Delayed antibody dependent enhancement of low passage dengue virus 4 isolates

被引:1
作者
Wikan N. [1 ]
Libsittikul S. [1 ]
Yoksan S. [1 ,2 ]
Auewarakul P. [2 ,3 ]
Smith D.R. [1 ,2 ]
机构
[1] Institute of Molecular Biosciences, Mahidol University, Salaya Campus, 25/25 Phuttamonthol Sai 4, Salaya, Nakorn Pathom
[2] Center for Emerging and Neglected Infectious Diseases, Mahidol University, Salaya Campus, 25/25 Phuttamonthol Sai 4, Salaya, Nakorn Pathom
[3] Department of Microbiology, Faculty of Medicine, Siriraj Hospital, Mahidol University, 2 Wanglang Road, Bangkoknoi, Bangkok
关键词
Antibody dependent enhancement; Dengue; Infection; U937; cells;
D O I
10.1186/s13104-015-1381-8
中图分类号
学科分类号
摘要
Background: The concept of antibody dependent enhancement (ADE) of dengue virus (DENV) infection is a cornerstone of our current understanding of dengue pathogenesis, although some questions as to the mechanism remain, particularly in regards to the behavior of low and high passage virus isolates. This study utilized two low passage DENV 4 isolates and a laboratory adapted DENV 4 isolate to investigate the potential of low passage isolates to undergo ADE. Results: Little or no ADE of infection was observed on day 2 post infection with low passage isolates, while high enhancement of infection was seen with the laboratory adapted virus. However, both of the low passage isolates showed high levels of infection (60-100 %) by day 5 post infection. Conclusions: These results show that low passage DENV 4 viruses undergo ADE mediated infection, but that the process is significantly temporally delayed as compared to laboratory adapted DENV 4. © 2015 Wikan et al.
引用
收藏
相关论文
共 24 条
[1]  
Bhatt S., Gething P.W., Brady O.J., Messina J.P., Farlow A.W., Moyes C.L., Drake J.M., Brownstein J.S., Hoen A.G., Sankoh O., Et al., The global distribution and burden of dengue, Nature, 496, pp. 504-507, (2013)
[2]  
Halstead S.B., Antibody, macrophages, dengue virus infection, shock, and hemorrhage: A pathogenetic cascade, Rev Infect Dis, 11, pp. S830-S839, (1989)
[3]  
Gubler D.J., Dengue and dengue hemorrhagic fever, Clin Microbiol Rev, 11, pp. 480-496, (1998)
[4]  
Halstead S.B., O'Rourke E.J., Dengue viruses and mononuclear phagocytes. I. Infection enhancement by non-neutralizing antibody, J Exp Med, 146, pp. 201-217, (1977)
[5]  
Halstead S.B., Porterfield J.S., O'Rourke E.J., Enhancement of dengue virus infection in monocytes by flavivirus antisera, Am J Trop Med Hyg, 29, pp. 638-642, (1980)
[6]  
Guzman M.G., Kouri G.P., Bravo J., Soler M., Vazquez S., Morier L., Dengue hemorrhagic fever in Cuba, 1981: A retrospective seroepidemiologic study, Am J Trop Med Hyg, 42, pp. 179-184, (1990)
[7]  
Rothman A.L., Cellular immunology of sequential dengue virus infection and its role in disease pathogenesis, Curr Top Microbiol Immunol, 338, pp. 83-98, (2010)
[8]  
Sangkawibha N., Rojanasuphot S., Ahandrik S., Viriyapongse S., Jatanasen S., Salitul V., Phanthumachinda B., Halstead S.B., Risk factors in dengue shock syndrome: A prospective epidemiologic study in Rayong, Thailand. I. The, 1980 outbreak, Am J Epidemiol, 120, pp. 653-669, (1984)
[9]  
Endy T.P., Human immune responses to dengue virus infection: Lessons learned from prospective cohort studies, Front Immunol, 5, (2014)
[10]  
Chaichana P., Okabayashi T., Puiprom O., Sasayama M., Sasaki T., Yamashita A., Ramasoota P., Kurosu T., Ikuta K., Low levels of antibody-dependent enhancement in vitro using viruses and plasma from dengue patients, PLoS One, 9, (2014)