Tsai Ming-Shan, François Sarah, Newman Chris, Macdonald David W, Buesching Christina D
Wildlife Conservation Research Unit, Recanati-Kaplan Centre, Department of Biology, University of Oxford, Tubney, Oxfordshire OX13 5QL, UK.
Department of Biology, University of Oxford, Peter Medawar Building, South Park Road, Oxford OX1 3SY, UK.
Pathogens. 2022 Oct 6;11(10):1154. doi: 10.3390/pathogens11101154.
Herpesviruses are ubiquitous pathogens infecting most animals. Although host immunity continually coevolves to combat virulence, viral variants with enhanced transmissibility or virulence occasionally emerge, resulting in disease burdens in host populations. Mustelid gammaherpesvirus 1 (MusGHV-1) is the only herpesvirus species identified thus far in European badgers, Meles meles. No MusGHV-1 associated pathomorbidity has been reported, but reactivation of MusGHV-1 in genital tracts is linked to impaired female reproductive success. An analysis of a short sequence from the highly conserved DNA polymerase (DNApol) gene previously identified two variants in a single host population. Here we compared genetic variance in blood samples from 66 known individuals of this same free-ranging badger population using a partial sequence comprising 2874 nucleotides of the DNApol gene, among which we identified 15 nucleotide differences resulting in 5 amino acid differences. Prevalence was 86% (59/66) for the common and 17% (11/66) for the novel variant, with 6% (4/66) of badgers presenting with coinfection. MusGHV-1 variants were distributed unevenly across the population, with individuals infected with the novel genotype clustered in 3 of 25 contiguous social groups. Individuals infected with the novel variant had significantly higher MusGHV-1 viral loads in their blood (p = 0.002) after adjusting for age (juveniles > adults, p < 0.001) and season (summer > spring and autumn, p = 0.005; mixed-effect linear regression), likely indicating higher virulence of the novel variant. Further genome-wide analyses of MusGHV-1 host resistance genes and host phenotypic variations are required to clarify the drivers and sequelae of this new MusGHV-1 variant.
疱疹病毒是感染大多数动物的普遍存在的病原体。尽管宿主免疫力不断共同进化以对抗病毒毒性,但偶尔会出现具有增强传播性或毒性的病毒变体,从而给宿主种群带来疾病负担。鼬科γ疱疹病毒1(MusGHV-1)是迄今为止在欧洲獾(Meles meles)中鉴定出的唯一疱疹病毒种类。尚未有关于MusGHV-1相关发病机制的报道,但MusGHV-1在生殖道中的重新激活与雌性生殖成功率受损有关。先前对高度保守的DNA聚合酶(DNApol)基因的短序列分析在单个宿主种群中鉴定出了两个变体。在这里,我们使用包含DNApol基因2874个核苷酸的部分序列,比较了来自同一自由放养獾种群的66个已知个体的血液样本中的遗传变异,其中我们鉴定出15个核苷酸差异,导致5个氨基酸差异。常见变体的流行率为86%(59/66),新变体的流行率为17%(11/66),6%(4/66)的獾呈现合并感染。MusGHV-1变体在整个种群中分布不均,感染新基因型的个体聚集在25个相邻社会群体中的3个群体中。在调整年龄(幼年>成年,p<0.001)和季节(夏季>春季和秋季,p=0.005;混合效应线性回归)后,感染新变体的个体血液中的MusGHV-1病毒载量显著更高(p=0.002),这可能表明新变体的毒性更高。需要对MusGHV-1宿主抗性基因和宿主表型变异进行进一步的全基因组分析,以阐明这种新的MusGHV-1变体的驱动因素和后遗症。