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DC Field | Value | Language |
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dc.contributor.author | Lothong M. | |
dc.contributor.author | Wattanaphansak S. | |
dc.contributor.author | Deachapunya C. | |
dc.contributor.author | Poonyachoti S. | |
dc.date.accessioned | 2021-04-05T03:02:22Z | - |
dc.date.available | 2021-04-05T03:02:22Z | - |
dc.date.issued | 2019 | |
dc.identifier.issn | 1256491 | |
dc.identifier.other | 2-s2.0-85085664117 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/12241 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85085664117&partnerID=40&md5=fc43fd9d0c31c4a1905b3ccad4a20a64 | |
dc.description.abstract | The underlying mechanism of porcine reproductive and respiratory syndrome virus (PRRSV) causing reproductive failure and re-circulation in herds has remained unclear. Endometrial cells primarily infected with PRRSV may serve as a significant target for PRRSV eradication. Primary endometrial (PE) cells from the porcine uterus were isolated and cultivated to pursue this possibility. Immunocytochemistry analysis revealed the protein expression of classical estrogen receptors (ER-α and ER-β), but not PRRSV receptors, CD163 and sialoadhesin in PE cells. PE cells were apically/basolaterally inoculated with PRRSV type I/type II isolated from PRRSV infected lungs or mock infection. Cytopathic effects (CPE) and PRRSV-GP5 positive cells were detected in PE cells incubated with PRRSV inoculum (107 TCID50/ml) beginning at 4 days post inoculation (dpi). Only apical inoculation produced effects, suggesting route dependence of PRRSV infectivity in PE cells (p<0.05). PRRSV type II produced overall effects i.e., CPE, PRRSV-GP5 positive cells and a viral load higher than type I (p<0.05) during 2-6 dpi. In accordance with these effects, the tissue epithelial resistance (TER) of type II inoculated PE cells was lower than that of mock or type I inoculated cells (p<0.05). In addition, all the PE cells and media samples collected from PRRSV-inoculated PE cells persistently revealed PRRSVGP5 protein and viral copies (102-108 TCID50/ml) accessed by infecting MARC-145 cells. These findings provided the first evidence that PE cells can be directly infected with PRRSV, favorably by type II at the apical side. However, all PRRSV contaminated PE cells persistently carry the progeny virus. © 2019 Chulalongkorn University Printing House. All rights reserved. | |
dc.subject | CD163 antigen | |
dc.subject | estrogen receptor alpha | |
dc.subject | estrogen receptor beta | |
dc.subject | sialoadhesin | |
dc.subject | animal cell | |
dc.subject | apical surface | |
dc.subject | Article | |
dc.subject | cell culture | |
dc.subject | cell isolation | |
dc.subject | cell surface | |
dc.subject | Classical swine fever virus | |
dc.subject | controlled study | |
dc.subject | cytopathogenic effect | |
dc.subject | data analysis | |
dc.subject | endometrium cell | |
dc.subject | immunocytochemistry | |
dc.subject | immunoreactivity | |
dc.subject | inoculation | |
dc.subject | MARC-145 cell line | |
dc.subject | nonhuman | |
dc.subject | pig | |
dc.subject | Porcine reproductive and respiratory syndrome virus | |
dc.subject | real time reverse transcription polymerase chain reaction | |
dc.subject | reverse transcription polymerase chain reaction | |
dc.subject | RNA extraction | |
dc.subject | RNA isolation | |
dc.subject | transepithelial potential difference | |
dc.subject | transepithelial resistance | |
dc.subject | uterus tissue | |
dc.subject | virus entry | |
dc.subject | virus isolation | |
dc.subject | virus load | |
dc.subject | virus release | |
dc.subject | virus transmission | |
dc.title | Porcine reproductive and respiratory syndrome virus (PRRSV) preferentially infected the apical surface of primary endometrial cell monolayer | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Thai Journal of Veterinary Medicine. Vol 49, No.4 (2019), p.401-413 | |
Appears in Collections: | Scopus 1983-2021 |
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