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Screening and identification of host proteins interacting with Nsp8 of porcine epidemic diarrhea virus
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Yun TU1, Ruiming YU1, Liping ZHANG2, Yonglu WANG2, Li PAN2, Xia LIU1, Xiaohua DU1, *, Xinsheng LIU2, *
Acta Microbiologica Sinica | 2024, 64(10) : 3932 - 3944
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Acta Microbiologica Sinica | 2024, 64(10): 3932-3944
Research Articles
Screening and identification of host proteins interacting with Nsp8 of porcine epidemic diarrhea virus
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Yun TU1, Ruiming YU1, Liping ZHANG2, Yonglu WANG2, Li PAN2, Xia LIU1, Xiaohua DU1, *, Xinsheng LIU2, *
Affiliations
  • 1 College of Animal Medicine, Gansu Agricultural University, Lanzhou 730070, Gansu, China
  • 2 State Key Laboratory for Animal Disease Control and Prevention, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou 730046, Gansu, China
Published: 2024-06-18 doi: 10.13343/j.cnki.wsxb.20240237
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Porcine epidemic diarrhea virus (PEDV) is an enterovirus that can cause severe diarrhea and dehydration. The widespread epidemic of PEDV has caused huge economic losses to the pig breeding industry, which, however, lacks effective means for prevention and treatment. Nsp8 is an important non-structural protein involved in the replication of PEDV, while the host proteins interacting with Nsp8 remains unclear. [Objective] To screen the host proteins interacting with PEDV Nsp8 and explore the effects of the host proteins on the replication of PEDV, so as to provide a theoretical basis for discovering new key functional receptors or therapeutic targets of PEDV. [Methods] The eukaryotic expression plasmid of PEDV Nsp8 was successfully constructed with the eukaryotic expression vector pcDNA3.1(+). The host proteins interacting with PEDV Nsp8 were screened by co-immunoprecipitation, mass spectrometry, and laser confocal microscopy. The effects of the host proteins on PEDV replication were explored by overexpression and knockdown in LLC-PK cells. [Results] Thirty-six potential host proteins interacting with Nsp8 were screened by mass spectrometry, and the interaction between heat shock protein member 8 (HSPA8) and Nsp8 was verified. The overexpression of HSPA8 in LLC-PK cells inhibited the overexpression of Nsp8 in a dose-dependent manner. Meanwhile, it significantly inhibited the replication of PEDV in a dose-dependent manner at the protein and transcriptional levels. Interfering with endogenous HSPA8 expression significantly promoted the replication of PEDV. The 50% tissue culture infectious dose (TCID50) and indirect immunofluorescence further proved that HSPA8 inhibited PEDV replication. [Conclusion] This study screened out the host protein HSPA8 interacting with PEDV Nsp8 and proved that HSPA8 could significantly inhibit PEDV replication, which provided a new idea for the design of HSPA8-targeted drugs for the prevention or treatment of PEDV.

porcine epidemic diarrhea virus  /  Nsp8  /  co-immunoprecipitation  /  HSPA8
Yun TU, Ruiming YU, Liping ZHANG, Yonglu WANG, Li PAN, Xia LIU, Xiaohua DU, Xinsheng LIU. Screening and identification of host proteins interacting with Nsp8 of porcine epidemic diarrhea virus[J]. Acta Microbiologica Sinica, 2024 , 64 (10) : 3932 -3944 . DOI: 10.13343/j.cnki.wsxb.20240237
  • National Center of Technology Innovation for Pigs Project(NCTIP-XD/C 03)
Year 2024 volume 64 Issue 10
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Article Info
doi: 10.13343/j.cnki.wsxb.20240237
  • Receive Date:2024-04-15
  • Online Date:2026-03-21
  • Published:2024-06-18
Article Data
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History
  • Received:2024-04-15
  • Accepted:2024-06-11
Funding
National Center of Technology Innovation for Pigs Project(NCTIP-XD/C 03)
Affiliations
    1 College of Animal Medicine, Gansu Agricultural University, Lanzhou 730070, Gansu, China
    2 State Key Laboratory for Animal Disease Control and Prevention, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou 730046, Gansu, China

Corresponding:

*DU Xiaohua, E-mail:
LIU Xinsheng, E-mail:
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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