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基于合成VP1蛋白肽的酶联免疫吸附测定法的开发,用于检测抗猪博卡病毒3型抗体。

Development of a Synthetic VP1 Protein Peptide-Based ELISA to Detect Antibodies Against Porcine Bocavirus Group 3.

作者信息

Gong Chao, He Hui, Fu Yuguang, Li Baoyu, Yang Bin, Li Jianlong, He Xiaodong, Han Juncheng, Zhang Yi, Liu Guangliang, Guo Qingyong

机构信息

Xinjiang Key Laboratory of New Drug Study and Creation for Herbivorous Animals (XJ-KLNDSCHA), College of Veterinary Medicine, Xinjiang Agricultural University, Urumqi 830052, China.

State Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou University, Lanzhou 730000, China.

出版信息

Viruses. 2024 Dec 19;16(12):1946. doi: 10.3390/v16121946.

Abstract

Porcine bocavirus (PBoV), classified within the genus Bocaparvovirus, has been reported worldwide. PBoV has been divided into group 1, group 2, and group 3. PBoV group 3 (G3) viruses are the most prevalent in China. Currently, effective serological methods for the detection of antibodies against PBoV G3 are limited. In this study, we developed an indirect ELISA using a synthetic VP1 peptide designed on the basis of the conserved region of the PBoV VP1 protein as a coating antigen. Through matrix titration, the optimal coating concentration of the VP1 peptide (0.5 μg/mL), serum dilution (1:200), and working concentration of the secondary antibody (1:50,000) were determined. The cutoff value of this developed ELISA was set as 0.4239. Further investigations revealed that this developed ELISA had no cross-reactivity with positive serum antibodies against FMDV-O, FMDV-A, PRV, ASFV, SF, PCV2, PEDV, and TGEV. The detection limit of the method was a 1:1600 dilution of standard positive serum against PBoV G3. The coefficients of variation for both the intra- and interassay data were lower than 10%. A total of 1373 serum samples collected from 12 provinces in China between 2022 and 2023 were subjected to indirect ELISA. The results showed that 47.56% of the samples were PBoV G3 positive. These results reveal that peptide-based ELISA is a reliable and cost-effective method for detecting PBoV G3 antibodies. It also facilitates the investigation of the prevalence and distribution of PBoV G3.

摘要

猪博卡病毒(PBoV)属于博卡细小病毒属,已在全球范围内被报道。PBoV已被分为第1组、第2组和第3组。PBoV第3组(G3)病毒在中国最为普遍。目前,用于检测抗PBoV G3抗体的有效血清学方法有限。在本研究中,我们基于PBoV VP1蛋白的保守区域设计了一种合成VP1肽作为包被抗原,开发了一种间接ELISA。通过方阵滴定法,确定了VP1肽的最佳包被浓度(0.5μg/mL)、血清稀释度(1:200)和二抗工作浓度(1:50,000)。所开发的ELISA的临界值设定为0.4239。进一步研究表明,所开发的ELISA与抗口蹄疫病毒O型、口蹄疫病毒A型、伪狂犬病病毒、非洲猪瘟病毒、猪流感病毒、猪圆环病毒2型、猪流行性腹泻病毒和猪传染性胃肠炎病毒的阳性血清抗体无交叉反应。该方法的检测限为抗PBoV G3标准阳性血清的1:1600稀释度。批内和批间数据的变异系数均低于10%。对2022年至2023年期间从中国12个省份采集的1373份血清样本进行了间接ELISA检测。结果显示,47.56%的样本为PBoV G3阳性。这些结果表明,基于肽的ELISA是检测PBoV G3抗体的一种可靠且经济高效的方法。它也有助于调查PBoV G3的流行情况和分布。

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