Secreted portion of glycoprotein G of herpes simplex virus type 2 is a novel antigen for type-discriminating serology

被引:23
作者
Görander, S [1 ]
Svennerholm, B [1 ]
Liljeqvist, JÅ [1 ]
机构
[1] Gothenburg Univ, Dept Virol, S-41346 Gothenburg, Sweden
关键词
D O I
10.1128/JCM.41.8.3681-3686.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The secreted portion of glycoprotein G (sgG-2) of herpes simplex virus type 2 (HSV-2) was evaluated as a novel antigen in an enzyme-linked immunosorbent assay (ELISA) format for detection of type-specific immunoglobulin G (IgG) antibodies in HSV-2-infected patients. The results were compared with those obtained by a commercially available assay, the HerpeSelect 2 ELISA (the FOCUS2 assay). Five different panels of sera were analyzed: panel A consisted of 109 serum samples from patients with a culture-proven HSV-1 infection that were Western blotting (WB) negative for H,SV-2; panel B consisted of 106 serum samples from patients with a culture-proven recurrent HSV-2 infection that were WB positive for HSV-2; panel C consisted of 100 serum samples with no detectable IgG antibodies against HSV-1 and HSV-2; panel D consisted of 70 HSV-2 negative "tricky" serum samples containing antinuclear IgG antibodies or IgM antibodies against other viruses or bacteria; and panel E consisted of consecutive serum samples from 21 patients presenting with a first episode of HSV-2-induced lesions. When sera in panels A to C were analyzed, the sgG-2 ELISA and the FOCUS2 assay both showed sensitivities and specificities of :greater than or equal to98%. In total, among the samples in panel D, 13 serum samples (19%) were false positive by the FOCUS2 assay and I serum sample (1.4%) was false positive by the sgG-2 ELISA. When the sera in panel E were analyzed, the sgG-2 ELISA detected seroconversion, somewhat later than WB or the FOCUS2 assay did. We conclude that sgG-2 induces an HSV-2 type-specific antibody response and can be used for type-discriminating serology.
引用
收藏
页码:3681 / 3686
页数:6
相关论文
共 34 条
[1]   COMPARISON OF WESTERN BLOT (IMMUNOBLOT) AND GLYCOPROTEIN-G-SPECIFIC IMMUNODOT ENZYME ASSAY FOR DETECTING ANTIBODIES TO HERPES-SIMPLEX VIRUS TYPE-1 AND TYPE-2 IN HUMAN-SERA [J].
ASHLEY, RL ;
MILITONI, J ;
LEE, F ;
NAHMIAS, A ;
COREY, L .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (04) :662-667
[2]  
Ashley RL, 1999, CLIN MICROBIOL REV, V12, P1
[3]   Premarket evaluation of a commercial glycoprotein G-based enzyme immunoassay for herpes simplex virus type-specific antibodies [J].
Ashley, RL ;
Wu, LX ;
Pickering, JW ;
Tu, MC ;
Schnorenberg, L .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (01) :294-295
[4]   Sorting out the new HSV type specific antibody tests [J].
Ashley, RL .
SEXUALLY TRANSMITTED INFECTIONS, 2001, 77 (04) :232-237
[5]   SYNTHESIS AND PROCESSING OF GLYCOPROTEIN-GG OF HERPES-SIMPLEX VIRUS TYPE-2 [J].
BALACHANDRAN, N ;
HUTTFLETCHER, LM .
JOURNAL OF VIROLOGY, 1985, 54 (03) :825-832
[6]   Case-control study of sexually transmitted diseases as cofactors for HIV-1 transmission [J].
Beck, EJ ;
Mandalia, S ;
Leonard, K ;
Griffith, RJ ;
Harris, JRW ;
Miller, DL .
INTERNATIONAL JOURNAL OF STD & AIDS, 1996, 7 (01) :34-38
[7]   NEONATAL HERPES-SIMPLEX VIRUS-INFECTION IN RELATION TO ASYMPTOMATIC MATERNAL INFECTION AT THE TIME OF LABOR [J].
BROWN, ZA ;
BENEDETTI, J ;
ASHLEY, R ;
BURCHETT, S ;
SELKE, S ;
BERRY, S ;
VONTVER, LA ;
COREY, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (18) :1247-1252
[8]   The acquisition of herpes simplex virus during pregnancy [J].
Brown, ZA ;
Selke, S ;
Zeh, J ;
Kopelman, J ;
Maslow, A ;
Ashley, RL ;
Watts, DH ;
Berry, S ;
Herd, M ;
Corey, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (08) :509-515
[9]   Herpes simplex virus type-2 antibodies in pregnant women: the impact of the stage of pregnancy [J].
Eskild, A ;
Jeansson, S ;
Hagen, JA ;
Jenum, PA ;
Skrondal, A .
EPIDEMIOLOGY AND INFECTION, 2000, 125 (03) :685-692
[10]   Herpes simplex virus type 2 in the United States, 1976 TO 1994 [J].
Fleming, DT ;
McQuillan, GM ;
Johnson, RE ;
Nahmias, AJ ;
Aral, SO ;
Lee, FK ;
StLouis, ME .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (16) :1105-1111