Publication:
Porcine reproductive and respiratory syndrome virus (PRRSV) preferentially infected the apical surface of primary endometrial cell monolayer

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.date.issuedBE2562
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.format.mimetypeapplication/pdf
dc.identifier.citationThai Journal of Veterinary Medicine. Vol 49, No.4 (2019), p.401-413
dc.identifier.issn1256491
dc.identifier.other2-s2.0-85085664117
dc.identifier.urihttps://hdl.handle.net/20.500.14740/5066
dc.rights.holderScopus
dc.subject.otherCD163 antigen
dc.subject.otherEstrogen receptor alpha
dc.subject.otherEstrogen receptor beta
dc.subject.otherSialoadhesin
dc.subject.otherAnimal cell
dc.subject.otherApical surface
dc.subject.otherArticle
dc.subject.otherCell culture
dc.subject.otherCell isolation
dc.subject.otherCell surface
dc.subject.otherClassical swine fever virus
dc.subject.otherControlled study
dc.subject.otherCytopathogenic effect
dc.subject.otherData analysis
dc.subject.otherEndometrium cell
dc.subject.otherImmunocytochemistry
dc.subject.otherImmunoreactivity
dc.subject.otherInoculation
dc.subject.otherMARC-145 cell line
dc.subject.otherNonhuman
dc.subject.otherPig
dc.subject.otherPorcine reproductive and respiratory syndrome virus
dc.subject.otherReal time reverse transcription polymerase chain reaction
dc.subject.otherReverse transcription polymerase chain reaction
dc.subject.otherRNA extraction
dc.subject.otherRNA isolation
dc.subject.otherTransepithelial potential difference
dc.subject.otherTransepithelial resistance
dc.subject.otherUterus tissue
dc.subject.otherVirus entry
dc.subject.otherVirus isolation
dc.subject.otherVirus load
dc.subject.otherVirus release
dc.subject.otherVirus transmission
dc.titlePorcine reproductive and respiratory syndrome virus (PRRSV) preferentially infected the apical surface of primary endometrial cell monolayer
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85085664117&partnerID=40&md5=fc43fd9d0c31c4a1905b3ccad4a20a64

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