Application two-dimensional gel electrophoresis coupled with LC-MS/MS to identify candidate serodiagnostic antigens for early detection Psoroptes ovis var. cuniculi infection.

IF 2 2区 农林科学 Q2 PARASITOLOGY
X B Gu, Y Tian, C Y Zhang, J Xu, G Y Hao, F S Yang, Y E Li, Y P Liang, J Fan, F Y Wu, X Y Yao, M L He, R He, H Wang, Y Xie
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引用次数: 0

Abstract

Currently, the 'gold standard' for diagnosis of Psoroptes ovis infections is detecting Psoroptes mites or eggs in skin scrapings under microscopy, but it is prone to be mis-diagnosed for detecting early infection of P. ovis. Hence, seeking a reliable diagnostic technique for detecting early-stage mite infections is extremely desirable. Enzyme linked immunosorbent assay (ELISA) has proven to be useful for the diagnosis of early-stage P. ovis infection. Thus, the purpose of this study was to screen serodiagnostic candidate antigens that can detect early P. ovis infection. Psoroptes ovis var. cuniculi wash proteins (PsoWA), which contained an enriched source of secretory and excretory antigens, were separated by two-dimensional gel electrophoresis (2-DE) and screened by immunoblot using sera from rabbits with early-stage Psoroptes infection (1 week and 3 weeks). Immunogenic proteins were submitted for sequencing by liquid chromatography tandem-mass spectrometry (LC-MS/MS) analyses. Three potential diagnostic antigens were identified (PsoSP3, Pso14-3-3(1) and Pso14-3-3(2)) in this study. These were further expressed in E. coli expression system to evaluate the serodiagnostic potential of these recombinant proteins for detecting early-stage P. ovis infection using an indirect ELISA (iELISA). Western blotting showed that 34 protein spots were recognized by rabbit sera of 1 week post-infection (wpi) and 3 wpi. The 2-DE results showed that a total of 199 proteins were detected with molecular weights varying from 20 to 100 kDa and isoelectric point (pI) from 4.1 to 9.3. Among these, 90 proteins were detected both at 1 wpi sera and 3 wpi sera, and the numbers of the specific identified proteins were 27 for 1 wpi sera and 82 for 3wpi sera. Moreover, rPsoSP3 showed better diagnostic efficacy than rPso14-3-3(1) and rPso14-3-3(2) in detecting early-stage P. ovis infection for its higher values of sensitivity, specificity and area under the receiver operating characteristic curve. Our study describes the first immunoproteomic analysis to identify early diagnostic candidate antigens of P. ovis, and the identified antigens of Psoroptes in our study have significant implications for the development of early-stage diagnostic tests. PsoSP3 is a promising early diagnostic antigen for detecting P. ovis var. cuniculi infection.

应用双向凝胶电泳联用LC-MS/MS鉴定早期检测卵巢棘球绦虫感染的候选血清诊断抗原。
目前,诊断卵巢假单胞菌感染的“金标准”是在显微镜下检测皮肤刮痕中的疥螨或虫卵,但很容易被误诊为早期检测卵巢假单胞菌感染。因此,寻找一种可靠的诊断技术来检测早期螨虫感染是非常可取的。酶联免疫吸附试验(ELISA)已被证明是有用的早期卵巢假单胞菌感染的诊断。因此,本研究的目的是筛选血清诊断候选抗原,可以检测早期卵巢假单胞菌感染。利用兔早期(1周和3周)Psoroptes感染血清,用二维凝胶电泳(2-DE)分离和免疫印迹法筛选含有丰富分泌和排泄抗原来源的PsoWA。免疫原性蛋白通过液相色谱串联质谱(LC-MS/MS)分析进行测序。本研究鉴定出3种潜在的诊断抗原(PsoSP3、Pso14-3-3(1)和Pso14-3-3(2))。在大肠杆菌表达系统中进一步表达这些重组蛋白,利用间接ELISA (iELISA)评估这些重组蛋白检测早期卵巢假单胞菌感染的血清诊断潜力。Western blotting结果显示,感染后1周(wpi)和3周(wpi)兔血清可识别34个蛋白点。2-DE结果表明,共检测到199个蛋白,分子量在20 ~ 100 kDa之间,等电点(pI)在4.1 ~ 9.3之间。其中,在1 wpi和3wpi血清中均检测到90种蛋白,1 wpi血清中特异性鉴定蛋白27种,3wpi血清中特异性鉴定蛋白82种。此外,rPsoSP3在检测早期葡萄球菌感染方面的敏感性、特异性和受者工作特征曲线下面积均高于rPso14-3-3(1)和rPso14-3-3(2),表现出更好的诊断效果。我们的研究首次通过免疫蛋白质组学分析确定了绵羊假单胞菌的早期诊断候选抗原,并且在我们的研究中确定的Psoroptes抗原对早期诊断测试的发展具有重要意义。PsoSP3是一种很有前途的早期诊断抗原,可用于检测卵巢斑绦虫感染。
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来源期刊
Veterinary parasitology
Veterinary parasitology 农林科学-寄生虫学
CiteScore
5.30
自引率
7.70%
发文量
126
审稿时长
36 days
期刊介绍: The journal Veterinary Parasitology has an open access mirror journal,Veterinary Parasitology: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review. This journal is concerned with those aspects of helminthology, protozoology and entomology which are of interest to animal health investigators, veterinary practitioners and others with a special interest in parasitology. Papers of the highest quality dealing with all aspects of disease prevention, pathology, treatment, epidemiology, and control of parasites in all domesticated animals, fall within the scope of the journal. Papers of geographically limited (local) interest which are not of interest to an international audience will not be accepted. Authors who submit papers based on local data will need to indicate why their paper is relevant to a broader readership. Parasitological studies on laboratory animals fall within the scope of the journal only if they provide a reasonably close model of a disease of domestic animals. Additionally the journal will consider papers relating to wildlife species where they may act as disease reservoirs to domestic animals, or as a zoonotic reservoir. Case studies considered to be unique or of specific interest to the journal, will also be considered on occasions at the Editors'' discretion. Papers dealing exclusively with the taxonomy of parasites do not fall within the scope of the journal.
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