Lankester Felix, Lugelo Ahmed, Mnyambwa Nicholas, Ndabigaye Ahab, Keyyu Julius, Kazwala Rudovick, Grant Dawn M, Relf Valerie, Haig David M, Cleaveland Sarah, Russell George C
Boyd Orr Centre for Population and Ecosystem Health, Institute of Biodiversity, Animal Health & Comparative Medicine, University of Glasgow, Glasgow, G12 8QQ, United Kingdom; Paul G. Allen School for Global Animal Health, Washington State University, Pullman, WA, 99164, United States of America; School of Life Sciences and Bioengineering, Nelson Mandela African Institution of Science and Technology, Arusha, Tanzania.
Faculty of Veterinary Medicine, Sokoine University of Agriculture, Morogoro, Tanzania.
PLoS One. 2015 May 13;10(5):e0124121. doi: 10.1371/journal.pone.0124121. eCollection 2015.
Alcelaphine herpesvirus-1 (AlHV-1), a causative agent of malignant catarrhal fever in cattle, was detected in wildebeest (Connochaetes taurinus) placenta tissue for the first time. Although viral load was low, the finding of viral DNA in over 50% of 94 samples tested lends support to the possibility that placental tissue could play a role in disease transmission and that wildebeest calves are infected in utero. Two viral loci were sequenced to examine variation among virus samples obtained from wildebeest and cattle: the ORF50 gene, encoding the lytic cycle transactivator protein, and the A9.5 gene, encoding a novel polymorphic viral glycoprotein. ORF50 was well conserved with six newly discovered alleles differing at only one or two base positions. In contrast, while only three new A9.5 alleles were discovered, these differed by up to 13% at the nucleotide level and up to 20% at the amino acid level. Structural homology searching performed with the additional A9.5 sequences determined in this study adds power to recent analysis identifying the four-helix bundle cytokine interleukin-4 (IL4) as the major homologue. The majority of MCF virus samples obtained from Tanzanian cattle and wildebeest encoded A9.5 polypeptides identical to the previously characterized A9.5 allele present in the laboratory maintained AlHV-1 C500 strain. This supports the view that AlHV-1 C500 is suitable for the development of a vaccine for wildebeest-associated MCF.
首次在角马(牛羚)胎盘组织中检测到牛恶性卡他热的病原体——牛疱疹病毒1型(AlHV - 1)。尽管病毒载量很低,但在94个检测样本中超过50%发现了病毒DNA,这支持了胎盘组织可能在疾病传播中起作用以及角马幼崽在子宫内被感染的可能性。对两个病毒基因座进行了测序,以检查从角马和牛获得的病毒样本之间的变异情况:编码裂解周期反式激活蛋白的ORF50基因和编码一种新型多态性病毒糖蛋白的A9.5基因。ORF50高度保守,新发现的六个等位基因仅在一两个碱基位置上有所不同。相比之下,虽然仅发现了三个新的A9.5等位基因,但它们在核苷酸水平上的差异高达13%,在氨基酸水平上的差异高达20%。用本研究中确定的额外A9.5序列进行的结构同源性搜索,为最近将四螺旋束细胞因子白细胞介素-4(IL4)鉴定为主要同源物的分析提供了支持。从坦桑尼亚的牛和角马获得的大多数MCF病毒样本编码的A9.5多肽与实验室保存的AlHV - 1 C500菌株中先前鉴定的A9.5等位基因相同。这支持了AlHV - 1 C500适合开发与角马相关的MCF疫苗的观点。