Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/12241
Title: Porcine reproductive and respiratory syndrome virus (PRRSV) preferentially infected the apical surface of primary endometrial cell monolayer
Authors: Lothong M.
Wattanaphansak S.
Deachapunya C.
Poonyachoti S.
Keywords: CD163 antigen
estrogen receptor alpha
estrogen receptor beta
sialoadhesin
animal cell
apical surface
Article
cell culture
cell isolation
cell surface
Classical swine fever virus
controlled study
cytopathogenic effect
data analysis
endometrium cell
immunocytochemistry
immunoreactivity
inoculation
MARC-145 cell line
nonhuman
pig
Porcine reproductive and respiratory syndrome virus
real time reverse transcription polymerase chain reaction
reverse transcription polymerase chain reaction
RNA extraction
RNA isolation
transepithelial potential difference
transepithelial resistance
uterus tissue
virus entry
virus isolation
virus load
virus release
virus transmission
Issue Date: 2019
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.
URI: https://ir.swu.ac.th/jspui/handle/123456789/12241
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85085664117&partnerID=40&md5=fc43fd9d0c31c4a1905b3ccad4a20a64
ISSN: 1256491
Appears in Collections:Scopus 1983-2021

Files in This Item:
There are no files associated with this item.


Items in SWU repository are protected by copyright, with all rights reserved, unless otherwise indicated.