Evaluation of recombinant antigens in combination and single formula for diagnosis of feline toxoplasmosis

被引:25
作者
Abdelbaset, Abdelbaset Eweda [1 ,2 ]
Alhasan, Hend [1 ]
Salman, Doaa [3 ]
Karram, Mohamed Hassan [2 ]
Rushdi, Mahmoud Abd Ellah [2 ]
Xuan Xuenan [1 ]
Igarashi, Makoto [1 ]
机构
[1] Obihiro Univ Agr & Vet Med, Natl Res Ctr Protozoan Dis, 2-13 Inada Cho, Obihiro, Hokkaido 0808555, Japan
[2] Assiut Univ, Dept Anim Med, Fac Vet Med, Assiut, Egypt
[3] Sohag Univ, Dept Anim Med, Fac Vet Med, Sohag, Egypt
关键词
ELISA; Recombinant proteins; Serodiagnosis; Toxoplasmosis; IMMUNOGLOBULIN-G ANTIBODIES; LINKED-IMMUNOSORBENT-ASSAY; GONDII INFECTION; SERODIAGNOSIS; CATS; GRA7; SAG1;
D O I
10.1016/j.exppara.2016.11.003
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Cats are the only definitive hosts of Toxoplasma gondii and constitute an essential source of infection to all warm blooded animals and humans. Diagnosis of T gondii infection in cats is fundamental for proper management and control of infection in humans and animals. In the current study, we have evaluated the diagnostic performance of tachyzoite lysate antigen (TLA) and different T. gondii recombinant antigens including surface antigen 2 (SAG2), dense granule proteins 2, 6, 7, 15 (GRA2, GRA6, GRA7, GRA15) and microneme 10 protein (MIC10) in immunoglobulin G enzyme linked-immunosorbent assay (IgG ELISA) using cat serum samples, with reference to latex agglutination test (LAT). Remarkably, TLA showed better performance than other recombinant antigens in IgG ELISAs as compared to LAT, with concordance and Kappa values of 94.27% and 0.93, respectively. Furthermore, to improve the reactivity of the recombinant antigens, we have developed IgG ELISAs using different combinations with these recombinant antigens. Strikingly, a combination of SAG2 and GRAs has relatively similar performance as TLA evidenced by concordance and Kappa values of 94.27% and 0.81, respectively. The developed ELISA with a combination of recombinant antigens can be used as a promising diagnostic tool for routine testing of T. gondii infection and mass screening in cats. The major advantages of this assay are the high sensitivity and specificity, lower cost, safer production and easiness of standardization in various laboratories worldwide. (C) 2016 The Authors. Published by Elsevier Inc.
引用
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页码:1 / 4
页数:4
相关论文
共 24 条
  • [1] Recombinant antigens to detect Toxoplasma gondii-specific immunoglobulin G and immunoglobulin M in human sera by enzyme immunoassay
    Aubert, D
    Maine, GT
    Villena, I
    Hunt, JC
    Howard, L
    Sheu, M
    Brojanac, S
    Chovan, LE
    Nowlan, SF
    Pinon, JM
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (03) : 1144 - 1150
  • [2] Buxton D, 1998, VET RES, V29, P289
  • [3] EVALUATION OF AN INDIRECT ELISA USING RECOMBINANT GRANULE ANTIGEN GRA7 FOR SERODIAGNOSIS OF TOXOPLASMA GONDII INFECTION IN CATS
    Cai, Yufeng
    Wang, Zedong
    Li, Jiping
    Li, Nan
    Wei, Feng
    Liu, Quan
    [J]. JOURNAL OF PARASITOLOGY, 2015, 101 (01) : 37 - 40
  • [4] Cats and Toxoplasma: Implications for Public Health
    Dabritz, H. A.
    Conrad, P. A.
    [J]. ZOONOSES AND PUBLIC HEALTH, 2010, 57 (01) : 34 - 52
  • [5] Dubey J.P., 1988, TOXOPLASMOSIS ANIMAL
  • [6] Toxoplasma gondii: epidemiology, feline clinical aspects, and prevention
    Elmore, Stacey A.
    Jones, Jeffrey L.
    Conrad, Patricia A.
    Patton, Sharon
    Lindsay, David S.
    Dubey, J. P.
    [J]. TRENDS IN PARASITOLOGY, 2010, 26 (04) : 190 - 196
  • [7] Haung X, 2002, J PARASITOL, V88, P804, DOI 10.1645/0022-3395(2002)088[0804:DAEOAE]2.0.CO
  • [8] 2
  • [9] Toxoplasma gondii:: Enzyme-linked immunosorbent assay using different fragments of recombinant microneme protein 1 (MIC1) for detection of immunoglobulin G antibodies
    Holec, Lucyna
    Gasior, Atur
    Brillowska-Dabrowska, Anna
    Kur, Jozef
    [J]. EXPERIMENTAL PARASITOLOGY, 2008, 119 (01) : 1 - 6
  • [10] Toxoplasma gondii Recombinant Antigens as Tools for Serodiagnosis of Human Toxoplasmosis: Current Status of Studies
    Holec-Gasior, Lucyna
    [J]. CLINICAL AND VACCINE IMMUNOLOGY, 2013, 20 (09) : 1343 - 1351