Effective Infection with Dengue Virus in Experimental Neonate and Adult Mice through the Intranasal Route

• Published in: Viruses Vol. 14; no. 7; p. 1394
• Main Authors: Qiu, Minyue, Zhao, Lixin, Zhang, Junjie, Wang, Yalan, Liu, Minchi, Hua, Dong, Ding, Xiaoyan, Zhou, Xiaoyang, Zeng, Jie, Yan, Huacheng, Li, Jintao
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 26.06.2022; MDPI
• Subjects: A6 mice; Blood transfusion; Brain; Care and treatment; Control; Dengue fever; Dengue hemorrhagic fever; dengue virus; Dengue viruses; DENV-2; Diagnosis; Encephalitis; Epidemics; Genomes; Hemorrhagic fever; Homology; Identification and classification; Immunodeficiency; Infections; Infectivity; Inoculation; intranasal route; Laboratory animals; neonate mice; Patient outcomes; Spleen; Suckling behavior; Transplantation; Transplantation of organs, tissues, etc; Tropism; Vectors; Viremia; Viruses; West Nile virus; α-Interferon; China; United Kingdom > UK; United States > US; Japan
• DOI: 10.3390/v14071394
• ISSN: 1999-4915

Dengue virus, the causative agent of dengue fever, life-threatening hemorrhagic fever, and shock syndrome, is mainly transmitted to humans through mosquito vectors. It can also be transmitted through atypical routes, including needle stick injury, vertical transmission, blood transfusion, and organ transplantation. In addition, sporadic cases which have no clear infectious causes have raised the respiratory exposure concerns, and the risks remain unclear. Here, we analyze the respiratory infectivity of the dengue virus in BALB/c suckling and adult immunodeficient mice by the intranasal inoculation of dengue virus serotype 2. The infected mice presented with clinical symptoms, including excitement, emaciation, malaise, and death. Viremia was detected for 3 days post inoculation. Histopathological changes were observed in the brain, liver, and spleen. The virus showed evident brain tropism post inoculation and viral loads peaked at 7 days post inoculation. Furthermore, the virus was isolated from the infected mice; the sequence homology between the origin and isolates was 99.99%. Similar results were observed in adult IFN-α/β receptor-deficient mice. Overall, dengue virus can infect suckling mice and adult immune-deficient mice via the nasal route. This study broadens our perception of atypical dengue transmission routes and provides evidence of nasal transmission of dengue virus in the absence of mosquito vectors.