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用于检测感染犬中糖基磷脂酰肌醇锚定蛋白52(P52)抗体的间接酶联免疫吸附测定法的建立与应用

Establishment and Application of an Indirect Enzyme-Linked Immunosorbent Assay for Measuring GPI-Anchored Protein 52 (P52) Antibodies in -Infected Dogs.

作者信息

Liu Qin, Zhan Xueyan, Li Dongfang, Zhao Junlong, Wei Haiyong, Alzan Heba, He Lan

机构信息

State Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, China.

Key Laboratory of Preventive Veterinary Medicine in Hubei Province, Wuhan 430070, China.

出版信息

Animals (Basel). 2022 May 6;12(9):1197. doi: 10.3390/ani12091197.

DOI:10.3390/ani12091197
PMID:35565622
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9099545/
Abstract

is a malaria-like protozoan that parasitizes the red blood cells of canids to cause babesiosis. Due to its high expression and essential function in the survival of parasites, the Glycosylphosphatidylinositol (GPI) anchor protein family is considered an excellent immunodiagnostic marker. Herein, we identified a novel GPI-anchored protein named as BgGPI52-WH with a size of 52 kDa; the recombinant BgGPI52-WH with high antigenicity and immunogenicity was used as a diagnostic antigen to establish a new iELISA method. The iELISA had a sensitivity of 1:400, and no cross-reaction with other apicomplexan parasites occurred. We further demonstrated that the degree of variation was less than 10% using the same samples from the same or different batches of an enzyme-labeled strip. It was found that the method was able to detect early infection (6 days after infection) in the sera of the -infected experimental dogs in which antibody response to rBgGPI52-WH was evaluated. Clinical sera from pet hospitals were further tested, and the average positive rate was about 11.41% (17/149). The results indicate that BgGPI52-WH is a reliable diagnostic antigen, and the new iELISA could be used as a practical method for the early diagnosis of .

摘要

是一种类似疟疾的原生动物,寄生于犬科动物的红细胞中导致巴贝斯虫病。由于其在寄生虫存活中的高表达和基本功能,糖基磷脂酰肌醇(GPI)锚定蛋白家族被认为是一种优秀的免疫诊断标志物。在此,我们鉴定了一种名为BgGPI52-WH的新型GPI锚定蛋白,大小为52 kDa;具有高抗原性和免疫原性的重组BgGPI52-WH被用作诊断抗原,建立了一种新的间接ELISA方法。该间接ELISA的灵敏度为1:400,与其他顶复门寄生虫无交叉反应。我们进一步证明,使用来自相同或不同批次酶标条的相同样品,变异程度小于10%。结果发现,该方法能够在评估了对rBgGPI52-WH抗体反应的感染实验犬血清中检测到早期感染(感染后6天)。对宠物医院的临床血清进行了进一步检测,平均阳性率约为11.41%(17/149)。结果表明,BgGPI52-WH是一种可靠的诊断抗原,新的间接ELISA可作为早期诊断的实用方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8084/9099545/412bafacc854/animals-12-01197-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8084/9099545/56132d1081e7/animals-12-01197-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8084/9099545/be49452101fe/animals-12-01197-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8084/9099545/8b77a7f7992e/animals-12-01197-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8084/9099545/3344d0cddbb6/animals-12-01197-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8084/9099545/6af1e66ca1eb/animals-12-01197-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8084/9099545/272424daf233/animals-12-01197-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8084/9099545/412bafacc854/animals-12-01197-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8084/9099545/56132d1081e7/animals-12-01197-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8084/9099545/be49452101fe/animals-12-01197-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8084/9099545/8b77a7f7992e/animals-12-01197-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8084/9099545/3344d0cddbb6/animals-12-01197-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8084/9099545/6af1e66ca1eb/animals-12-01197-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8084/9099545/272424daf233/animals-12-01197-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8084/9099545/412bafacc854/animals-12-01197-g007.jpg

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本文引用的文献

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Trends Parasitol. 2022 Sep;38(9):815-816. doi: 10.1016/j.pt.2022.03.001. Epub 2022 Mar 23.
2
The Etiology, Incidence, Pathogenesis, Diagnostics, and Treatment of Canine Babesiosis Caused by Infection.由感染引起的犬巴贝斯虫病的病因、发病率、发病机制、诊断及治疗
Animals (Basel). 2022 Mar 16;12(6):739. doi: 10.3390/ani12060739.
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A universal ELISA assay for detecting six strains of ovine Babesia species in China.一种用于检测中国六种绵羊巴贝斯虫菌株的通用酶联免疫吸附测定法。
Vet Parasitol. 2021 Dec;300:109616. doi: 10.1016/j.vetpar.2021.109616. Epub 2021 Nov 4.
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Evaluation of GPI-anchored Protein 47 (BgGPI47-WH) as a Potential Diagnostic Antigen by Enzyme-Linked Immunosorbent Assay.通过酶联免疫吸附测定评估糖基磷脂酰肌醇锚定蛋白47(BgGPI47-WH)作为潜在诊断抗原的情况。
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Vaccination against babesiosis using recombinant GPI-anchored proteins.使用重组 GPI 锚定蛋白对抗巴贝斯虫病的疫苗接种。
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