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Detection of Acute Toxoplasmosis in Pigs Using Loop-Mediated Isothermal Amplification and Quantitative PCR

机译:用环介导的等温扩增和定量PCR检测猪的急性弓形虫病

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摘要

A loop-mediated isothermal amplification (LAMP) assay allows rapid diagnosis of Toxoplasma gondii infection. In the present study, the LAMP assay was evaluated using blood from both naturally and experimentally infected pigs. The sensitivity of the LAMP assay was compared with that of Q-PCR. Both assays detected T. gondii in the blood of experimentally infected pigs, with 100% agreement. In infected blood samples, the parasite was detected as early as 2 days post-infection and reached a peak in 3-5 days. In 216 field serum samples, the detection rates of LAMP and Q-PCR assays were 6.9% and 7.8%, respectively. This result indicates that the sensitivity of the LAMP assay was slightly lower than that of the Q-PCR assay. However, the LAMP may be an attractive diagnostic method in conditions where sophisticated and expensive equipment is unavailable. This assay could be a powerful supplement to current diagnostic methods.
机译:环介导的等温扩增(LAMP)分析可快速诊断弓形虫感染。在本研究中,使用自然和实验感染猪的血液对LAMP分析进行了评估。将LAMP分析的灵敏度与Q-PCR的灵敏度进行了比较。两种检测方法均以100%的一致性检测出实验感染猪血液中的弓形虫。在感染的血液样本中,寄生虫最早在感染后2天就被检测到,并在3-5天达到峰值。在216份田间血清样品中,LAMP和Q-PCR检测的检出率分别为6.9%和7.8%。该结果表明,LAMP测定法的灵敏度略低于Q-PCR测定法的灵敏度。但是,在无法使用复杂且昂贵的设备的情况下,LAMP可能是一种有吸引力的诊断方法。该测定法可以作为当前诊断方法的有力补充。

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