Rapamycin-induced autophagy restricts porcine epidemic diarrhea virus infectivity in porcine intestinal epithelial cells

被引:56
作者
Ko, Seongyeol [1 ,2 ]
Gu, Min Jeong [1 ,2 ]
Kim, Cheol Gyun [1 ,2 ]
Kye, Yoon Chul [1 ,2 ]
Lim, Younggap [1 ,2 ]
Lee, Ji Eun [1 ,2 ]
Park, Byung-Chul [3 ]
Chu, Hyuk [4 ]
Han, Seung Hyun [5 ]
Yun, Cheol-Heui [1 ,2 ,3 ]
机构
[1] Seoul Natl Univ, Dept Agr Biotechnol, 1 Gwanak Ro, Seoul 08826, South Korea
[2] Seoul Natl Univ, Res Inst Agr & Life Sci, Seoul 08826, South Korea
[3] Seoul Natl Univ, Inst Green Bio Sci Technol, Pyeongchang 23254, South Korea
[4] Korea Ctr Dis Control & Prevent, Natl Inst Hlth, Ctr Immunol & Pathol, Div Zoonoses, Osong 28159, South Korea
[5] Seoul Natl Univ, Sch Dent, Dept Oral Microbiol & Immunol, DRI & BK21 Plus Pro, Seoul 08826, South Korea
基金
新加坡国家研究基金会;
关键词
Porcine epidemic diarrhea virus; Rapamycin; Antiviral effect; Autophagy; IPEC-J2; CORONAVIRUS REPLICATION; INHIBITION; MECHANISMS; MATURATION; PROTEIN; TARGET; ENTRY;
D O I
10.1016/j.antiviral.2017.08.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Porcine epidemic diarrhea virus (PEDV) invades porcine intestinal epithelial cells (IECs) and causes diarrhea and dehydration in pigs. In the present study, we showed a suppression of PEDV infection in porcine jejunum intestinal epithelial cells (IPEC-J2) by an increase in autophagy. Autophagy was activated by rapamycin at a dose that does not affect cell viability and tight junction permeability. The induction of autophagy was examined by LC3I/LC3II conversion. To confirm the autophagic-flux (entire autophagy pathway), autophagolysosomes were examined by an immunofluorescence assay. Pretreatment with rapamycin significantly restricted not only a 1 h infection but also a longer infection (24 h) with PEDV, while this effect disappeared when autophagy was blocked. Co-localization of PEDV and autophagosomes suggests that PEDV could be a target of autophagy. Moreover, alleviation of PEDV-induced cell death in IPEC-J2 cells pretreated with rapamycin demonstrates a protective effect of rapamycin against PEDV-induced epithelial cell death. Collectively, the present study suggests an early prevention against PEDV infection in IPEC-J2 cells via autophagy that might be an effective strategy for the restriction of PEDV, and opens up the possibility of the use of rapamycin in vivo as an effective prophylactic and prevention treatment. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:86 / 95
页数:10
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