Analysis of recombinant dengue virus polypeptides for dengue diagnosis and evaluation of the humoral immune response

被引:15
作者
Dos Santos, FB
Miagostovich, MP
Nogueira, RMR
Schatzmayr, HG
Riley, LW
Harris, E
机构
[1] Fiocruz MS, Dept Virol, Inst Oswaldo Cruz, BR-21045900 Rio De Janeiro, Brazil
[2] Univ Calif Berkeley, Sch Publ Hlth, Div Infect Dis, Berkeley, CA 94720 USA
关键词
D O I
10.4269/ajtmh.2004.71.144
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Dengue is a serious cause of morbidity and mortality in tropical areas worldwide. We cloned and expressed recombinant polypeptides spanning the entire genome of a Brazilian dengue virus type 2 (DENV-2) strain in contiguous segments to generate antigens for dengue diagnosis and evaluation of the human humoral immune response. When analyzed by Western blot and an enzyme-linked immunosorbent assay (ELISA) using human sera, the most reactive polypeptide (pD2-3(E)) was located in the N-terminal portion of the envelope protein. The sensitivity of an IgG-ELISA using pD2-3(E) versus mouse brain antigen was 100% with convalescent sera and 79% with acute sera, with a specificity of 100%. Sera from patients infected with other DENV serotypes recognized pD2-3(E) equally well, whereas sera positive for yellow fever, rubella, and measles showed little or no reactivity. Using this novel approach, we identified a candidate antigen to facilitate diagnosis of DENV infections and observed a surprising variability in antibody patterns in the clinical response to DENV infections.
引用
收藏
页码:144 / 152
页数:9
相关论文
共 48 条
[31]   DENGUE EPIDEMIC IN THE STATE OF RIO-DE-JANEIRO, BRAZIL, 1990-1 - CO-CIRCULATION OF DENGUE-1 AND DENGUE-2 SEROTYPES [J].
NOGUEIRA, RMR ;
MIAGOSTOVICH, MP ;
LAMPE, E ;
SOUZA, RW ;
ZAGNE, SMO ;
SCHATZMAYR, HG .
EPIDEMIOLOGY AND INFECTION, 1993, 111 (01) :163-170
[32]   Evaluation of the MRL diagnostics dengue fever virus IgM capture ELISA and the PanBio Rapid Immunochromatographic Test for diagnosis of dengue fever in Jamaica [J].
Palmer, CJ ;
King, SD ;
Cuadrado, PR ;
Perez, E ;
Baum, M ;
Ager, AL .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (05) :1600-1601
[33]   Clinical evaluation of a rapid immunochromatographic test for the diagnosis of dengue virus infection [J].
Sang, CT ;
Hoon, LS ;
Cuzzubbo, A ;
Devine, P .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 1998, 5 (03) :407-409
[34]  
Se-Thoe SY, 1999, J MED VIROL, V57, P322, DOI 10.1002/(SICI)1096-9071(199903)57:3&lt
[35]  
322::AID-JMV17&gt
[36]  
3.0.CO
[37]  
2-5
[38]   Evaluation of recombinant dengue viral envelope B domain protein antigens for the detection of dengue complex-specific antibodies [J].
Simmons, M ;
Porter, KR ;
Escamilla, J ;
Graham, R ;
Watts, DM ;
Eckels, KH ;
Hayes, CG .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1998, 58 (02) :144-151
[39]   MICE IMMUNIZED WITH A DENGUE TYPE-2 VIRUS-E AND NS1 FUSION PROTEIN MADE IN ESCHERICHIA-COLI ARE PROTECTED AGAINST LETHAL DENGUE VIRUS-INFECTION [J].
SRIVASTAVA, AK ;
PUTNAK, JR ;
WARREN, RL ;
HOKE, CH .
VACCINE, 1995, 13 (13) :1251-1258
[40]   Affinity-purified dengue-2 virus envelope glycoprotein induces neutralizing antibodies and protective immunity in mice [J].
Staropoli, I ;
Frenkiel, MP ;
Megret, F ;
Deubel, V .
VACCINE, 1997, 15 (17-18) :1946-1954