Peña José, Chen-Harris Haiyin, Allen Jonathan E, Hwang Mona, Elsheikh Maher, Mabery Shalini, Bielefeldt-Ohmann Helle, Zemla Adam T, Bowen Richard A, Borucki Monica K
Lawrence Livermore National Laboratory, Livermore, CA, USA.
Australian Infectious Diseases Research Centre, University of Queensland , Brisbane, Australia; and.
Virus Evol. 2016 Apr 9;2(1):vew008. doi: 10.1093/ve/vew008. eCollection 2016 Jan.
serial passage of non-pathogenic viruses has been shown to lead to increased viral virulence, and although the precise mechanism(s) are not clear, it is known that both host and viral factors are associated with increased pathogenicity. Under- or overnutrition leads to a decreased or dysregulated immune response and can increase viral mutant spectrum diversity and virulence. The objective of this study was to identify the role of viral mutant spectra dynamics and host immunocompetence in the development of pathogenicity during passage. Because the nutritional status of the host has been shown to affect the development of viral virulence, the diet of animal model reflected two extremes of diets which exist in the global population, malnutrition and obesity. Sendai virus was serially passaged in groups of mice with differing nutritional status followed by transmission of the passaged virus to a second host species, guinea pigs. Viral population dynamics were characterized using deep sequence analysis and computational modeling. Histopathology, viral titer and cytokine assays were used to characterize viral virulence. Viral virulence increased with passage and the virulent phenotype persisted upon passage to a second host species. Additionally, nutritional status of mice during passage influenced the phenotype. Sequencing revealed the presence of several non-synonymous changes in the consensus sequence associated with passage, a majority of which occurred in the hemagglutinin-neuraminidase and polymerase genes, as well as the presence of persistent high frequency variants in the viral population. In particular, an N1124D change in the consensus sequences of the polymerase gene was detected by passage 10 in a majority of the animals. comparison of an 1124D plaque isolate to a clone with 1124N genotype indicated that 1124D was associated with increased virulence.
已证明非致病性病毒的连续传代可导致病毒毒力增强,尽管确切机制尚不清楚,但已知宿主和病毒因素均与致病性增加有关。营养不足或过剩会导致免疫反应降低或失调,并可能增加病毒突变谱的多样性和毒力。本研究的目的是确定病毒突变谱动态变化和宿主免疫能力在传代过程中致病性发展中的作用。由于已证明宿主的营养状况会影响病毒毒力的发展,因此动物模型的饮食反映了全球人群中存在的两种极端饮食情况,即营养不良和肥胖。将仙台病毒在营养状况不同的小鼠组中连续传代,然后将传代后的病毒传播给第二种宿主动物豚鼠。使用深度序列分析和计算模型来表征病毒种群动态。通过组织病理学、病毒滴度和细胞因子检测来表征病毒毒力。病毒毒力随传代而增加,并且毒力表型在传代至第二种宿主动物后持续存在。此外,传代过程中小鼠的营养状况影响了表型。测序揭示了与传代相关的共有序列中存在几种非同义变化,其中大多数发生在血凝素神经氨酸酶和聚合酶基因中,并且病毒种群中存在持续的高频变异。特别是,在大多数动物传代至第10代时,在聚合酶基因的共有序列中检测到N1124D变化。将1124D噬斑分离株与具有1124N基因型的克隆进行比较表明,1124D与毒力增加有关。