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由重组杆状病毒产生的猪博卡病毒病毒样颗粒可应用于血清流行病学研究。

Virus-like particles of porcine bocavirus generated by recombinant baculoviruses can be applied to sero-epidemic studies.

作者信息

Zhang Wenjing, Sano Natsuha, Kataoka Michiyo, Ami Yasushi, Suzaki Yuriko, Wakita Takaji, Ikeda Hidetoshi, Li Tian-Cheng

机构信息

Department of Clinical Laboratory, Qilu Hospital, Shandong University, Jinan 250012, China; Blood Group Reference and Research Laboratory, Blood Center of Shandong Province, East Shanshi Road 22, Jinan, Shandong, China.

Laboratory of Veterinary Hygiene, Graduate School of Veterinary Medicine and Life Science, Nippon Veterinary and Life Science University, Kyonan-cho 1-7-1, Musashino, Tokyo 180-8602, Japan.

出版信息

Virus Res. 2016 Jun 2;217:85-91. doi: 10.1016/j.virusres.2016.03.002. Epub 2016 Mar 6.

Abstract

Porcine bocaviruses (PBoVs), new members of the Bocavirus genus, have been identified in swine worldwide. However, the antigenicity and epidemiology of PBoVs are still unclear. Here we used a recombinant baculovirus expression system to express the main capsid protein VP2 of Japan strain JY31b in insect Tn5 cells, and successfully produced the virus-like particles of PBoV (PBoV-LPs). The diameter and densities of the PBoV-LPs were estimated to be 30nm and 1.300g/cm(3), respectively, which were similar to the values for the native virion of PBoV. Antigenic analysis demonstrated that the PBoV-LPs were not cross-reactive with porcine circovirus 2, but were cross-reactive with human bocavirus 1, 2, 3 and 4. An ELISA for detection of anti-PBoV IgG antibodies was established using PBoV-LPs as antigen, which proved to be useful for monitoring PBoV infection in both swine and wild boars. The preliminary epidemiology research showed that 90.7% of pigs and 59.5% of wild boars were positive for the anti-PBoV-IgG, suggesting that both species were also widely infected with PBoV. The seven PBoV strains detected in wild boars separated into four subgroups, demonstrating the genetic diversity of PBoV.

摘要

猪博卡病毒(PBoVs)是博卡病毒属的新成员,已在全球范围内的猪群中被发现。然而,PBoVs的抗原性和流行病学仍不清楚。在此,我们利用重组杆状病毒表达系统在昆虫Tn5细胞中表达日本株JY31b的主要衣壳蛋白VP2,并成功制备了PBoV的病毒样颗粒(PBoV-LPs)。PBoV-LPs的直径和密度估计分别为30nm和1.300g/cm³,与PBoV天然病毒粒子的值相似。抗原分析表明,PBoV-LPs与猪圆环病毒2无交叉反应,但与人类博卡病毒1、2、3和4有交叉反应。以PBoV-LPs为抗原建立了检测抗PBoV IgG抗体的ELISA方法,该方法被证明可用于监测猪和野猪中的PBoV感染。初步流行病学研究表明,90.7%的猪和59.5%的野猪抗PBoV-IgG呈阳性,表明这两个物种也广泛感染了PBoV。在野猪中检测到的7株PBoV毒株分为4个亚组,表明PBoV具有遗传多样性。

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