Neotropical primary bat cell lines show restricted dengue virus replication

Comparative Immunology, Microbiology and Infectious Diseases

Volumn 50, Issue , 2017, Pages 101-105

  Moreira Soto, Andrés ^a   Soto Garita, Claudio ^a   Corrales Aguilar, Eugenia ^a  

^a UNIVERSIDAD DE COSTA RICA   (Costa Rica)

Author keywords

Bats; Dengue; in vitro studies; Viral infection

Indexed keywords

ANIMAL CELL; ANIMAL TISSUE; ARTIBEUS JAMAICENSIS; ARTICLE; BAT; CELL LINE; CONTROLLED STUDY; DENGUE VIRUS; DENGUE VIRUS 1; DENGUE VIRUS 2; DENGUE VIRUS 3; DENGUE VIRUS 4; DESMODUS ROTUNDUS; EMBRYO; EMBRYO CELL; FETUS; INFECTION SENSITIVITY; MOLOSSUS SINALOAE; NONHUMAN; SEROTYPE; SPECIES DIFFERENCE; VIRUS REPLICATION; ANIMAL; CLASSIFICATION; PHYSIOLOGY; REAL TIME POLYMERASE CHAIN REACTION; VIROLOGY;

ANIMALS; CELL LINE; CHIROPTERA; DENGUE VIRUS; REAL-TIME POLYMERASE CHAIN REACTION; SEROGROUP; SPECIES SPECIFICITY; VIRUS REPLICATION;

EID: 85008385706     PISSN: 01479571     EISSN: 18781667     Source Type: Journal    
DOI: 10.1016/j.cimid.2016.12.004     Document Type: Article

References (29)

1. [1] Yacoub, S., Mongkolsapaya, J., Screaton, G., Recent advances in understanding dengue. F1000Research, 5, 2016, 10.12688/f1000research.6233.1.
2. [2] W.H. Organization, Dengue: Guidelines for Diagnosis, Treatment, Prevention and Control, Prev. Control. 409 (2009) 160. WHO/HTM/NTD/DEN/2009.1.
3. [3] Fagbami, A.H., Monath, T.P., Fabiyi, A., Dengue virus infections in Nigeria: a survey for antibodies in monkeys and humans. Trans. R. Soc. Trop. Med. Hyg. 71 (1977), 60–65.
4. [4] Vasilakis, N., Cardosa, J., Hanley, K.A., Holmes, E.C., Weaver, S.C., Fever from the forest: prospects for the continued emergence of sylvatic dengue virus and its impact on public health. Nat. Rev. Microbiol. 9 (2011), 532–541, 10.1038/nrmicro2595.
5. [5] de Thoisy, B., Lacoste, V., Germain, A., Muñoz-Jordán, J., Colón, C., Mauffrey, J.-F., Delaval, M., Catzeflis, F., Kazanji, M., Matheus, S., Dussart, P., Morvan, J., Setién, A.A., Deparis, X., Lavergne, A., Dengue infection in neotropical forest mammals. Vector Borne Zoonotic Dis. 9 (2009), 157–170, 10.1089/vbz.2007.0280.
6. [6] Platt, K., Mangiafico, J., Rocha, O., Zaldivar, M.E., Mora, J., Trueba, G., Rowley, W.A., Detection of dengue virus neutralizing antibodies in bats from Costa Rica and Ecuador. J. Med. Entomol. 37 (2000), 965–967.
7. [7] de Thoisy, B., Dussart, P., Kazanji, M., Wild terrestrial rainforest mammals as potential reservoirs for flaviviruses (yellow fever, dengue 2 and St Louis encephalitis viruses) in French Guiana. Trans. R. Soc. Trop. Med. Hyg. 98 (2004), 409–412, 10.1016/j.trstmh.2003.12.003.
8. [8] Calisher, C.H., Childs, J.E., Field, H.E., Holmes, K.V., Schountz, T., Bats: important reservoir hosts of emerging viruses. Clin. Microbiol. Rev. 19 (2006), 531–545, 10.1128/CMR.00017-06.
9. [9] Han, H.-J., Wen, H., Zhou, C.-M., Chen, F.-F., Luo, L.-M., Liu, J., Yu, X.-J., Bats as reservoirs of severe emerging infectious diseases. Virus Res. 205 (2015), 1–6, 10.1016/j.virusres.2015.05.006.
10. [10] Sotomayor-Bonilla, J., Chaves, A., Rico-Chávez, O., Rostal, M.K., Ojeda-Flores, R., Salas-Rojas, M., Aguilar-Setien, Á., Ibáñez-Bernal, S., Barbachano-Guerrero, A., Gutiérrez-Espeleta, G., Aguilar-Faisal, J.L., Aguirre, A.A., Daszak, P., Suzán, G., Dengue virus in bats from southeastern Mexico. Am. J. Trop. Med. Hyg. 91 (2014), 129–131, 10.4269/ajtmh.13-0524.
11. [11] Aguilar-Setién, A., Romero-Almaraz, M.L., Sánchez-Hernández, C., Figueroa, R., Juárez-Palma, L.P., García-Flores, M.M., Vázquez-Salinas, C., Salas-Rojas, M., Hidalgo-Martínez, A.C., Pierlé, S.A., García-Estrada, C., Ramos, C., Dengue virus in Mexican bats. Epidemiol. Infect. 136 (2008), 1678–1683, 10.1017/S0950268808000460.
12. [12] Thompson, N.N., Auguste, A.J., Travassos da Rosa, A.P.A., Carrington, C.V.F., Blitvich, B.J., Chadee, D.D., Tesh, R.B., Weaver, S.C., Adesiyun, A.A., Seroepidemiology of selected alphaviruses and flaviviruses in bats in trinidad. Zoonoses Public Health, 2014, 53–60, 10.1111/zph.12118.
13. [13] Lavergne, A., Lacoste, V., Germain, A., Matheus, S., Dussart, P., Deparis, X., D.T.B Infection par le virus de la dengue de mammifères sauvages en région néotropicale: hôtes accidentels ou réservoirs potentiels?. Médecine Trop. 69 (2009), 345–350.
14. [14] Machain-Williams, C., López-Uribe, M., Talavera-Aguilar, L., Carrillo-Navarrete, J., Vera-Escalante, L., Puerto-Manzano, F., Ulloa, A., Farfán-Ale, J.A., Garcia-Rejon, J., Blitvich, B.J., Loroño-Pino, M.A., Serologic evidence of flavivirus infection in bats in the Yucatan Peninsula of Mexico. J. Wildl. Dis. 49 (2013), 684–689, 10.7589/2012-12-318.
15. [15] Cabrera-Romo, S., Recio-Tótoro, B., Alcalá, A.C., Lanz, H., del Ángel, R.M., Sánchez-Cordero, V., Á. Rodríguez-Moreno, Ludert, J.E., Experimental inoculation of Artibeus jamaicensis bats with dengue virus serotypes 1 or 4 showed no evidence of sustained replication. Am. J. Trop. Med. Hyg. 91 (2014), 1227–1234, 10.4269/ajtmh.14-0361.
16. [16] Perea-Martínez, L., Moreno-Sandoval, H.N., Moreno-Altamirano, M.M., Salas-Rojas, M., García-Flores, M.M., Aréchiga-Ceballos, N., Tordo, N., Marianneau, P., Aguilar-Setién, A., Experimental infection of Artibeus intermedius bats with serotype-2 dengue virus. Comp. Immunol. Microbiol. Infect. Dis. 36 (2013), 193–198, 10.1016/j.cimid.2012.12.002.
17. [17] Cabrera-Romo, S., Max Ramirez, C., Recio-Tótoro, B., Tolentino-Chi, J., Lanz, H., del Ángel, R.M., Sánchez-Cordero, V., Rodríguez-Moreno, Á., Ludert, J.E., No evidence of dengue virus infections in several species of bats captured in central and southern Mexico. Zoonoses Public Health 63 (2016), 579–583, 10.1111/zph.12276.
18. [18] Barr, K.L., Anderson, B.D., Heil, G.L., Friary, J. a., Gray, G.C., Focks, D. a., Dengue serotypes 1–4 exhibit unique host specificity in vitro. Virus Adapt. Treat. 4 (2012), 65–73, 10.2147/VAAT.S36856.
19. [19] Mourya, D.T., Lakra, R.J., Yadav, P.D., Tyagi, P., Raut, C.G., Shete, A.M., Singh, D.K., Establishment of cell line from embryonic tissue of Pipistrellus ceylonicus bat species from India & its susceptibility to different viruses. Indian J. Med. Res. 138 (2013), 224–231.
20. [20] Crameri, G., Todd, S., Grimley, S., McEachern, J.A., Marsh, G.A., Smith, C., Tachedjian, M., De Jong, C., Virtue, E.R., Yu, M., Bulach, D., Liu, J.-P., Michalski, W.P., Middleton, D., Field, H.E., Wang, L.-F., Establishment, immortalisation and characterisation of pteropid bat cell lines. PLoS One, 4, 2009, e8266, 10.1371/journal.pone.0008266.
21. [21] Angel-Ambrocio, A.H., Soto-Acosta, R., Tammineni, E.R., Carrillo, E.D., Bautista-Carbajal, P., Hernández, A., Sánchez, J.A., del Angel, R.M., An embryonic heart cell line is susceptible to dengue virus infection. Virus Res. 198 (2015), 53–58, 10.1016/j.virusres.2015.01.004.
22. [22] Balsitis, S.J., Coloma, J., Castro, G., Alava, A., Flores, D., McKerrow, J.H., Beatty, P.R., Harris, E., Tropism of dengue virus in mice and humans defined by viral nonstructural protein 3-specific immunostaining. Am. J. Trop. Med. Hyg. 80 (2009), 416–424 http://www.ncbi.nlm.nih.gov/pubmed/19270292 (Accessed 5 December 2016).
23. [23] Jennings, J.B., Best, T.L., Burnett, S.E., Rainey, J.C., Molossus sinaloae. Mamm. Species 691 (2002), 1–5, 10.1644/1545-1410(2002)691<0001:MS>2.0. CO;2.
24. [24] Halstead, S.B., Heinz, F.X., Barrett, A.D.T., Roehrig, J.T., Dengue virus: molecular basis of cell entry and pathogenesis, 25–27 June 2003, Vienna, Austria. Vaccine 23 (2005), 849–856, 10.1016/j.vaccine.2004.03.069.
25. [25] Schmid, M.A., Diamond, M.S., Harris, E., Dendritic cells in dengue virus infection: targets of virus replication and mediators of immunity. Front. Immunol., 5, 2014, 647, 10.3389/fimmu.2014.00647.
26. [26] Ho, L.J., Wang, J.J., Shaio, M.F., Kao, C.L., Chang, D.M., Han, S.W., Lai, J.H., Infection of human dendritic cells by dengue virus causes cell maturation and cytokine production. J. Immunol. 166 (2001), 1499–1506 ( http://www.ncbi.nlm.nih.gov/pubmed/11160189).
27. [27] Tassaneetrithep, B., Burgess, T.H., Granelli-Piperno, A., Trumpfheller, C., Finke, J., Sun, W., Eller, M.A., Pattanapanyasat, K., Sarasombath, S., Birx, D.L., Steinman, R.M., Schlesinger, S., Marovich, M.A., DC-SIGN (CD209) mediates dengue virus infection of human dendritic cells. J. Exp. Med. 197 (2003), 823–829, 10.1084/jem.20021840.
28. [28] Perera-Lecoin, M., Meertens, L., Carnec, X., Amara, A., Flavivirus entry receptors: an update. Viruses 6 (2013), 69–88, 10.3390/v6010069.
29. [29] Vaughan, K., Greenbaum, J., Blythe, M., Peters, B., Sette, A., Meta-analysis of all immune epitope data in the Flavivirus genus: inventory of current immune epitope data status in the context of virus immunity and immunopathology. Viral Immunol. 23 (2010), 259–284, 10.1089/vim.2010.0006.