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通过 ELISA 开发一种有前景的抗原混合物,用于全球检测马巴贝斯虫。

Development of a promising antigenic cocktail for the global detection of Babesia caballi in horse by ELISA.

机构信息

National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Hokkaido, Japan.

Department of Biochemistry and Chemistry of Nutrition, Faculty of Veterinary Medicine, Mansoura University, Mansoura, Egypt.

出版信息

PLoS One. 2023 Apr 14;18(4):e0284535. doi: 10.1371/journal.pone.0284535. eCollection 2023.

Abstract

In this study, we designed novel truncated Babesia caballi (B. caballi) recombinant proteins from the previously used B. caballi proteins; 134-Kilodalton Protein (rBC134) and Merozoite Rhoptry 48 Protein (rBC48). Then, we evaluated the diagnostic performance of the newly designed proteins when used as a single antigen or when used as cocktail antigen consists of rBC134 full length (rBC134f) + newly designed rBC48 (rBC48t) or newly designed rBC134 (rBC134t) + rBC48t for the detection of B. caballi infection in horse using indirect enzyme-linked immunosorbent assay (iELISA). We used one dose and a half of each antigen in the cocktail formulas. The serum samples were collected from different endemic areas in addition to the sera collected from horses experimentally infected with B. caballi were used in the present study. Cocktail antigen in full dose of (rBC134f + rBC48t) exhibited the highest optical density (OD) values with B. caballi-infected sera and showed the lowest OD values with normal equine sera or B. caballi, and Theileria equi mixed infected sera in comparison with the single antigen. Interestingly, the same cocktail antigen exhibited the highest concordance rate (76.74%) and kappa value (0.79) in the screening of 200 field serum samples collected from five B. caballi endemic countries, including South Africa (n = 40), Ghana (n = 40), Mongolia (n = 40), Thailand (n = 40), and China (n = 40) using iELISA and the results were compared to those of indirect fluorescent antibody test (IFAT) as a reference. Moreover, the identified promising cocktail full dose antigen (rBC134f + rBC48t) showed that it can detect the infection as early as the 4th day post-infection in sera collected from experimentally infected horses. The obtained results revealed the reliability of the rBC134f + rBC48t cocktail antigen when used in full dose for the detection of specific antibodies to B. caballi in horses which will be useful for epidemiological surveys and control of equine babesiosis.

摘要

在这项研究中,我们设计了新型截短的巴贝斯虫(B. caballi)重组蛋白,这些蛋白来自先前使用的巴贝斯虫蛋白,即 134 千道尔顿蛋白(rBC134)和裂殖体 rhoptry48 蛋白(rBC48)。然后,我们评估了新设计的蛋白作为单一抗原或作为鸡尾酒抗原的诊断性能,该鸡尾酒抗原由全长 rBC134(rBC134f)+新设计的 rBC48(rBC48t)或新设计的 rBC134(rBC134t)+rBC48t 组成,用于检测马中的巴贝斯虫感染使用间接酶联免疫吸附试验(iELISA)。我们在鸡尾酒配方中使用了每种抗原的一剂半。血清样本来自不同的流行地区,此外,还使用了从实验感染巴贝斯虫的马中收集的血清。与单一抗原相比,全剂量鸡尾酒抗原(rBC134f+rBC48t)与感染巴贝斯虫的血清具有最高的光密度(OD)值,与正常马血清或巴贝斯虫和泰勒虫混合感染的血清具有最低的 OD 值。有趣的是,在使用 iELISA 筛查来自南非(n=40)、加纳(n=40)、蒙古(n=40)、泰国(n=40)和中国(n=40)等五个巴贝斯虫流行国家的 200 份现场血清样本时,相同的鸡尾酒抗原表现出最高的一致性率(76.74%)和 Kappa 值(0.79),结果与间接荧光抗体试验(IFAT)作为参考进行比较。此外,鉴定出的有前途的鸡尾酒全剂量抗原(rBC134f+rBC48t)表明,它可以在从实验感染马采集的血清中检测到感染,最早可在感染后第 4 天。研究结果表明,rBC134f+rBC48t 鸡尾酒抗原在全剂量使用时用于检测马对巴贝斯虫的特异性抗体是可靠的,这将有助于进行流行病学调查和控制马巴贝斯虫病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5246/10104287/2b790a61b90d/pone.0284535.g001.jpg

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