Author:
ProCite
RefWorks
Reference Manager
BibTeX
Zotero
EndNote
-
1
Guzman MG, Kouri G, 2002. Dengue: an update. Lancet Infect Dis 2 :33–42.
-
2
Jacobs M, 2000. Dengue: emergence as a global public health problem and prospects for control. Trans R Soc Trop Med Hyg 94 :7–8.
-
3
Ramos C, 1989. Biología de la Infección causada por el virus del dengue. Salud Publica Mex 31 :100–105.
-
4
Reinert JF, Harbach RE, 2005. Generic and subgeneric status of aedine mosquito species (Diptera: Culicidae: Aedini) occurring in the Australasian region. Zootaxa 887 :1–10.
-
5
Salas-Benito JS, del Angel RM, 1997. Identification of two surface proteins from C6/36 cells that bind dengue type 4 virus. J Virol 71 :7246–7252.
-
6
Igarashi A, 1978. Isolation of a Singh’s Aedes albopictus cell clone sensitive to dengue and chikungunya viruses. J Gen Virol 40 :531–544.
-
7
Mendoza YM, Salas-Benito JS, Lanz-Mendoza H, Hernandez-Martinez S, del Angel RM, 2002. A putative receptor for dengue virus in mosquito tissues: localization of a 45-kDa glyco-protein. Am J Trop Med Hyg 67 :76–84.
-
8
Triantafilou K, Fradelizi D, Wilson K, Triantafilou M, 2002. GRP78, a coreceptor for coxsackievirus A9, interacts with major histocompatibility complex class I molecules which mediate virus internalization. J Virol 76 :633–643.
-
9
Guerrero CA, Bouyssounade D, Zárate S, Isa P, López T, Espinosa R, Romero P, Méndez E, López S, Arias CF, 2002. Heat shock cognate protein 70 is involved in rotavirus cell entry. J Virol 76 :4096–4102.
-
10
Zárate S, Cuadras MA, Espinosa R, Romero P, Juárez KO, Camacho-Nuez M, Arias CF, López S, 2003. Interaction of rotaviruses with Hsc70 during cell entry is mediated by VP5. J Virol 77 :7254–7260.
-
11
Reyes del Valle J, Chavez-Salinas S, Medina F, del Angel RM, 2005. Heat shock protein 90 and heat shock protein 70 are components of dengue virus receptor complex in human cells. J Virol 79 :4547–4567.
-
12
Jindadamrongwech S, Thepparit C, Smith DR, 2004. Identification of GRP 78 (BiP) as a liver cell expressed receptor element for dengue virus serotype 2. Arch Virol 149 :915–927.
-
13
Craig EA, Gross CA, 1991. Is hsp70 the cellular thermometer? Trends Biochem Sci 16 :135–140.
-
14
Lindquist S, Craig EA, 1988. The heat shock proteins. Annu Rev Genet 22 :631–677.
-
15
Gould EA, Clegg JCS, 1991. Growth, titration and purification of alphaviruses and flaviviruses. Mahy BWJ, editor. Virology: A Practical Approach. Oxford, United Kingdom: IRL Press, 43–78.
-
16
Kuno G, Oliver A, 1989. Maintaining mosquito cell lines at high temperatures: effects on the replication of flaviviruses. In Vitro Cell Dev Biol 25 :193–196.
-
17
Reyes del Valle J, del Angel RM, 2004. Isolation of putative dengue virus receptor molecules by affinity chromatography using a recombinant E protein ligand. J Virol Methods 116 :95–102.
-
18
Triantafilou K, Triantafilou M, 2004. Coxsackievirus B4-induced cytokine production in pancreatic cells is mediated through toll-like receptor 4. J Virol 78 :11313–11320.
-
19
Riehl RM, Sullivan WP, Vroman BT, Bauer VJ, Pearson GR, Toft, DO, 1985. Immunological evidence that the nonhormone binding component of avian steroid receptors exists in a wide range of tissues and species. Biochemistry 24 :6586–6591.
-
20
Mercado-Curiel RF, Esquinca-Avilés HA, Tovar R, Díaz-Badillo A, Camacho-Nuez M, Muñoz ML, 2006. The four serotypes of dengue recognize the same putative receptors in Aedes aegypti midgut and Ae. albopictus cells. BMC Microbiol 6 :85–95.
-
21
Chu JJ, Leong PW, Ng ML, 2005. Characterization of plasma membrane-associated proteins from Aedes albopictus mosquito (C6/36) cells that mediate West Nile virus binding and infection. Virology 339 :249–260.
-
22
Muñoz ML, Cisneros A, Cruz J, Das P, Tovar R, Ortega A, 1988. Putative dengue virus receptors from mosquito cells. FEMS Microbiol Lett 168 :251–258.
-
23
Sakoonwatanyoo P, Boonsanay V, Smith DR, 2006. Growth and production of the dengue virus in C6/36 cells and identification of a laminin-binding protein as a candidate serotype 3 and 4 receptor protein. Intervirology 49 :161–172.
-
24
Gilman A, 1987. G proteins: transducers of receptor-generated signals. Annu Rev Biochem 56 :615–649.
-
25
Pearl LH, Prodromou C, 2006. Structure and mechanism of the Hsp90 molecular chaperone machinery. Annu Rev Biochem 75 :271–295.
-
26
Sales K, Brandt W, Rumbak E, Lindsey G, 2000. The LEA-like protein HSP 12 in Saccharomyces cerevisiae has a plasma membrane location and protects membranes against desiccation and ethanol-induced stress. Biochim Biophys Acta 1463 :267–278.
-
27
Trent JD, Kagawa HK, Paavola CD, McMillan RA, Howard J, Jahnke L, Lavin C, Embaye T, Henze CE, 2003. Intracellular localization of a group II chaperonin indicates a membrane-related function. Proc Natl Acad Sci USA 100 :15589–15594.
-
28
Pfister G, Stroh CM, Perschinka H, Kind M, Knoflach M, Hinterdorfer P, Wick G, 2005. Detection of HSP60 on the membrane surface of stressed human endothelial cells by atomic force and confocal microscopy. J Cell Sci 118 :1587–1594.
-
29
Gakhar SK, Shandilya H, 1999. Heat shock response during development of the malaria vector Anopheles stephensi (Culicidae: Diptera). Cytobios 99 :173–182.
-
30
Mourya DT, Yadav P, Mishra AC, 2004. Effect of temperature stress on immature stages and susceptibility of Aedes aegypti mosquitoes to Chikungunya virus. Am J Trop Med Hyg 70 :346–350.
-
31
Cripe T, Delos PE, Estes PA, Garcea RL, 1995. In vivo and in vitro association of Hsc70 with polyoma virus capsid proteins. J Virol 69 :7807–7813.
-
32
Florin L, Becker KA, Sapp C, Lambert C, Sirma H, Müller M, Streeck RE, Sapp M, 2004. Nuclear translocation of papillomavirus minor capsid protein L2 requires Hsc70. J Virol 78 :5546–5553.
-
33
Jindal S, Young RA, 1992. Vaccinia virus infection induce stress response that leads to association of hsp70 with viral proteins. J Virol 66 :5357–5362.
-
34
Macejak DG, Sarnow P, 1992. Association of heat shock protein 70 with enterovirus capsid precursor P1 in infected human cell. J Virol 66 :1520–1527.
-
35
Ohgitani E, Kobayashi K, Takeshita K, Imanishi J, 1999. Biphasic translocation of a 70 kDa heat shock protein in human cytomegalovirus infected cells. J Gen Virol 80 :63–68.
-
36
Prange R, Werr M, Loffler-Mary M, 1999. Chaperones involved in hepatitis B virus morphogenesis. Biol Chem 380 :305–314.
-
37
Sagara Y, Ishida C, Inouse Y, Shiraki H, Maeda Y, 1998. 71-kilodalton heat shock cognate protein acts as cellular receptor for syncytium formation induced by human T cell lymphotropic virus type 1. J Virol 72 :535–541.
-
38
Speth C, Prohaszka M, Mair M, Stockl G, Zhu X, Jobstl B, Gerace L, 1999. A 60 kDa heat shock protein-like molecule interacts with the HIV transmembrane glycoprotein gp41. Mol Immunol 36 :619–623.
| Past two years | Past Year | Past 30 Days | |
|---|---|---|---|
| Abstract Views | 432 | 357 | 246 |
| Full Text Views | 108 | 1 | 0 |
| PDF Downloads | 24 | 2 | 0 |
Evidence that the 45-kD Glycoprotein, Part of a Putative Dengue Virus Receptor Complex in the Mosquito Cell Line C6/36, Is a Heat-Shock–Related Protein
Juan Salas-Benito
Juan Salas-Benito
Programa Institucional de Biomedicina Molecular, Escuela Nacional de Medicina y Homeopatía del Instituto Politénico Nacional, Mexico City, Mexico; Departamento de Patología Experimental, Centro de Investigación y de Estudios Avanzados del Instituto Politénico Nacional, Mexico City, Mexico
Search for other papers by Juan Salas-Benito in
Current site
Google Scholar
PubMed
Search for other papers by Juan Salas-Benito in
Current site
Google Scholar
PubMed
Jorge Reyes-Del Valle
Jorge Reyes-Del Valle
Programa Institucional de Biomedicina Molecular, Escuela Nacional de Medicina y Homeopatía del Instituto Politénico Nacional, Mexico City, Mexico; Departamento de Patología Experimental, Centro de Investigación y de Estudios Avanzados del Instituto Politénico Nacional, Mexico City, Mexico
Search for other papers by Jorge Reyes-Del Valle in
Current site
Google Scholar
PubMed
Search for other papers by Jorge Reyes-Del Valle in
Current site
Google Scholar
PubMed
Mariana Salas-Benito
Mariana Salas-Benito
Programa Institucional de Biomedicina Molecular, Escuela Nacional de Medicina y Homeopatía del Instituto Politénico Nacional, Mexico City, Mexico; Departamento de Patología Experimental, Centro de Investigación y de Estudios Avanzados del Instituto Politénico Nacional, Mexico City, Mexico
Search for other papers by Mariana Salas-Benito in
Current site
Google Scholar
PubMed
Search for other papers by Mariana Salas-Benito in
Current site
Google Scholar
PubMed
Ivonne Ceballos-Olvera
Ivonne Ceballos-Olvera
Programa Institucional de Biomedicina Molecular, Escuela Nacional de Medicina y Homeopatía del Instituto Politénico Nacional, Mexico City, Mexico; Departamento de Patología Experimental, Centro de Investigación y de Estudios Avanzados del Instituto Politénico Nacional, Mexico City, Mexico
Search for other papers by Ivonne Ceballos-Olvera in
Current site
Google Scholar
PubMed
Search for other papers by Ivonne Ceballos-Olvera in
Current site
Google Scholar
PubMed
Clemente Mosso
Clemente Mosso
Programa Institucional de Biomedicina Molecular, Escuela Nacional de Medicina y Homeopatía del Instituto Politénico Nacional, Mexico City, Mexico; Departamento de Patología Experimental, Centro de Investigación y de Estudios Avanzados del Instituto Politénico Nacional, Mexico City, Mexico
Search for other papers by Clemente Mosso in
Current site
Google Scholar
PubMed
Search for other papers by Clemente Mosso in
Current site
Google Scholar
PubMed
Rosa M. del Angel
Rosa M. del Angel
Programa Institucional de Biomedicina Molecular, Escuela Nacional de Medicina y Homeopatía del Instituto Politénico Nacional, Mexico City, Mexico; Departamento de Patología Experimental, Centro de Investigación y de Estudios Avanzados del Instituto Politénico Nacional, Mexico City, Mexico
Search for other papers by Rosa M. del Angel in
Current site
Google Scholar
PubMed
Search for other papers by Rosa M. del Angel in
Current site
Google Scholar
PubMed
Dengue virus (DENV) is transmitted to humans by mosquitoes of the genus Aedes. Although several molecules have been described as part of DENV receptor complex in mosquito cells, none of them have been identified. Our group characterized two glycoproteins (40 and 45 kD) as part of the DENV receptor complex in C6/36 cells. Because identification of the mosquito cell receptor has been unsuccessful and some cell receptors described for DENV in mammalian cells are heat-shock proteins (HSPs), the role of HSPs in DENV binding and infection in C6/36 cells was evaluated. Our results indicate that gp45 and a 74-kD molecule (p74), which interact with DENV envelope protein, are immunologically related to HSP90. Although p74 is induced by heat shock, gp45 apparently is not. However, these proteins are relocated to the cell surface after heat-shock treatment, causing an increase in virus binding without any effect on virus yield.
Author Notes
ProCite
RefWorks
Reference Manager
BibTeX
Zotero
EndNote
-
1
Guzman MG, Kouri G, 2002. Dengue: an update. Lancet Infect Dis 2 :33–42.
-
2
Jacobs M, 2000. Dengue: emergence as a global public health problem and prospects for control. Trans R Soc Trop Med Hyg 94 :7–8.
-
3
Ramos C, 1989. Biología de la Infección causada por el virus del dengue. Salud Publica Mex 31 :100–105.
-
4
Reinert JF, Harbach RE, 2005. Generic and subgeneric status of aedine mosquito species (Diptera: Culicidae: Aedini) occurring in the Australasian region. Zootaxa 887 :1–10.
-
5
Salas-Benito JS, del Angel RM, 1997. Identification of two surface proteins from C6/36 cells that bind dengue type 4 virus. J Virol 71 :7246–7252.
-
6
Igarashi A, 1978. Isolation of a Singh’s Aedes albopictus cell clone sensitive to dengue and chikungunya viruses. J Gen Virol 40 :531–544.
-
7
Mendoza YM, Salas-Benito JS, Lanz-Mendoza H, Hernandez-Martinez S, del Angel RM, 2002. A putative receptor for dengue virus in mosquito tissues: localization of a 45-kDa glyco-protein. Am J Trop Med Hyg 67 :76–84.
-
8
Triantafilou K, Fradelizi D, Wilson K, Triantafilou M, 2002. GRP78, a coreceptor for coxsackievirus A9, interacts with major histocompatibility complex class I molecules which mediate virus internalization. J Virol 76 :633–643.
-
9
Guerrero CA, Bouyssounade D, Zárate S, Isa P, López T, Espinosa R, Romero P, Méndez E, López S, Arias CF, 2002. Heat shock cognate protein 70 is involved in rotavirus cell entry. J Virol 76 :4096–4102.
-
10
Zárate S, Cuadras MA, Espinosa R, Romero P, Juárez KO, Camacho-Nuez M, Arias CF, López S, 2003. Interaction of rotaviruses with Hsc70 during cell entry is mediated by VP5. J Virol 77 :7254–7260.
-
11
Reyes del Valle J, Chavez-Salinas S, Medina F, del Angel RM, 2005. Heat shock protein 90 and heat shock protein 70 are components of dengue virus receptor complex in human cells. J Virol 79 :4547–4567.
-
12
Jindadamrongwech S, Thepparit C, Smith DR, 2004. Identification of GRP 78 (BiP) as a liver cell expressed receptor element for dengue virus serotype 2. Arch Virol 149 :915–927.
-
13
Craig EA, Gross CA, 1991. Is hsp70 the cellular thermometer? Trends Biochem Sci 16 :135–140.
-
14
Lindquist S, Craig EA, 1988. The heat shock proteins. Annu Rev Genet 22 :631–677.
-
15
Gould EA, Clegg JCS, 1991. Growth, titration and purification of alphaviruses and flaviviruses. Mahy BWJ, editor. Virology: A Practical Approach. Oxford, United Kingdom: IRL Press, 43–78.
-
16
Kuno G, Oliver A, 1989. Maintaining mosquito cell lines at high temperatures: effects on the replication of flaviviruses. In Vitro Cell Dev Biol 25 :193–196.
-
17
Reyes del Valle J, del Angel RM, 2004. Isolation of putative dengue virus receptor molecules by affinity chromatography using a recombinant E protein ligand. J Virol Methods 116 :95–102.
-
18
Triantafilou K, Triantafilou M, 2004. Coxsackievirus B4-induced cytokine production in pancreatic cells is mediated through toll-like receptor 4. J Virol 78 :11313–11320.
-
19
Riehl RM, Sullivan WP, Vroman BT, Bauer VJ, Pearson GR, Toft, DO, 1985. Immunological evidence that the nonhormone binding component of avian steroid receptors exists in a wide range of tissues and species. Biochemistry 24 :6586–6591.
-
20
Mercado-Curiel RF, Esquinca-Avilés HA, Tovar R, Díaz-Badillo A, Camacho-Nuez M, Muñoz ML, 2006. The four serotypes of dengue recognize the same putative receptors in Aedes aegypti midgut and Ae. albopictus cells. BMC Microbiol 6 :85–95.
-
21
Chu JJ, Leong PW, Ng ML, 2005. Characterization of plasma membrane-associated proteins from Aedes albopictus mosquito (C6/36) cells that mediate West Nile virus binding and infection. Virology 339 :249–260.
-
22
Muñoz ML, Cisneros A, Cruz J, Das P, Tovar R, Ortega A, 1988. Putative dengue virus receptors from mosquito cells. FEMS Microbiol Lett 168 :251–258.
-
23
Sakoonwatanyoo P, Boonsanay V, Smith DR, 2006. Growth and production of the dengue virus in C6/36 cells and identification of a laminin-binding protein as a candidate serotype 3 and 4 receptor protein. Intervirology 49 :161–172.
-
24
Gilman A, 1987. G proteins: transducers of receptor-generated signals. Annu Rev Biochem 56 :615–649.
-
25
Pearl LH, Prodromou C, 2006. Structure and mechanism of the Hsp90 molecular chaperone machinery. Annu Rev Biochem 75 :271–295.
-
26
Sales K, Brandt W, Rumbak E, Lindsey G, 2000. The LEA-like protein HSP 12 in Saccharomyces cerevisiae has a plasma membrane location and protects membranes against desiccation and ethanol-induced stress. Biochim Biophys Acta 1463 :267–278.
-
27
Trent JD, Kagawa HK, Paavola CD, McMillan RA, Howard J, Jahnke L, Lavin C, Embaye T, Henze CE, 2003. Intracellular localization of a group II chaperonin indicates a membrane-related function. Proc Natl Acad Sci USA 100 :15589–15594.
-
28
Pfister G, Stroh CM, Perschinka H, Kind M, Knoflach M, Hinterdorfer P, Wick G, 2005. Detection of HSP60 on the membrane surface of stressed human endothelial cells by atomic force and confocal microscopy. J Cell Sci 118 :1587–1594.
-
29
Gakhar SK, Shandilya H, 1999. Heat shock response during development of the malaria vector Anopheles stephensi (Culicidae: Diptera). Cytobios 99 :173–182.
-
30
Mourya DT, Yadav P, Mishra AC, 2004. Effect of temperature stress on immature stages and susceptibility of Aedes aegypti mosquitoes to Chikungunya virus. Am J Trop Med Hyg 70 :346–350.
-
31
Cripe T, Delos PE, Estes PA, Garcea RL, 1995. In vivo and in vitro association of Hsc70 with polyoma virus capsid proteins. J Virol 69 :7807–7813.
-
32
Florin L, Becker KA, Sapp C, Lambert C, Sirma H, Müller M, Streeck RE, Sapp M, 2004. Nuclear translocation of papillomavirus minor capsid protein L2 requires Hsc70. J Virol 78 :5546–5553.
-
33
Jindal S, Young RA, 1992. Vaccinia virus infection induce stress response that leads to association of hsp70 with viral proteins. J Virol 66 :5357–5362.
-
34
Macejak DG, Sarnow P, 1992. Association of heat shock protein 70 with enterovirus capsid precursor P1 in infected human cell. J Virol 66 :1520–1527.
-
35
Ohgitani E, Kobayashi K, Takeshita K, Imanishi J, 1999. Biphasic translocation of a 70 kDa heat shock protein in human cytomegalovirus infected cells. J Gen Virol 80 :63–68.
-
36
Prange R, Werr M, Loffler-Mary M, 1999. Chaperones involved in hepatitis B virus morphogenesis. Biol Chem 380 :305–314.
-
37
Sagara Y, Ishida C, Inouse Y, Shiraki H, Maeda Y, 1998. 71-kilodalton heat shock cognate protein acts as cellular receptor for syncytium formation induced by human T cell lymphotropic virus type 1. J Virol 72 :535–541.
-
38
Speth C, Prohaszka M, Mair M, Stockl G, Zhu X, Jobstl B, Gerace L, 1999. A 60 kDa heat shock protein-like molecule interacts with the HIV transmembrane glycoprotein gp41. Mol Immunol 36 :619–623.
| Past two years | Past Year | Past 30 Days | |
|---|---|---|---|
| Abstract Views | 432 | 357 | 246 |
| Full Text Views | 108 | 1 | 0 |
| PDF Downloads | 24 | 2 | 0 |