新型Tc-24重组抗原ELISA检测犬克氏锥虫血清学的初步研究

IF 1.7 3区 农林科学 Q2 VETERINARY SCIENCES
Rojelio Mejia, Guilherme G Verocai, Ilana A Mosley, Ashley B Saunders, Bin Zhan, Lindsey Vongthavaravat, Rachel E Busselman, Sarah A Hamer
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引用次数: 0

摘要

恰加斯病由原生动物克氏锥虫引起,是犬类健康面临的重大挑战,诊断工具有限。本研究评估了一种新型Tc-24重组抗原ELISA的性能,并将其与三种商业诊断检测方法进行了比较。与间接荧光抗体(IFA)检测相比,Tc-24 ELISA具有较高的灵敏度(87.5%)和特异性(91.2%),阳性和阴性Tc-24光密度(OD)差异显著(0.607比0.089,p < 0.001)。与Chagas Stat-Pak (SP)相比,Tc-24 ELISA的敏感性和特异性分别为82.1%和86.7% (p < 0.001)。对于Chagas Detect Plus (IB),该方法的灵敏度为80.0%,特异性为93.1% (p < 0.001)。Spearman相关分析显示,Tc-24 OD与SP (r = 1.0, p = 0.0167)、IB (r = 0.9, p = 0.0833)、IFA (r = 0.6273, p = 0.044)有显著相关。商业试剂盒(SP或IB)中免疫层析值升高与Tc-24 OD相关(1.17 vs. 0.039, p < 0.001),基于商业试剂盒的阳性结果,达到100%的灵敏度和95.8%的特异性。这些结果表明,Tc-24酶联免疫吸附试验是一种可靠、准确的犬克氏t型虫感染血清学诊断工具,具有提高兽医学诊断能力的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evaluation of a Novel Tc-24 Recombinant Antigen ELISA for Serologic Detection of Trypanosoma cruzi Infection in Dogs: A Pilot Study.

Evaluation of a Novel Tc-24 Recombinant Antigen ELISA for Serologic Detection of Trypanosoma cruzi Infection in Dogs: A Pilot Study.

Evaluation of a Novel Tc-24 Recombinant Antigen ELISA for Serologic Detection of Trypanosoma cruzi Infection in Dogs: A Pilot Study.

Evaluation of a Novel Tc-24 Recombinant Antigen ELISA for Serologic Detection of Trypanosoma cruzi Infection in Dogs: A Pilot Study.

Chagas disease, caused by the protozoan Trypanosoma cruzi, is a significant challenge for canine health, with limited diagnostic tools. This study assessed the performance of a novel Tc-24 recombinant antigen ELISA compared to three commercial diagnostic tests on 70 serum samples from kennel dogs in Texas. The Tc-24 ELISA demonstrated high sensitivity (87.5%) and specificity (91.2%) compared to Indirect Fluorescent Antibody (IFA) testing, with significant differences in Tc-24 optical density (OD) between positives and negatives (0.607 vs. 0.089, p < 0.001). When compared to Chagas Stat-Pak (SP), Tc-24 ELISA showed sensitivity and specificity values of 82.1% and 86.7%, respectively (p < 0.001). For Chagas Detect Plus (IB), the assay achieved a sensitivity of 80.0% and specificity of 93.1% (p < 0.001). Spearman correlation analysis revealed significant associations between Tc-24 OD and SP (r = 1.0, p = 0.0167), IB (r = 0.9, p = 0.0833) and IFA (r = 0.6273, p = 0.044). Elevated immunochromatographic values in commercial kits (SP or IB) correlated with Tc-24 OD (1.17 vs. 0.039, p < 0.001), achieving 100% sensitivity and 95.8% specificity based on positive results from commercial kits. These findings suggest that Tc-24 ELISA is a reliable and accurate serological tool for diagnosing T. cruzi infection in dogs, with the potential to enhance diagnostic capabilities in veterinary medicine.

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来源期刊
Veterinary Medicine and Science
Veterinary Medicine and Science Veterinary-General Veterinary
CiteScore
3.00
自引率
0.00%
发文量
296
期刊介绍: Veterinary Medicine and Science is the peer-reviewed journal for rapid dissemination of research in all areas of veterinary medicine and science. The journal aims to serve the research community by providing a vehicle for authors wishing to publish interesting and high quality work in both fundamental and clinical veterinary medicine and science. Veterinary Medicine and Science publishes original research articles, systematic reviews, meta-analyses, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented in the paper. We aim to be a truly global forum for high-quality research in veterinary medicine and science, and believe that the best research should be published and made widely accessible as quickly as possible. Veterinary Medicine and Science publishes papers submitted directly to the journal and those referred from a select group of prestigious journals published by Wiley-Blackwell. Veterinary Medicine and Science is a Wiley Open Access journal, one of a new series of peer-reviewed titles publishing quality research with speed and efficiency. For further information visit the Wiley Open Access website.
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