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Journal articles on the topic 'Dengue viruses'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 January 2023

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1

Aaskov, John. "Dengue viruses." Pathology 25 (1993): 19. http://dx.doi.org/10.1016/s0031-3025(16)35773-7.

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2

Henchal, E. A., and J. R. Putnak. "The dengue viruses." Clinical Microbiology Reviews 3, no. 4 (1990): 376–96. http://dx.doi.org/10.1128/cmr.3.4.376.

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Dengue, a major public health problem throughout subtropical and tropical regions, is an acute infectious disease characterized by biphasic fever, headache, pain in various parts of the body, prostration, rash, lymphadenopathy, and leukopenia. In more severe or complicated dengue, patients present with a severe febrile illness characterized by abnormalities of hemostasis and increased vascular permeability, which in some instances results in a hypovolemic shock. Four distinct serotypes of the dengue virus (dengue-1, dengue-2, dengue-3, and dengue-4) exist, with numerous virus strains found wor

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3

Henchal, E. A., and J. R. Putnak. "The dengue viruses." Clinical Microbiology Reviews 3, no. 4 (1990): 376–96. http://dx.doi.org/10.1128/cmr.3.4.376-396.1990.

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4

Tuiskunen Bäck, Anne, and Åke Lundkvist. "Dengue viruses – an overview." Infection Ecology & Epidemiology 3, no. 1 (2013): 19839. http://dx.doi.org/10.3402/iee.v3i0.19839.

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5

Vasilakis, N., J. Cardosa, M. Diallo, et al. "Sylvatic Dengue Viruses Share the Pathogenic Potential of Urban/Endemic Dengue Viruses." Journal of Virology 84, no. 7 (2010): 3726–28. http://dx.doi.org/10.1128/jvi.02640-09.

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6

Gubler, Duane J. "Cities spawn epidemic dengue viruses." Nature Medicine 10, no. 2 (2004): 129–30. http://dx.doi.org/10.1038/nm0204-129.

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7

Aaskov, John, Katie Buzacott, Emma Field, Kym Lowry, Alain Berlioz-Arthaud, and Edward C. Holmes. "Multiple recombinant dengue type 1 viruses in an isolate from a dengue patient." Journal of General Virology 88, no. 12 (2007): 3334–40. http://dx.doi.org/10.1099/vir.0.83122-0.

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Between 2000 and 2004, dengue virus type 1 (DENV-1) genotypes I and II from Asia were introduced into the Pacific region and co-circulated in some localities. Envelope protein gene sequences of DENV-1 from 12 patients infected on the island of New Caledonia were obtained, five of which carried genotype I viruses and six, genotype II viruses. One patient harboured a mixed infection, containing viruses assigned to both genotypes I and II, as well as a number of inter-genotypic recombinants. This is the first report of a population of dengue viruses isolated from a patient containing both parenta

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8

Chungue, E., O. Cassar, M. T. Drouet, et al. "Molecular epidemiology of dengue-1 and dengue-4 viruses." Journal of General Virology 76, no. 7 (1995): 1877–84. http://dx.doi.org/10.1099/0022-1317-76-7-1877.

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9

Nogueira, Rita Maria Ribeiro, Josélio Maria Galvão de Araújo, and Hermann Gonçalves Schatzmayr. "Dengue viruses in Brazil, 1986-2006." Revista Panamericana de Salud Pública 22, no. 5 (2007): 358–63. http://dx.doi.org/10.1590/s1020-49892007001000009.

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10

Castro, José Adail Fonseca de, Hélida Monteiro de Andrade, Semiramis Jamil Hadad do Monte, et al. "Dengue viruses activity in Piauí, Brazil." Memórias do Instituto Oswaldo Cruz 98, no. 8 (2003): 1021–23. http://dx.doi.org/10.1590/s0074-02762003000800007.

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11

Rohani, Pejman, and John M. Drake. "Untangling the evolution of dengue viruses." Science 374, no. 6570 (2021): 941–42. http://dx.doi.org/10.1126/science.abm6812.

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12

Nicoletti, Loredana, Massimo Ciccozzi, Antonella Marchi, et al. "Chikungunya and Dengue Viruses in Travelers." Emerging Infectious Diseases 14, no. 1 (2008): 177–78. http://dx.doi.org/10.3201/eid1401.070618.

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13

Chan, Miranda, and Michael A. Johansson. "The Incubation Periods of Dengue Viruses." PLoS ONE 7, no. 11 (2012): e50972. http://dx.doi.org/10.1371/journal.pone.0050972.

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14

Lewis, Joyce A., Gwong-Jen Chang, Robert S. Lanciotti, Richard M. Kinney, Leonard W. Mayer, and Dennis W. Trent. "Phylogenetic Relationships of Dengue-2 Viruses." Virology 197, no. 1 (1993): 216–24. http://dx.doi.org/10.1006/viro.1993.1582.

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15

Cologna, Raymond, Philip M. Armstrong, and Rebeca Rico-Hesse. "Selection for Virulent Dengue Viruses Occurs in Humans and Mosquitoes." Journal of Virology 79, no. 2 (2005): 853–59. http://dx.doi.org/10.1128/jvi.79.2.853-859.2005.

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ABSTRACT Dengue is the most common mosquito-borne viral disease in humans. The spread of both mosquito vectors and viruses has led to the resurgence of epidemic dengue fever (a self-limited flu-like syndrome) and the emergence of dengue hemorrhagic fever (severe dengue with bleeding abnormalities) in urban centers of the tropics. There are no animal or laboratory models of dengue disease; indirect evidence suggests that dengue viruses differ in virulence, including their pathogenicities for humans and epidemic potential. We developed two assay systems (using human dendritic cells and Aedes aeg

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16

Chambers, Thomas J., Yan Liang, Deborah A. Droll, et al. "Yellow Fever Virus/Dengue-2 Virus and Yellow Fever Virus/Dengue-4 Virus Chimeras: Biological Characterization, Immunogenicity, and Protection against Dengue Encephalitis in the Mouse Model." Journal of Virology 77, no. 6 (2003): 3655–68. http://dx.doi.org/10.1128/jvi.77.6.3655-3668.2003.

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ABSTRACT Two yellow fever virus (YFV)/dengue virus chimeras which encode the prM and E proteins of either dengue virus serotype 2 (dengue-2 virus) or dengue-4 virus within the genome of the YFV 17D strain (YF5.2iv infectious clone) were constructed and characterized for their properties in cell culture and as experimental vaccines in mice. The prM and E proteins appeared to be properly processed and glycosylated, and in plaque reduction neutralization tests and other assays of antigenic specificity, the E proteins exhibited profiles which resembled those of the homologous dengue virus serotype

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17

Muturi, Ephantus J., Eva Buckner, and Jeffrey Bara. "Superinfection interference between dengue-2 and dengue-4 viruses inAedes aegyptimosquitoes." Tropical Medicine & International Health 22, no. 4 (2017): 399–406. http://dx.doi.org/10.1111/tmi.12846.

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18

Huang, Claire Y. H., Siritorn Butrapet, Dennis J. Pierro, et al. "Chimeric Dengue Type 2 (Vaccine Strain PDK-53)/Dengue Type 1 Virus as a Potential Candidate Dengue Type 1 Virus Vaccine." Journal of Virology 74, no. 7 (2000): 3020–28. http://dx.doi.org/10.1128/jvi.74.7.3020-3028.2000.

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ABSTRACT We constructed chimeric dengue type 2/type 1 (DEN-2/DEN-1) viruses containing the nonstructural genes of DEN-2 16681 virus or its vaccine derivative, strain PDK-53, and the structural genes (encoding capsid protein, premembrane protein, and envelope glycoprotein) of DEN-1 16007 virus or its vaccine derivative, strain PDK-13. We previously reported that attenuation markers of DEN-2 PDK-53 virus were encoded by genetic loci located outside the structural gene region of the PDK-53 virus genome. Chimeric viruses containing the nonstructural genes of DEN-2 PDK-53 virus and the structural g

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19

Nogueira, Rita Maria Ribeiro, Marize Pereira Miagostovich, and Hermann Gonçalves Schatzmayr. "Molecular epidemiology of dengue viruses in Brazil." Cadernos de Saúde Pública 16, no. 1 (2000): 205–11. http://dx.doi.org/10.1590/s0102-311x2000000100021.

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Dengue viruses (DEN) are found as four antigenically distinct serotypes designated DEN-1, 2, 3, and 4. Laboratory evidence that strain-intratypical variation occurs among DEN viruses has been demonstrated since the 1970s, although only with the advances in molecular technologies has it been possible to determine the genetic variability of each serotype. Genotypical identification has proven to be a useful tool for determining the origin and spread of epidemics and to correlate virulence of strains. In this report we present the results of molecular epidemiological studies with the DEN-1 and DE

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20

Basu, Atanu, and Umesh C. Chaturvedi. "Vascular endothelium: the battlefield of dengue viruses." FEMS Immunology & Medical Microbiology 53, no. 3 (2008): 287–99. http://dx.doi.org/10.1111/j.1574-695x.2008.00420.x.

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21

Putnak, J. Robert, Niranjan Kanesa-Thasan, and Bruce L. Innis. "A putative cellular receptor for dengue viruses." Nature Medicine 3, no. 8 (1997): 828–29. http://dx.doi.org/10.1038/nm0897-828.

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22

Reyes-Sandoval, Arturo. "Tackling the dengue, Zika and Chikungunya viruses." Impact 2018, no. 7 (2018): 31–33. http://dx.doi.org/10.21820/23987073.2018.7.31.

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23

Blok, J., A. J. Gibbs, S. M. McWilliam, and U. T. Vitarana. "NS 1 gene sequences from eight dengue-2 viruses and their evolutionary relationships with other dengue-2 viruses." Archives of Virology 118, no. 3-4 (1991): 209–23. http://dx.doi.org/10.1007/bf01314031.

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24

Huang, Claire Y. H., Siritorn Butrapet, Kiyotaka R. Tsuchiya, Natth Bhamarapravati, Duane J. Gubler, and Richard M. Kinney. "Dengue 2 PDK-53 Virus as a Chimeric Carrier for Tetravalent Dengue Vaccine Development." Journal of Virology 77, no. 21 (2003): 11436–47. http://dx.doi.org/10.1128/jvi.77.21.11436-11447.2003.

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ABSTRACT Attenuation markers of the candidate dengue 2 (D2) PDK-53 vaccine virus are encoded by mutations that reside outside of the structural gene region of the genome. We engineered nine dengue virus chimeras containing the premembrane (prM) and envelope (E) genes of wild-type D1 16007, D3 16562, or D4 1036 virus within the genetic backgrounds of wild-type D2 16681 virus and the two genetic variants (PDK53-E and PDK53-V) of the D2 PDK-53 vaccine virus. Expression of the heterologous prM-E genes in the genetic backgrounds of the two D2 PDK-53 variants, but not that of wild-type D2 16681 viru

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25

Saluzzo, J. F., M. Cornet, P. Castagnet, C. Rey, and J. P. Digoutte. "Isolation of dengue 2 and dengue 4 viruses from patients in Senegal." Transactions of the Royal Society of Tropical Medicine and Hygiene 80, no. 1 (1986): 5. http://dx.doi.org/10.1016/0035-9203(86)90182-3.

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26

Megawati, Dewi, Sri Masyeni, Benediktus Yohan, et al. "Dengue in Bali: Clinical characteristics and genetic diversity of circulating dengue viruses." PLOS Neglected Tropical Diseases 11, no. 5 (2017): e0005483. http://dx.doi.org/10.1371/journal.pntd.0005483.

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27

Cecílio, AB, ES Campanelli, KPR Souza, LB Figueiredo, and MC Resende. "Natural vertical transmission by Stegomyia albopicta as dengue vector in Brazil." Brazilian Journal of Biology 69, no. 1 (2009): 123–27. http://dx.doi.org/10.1590/s1519-69842009000100015.

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The mosquito Stegomyia albopicta is among the most important arbovirus vectors in the world, particularly for Dengue viruses. Their natural history suggests that biologically these viruses are highly adapted to their mosquito hosts and they were most likely mosquito viruses prior to becoming adapted to lower primates and humans. As well as being maintained by transmission among susceptible humans, Dengue viruses may also be maintained by vertical transmission in mosquitoes during inter-epidemic periods. The larvae and mosquitoes of Stegomyia albopicta were used to identify the vertical transmi

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28

Katzelnick, Leah C., Ana Coello Escoto, Angkana T. Huang, et al. "Antigenic evolution of dengue viruses over 20 years." Science 374, no. 6570 (2021): 999–1004. http://dx.doi.org/10.1126/science.abk0058.

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Variations in disease enhancement Secondary Dengue virus (DENV) infections can be dangerous if levels of antibodies from prior infection are inadequate to clear the virus. This RNA flavivirus exploits the presence of lower levels of heterotypic antibodies to infect immunoglobulin Fcγ receptor–bearing cells. Many RNA viruses also exhibit antigenic variation, which classically allows evasion of immune responses. Katzelnick et al . investigated whether antigenic variation in DENV has a biological function in a virus that courts immune responses to enhance replication (see the Perspective by Rohan

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29

Leon, Rosen. "Sexual Transmission of Dengue Viruses by Aedes Albopictus." American Journal of Tropical Medicine and Hygiene 37, no. 2 (1987): 398–402. http://dx.doi.org/10.4269/ajtmh.1987.37.398.

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30

Freier, Jerome E., and Leon Rosen. "Vertical Transmission of Dengue Viruses by Aedes Mediovittatus." American Journal of Tropical Medicine and Hygiene 39, no. 2 (1988): 218–22. http://dx.doi.org/10.4269/ajtmh.1988.39.218.

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31

Choudhury, Md Abu, William B. Lott, and John Aaskov. "Distribution of Fitness in Populations of Dengue Viruses." PLoS ONE 9, no. 9 (2014): e107264. http://dx.doi.org/10.1371/journal.pone.0107264.

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32

Vasilakis, Nikos, Robert B. Tesh, Anna P. Durbin, Jorge L. Munoz-Jordan, Amelia P. A. Travassos da Rosa, and Scott C. Weaver. "Antigenic Relationships between Sylvatic and Endemic Dengue Viruses." American Journal of Tropical Medicine and Hygiene 79, no. 1 (2008): 128–32. http://dx.doi.org/10.4269/ajtmh.2008.79.128.

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33

Vasilakis, Nikos, Edward C. Holmes, Eric B. Fokam, et al. "Evolutionary Processes among Sylvatic Dengue Type 2 Viruses." Journal of Virology 81, no. 17 (2007): 9591–95. http://dx.doi.org/10.1128/jvi.02776-06.

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ABSTRACT Sylvatic dengue viruses (DENV) are transmitted in an enzootic cycle between nonhuman primates and arboreal Aedes mosquitoes in Southeast Asia and West Africa. Although previous analyses have revealed the evolutionary processes among endemic (human) DENV, little is known about viral evolution in the sylvatic cycle. Through an analysis of 14 complete coding regions of sylvatic Dengue type 2 virus sampled over a 33-year period, we show that both the rate of evolutionary change and the pattern of natural selection are similar among endemic and sylvatic DENV, although the latter have a uni

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34

Lanciotti, R. S., J. G. Lewis, D. J. Gubler, and D. W. Trent. "Molecular evolution and epidemiology of dengue-3 viruses." Journal of General Virology 75, no. 1 (1994): 65–75. http://dx.doi.org/10.1099/0022-1317-75-1-65.

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35

Lanciotti, R. S., D. W. Trent, and D. J. Gubler. "Molecular evolution and phylogeny of dengue-4 viruses." Journal of General Virology 78, no. 9 (1997): 2279–84. http://dx.doi.org/10.1099/0022-1317-78-9-2279.

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36

WEI, Y., S. WANG, and X. WANG. "Vectors expressing chimeric Japanese encephalitis dengue 2 viruses." Acta virologica 58, no. 04 (2014): 340–47. http://dx.doi.org/10.4149/av_2014_04_340.

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37

Harrison, Stephen C. "Immunogenic cross-talk between dengue and Zika viruses." Nature Immunology 17, no. 9 (2016): 1010–12. http://dx.doi.org/10.1038/ni.3539.

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38

Vorndam, V., R. M. R. Nogueira, and D. W. Trent. "Restriction enzyme analysis of American region dengue viruses." Archives of Virology 136, no. 1-2 (1994): 191–96. http://dx.doi.org/10.1007/bf01538828.

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39

Nusa, Roy, Heni Prasetyowati, Febrina Meutiawati, et al. "Molecular surveillance of Dengue in Sukabumi, West Java province, Indonesia." Journal of Infection in Developing Countries 8, no. 06 (2014): 733–41. http://dx.doi.org/10.3855/jidc.3959.

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Introduction: Dengue is endemic and affects people in all Indonesian provinces. Increasing dengue cases have been observed every year in Sukabumi in West Java province. Despite the endemicity, limited data is available on the genetic of dengue viruses (DENV) circulating in the country. To understand the dynamics of dengue disease, we performed molecular and serological surveillance of dengue in Sukabumi. Methodology: A total of 113 patients were recruited for this study. Serological data were obtained using anti-dengue IgM and IgG tests plus dengue NS1 antigen detection. Dengue detection and s

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40

Mantel, N., Y. Girerd, C. Geny, et al. "Genetic stability of a dengue vaccine based on chimeric yellow fever/dengue viruses." Vaccine 29, no. 38 (2011): 6629–35. http://dx.doi.org/10.1016/j.vaccine.2011.06.101.

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41

Sharma, Shashi, Paban Kumar Dash, Surekha Agarwal, Jyoti Shukla, M. M. Parida, and P. V. L. Rao. "Comparative complete genome analysis of dengue virus type 3 circulating in India between 2003 and 2008." Journal of General Virology 92, no. 7 (2011): 1595–600. http://dx.doi.org/10.1099/vir.0.030437-0.

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Dengue is endemic in most parts of the tropics including India. So far, complete genome information for Indian dengue isolates is not available. In the present study, we characterized the genome of three dengue type 3 viruses isolated from India. The genomes of all three viruses were found to be 10 707 bp long with an ORF encoding 3390 aa. Extensive molecular phylogenetic analysis based on comparison of the complete genome and envelope gene classified the recent Indian viruses into genotype III (lineage III), revealing a shift of lineage from lineage V. The sequence analysis revealed several n

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42

Gubler, Duane J. "Dengue and Dengue Hemorrhagic Fever." Clinical Microbiology Reviews 11, no. 3 (1998): 480–96. http://dx.doi.org/10.1128/cmr.11.3.480.

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SUMMARY Dengue fever, a very old disease, has reemerged in the past 20 years with an expanded geographic distribution of both the viruses and the mosquito vectors, increased epidemic activity, the development of hyperendemicity (the cocirculation of multiple serotypes), and the emergence of dengue hemorrhagic fever in new geographic regions. In 1998 this mosquito-borne disease is the most important tropical infectious disease after malaria, with an estimated 100 million cases of dengue fever, 500,000 cases of dengue hemorrhagic fever, and 25,000 deaths annually. The reasons for this resurgence

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43

BAIG, SHAHBAZ, ABDUL SATTAR, and SHAHBAZ AHMAD. "DENGUE FEVER;." Professional Medical Journal 19, no. 05 (2012): 688–94. http://dx.doi.org/10.29309/tpmj/2012.19.05.2398.

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Dengue infection is one of the most common mosquito borne viral diseases of public health significance. It has been identifiedas a clinical entity since 1780. Dengue is caused by viruses that are small enveloped viruses and are members of the family Flaviviridae genusFlavivirus. It is a vector borne disease and is a global health threat. In Pakistan first epidemic was reported in 1994 and since then cases arereported every years. This year dengue infection raised the number of patients and increased the deaths. Objectives: To assess theknowledge, attitude and practices of the people regarding

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44

Raut, Rajendra, and Aravinda M. de Silva. "Structural differences between dengue viruses circulating in humans and viruses used for vaccine research." Future Virology 14, no. 6 (2019): 379–81. http://dx.doi.org/10.2217/fvl-2019-0048.

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45

Kobayashi, N., K. Oda, Z. Saat, et al. "Type-3 dengue viruses responsible for the dengue epidemic in Malaysia during 1993-1994." American Journal of Tropical Medicine and Hygiene 60, no. 6 (1999): 904–9. http://dx.doi.org/10.4269/ajtmh.1999.60.904.

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46

Feldstein, Leora R., John S. Brownstein, Oliver J. Brady, Simon I. Hay, and Michael A. Johansson. "Dengue on islands: a Bayesian approach to understanding the global ecology of dengue viruses." Transactions of The Royal Society of Tropical Medicine and Hygiene 109, no. 5 (2015): 303–12. http://dx.doi.org/10.1093/trstmh/trv012.

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47

Hanley, Kathryn A., Laura B. Goddard, Lara E. Gilmore, et al. "Infectivity of West Nile/Dengue Chimeric Viruses for West Nile and Dengue Mosquito Vectors." Vector-Borne and Zoonotic Diseases 5, no. 1 (2005): 1–10. http://dx.doi.org/10.1089/vbz.2005.5.1.

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48

Bhavya, M., M. Ramya, N. Nagarjun, Nagarathna Amresh, and Balasubramanian Sathyamurthy. "Docking study of Selected Vinis vitifera seeds constituents on Dengue viral proteins – An In Silico approach." Indian Journal of Pharmaceutical and Biological Research 6, no. 04 (2018): 25–31. http://dx.doi.org/10.30750/ijpbr.6.4.5.

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Dengue is a mosquito-borne systemic viral infection caused by any of the four antigenically related dengue viruses (DENV).The dengue virus belongs to the Flaviviridae family of viruses that cause diseases in humans.A virtual screening analysis of phytochemical structures with dengue virus protein targets has been carried out using a molecular docking approach with vins vinifera seeds. Grapes (Vinis vitifera) are believed to have health benefits due to their antioxidant activity and polyphenols. In this study we examined the binding affinities of 14 ligands with seven non structural Dengu viral

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49

Raviprakash, Kanakatte, Danher Wang, Dan Ewing, et al. "A Tetravalent Dengue Vaccine Based on a Complex Adenovirus Vector Provides Significant Protection in Rhesus Monkeys against All Four Serotypes of Dengue Virus." Journal of Virology 82, no. 14 (2008): 6927–34. http://dx.doi.org/10.1128/jvi.02724-07.

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ABSTRACT Nearly a third of the human population is at risk of infection with the four serotypes of dengue viruses, and it is estimated that more than 100 million infections occur each year. A licensed vaccine for dengue viruses has become a global health priority. A major challenge to developing a dengue vaccine is the necessity to produce fairly uniform protective immune responses to all four dengue virus serotypes. We have developed two bivalent dengue virus vaccines, using a complex adenovirus vector, by incorporating the genes expressing premembrane (prM) and envelope (E) proteins of dengu

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50

Tripathy, Mr Chandra Sekhar, Dr Anil Kumar, Dr Santosh Kumar Behera, et al. "DengueVrsEllagic Acid & Ferric Carboxymaltose: InSilico." Saudi Journal of Biomedical Research 7, no. 7 (2022): 211–18. http://dx.doi.org/10.36348/sjbr.2022.v07i07.001.

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Backgrounds: Dengue viruses are transmitted to humans via mosquito bites from infected Aedes species (Aedesaegypti or Aedesalbopictus). Dengue fever affects over half of the world's population, or about 4 billion people. Dengue fever is a common cause of sickness in high-risk settings. Methods: In the current study two serotypes of Dengue viruses namely DENV1 and DENV2 taken for the study. Here two important compounds namely Ellagic acid and Ferric Carboxymaltose chosen for the targets to be inhibited. In silico docking approach performed to dock the two compounds against the DENV1 and DENV2 v

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