Establishment and Comparison of Pathogenicity and Related Neurotropism in Two Age Groups of Immune Competent Mice, C57BL/6J Using an Indian Isolate of Chikungunya Virus (CHIKV)

• Published in: Viruses Vol. 11; no. 6; p. 578
• Main Authors: Jain, Jaspreet, Narayanan, Vimal, Kumar, Ankit, Shrinet, Jatin, Srivastava, Priyanshu, Chaturvedi, Shivam, Sunil, Sujatha
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 25.06.2019; MDPI
• Subjects: Age; Age groups; animal model; Animals; Arthritis; Asymptomatic; Asymptomatic infection; C57BL/6J mice; Chikungunya virus; Chronic illnesses; Chronic infection; Clinical isolates; Disease; disease progression; Encephalitis; Epidemics; Genotypes; Immune clearance; Infections; Morbidity; Pathogenesis; Pathogenicity; Population studies; Public health; Vaccines; Viruses; Young adults; Germany; pathogenicity; C57BL/6J mice; chikungunya virus; disease progression; animal model
• ISSN: 1999-4915; 1999-4915
• DOI: 10.3390/v11060578

Chikungunya (CHIK) is a febrile arboviral illness caused by chikungunya virus (CHIKV) and has been identified in more than 60 countries across the globe. A major public health concern, the infection occurs as an acute febrile phase and a chronic arthralgic phase. The disease manifests differently in different age groups that can range from asymptomatic infection in the younger age group to a prolonged chronic phase in the elderly population. The present study was undertaken to evaluate strain-specific pathogenesis of ECSA genotype of CHIKV strains derived from clinical isolates in adult C57BL/6J mice model. The strain that was pathogenic and developed distinct acute and post-acute phase of CHIK infection was further evaluated for dose-dependent pathogenesis. Upon arriving on the optimal dose to induce clinical symptoms in the mice, the disease progression was evaluated across the acute and the post-acute phase of infection for a period of 15 days post-infection in two age groups of mice, namely eight weeks old and 20 weeks old mice groups. Biochemical, hematological, and virology attributes were measured and correlated to morbidity and linked neurotropism and limb thickness in the two age groups. Our results show that CHIKV exhibit strain-specific pathogenesis in C57BL/6J mice. Distinct dissimilarities were observed between the two age groups in terms of pathogenesis, viral clearance and host response to CHIKV infection.