首页> 外国专利> ATTENUATED AFRICAN SWINE FEVER VIRUS STRAIN INDUCES PROTECTION AGAINST CHALLENGE WITH HOMOLOGOUS VIRULENT PARENTAL VIRUS GEORGIA 2007 ISOLATE

ATTENUATED AFRICAN SWINE FEVER VIRUS STRAIN INDUCES PROTECTION AGAINST CHALLENGE WITH HOMOLOGOUS VIRULENT PARENTAL VIRUS GEORGIA 2007 ISOLATE

机译:减毒的非洲猪瘟病毒菌株可抵抗同种毒物的毒株感染佐治亚州2007年孤立

摘要

African swine fever virus (ASFV) is the etiological agent of a contagious and often lethal viral disease of domestic pigs that has significant economic consequences for swine breeding. Control of ASF has been hampered by the unavailability of vaccines. Recombinant viruses harboring engineered deletions of specific virulence-associated genes induce solid protection against the challenge with parental viruses. Here we report the construction of a recombinant Δ9GL virus derived from the highly virulent ASFV Georgia 2007 (ASFV-G) isolate. In vivo, ASFV-G Δ9GL administered intramuscularly (IM) to swine at relatively high doses (104 HAD50) retains a virulent phenotype practically indistinguishable from the parental virus. Conversely, at low IM doses (102 or 103 HAD50), ASFV-G Δ9GL does not induce disease. Importantly, animals infected with 103 HAD50 are protected against the presentation of clinical disease when challenge at 28 days post infection with the virulent parental strain Georgia 2007.
机译:非洲猪瘟病毒(ASFV)是家猪具有传染性和致命性的病毒性疾病的病原体,对猪的繁殖具有重大的经济影响。无法获得疫苗阻碍了对ASF的控制。带有特定毒力相关基因的工程缺失的重组病毒诱导出针对父母病毒攻击的坚固保护。在这里,我们报告从高毒力的ASFV Georgia 2007(ASFV-G)分离株衍生的重组Δ9GL病毒的构建。在体内,以较高剂量(104 HAD50)肌内(IM)给予猪ASFV-GΔ9GL保留了实际上与亲本病毒没有区别的强毒表型。相反,在低IM剂量(102或103 HAD50)下,ASFV-GΔ9GL不会诱发疾病。重要的是,感染了103种HAD50的动物在感染后28天受到有毒的亲本佐治亚州佐治亚州2007的攻击时,可以防止出现临床疾病。

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