Genomic Mutations in SARS-CoV-2 Genome following Infection in Syrian Golden Hamster and Associated Lung Pathologies

• Published in: Pathogens (Basel) 2023-11, Vol.12 (11), p.1328
• Main Authors: Rudramurthy, Gudepalya Renukaiah, Naveenkumar, Chakenahalli N, Bharathkumar, Kumaraswamy, Shandil, Radha K, Narayanan, Shridhar
• Format: Article
• Language: English
• Subjects: Accumulation; Alveoli; ancestral Wuhan strain; Animals; Antibodies; antiviral; Antiviral agents; COVID-19; COVID-19 vaccines; Cross-protection; Degeneration; Development and progression; Disease transmission; Edema; Effectiveness; Epithelium; Females; Gene mutations; Genetic aspects; Genomes; Genomics; Hamsters; Histopathology; Immune response; Immune response (humoral); Infections; Inflammation; Lung diseases; Lungs; Males; Mutation; Necrosis; Next-generation sequencing; NGS; Nucleotides; Pandemics; Physiological aspects; Proteins; S protein; Severe acute respiratory syndrome coronavirus 2; Single-nucleotide polymorphism; Vaccines; Viral diseases; Virus research; Viruses
• ISSN: 2076-0817; 2076-0817
• DOI: 10.3390/pathogens12111328

The continuous evolution of the SARS-CoV-2 virus led to constant developments and efforts in understanding the significance and impacts of SARS-CoV-2 variants on human health. Our study aimed to determine the accumulation of genetic mutations and associated lung pathologies in male and female hamsters infected with the ancestral Wuhan strain of SARS-CoV-2. The present study showed no significant difference in the viral load between male and female hamsters and peak infection was found to be on day four post infection in both sexes of the animals. Live virus particles were detected up to 5 days post infection (dpi) through the TCID-50 assay, while qRT-PCR could detect viral RNA up to 14 dpi from all the infected animals. Further, the determination of the neutralizing antibody titer showed the onset of the humoral immune response as early as 4 dpi in both sexes against SARS-CoV-2, and a significant cross-protection against the delta variant of SARS-CoV-2 was observed. Histopathology showed edema, inflammation, inflammatory cell infiltration, necrosis, and degeneration of alveolar and bronchial epithelium cells from 3 dpi to 14 dpi in both sexes. Furthermore, next-generation sequencing (NGS) showed up to 10 single-nucleotide polymorphisms (SNPs) in the SARS-CoV-2 (ancestral Wuhan strain) genome isolated from both male and female hamsters. The mutation observed at the 23014 position (Glu484Asp) in the SARS-CoV-2 genome isolated from both sexes of the hamsters plays a significant role in the antiviral efficacy of small molecules, vaccines, and the Mabs-targeting S protein. The present study shows that either of the genders can be used in the pre-clinical efficacy of antiviral agents against SARS-CoV-2 in hamsters. However, considering the major mutation in the S protein, the understanding of the genetic mutation in SARS-CoV-2 after passing through hamsters is crucial in deciding the efficacy of the antiviral agents targeting the S protein. Importance: Our study findings indicate the accumulation of genomic mutations in SARS-CoV-2 after passing through the Syrian golden hamsters. Understanding the genomic mutations showed that either of the hamster genders can be used in the pre-clinical efficacy of antiviral agents and vaccines.