Cell culture isolation and sequence analysis of genetically diverse US porcine epidemic diarrhea virus strains including a novel strain with a large deletion in the spike gene

•We isolated a novel PEDV strain with a large deletion (197aa) in the spike gene.•We isolated US PEDV INDEL variant in Vero cells.•We isolated multiple original highly virulent US PEDV strains in Vero cells.•Genomic sequences of the isolated PEDV strains were analyzed.•The isolated genetically diver...

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Veröffentlicht in:Veterinary microbiology 2014-10, Vol.173 (3-4), p.258-269
Hauptverfasser: Oka, Tomoichiro, Saif, Linda J., Marthaler, Douglas, Esseili, Malak A., Meulia, Tea, Lin, Chun-Ming, Vlasova, Anastasia N., Jung, Kwonil, Zhang, Yan, Wang, Qiuhong
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container_end_page 269
container_issue 3-4
container_start_page 258
container_title Veterinary microbiology
container_volume 173
creator Oka, Tomoichiro
Saif, Linda J.
Marthaler, Douglas
Esseili, Malak A.
Meulia, Tea
Lin, Chun-Ming
Vlasova, Anastasia N.
Jung, Kwonil
Zhang, Yan
Wang, Qiuhong
description •We isolated a novel PEDV strain with a large deletion (197aa) in the spike gene.•We isolated US PEDV INDEL variant in Vero cells.•We isolated multiple original highly virulent US PEDV strains in Vero cells.•Genomic sequences of the isolated PEDV strains were analyzed.•The isolated genetically diverse PEDV strains can be used for attenuated vaccine development. The highly contagious and deadly porcine epidemic diarrhea virus (PEDV) first appeared in the US in April 2013. Since then the virus has spread rapidly nationwide and to Canada and Mexico causing high mortality among nursing piglets and significant economic losses. Currently there are no efficacious preventive measures or therapeutic tools to control PEDV in the US. The isolation of PEDV in cell culture is the first step toward the development of an attenuated vaccine, to study the biology of PEDV and to develop in vitro PEDV immunoassays, inactivation assays and screen for PEDV antivirals. In this study, nine of 88 US PEDV strains were isolated successfully on Vero cells with supplemental trypsin and subjected to genomic sequence analysis. They differed genetically mainly in the N-terminal S protein region as follows: (1) strains (n=7) similar to the highly virulent US PEDV strains; (2) one similar to the reportedly US S INDEL PEDV strain; and (3) one novel strain most closely related to highly virulent US PEDV strains, but with a large (197aa) deletion in the S protein. Representative strains of these three genetic groups were passaged serially and grew to titers of ∼5–6log10 plaque forming units/mL. To our knowledge, this is the first report of the isolation in cell culture of an S INDEL PEDV strain and a PEDV strain with a large (197aa) deletion in the S protein. We also designed primer sets to detect these genetically diverse US PEDV strains.
doi_str_mv 10.1016/j.vetmic.2014.08.012
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The highly contagious and deadly porcine epidemic diarrhea virus (PEDV) first appeared in the US in April 2013. Since then the virus has spread rapidly nationwide and to Canada and Mexico causing high mortality among nursing piglets and significant economic losses. Currently there are no efficacious preventive measures or therapeutic tools to control PEDV in the US. The isolation of PEDV in cell culture is the first step toward the development of an attenuated vaccine, to study the biology of PEDV and to develop in vitro PEDV immunoassays, inactivation assays and screen for PEDV antivirals. In this study, nine of 88 US PEDV strains were isolated successfully on Vero cells with supplemental trypsin and subjected to genomic sequence analysis. They differed genetically mainly in the N-terminal S protein region as follows: (1) strains (n=7) similar to the highly virulent US PEDV strains; (2) one similar to the reportedly US S INDEL PEDV strain; and (3) one novel strain most closely related to highly virulent US PEDV strains, but with a large (197aa) deletion in the S protein. Representative strains of these three genetic groups were passaged serially and grew to titers of ∼5–6log10 plaque forming units/mL. To our knowledge, this is the first report of the isolation in cell culture of an S INDEL PEDV strain and a PEDV strain with a large (197aa) deletion in the S protein. 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All rights reserved.</rights><rights>Copyright © 2014 Elsevier B.V. Published by Elsevier B.V. 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The highly contagious and deadly porcine epidemic diarrhea virus (PEDV) first appeared in the US in April 2013. Since then the virus has spread rapidly nationwide and to Canada and Mexico causing high mortality among nursing piglets and significant economic losses. Currently there are no efficacious preventive measures or therapeutic tools to control PEDV in the US. The isolation of PEDV in cell culture is the first step toward the development of an attenuated vaccine, to study the biology of PEDV and to develop in vitro PEDV immunoassays, inactivation assays and screen for PEDV antivirals. In this study, nine of 88 US PEDV strains were isolated successfully on Vero cells with supplemental trypsin and subjected to genomic sequence analysis. 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We also designed primer sets to detect these genetically diverse US PEDV strains.</description><subject>Animals</subject><subject>Base Sequence</subject><subject>Cell culture isolation</subject><subject>Cell Culture Techniques - veterinary</subject><subject>Chlorocebus aethiops</subject><subject>Complete genome analysis</subject><subject>Coronavirus Infections - epidemiology</subject><subject>Coronavirus Infections - veterinary</subject><subject>DNA Primers - genetics</subject><subject>Fluorescent Antibody Technique, Indirect - veterinary</subject><subject>Genetic Variation</subject><subject>Large deletion in S protein</subject><subject>Microscopy, Electron, Transmission - veterinary</subject><subject>Midwestern United States - epidemiology</subject><subject>Molecular Sequence Data</subject><subject>PEDV variants</subject><subject>Phylogeny</subject><subject>Porcine epidemic diarrhea virus (PEDV)</subject><subject>Porcine epidemic diarrhea virus - genetics</subject><subject>Porcine epidemic diarrhea virus - isolation &amp; purification</subject><subject>Porcine epidemic diarrhea virus - pathogenicity</subject><subject>Real-Time Polymerase Chain Reaction - veterinary</subject><subject>Reverse Transcriptase Polymerase Chain Reaction - veterinary</subject><subject>Sequence Analysis, DNA - veterinary</subject><subject>Sequence Deletion - genetics</subject><subject>Species Specificity</subject><subject>Spike Glycoprotein, Coronavirus - genetics</subject><subject>Swine</subject><subject>Swine Diseases - epidemiology</subject><subject>Swine Diseases - virology</subject><subject>Vero Cells</subject><subject>Virulence</subject><issn>0378-1135</issn><issn>1873-2542</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kd1uEzEQhS0EoqHtGyDkF8jWf7ve3iChiJ9KlbgovbYcezaZ4HgXe3dRnopXxGlKgZteWeOjc-aMPkLeclZxxpurXTXDuEdXCcZVxdqKcfGCLHir5VLUSrwkCyZ1u-Rc1mfkTc47xpi6bthrciZqwbVibEF-rSAE6qYwTgko5j7YEftIbfQ0w48JooMy2HDImGnf0Q1EGNHZEA7U4wwpA72_o0OfHEagMKCH0qpoNqUtWDpjmjLNY7IYM8XowuQxbqilsZ8hPCr0J47b8hds2gD1EOChRhHGLdA84Hd4WH1BXnU2ZLh8fM_J_aeP31ZflrdfP9-sPtwunWrkWI7uXAOt7zQT0reyYW2nFV-Dbxgozeq1VdZJzWshuebSeeXltdMemjWXnZPn5P0pd5jWe_AOYqkZzJBwb9PB9BbN_0rErdn0s9FcNII3JUCdAlzqc07QPXk5M0eAZmdOAM0RoGGtKQCL7d2_e59Mf4j9LQbl-hkhmezwSMljAjca3-PzG34Dw0W0aA</recordid><startdate>20141010</startdate><enddate>20141010</enddate><creator>Oka, Tomoichiro</creator><creator>Saif, Linda J.</creator><creator>Marthaler, Douglas</creator><creator>Esseili, Malak A.</creator><creator>Meulia, Tea</creator><creator>Lin, Chun-Ming</creator><creator>Vlasova, Anastasia N.</creator><creator>Jung, Kwonil</creator><creator>Zhang, Yan</creator><creator>Wang, Qiuhong</creator><general>Elsevier B.V</general><general>Elsevier B.V. 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The highly contagious and deadly porcine epidemic diarrhea virus (PEDV) first appeared in the US in April 2013. Since then the virus has spread rapidly nationwide and to Canada and Mexico causing high mortality among nursing piglets and significant economic losses. Currently there are no efficacious preventive measures or therapeutic tools to control PEDV in the US. The isolation of PEDV in cell culture is the first step toward the development of an attenuated vaccine, to study the biology of PEDV and to develop in vitro PEDV immunoassays, inactivation assays and screen for PEDV antivirals. In this study, nine of 88 US PEDV strains were isolated successfully on Vero cells with supplemental trypsin and subjected to genomic sequence analysis. They differed genetically mainly in the N-terminal S protein region as follows: (1) strains (n=7) similar to the highly virulent US PEDV strains; (2) one similar to the reportedly US S INDEL PEDV strain; and (3) one novel strain most closely related to highly virulent US PEDV strains, but with a large (197aa) deletion in the S protein. Representative strains of these three genetic groups were passaged serially and grew to titers of ∼5–6log10 plaque forming units/mL. To our knowledge, this is the first report of the isolation in cell culture of an S INDEL PEDV strain and a PEDV strain with a large (197aa) deletion in the S protein. We also designed primer sets to detect these genetically diverse US PEDV strains.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>25217400</pmid><doi>10.1016/j.vetmic.2014.08.012</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0378-1135
ispartof Veterinary microbiology, 2014-10, Vol.173 (3-4), p.258-269
issn 0378-1135
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language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7126216
source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Animals
Base Sequence
Cell culture isolation
Cell Culture Techniques - veterinary
Chlorocebus aethiops
Complete genome analysis
Coronavirus Infections - epidemiology
Coronavirus Infections - veterinary
DNA Primers - genetics
Fluorescent Antibody Technique, Indirect - veterinary
Genetic Variation
Large deletion in S protein
Microscopy, Electron, Transmission - veterinary
Midwestern United States - epidemiology
Molecular Sequence Data
PEDV variants
Phylogeny
Porcine epidemic diarrhea virus (PEDV)
Porcine epidemic diarrhea virus - genetics
Porcine epidemic diarrhea virus - isolation & purification
Porcine epidemic diarrhea virus - pathogenicity
Real-Time Polymerase Chain Reaction - veterinary
Reverse Transcriptase Polymerase Chain Reaction - veterinary
Sequence Analysis, DNA - veterinary
Sequence Deletion - genetics
Species Specificity
Spike Glycoprotein, Coronavirus - genetics
Swine
Swine Diseases - epidemiology
Swine Diseases - virology
Vero Cells
Virulence
title Cell culture isolation and sequence analysis of genetically diverse US porcine epidemic diarrhea virus strains including a novel strain with a large deletion in the spike gene
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