Burrage T G, Lu Z, Neilan J G, Rock D L, Zsak L
Plum Island Animal Disease Center, Agricultural Research Service, U.S. Department of Agriculture, Greenport, New York 11944-0848, USA.
J Virol. 2004 Mar;78(5):2445-53. doi: 10.1128/jvi.78.5.2445-2453.2004.
Recently, we reported that African swine fever virus (ASFV) multigene family (MGF) 360 and 530 genes are significant swine macrophage host range determinants that function by promoting infected-cell survival. To examine the function of these genes in ASFV's arthropod host, Ornithodoros porcinus porcinus, an MGF360/530 gene deletion mutant (Pr4Delta35) was constructed from an ASFV isolate of tick origin, Pr4. Pr4Delta35 exhibited a significant growth defect in ticks. The deletion of six MGF360 and two MGF530 genes from Pr4 markedly reduced viral replication in infected ticks 100- to 1,000-fold. To define the minimal set of MGF360/530 genes required for tick host range, additional gene deletion mutants lacking individual or multiple MGF genes were constructed. The deletion mutant Pr4Delta3-C2, which lacked three MGF360 genes (3HL, 3Il, and 3LL), exhibited reduced viral growth in ticks. Pr4Delta3-C2 virus titers in ticks were significantly reduced 100- to 1,000-fold compared to control values at various times postinfection. In contrast to the parental virus, with which high levels of virus replication were observed in the tissues of infected adults, Pr4Delta3-C2 replication was not detected in the midgut, hemolymph, salivary gland, coxal gland, or reproductive organs at 15 weeks postinfection. These data indicate that ASFV MGF360 genes are significant tick host range determinants and that they are required for efficient virus replication and generalization of infection. The impaired virus replication of Pr4Delta3-C2 in the tick midgut likely accounts for the absence of the generalized infection that is necessary for the natural transmission of virus from ticks to pigs.
最近,我们报道非洲猪瘟病毒(ASFV)多基因家族(MGF)360和530基因是重要的猪巨噬细胞宿主范围决定因素,其通过促进受感染细胞存活发挥作用。为了研究这些基因在ASFV节肢动物宿主——猪钝缘蜱中的功能,从蜱源ASFV分离株Pr4构建了一个MGF360/530基因缺失突变体(Pr4Delta35)。Pr4Delta35在蜱中表现出显著的生长缺陷。从Pr4中缺失六个MGF360基因和两个MGF530基因,使感染蜱中的病毒复制显著降低了100至1000倍。为了确定蜱宿主范围所需的MGF360/530基因的最小集合,构建了缺失单个或多个MGF基因的其他基因缺失突变体。缺失三个MGF360基因(3HL、3Il和3LL)的缺失突变体Pr4Delta3-C2在蜱中的病毒生长减少。与感染后不同时间的对照值相比,Pr4Delta3-C2在蜱中的病毒滴度在感染后15周时显著降低了100至1000倍。与在感染成年动物组织中观察到高水平病毒复制的亲本病毒相比,在感染后15周时,在中肠、血淋巴、唾液腺、基节腺或生殖器官中未检测到Pr4Delta3-C2的复制。这些数据表明,ASFV MGF360基因是重要的蜱宿主范围决定因素,并且它们是病毒有效复制和感染传播所必需的。Pr4Delta3-C2在蜱中肠中的病毒复制受损,可能是导致病毒从蜱自然传播到猪所需的全身性感染缺失的原因。