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Baculovirus Utilizes Cholesterol Transporter NIEMANN–Pick C1 for Host Cell Entry
The dual roles of baculovirus for the control of natural insect populations as an insecticide, and as a tool for foreign gene expression and delivery, have called for a comprehensive understanding of the molecular mechanisms governing viral infection. Here, we demonstrate that the Bombyx mori Nieman...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906155/ https://www.ncbi.nlm.nih.gov/pubmed/31866985 http://dx.doi.org/10.3389/fmicb.2019.02825 |
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author | Li, Zhihong Fan, Youpeng Wei, Junhong Mei, Xionge He, Qiang Zhang, Yonghua Li, Tian Long, Mengxian Chen, Jie Bao, Jialing Pan, Guoqing Li, Chunfeng Zhou, Zeyang |
author_facet | Li, Zhihong Fan, Youpeng Wei, Junhong Mei, Xionge He, Qiang Zhang, Yonghua Li, Tian Long, Mengxian Chen, Jie Bao, Jialing Pan, Guoqing Li, Chunfeng Zhou, Zeyang |
author_sort | Li, Zhihong |
collection | PubMed |
description | The dual roles of baculovirus for the control of natural insect populations as an insecticide, and as a tool for foreign gene expression and delivery, have called for a comprehensive understanding of the molecular mechanisms governing viral infection. Here, we demonstrate that the Bombyx mori Niemann-Pick C1 (BmNPC1) is essential for baculovirus infection in insect cells. Both pretreatment of B. mori embryonic cells (BmE) with NPC1 antagonists (imipramine or U18666A) and down-regulation of NPC1 expression resulted in a significant reduction in baculovirus BmNPV (B. mori nuclear polyhedrosis virus) infectivity. Disruption of BmNPC1 could decrease viral entry (2 hpi) rather than reduce the viral binding to the BmE cells. Furthermore, our results showed that NPC1 domain C binds directly and specifically to the viral glycoprotein GP64, which is responsible for both receptor binding and fusion. Antibody blocking assay also revealed that the domain C specific polyclonal antibody inhibited BmNPV infection, indicating that NPC1 domain C most likely plays a role during viral fusion in endosomal compartments. Our results, combined with previous studies identifying an essential role of human NPC1 (hNPC1) in filovirus infection, suggest that the glycoprotein of several enveloped viruses possess a shared strategy of exploiting host NPC1 proteins during virus intracellular entry events. |
format | Online Article Text |
id | pubmed-6906155 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69061552019-12-20 Baculovirus Utilizes Cholesterol Transporter NIEMANN–Pick C1 for Host Cell Entry Li, Zhihong Fan, Youpeng Wei, Junhong Mei, Xionge He, Qiang Zhang, Yonghua Li, Tian Long, Mengxian Chen, Jie Bao, Jialing Pan, Guoqing Li, Chunfeng Zhou, Zeyang Front Microbiol Microbiology The dual roles of baculovirus for the control of natural insect populations as an insecticide, and as a tool for foreign gene expression and delivery, have called for a comprehensive understanding of the molecular mechanisms governing viral infection. Here, we demonstrate that the Bombyx mori Niemann-Pick C1 (BmNPC1) is essential for baculovirus infection in insect cells. Both pretreatment of B. mori embryonic cells (BmE) with NPC1 antagonists (imipramine or U18666A) and down-regulation of NPC1 expression resulted in a significant reduction in baculovirus BmNPV (B. mori nuclear polyhedrosis virus) infectivity. Disruption of BmNPC1 could decrease viral entry (2 hpi) rather than reduce the viral binding to the BmE cells. Furthermore, our results showed that NPC1 domain C binds directly and specifically to the viral glycoprotein GP64, which is responsible for both receptor binding and fusion. Antibody blocking assay also revealed that the domain C specific polyclonal antibody inhibited BmNPV infection, indicating that NPC1 domain C most likely plays a role during viral fusion in endosomal compartments. Our results, combined with previous studies identifying an essential role of human NPC1 (hNPC1) in filovirus infection, suggest that the glycoprotein of several enveloped viruses possess a shared strategy of exploiting host NPC1 proteins during virus intracellular entry events. Frontiers Media S.A. 2019-12-05 /pmc/articles/PMC6906155/ /pubmed/31866985 http://dx.doi.org/10.3389/fmicb.2019.02825 Text en Copyright © 2019 Li, Fan, Wei, Mei, He, Zhang, Li, Long, Chen, Bao, Pan, Li and Zhou. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Li, Zhihong Fan, Youpeng Wei, Junhong Mei, Xionge He, Qiang Zhang, Yonghua Li, Tian Long, Mengxian Chen, Jie Bao, Jialing Pan, Guoqing Li, Chunfeng Zhou, Zeyang Baculovirus Utilizes Cholesterol Transporter NIEMANN–Pick C1 for Host Cell Entry |
title | Baculovirus Utilizes Cholesterol Transporter NIEMANN–Pick C1 for Host Cell Entry |
title_full | Baculovirus Utilizes Cholesterol Transporter NIEMANN–Pick C1 for Host Cell Entry |
title_fullStr | Baculovirus Utilizes Cholesterol Transporter NIEMANN–Pick C1 for Host Cell Entry |
title_full_unstemmed | Baculovirus Utilizes Cholesterol Transporter NIEMANN–Pick C1 for Host Cell Entry |
title_short | Baculovirus Utilizes Cholesterol Transporter NIEMANN–Pick C1 for Host Cell Entry |
title_sort | baculovirus utilizes cholesterol transporter niemann–pick c1 for host cell entry |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906155/ https://www.ncbi.nlm.nih.gov/pubmed/31866985 http://dx.doi.org/10.3389/fmicb.2019.02825 |
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