Detection of Toxoplasma gondii Infection in Small Ruminants: Old Problems, and Current Solutions

被引:9
作者
Holec-Gasior, Lucyna [1 ]
Solowinska, Karolina [1 ]
机构
[1] Gdansk Univ Technol, Fac Chem, Dept Mol Biotechnol & Microbiol, 11-12 Narutowicza Str, PL-80233 Gdansk, Poland
基金
英国科研创新办公室;
关键词
Toxoplasma gondii; sheep; goat; toxoplasmosis; molecular detection; serological detection; recombinant antigen; LINKED-IMMUNOSORBENT-ASSAY; RISK-FACTORS; IMMUNOGLOBULIN-M; RECOMBINANT ANTIGENS; MOLECULAR-DETECTION; NEOSPORA-CANINUM; CONGENITAL TRANSMISSION; GOATS SEROPREVALENCE; OVINE TOXOPLASMOSIS; CHIMERIC ANTIGEN;
D O I
10.3390/ani13172696
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Toxoplasmosis is a parasitic zoonosis of veterinary importance, with implications for public health. Toxoplasma gondii infection causes abortion or congenital disease in small ruminants. Moreover, the consumption of infected meat, cured meat products, or unpasteurized milk and dairy products can facilitate zoonotic transmission. Serological studies conducted in various European countries have shown the high seroprevalence of specific anti-T. gondii antibodies in sheep and goats related to the presence of oocysts in the environment, as well as climatic conditions. This article presents the current status of the detection possibilities for T. gondii infection in small ruminants and their milk. Serological testing is considered the most practical method for diagnosing toxoplasmosis; therefore, many studies have shown that recombinant antigens as single proteins, mixtures of various antigens, or chimeric proteins can be successfully used as an alternative to Toxoplasma lysate antigens (TLA). Several assays based on DNA amplification have been developed as alternative diagnostic methods, which are especially useful when serodiagnosis is not possible, e.g., the detection of intrauterine T. gondii infection when the fetus is not immunocompetent. These techniques employ multicopy sequences highly conserved among different strains of T. gondii in conventional, nested, competitive, and quantitative reverse transcriptase-PCR.
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页数:20
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