Cargando…
Ultrastructural Characterization of Membrane Rearrangements Induced by Porcine Epidemic Diarrhea Virus Infection
The porcine epidemic diarrhea virus (PEDV) is a coronavirus (CoV) belonging to the α-CoV genus and it causes high mortality in infected sucking piglets, resulting in substantial losses in the farming industry. CoV trigger a drastic reorganization of host cell membranes to promote their replication a...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618017/ https://www.ncbi.nlm.nih.gov/pubmed/28872588 http://dx.doi.org/10.3390/v9090251 |
_version_ | 1783267092763508736 |
---|---|
author | Zhou, Xingdong Cong, Yingying Veenendaal, Tineke Klumperman, Judith Shi, Dongfang Mari, Muriel Reggiori, Fulvio |
author_facet | Zhou, Xingdong Cong, Yingying Veenendaal, Tineke Klumperman, Judith Shi, Dongfang Mari, Muriel Reggiori, Fulvio |
author_sort | Zhou, Xingdong |
collection | PubMed |
description | The porcine epidemic diarrhea virus (PEDV) is a coronavirus (CoV) belonging to the α-CoV genus and it causes high mortality in infected sucking piglets, resulting in substantial losses in the farming industry. CoV trigger a drastic reorganization of host cell membranes to promote their replication and egression, but a detailed description of the intracellular remodeling induced by PEDV is still missing. In this study, we examined qualitatively and quantitatively, using electron microscopy, the intracellular membrane reorganization induced by PEDV over the course of an infection. With our ultrastructural approach, we reveal that, as most of CoV, PEDV initially forms double-membrane vesicles (DMVs) and convoluted membranes (CMs), which probably serve as replication/transcription platforms. Interestingly, we also found that viral particles start to form almost simultaneously in both the endoplasmic reticulum and the large virion-containing vacuoles (LVCVs), which are compartments originating from the Golgi, confirming that α-CoV assemble indistinguishably in two different organelles of the secretory pathway. Moreover, PEDV virons appear to have an immature and a mature form, similar to another α-CoV the transmissible gastroenteritis coronavirus (TGEV). Altogether, our study underlies the similarities and differences between the lifecycle of α-CoV and that of viruses belonging to other CoV subfamilies. |
format | Online Article Text |
id | pubmed-5618017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-56180172017-09-29 Ultrastructural Characterization of Membrane Rearrangements Induced by Porcine Epidemic Diarrhea Virus Infection Zhou, Xingdong Cong, Yingying Veenendaal, Tineke Klumperman, Judith Shi, Dongfang Mari, Muriel Reggiori, Fulvio Viruses Article The porcine epidemic diarrhea virus (PEDV) is a coronavirus (CoV) belonging to the α-CoV genus and it causes high mortality in infected sucking piglets, resulting in substantial losses in the farming industry. CoV trigger a drastic reorganization of host cell membranes to promote their replication and egression, but a detailed description of the intracellular remodeling induced by PEDV is still missing. In this study, we examined qualitatively and quantitatively, using electron microscopy, the intracellular membrane reorganization induced by PEDV over the course of an infection. With our ultrastructural approach, we reveal that, as most of CoV, PEDV initially forms double-membrane vesicles (DMVs) and convoluted membranes (CMs), which probably serve as replication/transcription platforms. Interestingly, we also found that viral particles start to form almost simultaneously in both the endoplasmic reticulum and the large virion-containing vacuoles (LVCVs), which are compartments originating from the Golgi, confirming that α-CoV assemble indistinguishably in two different organelles of the secretory pathway. Moreover, PEDV virons appear to have an immature and a mature form, similar to another α-CoV the transmissible gastroenteritis coronavirus (TGEV). Altogether, our study underlies the similarities and differences between the lifecycle of α-CoV and that of viruses belonging to other CoV subfamilies. MDPI 2017-09-05 /pmc/articles/PMC5618017/ /pubmed/28872588 http://dx.doi.org/10.3390/v9090251 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhou, Xingdong Cong, Yingying Veenendaal, Tineke Klumperman, Judith Shi, Dongfang Mari, Muriel Reggiori, Fulvio Ultrastructural Characterization of Membrane Rearrangements Induced by Porcine Epidemic Diarrhea Virus Infection |
title | Ultrastructural Characterization of Membrane Rearrangements Induced by Porcine Epidemic Diarrhea Virus Infection |
title_full | Ultrastructural Characterization of Membrane Rearrangements Induced by Porcine Epidemic Diarrhea Virus Infection |
title_fullStr | Ultrastructural Characterization of Membrane Rearrangements Induced by Porcine Epidemic Diarrhea Virus Infection |
title_full_unstemmed | Ultrastructural Characterization of Membrane Rearrangements Induced by Porcine Epidemic Diarrhea Virus Infection |
title_short | Ultrastructural Characterization of Membrane Rearrangements Induced by Porcine Epidemic Diarrhea Virus Infection |
title_sort | ultrastructural characterization of membrane rearrangements induced by porcine epidemic diarrhea virus infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618017/ https://www.ncbi.nlm.nih.gov/pubmed/28872588 http://dx.doi.org/10.3390/v9090251 |
work_keys_str_mv | AT zhouxingdong ultrastructuralcharacterizationofmembranerearrangementsinducedbyporcineepidemicdiarrheavirusinfection AT congyingying ultrastructuralcharacterizationofmembranerearrangementsinducedbyporcineepidemicdiarrheavirusinfection AT veenendaaltineke ultrastructuralcharacterizationofmembranerearrangementsinducedbyporcineepidemicdiarrheavirusinfection AT klumpermanjudith ultrastructuralcharacterizationofmembranerearrangementsinducedbyporcineepidemicdiarrheavirusinfection AT shidongfang ultrastructuralcharacterizationofmembranerearrangementsinducedbyporcineepidemicdiarrheavirusinfection AT marimuriel ultrastructuralcharacterizationofmembranerearrangementsinducedbyporcineepidemicdiarrheavirusinfection AT reggiorifulvio ultrastructuralcharacterizationofmembranerearrangementsinducedbyporcineepidemicdiarrheavirusinfection |