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猪肺泡巨噬细胞极化对猪瘟病毒复制的影响 被引量:2

Effects of porcine alveolar macrophage polarization on the replication of classical swine fever virus
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摘要 为探究猪肺泡巨噬细胞(PAM)极化与猪瘟病毒(CSFV)复制之间的关系,本研究首先通过支气管肺泡灌洗液法建立了高纯度原代肺泡巨噬细胞的培养体系。通过western blot确立了PAM向M1和M2型巨噬细胞极化的鉴别体系,并用CCK8法检测巨噬细胞极化后的细胞活性。在此基础上,通过间接免疫荧光试验和荧光定量PCR分别检测感染不同亚型PAM的CSFV E2蛋白的表达及其E2基因的转录水平,显示PAM向M1型的极化可减少CSFV E2蛋白的表达,从而抑制病毒的复制。本研究不仅为研究宿主对CSFV的免疫机制提供了重要线索,而且为设计基于巨噬细胞极化亚型防制CSF新策略提供一定依据。 To explore the relationship between porcine alveolar macrophage (PAM) polarization and classical swine fever virus (CSFV) replication. Firstly, the culture system for highly pure primary alveolar pulmonary macrophages was established by the method of porcine bronchoalveolar lavage fluid. Secondly, the identification system for alveolar macrophage to M1 and M2 polarization by western blot, and the viability of different subtype PAM was detected by CCK-8. Based on the above methods, the expression of CSFV E2 protein and the transcriptional level of CSFV in CSFV infected different sultypes PAM CSFV in different subtypes of PAM infected with CSFV were detected by indirect immunofluorescence assay and real-time PCR. The results showed that the polarization of macrophages to M1 could inhilit the expression of CSFV E2 protein, thereby inhibiting the viral replication. This study not only provides an important clue for studying the immune mechenism of host to CSFV, but also provides a basis for the design of the new strategy for controlling CSFV based on macrophage polarization subtype.
出处 《中国预防兽医学报》 CAS CSCD 北大核心 2018年第2期91-95,共5页 Chinese Journal of Preventive Veterinary Medicine
基金 中国农业科学院哈尔滨兽医研究所兽医生物技术国家重点实验室开放基金项目(SKLVBP201430)
关键词 猪瘟病毒 肺泡巨噬细胞 极化 病毒复制 Classical swine fever virus pulmonary alveolar macrophage polarization viral replication
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  • 1罗廷荣,莫扬,吴文德,黄玉华,黄伟坚,秦爱珍,刘芳,温荣辉,陆芹章,余克伦.RT-PCR技术检测猪瘟病毒的应用研究[J].中国预防兽医学报,2004,26(4):307-309. 被引量:34
  • 2李艳,仇华吉,王秀荣,张守发,朱庆虎,李娜,李国新,童光志.鉴别猪瘟强毒和弱毒的反转录-复合套式聚合酶链式反应(RT-nPCR)检测方法的建立[J].中国农业科学,2006,39(9):1907-1914. 被引量:26
  • 3Bhudevi B, Weinstock D. Fluorogenic RT PCR assay (TaqMan) for detection and classification of bovine viral diarrhea virus [J]. Vet Microbiol, 2001, 83:1-10.
  • 4Glodrickma, Lowings J P,Ibala G. A novel approach to the detection of classical swine fever virus by RT PCR with a fluorogenic probe (Tagman) [J]. J Virol Methods, 1998,72(2) : 125- 135.
  • 5Krassnig R, Schuller W, Heinrich J, et al. Isolation of the agent of European swine plague from imported frozen wild boar meat. Dtsch Tierarztl Wochenschr, 1995,102(1 ) : 56.
  • 6McGoldrick A, Lowings J P, Ibata G, et al. A novel approach to the detection of classical swine fever virus by RT-PCR with a fluorogenic probe (TaqMan)[J]. J Virol Methods, 1998, 72:125-135.
  • 7Mennig V. Pestivi ruses : a review. Vet Microbiol, 19 9 O, 2 3 ( 1 - 4) : 35-54.
  • 8Nellemann C, Vinggaard A M, Dalgaard M, et al. Quantlfiea tion of antiandrogen effect determined by lightcycler technology[J]. Toxicology, 2001, 163:29-38.
  • 9Sandvikt,Paton D J, I.owings P J. Detection and identification of ruminal and porcine pestiviruses by nested amplification of 5 ’ un translated coding regions[J]. J Virol Methods, 1997,64:43- 56.
  • 10Stegeman A,Elbers A,De Smit H,et al. The 1997-1998 epidemic of classical swine fever in the Netherlands. Vet Microbiol,2000, 73(2-3) : 183- 196.

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