Kondo Yume, Komiya Tomoyoshi
Faculty of Health and Medical Sciences, Hokuriku University, 1-1, Taiyogaoka, Kanazawa 920-1180, Ishikawa, Japan.
Trop Med Infect Dis. 2024 May 16;9(5):117. doi: 10.3390/tropicalmed9050117.
Japanese encephalitis virus (JEV) has a positive-sense single-stranded RNA genome and belongs to the genus of the family . Persistent JEV infection was previously shown in pig blood cells, which act as a natural reservoir of this virus. We aimed to determine the pathogenicity factors involved in persistent JEV infection by analyzing the pathogenicity and genome sequences of a virus isolated from a persistent infection model. We established persistent JEV infections in cells by inoculating mouse fetus primary cell cultures with the Beijing-1 strain of JEV and then performing repeated infected cell passages, harvesting viruses after each passage while monitoring the plaque size over 100 generations. The virus growth rate was compared among Vero, C6/36, and Neuro-2a cells. The pathogenicity was examined in female ICR mice at several ages. Additionally, we determined the whole-genome sequences. The 134th Beijing-1-derived persistent virus (ME134) grew in Vero cells at a similar rate to the parent strain but did not grow well in C6/36 or Neuro-2a cells. No differences were observed in pathogenicity after intracerebral inoculation in mice of different ages, but the survival time was extended in older mice. Mutations in the persistent virus genomes were found across all regions but were mainly focused in the NS3, NS4b, and 3'NCR regions, with a 34-base-pair deletion found in the variable region. The short deletion in the 3'NCR region appeared to be responsible for the reduced pathogenicity and growth efficiency.
日本脑炎病毒(JEV)具有正链单链RNA基因组,属于 科的 属。先前已在猪血细胞中发现JEV持续感染,猪血细胞是该病毒的天然宿主。我们旨在通过分析从持续感染模型中分离出的病毒的致病性和基因组序列,确定参与JEV持续感染的致病因素。我们通过用JEV北京-1株接种小鼠胎儿原代细胞培养物,然后进行反复的感染细胞传代,在每次传代后收获病毒,同时监测100代以上的噬斑大小,从而在细胞中建立JEV持续感染。比较了Vero、C6/36和Neuro-2a细胞中的病毒生长速率。在几个年龄段的雌性ICR小鼠中检测了致病性。此外,我们还确定了全基因组序列。第134代北京-1衍生的持续病毒(ME134)在Vero细胞中的生长速率与亲本毒株相似,但在C6/36或Neuro-2a细胞中生长不佳。在不同年龄的小鼠脑内接种后,未观察到致病性差异,但老年小鼠的存活时间延长。在持续病毒基因组的所有区域均发现了突变,但主要集中在NS3、NS4b和3'NCR区域,在可变区域发现了一个34个碱基对的缺失。3'NCR区域的短缺失似乎是致病性和生长效率降低的原因。