunha, D., et al. Zika virus infection in pregnant women in Rio de Janeiro—preliminary report. N. Engl. J. Med., 2016, 10.1056/NEJMoa1602412.
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Cotrim da Cunha, D.10
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3
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84964276686
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Zika virus and birth defects—reviewing the evidence for causality
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The authors analyzed available epidemiological data to establish that fetal anomalies are caused by ZIKV infection during the first trimester.
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3• Rasmussen, S.A., Jamieson, D.J., Honein, M.A., Petersen, L.R., Zika virus and birth defects—reviewing the evidence for causality. N. Engl. J. Med. 374 (2016), 1981–1987 The authors analyzed available epidemiological data to establish that fetal anomalies are caused by ZIKV infection during the first trimester.
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4
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Miscarriage associated with Zika virus infection
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4 van der Eijk, A.A., van Genderen, P.J., Verdijk, R.M., Reusken, C.B., Mögling, R., van Kampen, J.J.A., Widagdo, W., Aron, G.I., GeurtsvanKessel, C.H., Pas, S.D., et al. Miscarriage associated with Zika virus infection. N. Engl. J. Med. 375 (2016), 1002–1004.
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5
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Analysis of blood from Zika virus-infected fetuses: a prospective case series
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5 Schaub, B., Vouga, M., Najioullah, F., Gueneret, M., Monthieux, A., Harte, C., Muller, F., Jolivet, E., Analysis of blood from Zika virus-infected fetuses: a prospective case series. Lancet 3099 (2017), 26–28.
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6
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85008419401
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Birth defects among fetuses and infants of US women with evidence of possible Zika virus infection during pregnancy
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6 Honein, M.A., Dawson, A.L., Petersen, E.E., Jones, A.M., Lee, E.H., Yazdy, M.M., Ahmad, N., Macdonald, J., Evert, N., Bingham, A., et al. Birth defects among fetuses and infants of US women with evidence of possible Zika virus infection during pregnancy. JAMA 30333 (2016), 59–68.
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Honein, M.A.1
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Bingham, A.10
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7
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Guillain–Barré Syndrome outbreak associated with Zika virus infection in French Polynesia: a case-control study
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7 Cao-Lormeau, V.-M., Blake, A., Mons, S., Lastère, S., Roche, C., Vanhomwegen, J., Dub, T., Baudouin, L., Teissier, A., Larre, P., et al. Guillain–Barré Syndrome outbreak associated with Zika virus infection in French Polynesia: a case-control study. Lancet 387 (2016), 1531–1539.
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Cao-Lormeau, V.-M.1
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8
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Zika virus and the Guillain–Barró Syndrome—case series from seven countries
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8 dos Santos, T., Rodriguez, A., Almiron, M., Sanhueza, A., Ramon, P., de Oliveira, W.K., Coelho, G.E., Badaró, R., Cortez, J., Ospina, M., et al. Zika virus and the Guillain–Barró Syndrome—case series from seven countries. N. Engl. J. Med. 375 (2016), 1598–1601.
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dos Santos, T.1
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9
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Case report: Guillain–Barrô Syndrome after Zika virus infection in Brazil
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9 Santana do Rosario, M., Antonio Pereira de Jesus, P., Vasilakis, N., Farias, D.S., Antônio Caires Novaes, M., Rodrigues, S.G., Martins, L.C., Fernando da Costa Vasconcelos, P., Ko, A.I., Carlos Junior Alcantara, L., et al. Case report: Guillain–Barrô Syndrome after Zika virus infection in Brazil. Am. J. Trop. Med. Hyg. 95 (2016), 1157–1160.
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Santana do Rosario, M.1
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Martins, L.C.7
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Ko, A.I.9
Carlos Junior Alcantara, L.10
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10
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Guillain–Barre Syndrome associated with Zika virus infection in Colombia
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10 Parra, B., Lizarazo, J., Jimenez- Arango, J.A., Zea- Vera, A.F., Manrique, G.G., Vargas, J., Angarita, J.A., Zuñiga, G., Gonzalez, R.L., Beltran, C.L., et al. Guillain–Barre Syndrome associated with Zika virus infection in Colombia. N. Engl. J. Med. 373 (2016), 1513–1523.
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11 Dick, G.W., Kitchen, S., Haddow, A., Zika virus (I): isolations and serological specificity. Trans. R. Soc. Trop. Med. Hyg. 46 (1952), 509–520.
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12 Dick, G.W.A., Zika virus (II): pathogenicity and physical properties. Trans. R. Soc. Trop. Med. Hyg. 46 (1952), 521–534.
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16 Frieden, T.R., Zika virus 6 months later. JAMA 30333 (2017), 2016–2017.
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18 Grard, G., Caron, M., Mombo, I.M., Nkoghe, D., Mboui Ondo, S., Jiolle, D., Fontenille, D., Paupy, C., Leroy, E.M., Zika virus in Gabon (Central Africa)—2007: a new threat from Aedes albopictus?. PLoS Negl. Trop. Dis. 8 (2014), 1–6.
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21 Russell, K., Hills, S.L., Oster, A.M., Porse, C.C., Danyluk, G., Cone, M., Brooks, R., Scotland, S., Schiffman, E., Fredette, C., et al. Male-to-female sexual transmission of Zika virus—United States, January–April. Clin. Infect. Dis., 64, 2016, ciw692.
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23 Deckard, D.T., Chung, W.M., Brooks, J.T., Smith, J.C., Woldai, S., Hennessey, M., Kwit, N., Mead, P., Male-to-male sexual transmission of Zika virus—Texas, January 2016. MMWR Morb. Mortal. Wkly. Rep. 65 (2016), 372–374.
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24 Gornet, M., Bracero, N., Segars, J., Zika virus in semen: what we know and what we need to know?. Semin. Reprod. Med. 34 (2016), 285–292.
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26 Murray, K.O., Gorchakov, R., Carlson, A.R., Berry, R., Lai, L., Natrajan, M., Garcia, M.N., Correa, A., Patel, S.M., Aagaard, K., et al. Prolonged detection of Zika virus in vaginal secretions and whole blood. Emerg. Infect. Dis. 23 (2017), 99–101.
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28 Shen, S., Shi, J., Wang, J., Tang, S., Wang, H., Hu, Z., Deng, F., Phylogenetic analysis revealed the central roles of two African countries in the evolution and worldwide spread of Zika virus. Virol. Sin. 31 (2016), 118–130.
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29 Dowd, K.A., DeMaso, C.R., Pelc, R.S., Speer, S.D., Smith, A.R.Y., Goo, L., Platt, D.J., Mascola, J.R., Graham, B.S., Mulligan, M.J., et al. Broadly neutralizing activity of Zika virus-immune Sera identifies a single viral serotype. Nature 11 (2016), 1485–1491.
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The authors showed that plasma from DENV-infected individuals could cross-react with and augment cellular infection of ZIKV at low concentrations. They determined this was due to antibody-dependent enhancement of infection. This study highlights the potential for ZIKV disease enhancement by cross-reactive anti-DENV antibodies.
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30•• Dejnirattisai, W., Supasa, P., Wongwiwat, W., Rouvinski, A., Barba-spaeth, G., Duangchinda, T., Sakuntabhai, A., Malasit, P., Rey, F.A., Mongkolsapaya, J., et al. Dengue virus sero-cross-reactivity drives antibody-dependent enhancement of infection with Zika virus. Nature Immunol. 17 (2016), 1102–1108 The authors showed that plasma from DENV-infected individuals could cross-react with and augment cellular infection of ZIKV at low concentrations. They determined this was due to antibody-dependent enhancement of infection. This study highlights the potential for ZIKV disease enhancement by cross-reactive anti-DENV antibodies.
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31 Priyamvada, L., Quicke, K.M., Hudson, W.H., Onlamoon, N., Sewatanon, J., Edupuganti, S., Pattanapanyasat, K., Chokephaibulkit, K., Mulligan, M.J., Wilson, P.C., et al. Human antibody responses after dengue virus infection are highly cross-reactive to Zika virus. Proc. Natl. Acad. Sci. U. S. A. 113 (2016), 7852–7857.
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The authors isolated human monoclonal antibodies agains ZIKV, defined a new protective epitope at the inter-dimer interface, and showed that passive prophylaxis or therapy can protect the fetus against infection.
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32•• Sapparapu, G., Fernandez, E., Kose, N., Bin Cao, Fox, J.M., Bombardi, R.G., Zhao, H., Nelson, C.A., Bryan, A.L., Barnes, T., et al. Neutralizing human antibodies prevent Zika virus replication and fetal disease in mice. Nature 540 (2016), 443–447 The authors isolated human monoclonal antibodies agains ZIKV, defined a new protective epitope at the inter-dimer interface, and showed that passive prophylaxis or therapy can protect the fetus against infection.
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The authors identified a panel of ZIKV-specific human antibodies, some of which can protect against ZIKV infection in mice. X-ray crystal structures of the antibodies with ZIKV E protein identfied three epitopes that were distinct from those reported previously for other flavivirues.
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33• Wang, Q., Yang, H., Liu, X., Dai, L., Ma, T., Qi, J., Wong, G., Peng, R., Liu, S., Li, J., et al. Molecular determinants of human neutralizing antibodies isolated from a patient infected with Zika virus. Sci. Transl. Med. 8 (2016), 1–11 The authors identified a panel of ZIKV-specific human antibodies, some of which can protect against ZIKV infection in mice. X-ray crystal structures of the antibodies with ZIKV E protein identfied three epitopes that were distinct from those reported previously for other flavivirues.
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34 Vogt, M.R., Moesker, B., Goudsmit, J., Jongeneelen, M., Austin, S.K., Oliphant, T., Nelson, S., Pierson, T.C., Wilschut, J., Throsby, M., et al. Human monoclonal antibodies against West Nile virus induced by natural infection neutralize at a postattachment step. J. Virol. 83 (2009), 6494–6507.
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