Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/12241
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dc.contributor.authorLothong M.
dc.contributor.authorWattanaphansak S.
dc.contributor.authorDeachapunya C.
dc.contributor.authorPoonyachoti S.
dc.date.accessioned2021-04-05T03:02:22Z-
dc.date.available2021-04-05T03:02:22Z-
dc.date.issued2019
dc.identifier.issn1256491
dc.identifier.other2-s2.0-85085664117
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/12241-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85085664117&partnerID=40&md5=fc43fd9d0c31c4a1905b3ccad4a20a64
dc.description.abstractThe 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.subjectCD163 antigen
dc.subjectestrogen receptor alpha
dc.subjectestrogen receptor beta
dc.subjectsialoadhesin
dc.subjectanimal cell
dc.subjectapical surface
dc.subjectArticle
dc.subjectcell culture
dc.subjectcell isolation
dc.subjectcell surface
dc.subjectClassical swine fever virus
dc.subjectcontrolled study
dc.subjectcytopathogenic effect
dc.subjectdata analysis
dc.subjectendometrium cell
dc.subjectimmunocytochemistry
dc.subjectimmunoreactivity
dc.subjectinoculation
dc.subjectMARC-145 cell line
dc.subjectnonhuman
dc.subjectpig
dc.subjectPorcine reproductive and respiratory syndrome virus
dc.subjectreal time reverse transcription polymerase chain reaction
dc.subjectreverse transcription polymerase chain reaction
dc.subjectRNA extraction
dc.subjectRNA isolation
dc.subjecttransepithelial potential difference
dc.subjecttransepithelial resistance
dc.subjectuterus tissue
dc.subjectvirus entry
dc.subjectvirus isolation
dc.subjectvirus load
dc.subjectvirus release
dc.subjectvirus transmission
dc.titlePorcine reproductive and respiratory syndrome virus (PRRSV) preferentially infected the apical surface of primary endometrial cell monolayer
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationThai Journal of Veterinary Medicine. Vol 49, No.4 (2019), p.401-413
Appears in Collections:Scopus 1983-2021

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