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Functional Analysis of lncRNA663 Regulating CLDN10 Expression and Porcine Epidemic Diarrhea Virus Replication
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Zuolin WU, Haijiang LIANG, Zheyu WU, Songbai YANG, Ayong ZHAO, Weiyun QIN
Acta Veterinaria et Zootechnica Sinica | 2026, 57(2) : 945 - 954
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Acta Veterinaria et Zootechnica Sinica | 2026, 57(2): 945-954
• PREVENTIVE VETERINARY MEDICINE •
Functional Analysis of lncRNA663 Regulating CLDN10 Expression and Porcine Epidemic Diarrhea Virus Replication
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Zuolin WU, Haijiang LIANG, Zheyu WU, Songbai YANG, Ayong ZHAO, Weiyun QIN
Affiliations
  • College of Animal Science and Technology·College of Veterinary Medicine,Zhejiang A&F University,Hangzhou 311300,China
Published: 2026-02-23 doi: 10.11843/j.issn.0366-6964.2026.02.031
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Porcine epidemic diarrhea virus (PEDV) is a coronavirus that causes acute diarrhea, vomiting, and dehydration in piglets, among other clinical signs, and has caused severe economic losses to the global swine farming industry. More and more studies have reported that long non-coding RNAs (lncRNAs) play important regulatory roles in porcine coronaviruses, however, the role and mechanism of lncRNA 663 in PEDV infection remain unclear. Based on prior transcriptome sequencing, we identified a co-expression pattern between lncRNA 663 and the tight junction protein CLDN10. This study aimed to explore their roles and regulatory relationship during PEDV infection. The qRT-PCR and Western blot results showed that the expression levels of lncRNA 663 and CLDN10 were up-regulated after PEDV infection of IPEC-J2 cells (P<0.05), DSS treatment significantly reduced the expression levels of lncRNA 663 and CLDN10 (P<0.05). Subcellular localization prediction revealed that lncRNA 663 was mainly localized in the cytoplasm, and RPISeq prediction revealed that lncRNA663 and CLDN10 were highly interoperable (SVM: 0.98, RF: 0.8). Functional experiments demonstrated that siRNA-mediated knockdown of lncRNA 663 led to a significant decrease in both CLDN10 expression and PEDV replication (P<0.05). Furthermore, structure prediction using AlphaFold3 and ChimeraX revealed potential hydrogen bond interactions between CLDN10 and the PEDV spike (S) protein, suggesting a role in viral entry or infection. Collectively, these results suggest that lncRNA 663 may promote PEDV replication by regulating CLDN10 expression. These findings expand our understanding of PEDV-host interactions and provide a theoretical basis for future antiviral strategies targeting host non-coding RNAs.

porcine epidemic diarrhea virus  /  long chain non-coding RNA  /  CLDN10  /  intestinal barrier
吴作林, 梁海江, 吴哲豫, 杨松柏, 赵阿勇, 钦伟云. lncRNA663调控CLDN10表达及猪流行性腹泻病毒复制的功能分析. 畜牧兽医学报, 2026 , 57 (2) : 945 -954 . DOI: 10.11843/j.issn.0366-6964.2026.02.031
Zuolin WU, Haijiang LIANG, Zheyu WU, Songbai YANG, Ayong ZHAO, Weiyun QIN. Functional Analysis of lncRNA663 Regulating CLDN10 Expression and Porcine Epidemic Diarrhea Virus Replication[J]. Acta Veterinaria et Zootechnica Sinica, 2026 , 57 (2) : 945 -954 . DOI: 10.11843/j.issn.0366-6964.2026.02.031
Year 2026 volume 57 Issue 2
156
70
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doi: 10.11843/j.issn.0366-6964.2026.02.031
  • Receive Date:2025-05-27
  • Online Date:2026-09-16
  • Published:2026-02-23
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  • Received:2025-05-27
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    College of Animal Science and Technology·College of Veterinary Medicine,Zhejiang A&F University,Hangzhou 311300,China

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QIN Weiyun, E-mail:
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
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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