Impact of PRRSV strains of different in vivo virulence on the macrophage population of the thymus.
Animals
Antigens, CD
/ genetics
Antigens, Differentiation, Myelomonocytic
/ genetics
Lung
/ pathology
Macrophages
/ immunology
Porcine Reproductive and Respiratory Syndrome
/ immunology
Porcine respiratory and reproductive syndrome virus
/ immunology
Receptors, Cell Surface
/ genetics
Swine
Thymus Gland
/ immunology
Viral Load
Viral Vaccines
/ therapeutic use
Virulence
Cell death
Macrophages
PRRSV
Thymus
Virulence
Journal
Veterinary microbiology
ISSN: 1873-2542
Titre abrégé: Vet Microbiol
Pays: Netherlands
ID NLM: 7705469
Informations de publication
Date de publication:
May 2019
May 2019
Historique:
received:
10
01
2019
revised:
25
03
2019
accepted:
11
04
2019
entrez:
30
4
2019
pubmed:
30
4
2019
medline:
6
6
2019
Statut:
ppublish
Résumé
The emergence of "highly pathogenic" isolates of porcine reproductive and respiratory syndrome virus (HP-PRRSV) has raised new concerns about PRRS control. Cells from the porcine monocyte-macrophage lineage represent the target for this virus, which replicates mainly in the lung, and especially in HP-PRRSV strains, also in lymphoid organs, such as the thymus. This study aimed at evaluating the impact of two PRRSV strains of different virulence on thymic macrophages as well as after heterologous vaccination. After experimental infection with PR11 and PR40 PRRSV1 subtype 1 strains (low and high virulent, respectively) samples from thymus were analysed by histopathology and immunohistochemistry for PRRSV N protein, TUNEL, CD172a, CD163, CD107a and BA4D5 expression. Mortality was similar in both infected groups, but lung lesions and thymus atrophy were more intense in PR40 group. Animals died at 10-14 dpi after PR11 or PR40 infection showed the most severe histopathological lesions, with a strong inflammatory response of the stroma and extensive cell death phenomena in the cortex. These animals presented an increase in the number of N protein, CD172a, CD163 and BA4D5 positive cells in the stroma and the cortex together with a decrease in the number of CD107a positive cells. Our results highlight the recruitment of macrophages in the thymus, the increase in the expression of CD163 and the regulation of the host cytotoxic activity by macrophages. However, no marked differences were observed between PR11- and PR40-infected animals. Heterologous vaccination restrained virus spread and lesions extent in the thymus of PR40-infected animals.
Identifiants
pubmed: 31030838
pii: S0378-1135(19)30045-8
doi: 10.1016/j.vetmic.2019.04.016
pii:
doi:
Substances chimiques
Antigens, CD
0
Antigens, Differentiation, Myelomonocytic
0
CD163 antigen
0
Receptors, Cell Surface
0
Viral Vaccines
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
137-145Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.