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PI3KC3-dependent autophagosomes formation pathway is of crucial importance to anti-DHAV activity of Chrysanthemum indicum polysaccharide.

Identifieur interne : 000263 ( Main/Exploration ); précédent : 000262; suivant : 000264

PI3KC3-dependent autophagosomes formation pathway is of crucial importance to anti-DHAV activity of Chrysanthemum indicum polysaccharide.

Auteurs : Ke Ming [République populaire de Chine] ; Wenjuan Yuan [République populaire de Chine] ; Yun Chen [République populaire de Chine] ; Hongxu Du [République populaire de Chine] ; Miao He [République populaire de Chine] ; Yuanliang Hu [République populaire de Chine] ; Deyun Wang [République populaire de Chine] ; Yi Wu [République populaire de Chine] ; Jiaguo Liu [République populaire de Chine]

Source :

RBID : pubmed:30658794

Descripteurs français

English descriptors

Abstract

We previously reported that Chrysanthemum indicum polysaccharide (CIPS) effectively inhibited the replication of duck hepatitis A virus (DHAV). However, the inhibition mechanisms are still unclear. Autophagy plays important role in virus genomic replication. Therefore, in present study, the effect of autophagy on DHAV genome replication as well as the influence of CIPS on autophagy were studied. qPCR, western blot, and ELISA methods were applied to observe the autophagy and analyze the inhibition mechanisms of CIPS on DHAV. Results showed that DHAV infection increased the expression level of LC3-II and interdicted the degradation of p62. Treating with rapamycin benefited DHAV gene expression level. What's more, DHAV infection and rapamycin treatment also promoted the expression of PI3KC3 and increased the concentration of PI3P. However, CIPS treatment significantly downregulated the expressions of LC3-II and PI3KC3 induced by DHAV and rapamycin, and consequently inhibited autophagosomes formation. As a result, DHAV replication was inhibited.

DOI: 10.1016/j.carbpol.2018.12.035
PubMed: 30658794


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<term>Autophagosomes</term>
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<div type="abstract" xml:lang="en">We previously reported that Chrysanthemum indicum polysaccharide (CIPS) effectively inhibited the replication of duck hepatitis A virus (DHAV). However, the inhibition mechanisms are still unclear. Autophagy plays important role in virus genomic replication. Therefore, in present study, the effect of autophagy on DHAV genome replication as well as the influence of CIPS on autophagy were studied. qPCR, western blot, and ELISA methods were applied to observe the autophagy and analyze the inhibition mechanisms of CIPS on DHAV. Results showed that DHAV infection increased the expression level of LC3-II and interdicted the degradation of p62. Treating with rapamycin benefited DHAV gene expression level. What's more, DHAV infection and rapamycin treatment also promoted the expression of PI3KC3 and increased the concentration of PI3P. However, CIPS treatment significantly downregulated the expressions of LC3-II and PI3KC3 induced by DHAV and rapamycin, and consequently inhibited autophagosomes formation. As a result, DHAV replication was inhibited.</div>
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<AbstractText>We previously reported that Chrysanthemum indicum polysaccharide (CIPS) effectively inhibited the replication of duck hepatitis A virus (DHAV). However, the inhibition mechanisms are still unclear. Autophagy plays important role in virus genomic replication. Therefore, in present study, the effect of autophagy on DHAV genome replication as well as the influence of CIPS on autophagy were studied. qPCR, western blot, and ELISA methods were applied to observe the autophagy and analyze the inhibition mechanisms of CIPS on DHAV. Results showed that DHAV infection increased the expression level of LC3-II and interdicted the degradation of p62. Treating with rapamycin benefited DHAV gene expression level. What's more, DHAV infection and rapamycin treatment also promoted the expression of PI3KC3 and increased the concentration of PI3P. However, CIPS treatment significantly downregulated the expressions of LC3-II and PI3KC3 induced by DHAV and rapamycin, and consequently inhibited autophagosomes formation. As a result, DHAV replication was inhibited.</AbstractText>
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<Keyword MajorTopicYN="N">Chrysanthemum indicum polysaccharide</Keyword>
<Keyword MajorTopicYN="N">Duck hepatitis A virus</Keyword>
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<Month>10</Month>
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<name sortKey="Ming, Ke" sort="Ming, Ke" uniqKey="Ming K" first="Ke" last="Ming">Ke Ming</name>
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<name sortKey="Chen, Yun" sort="Chen, Yun" uniqKey="Chen Y" first="Yun" last="Chen">Yun Chen</name>
<name sortKey="Du, Hongxu" sort="Du, Hongxu" uniqKey="Du H" first="Hongxu" last="Du">Hongxu Du</name>
<name sortKey="He, Miao" sort="He, Miao" uniqKey="He M" first="Miao" last="He">Miao He</name>
<name sortKey="Hu, Yuanliang" sort="Hu, Yuanliang" uniqKey="Hu Y" first="Yuanliang" last="Hu">Yuanliang Hu</name>
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