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  2. College of Bioresources and Agriculture / 生物資源暨農學院
  3. School of Veterinary Medicine / 獸醫專業學院
  4. Molecular and Comparative Pathobiology / 分子暨比較病理生物學研究所
  5. Impairment of oxidative burst in porcine neutrophils induced by pseudorabies virus
 
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Impairment of oxidative burst in porcine neutrophils induced by pseudorabies virus

Journal
Veterinary Immunology and Immunopathology
Journal Volume
101
Journal Issue
1-2
Pages
123-130
Date Issued
2004
Author(s)
FUN-IN WANG  
DOI
10.1016/j.vetimm.2004.04.018
URI
http://www.scopus.com/inward/record.url?eid=2-s2.0-3142518024&partnerID=MN8TOARS
http://scholars.lib.ntu.edu.tw/handle/123456789/306926
Abstract
Industrial swine production is affected by several serious viral diseases, such as pseudorabies, hog cholera, porcine reproductive and respiratory syndrome, which are frequently complicated with the increased incidence of bacterial complications such as Actinobacillus pleuropneumoniae (APP). This clinical observation is suggestive of a virus-bacteria synergism on the pathogenesis. One hypothesis is that viruses induce polymorphonuclear cell (PMNs, primarily neutrophils) dysfunction resulting in defective antibacterial resistance. The purpose of this study was to use the pseudorabies virus (PrV) as a model to explore the possibility of virus-induced PMN dysfunctions in pigs. The goals were to evaluate, in ex vivo settings, the oxidative burst (OB) function of pig PMNs, and to evaluate whether PrV could affect these responses to APP. We found that PrV served as a mild OB stimulant (2-fold) to pig PMNs, which also launched a significant burst to phorbol 12-myristate 13-diacetate (PMA; 61-fold), to non-opsonized, heat-killed and formaldehyde-fixed APP (8-fold), and to normal pig serum-opsonized APP (34-fold). Interestingly, the PMA-induced OB could be reduced 50-70% by preincubating PMNs with PrV, and the critical target was not likely the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase itself. Inactivated PrV was as efficient as viable PrV at exerting the inhibitory effect. On the other hand, PrV exerted a primarily additive effect on APP-induced OB, when the cytotoxic effect of APP on PMNs was avoided. The current finding suggests the possibility that activated PMNs are susceptible to PrV-induced dysfunction, and that the PrV-APP synergism may require upstream stimuli of PMNs to be initiated. ? 2004 Elsevier B.V. All rights reserved.
Subjects
2′,7′-dichlorofluorescin diacetate; Actinobacillus pleuropneumoniae; analysis of variance; ANOVA; APP; BEI; BHV-1; bovine herpesvirus type 1; bromoethylimine; Con, con; DCFH-DA, DCFH; DHR; negative control(s), background fluorescence
SDGs

[SDGs]SDG3

Other Subjects
formaldehyde; phorbol 13 acetate 12 myristate; reduced nicotinamide adenine dinucleotide phosphate oxidase; Actinobacillus pleuropneumoniae; animal cell; article; cell damage; controlled study; heat; incubation time; neutrophil; nonhuman; opsonization; polymorphonuclear cell; Pseudorabies herpetovirus; respiratory burst; swine; virus inactivation; Actinobacillus Infections; Actinobacillus pleuropneumoniae; Animals; Flow Cytometry; Herpesvirus 1, Suid; Hydrogen Peroxide; Neutrophil Activation; Neutrophils; Respiratory Burst; Superoxides; Swine; Swine Diseases; Tetradecanoylphorbol Acetate; Actinobacillus; Actinobacillus pleuropneumoniae; Bacteria (microorganisms); Bovinae; Bovine herpesvirus 1; Herpesviridae; Suid herpesvirus 1; Suidae; Sus scrofa
Type
journal article

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