Different routes and doses influence protection in pigs immunised with the naturally attenuated African swine fever virus isolate OURT88/3

被引:84
作者
Sanchez-Cordon, Pedro J. [1 ]
Chapman, Dave [1 ]
Jabbar, Tamara [1 ]
Reis, Ana L. [1 ]
Goatley, Lynnette [1 ]
Netherton, Christopher L. [1 ]
Taylor, Geraldine [1 ]
Montoya, Maria [1 ]
Dixon, Linda [1 ]
机构
[1] Pirbright Inst, Ash Rd, Woking, Surrey, England
基金
英国生物技术与生命科学研究理事会;
关键词
African swine fever; Pigs; Immunisation routes; Protection; Cytokines; DOMESTIC PIGS; PROINFLAMMATORY CYTOKINES; CHALLENGE; MACROPHAGES; VIRULENCE; MECHANISMS; EXPRESSION; DELIVERY; DELETION; GENES;
D O I
10.1016/j.antiviral.2016.11.021
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study compares different combinations of doses and routes of immunisation of pigs with low virulent African swine fever virus (ASFV) genotype I isolate OURT88/3, including the intramuscular and intranasal route, the latter not previously tested. Intranasal immunisations with low and moderate doses (10(3) and 10(4) TCID50) of OURT88/3 provided complete protection (100%) against challenge with virulent genotype I OURT88/1 isolate. Only mild and transient clinical reactions were observed in protected pigs. Transient moderate virus genome levels were detected in blood samples after challenge that decreased, but persisted until the end of the experiment in some animals. In contrast, pigs immunised intramuscularly with low and moderate doses (10(3) and 10(4) TCID50) displayed lower percentages of protection (50-66%), and low or undetectable levels of virus genome were detected in blood samples throughout the study. In addition, clinical courses observed in protected pigs were asymptomatic. In pigs that were not protected and developed acute ASF, an exacerbated increase of IL-10 sometimes accompanied by an increase of IFN gamma was observed before euthanasia. These results showed that factors including delivery route and dose determine the outcome of immunisation with the naturally attenuated isolate OURT88/3. (C) 2016 The Authors. Published by Elsevier B.V.
引用
收藏
页码:1 / 8
页数:8
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