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About:
Successive Passage In Vitro Led to Lower Virulence and Higher Titer of A Variant Porcine Epidemic Diarrhea Virus
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schema:ScholarlyArticle
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covidontheweb.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Successive Passage In Vitro Led to Lower Virulence and Higher Titer of A Variant Porcine Epidemic Diarrhea Virus
Creator
He, Hongbin
Guo, Xiaozhen
Zhao, Pengwei
Wu, Jiaqiang
Wang, Song
Chen, Zhi
Liu, Yueyue
Yu, Jiang
Xu, Guanlong
Li, Jinxiang
Zhao, Lu
Qiu, Wenbin
Tang, Rongzhi
Source
Medline; PMC
abstract
A highly virulent porcine epidemic diarrhea virus (PEDV) appeared in China and spread rapidly to neighbor countries, which have led to great economic losses to the pig industry. In the present study, we isolated a PEDV using Vero cells and serially propagated 100 passages. PEDV SDSX16 was characterized in vitro and in vivo. The viral titers increased to 10(7.6) TCID(50)/mL (100th) by serial passages. The spike (S) gene and the whole gene of the SDSX16 virus was fully sequenced to assess the genetic stability and relatedness to previously identified PEDV. Along with successive passage in vitro, there were 18 nucleotides (nt) deletion occurred in the spike (S) gene resulting in a deletion of six amino acids when the SDSX16 strain was passaged to the 64th generation, and this deletion was stable until the P100. However, the ORF1a/b, M, N, E, and ORF3 genes had only a few point mutations in amino acids and no deletions. According to growth kinetics experiments, the SDSX16 deletion strain significantly enhanced its replication in Vero cells since it was passaged to the 64th generation. The animal studies showed that PEDV SDSX16-P10 caused more severe diarrhea and vomiting, fecal shedding, and acute atrophic enteritis than SDSX16-P75, indicating that SDSX16-P10 is enteropathogenic in the natural host, and the pathogenicity of SDSX16 decreased with successive passage in vitro. However, SDSX16-P10 was found to cause lower levels of cytokine expression than SDSX16-P75 using real-time PCR and flow cytometry, such as IL1β, IL6, IFN-β, TNF-α, indicating that SDSX16-P10 might inhibit the expression of cytokines. Our data indicated that successive passage in vitro resulted in virulent attenuation in vivo of the PEDV variant strain SDSX16.
has issue date
2020-04-01
(
xsd:dateTime
)
bibo:doi
10.3390/v12040391
bibo:pmid
32244640
has license
cc-by
sha1sum (hex)
dc61db3f0571d3a11a3451ebd58997cada9d988a
schema:url
https://doi.org/10.3390/v12040391
resource representing a document's title
Successive Passage In Vitro Led to Lower Virulence and Higher Titer of A Variant Porcine Epidemic Diarrhea Virus
has PubMed Central identifier
PMC7232491
has PubMed identifier
32244640
schema:publication
Viruses
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covid:dc61db3f0571d3a11a3451ebd58997cada9d988a#body_text
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schema:about
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named entity 'IL1'
named entity 'TNF'
named entity 'PATHOGENICITY'
covid:arg/dc61db3f0571d3a11a3451ebd58997cada9d988a
named entity 'passaged'
named entity 'atrophic'
named entity 'PEDV'
named entity 'porcine epidemic diarrhea virus'
named entity 'genetic stability'
named entity 'China'
named entity 'pathogenicity'
named entity 'severe diarrhea'
named entity 'nucleotides'
named entity 'cytokine'
named entity 'point mutations'
named entity 'pig'
named entity 'PBS'
named entity 'pro-inflammatory cytokines'
named entity 'reverse transcription'
named entity 'cloned'
named entity 'IIb'
named entity 'TNF-α'
named entity 'TNF-α'
named entity 'Pro-inflammatory cytokines'
named entity 'intestinal epithelial cells'
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named entity 'virus'
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named entity 'OsO4'
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named entity 'TaKaRa Bio'
named entity 'feces'
named entity 'antigen'
named entity 'monoclonal antibody'
named entity 'Statistically significant'
named entity 'gene'
named entity 'coronaviruses'
named entity 'significant difference'
named entity 'titer'
named entity 'mRNA expression'
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named entity 'type I IFNs'
named entity 'cDNA'
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named entity 'GenBank'
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named entity 'innate immune response'
named entity 'microscope'
named entity 'Toll-like receptors'
named entity 'diarrhea'
named entity 'Figure 8'
named entity 'Germany'
named entity 'tissue culture'
named entity 'Vero'
named entity 'Shandong Province'
named entity 'Sigma-Aldrich'
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named entity 'phosphate-buffered saline'
named entity 'pathogenicity'
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