Altered enzyme-linked immunosorbent assay immunoglobulin M (IgM)/IgG optical density ratios can correctly classify all primary or secondary dengue virus infections 1 day after the onset of symptoms, when all of the viruses can be isolated

被引:51
作者
Falconar, Andrew K. I.
de Plata, Elsa
Romero-Vivas, Claudia M. E.
机构
[1] Univ Norte, Grp Invest Enfermedades Trop, Dept Ciencias Basicas Med, Barranquilla, Colombia
[2] Oficina Distrital Salud Publ Barranquilla, Barranquilla, Colombia
关键词
D O I
10.1128/CVI.00105-06
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We compared dengue virus (DV) isolation rates and tested whether acute primary (P) and acute/probable acute secondary (S/PS) DV infections could be correctly classified serologically when the patients' first serum (SI) samples were obtained 1 to 3 days after the onset of symptoms (AOS). DV envelope/membrane proteinspecific immunoglobulin M IgM) capture and IgG capture enzyme-linked immunosorbent assay (ELISA) titrations (1/log(10) 1.7 to 1 log(10) 6.6 dilutions) were performed on 100 paired S1 and S2 samples from suspected DV infections. The serologically confirmed S/PS infections were divided into six subgroups based on their different IgM and IgG responses. Because of their much greater dynamic ranges, IgG/IgM ELISA titer ratios were more accurate and reliable than IgM/IgG optical density (OD) ratios recorded at a single cutoff dilution for discriminating between P and S/PS infections. However, 62% of these patients' S1 samples were DV IgM and IgG titer negative (< ODmax/2 titer threshold), and in 35% of the S/PS infections, the patients' S1 and S2 samples were IgM titer negative. The IgM OD values were, however, much higher than those of IgG in the S1 samples of many of these, and the other, S/PS infections. This necessitated using higher (>= 2.60 and < 2.60) discriminatory IgM/IgG OD (DOD) ratios on these S1 samples than those published previously to correctly classify the highest percentage of these P and S/PS infections. The DV isolation rate was highest (12/12; 100%) using IgG and IgM titer-negative S1 samples collected 1 day AOS, when 100% of them were correctly classified as P or S/PS infections using these higher DOD ratios.
引用
收藏
页码:1044 / 1051
页数:8
相关论文
共 24 条
[1]   Enzyme-linked immunosorbent assay specific to dengue virus type 1 nonstructural protein NS1 reveals circulation of the antigen in the blood during the experiencing primary acute phase of disease in patients or secondary infections [J].
Alcon, S ;
Talarmin, A ;
Debruyne, M ;
Falconar, A ;
Deubel, V ;
Flamand, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (02) :376-381
[2]   Analysis of specific IgM responses in secondary dengue virus infections: levels and positive rates in comparison with primary infections [J].
Chanama, S ;
Anantapreecha, S ;
A-nuegoonpipat, A ;
Sa-gnasang, A ;
Kurane, I ;
Sawanpanyalert, P .
JOURNAL OF CLINICAL VIROLOGY, 2004, 31 (03) :185-189
[3]   COMPARISON OF IMMUNOGLOBULIN-G ENZYME-LINKED IMMUNOSORBENT-ASSAY (IGG-ELISA) AND HEMAGGLUTINATION INHIBITION (HI) TEST FOR THE DETECTION OF DENGUE ANTIBODIES - PREVALENCE OF DENGUE IGG-ELISA ANTIBODIES IN TAHITI [J].
CHUNGUE, E ;
MARCHE, G ;
PLICHART, R ;
BOUTIN, JP ;
ROUX, J .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1989, 83 (05) :708-711
[4]  
Falconar A. K. I., 1999, Recent Research Developments in Virology, V1, P437
[5]   PRODUCTION OF DIMER-SPECIFIC AND DENGUE VIRUS GROUP CROSS-REACTIVE MOUSE MONOCLONAL-ANTIBODIES TO THE DENGUE-2 VIRUS NONSTRUCTURAL GLYCOPROTEIN NS1 [J].
FALCONAR, AKI ;
YOUNG, PR .
JOURNAL OF GENERAL VIROLOGY, 1991, 72 :961-965
[6]   Identification of an epitope on the dengue virus membrane (M) protein defined by cross-protective monoclonal antibodies: design of an improved epitope sequence based on common determinants present in both envelope (E and M) proteins [J].
Falconar, AKI .
ARCHIVES OF VIROLOGY, 1999, 144 (12) :2313-2330
[7]  
Gubler D. J., 1996, Dengue Bulletin, V20, P20
[8]   Dengue and dengue hemorrhagic fever [J].
Gubler, DJ .
CLINICAL MICROBIOLOGY REVIEWS, 1998, 11 (03) :480-+
[9]   DENGUE VIRUS-SPECIFIC AND FLAVIVIRUS GROUP DETERMINANTS IDENTIFIED WITH MONOCLONAL-ANTIBODIES BY INDIRECT IMMUNOFLUORESCENCE [J].
HENCHAL, EA ;
GENTRY, MK ;
MCCOWN, JM ;
BRANDT, WE .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1982, 31 (04) :830-836
[10]   AN ENZYME-LINKED IMMUNOSORBENT-ASSAY TO CHARACTERIZE DENGUE INFECTIONS WHERE DENGUE AND JAPANESE ENCEPHALITIS CO-CIRCULATE [J].
INNIS, BL ;
NISALAK, A ;
NIMMANNITYA, S ;
KUSALERDCHARIYA, S ;
CHONGSWASDI, V ;
SUNTAYAKORN, S ;
PUTTISRI, P ;
HOKE, CH .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1989, 40 (04) :418-427