The Impact of Athymic Nude Mouse Stock and Colony Source on the Severity of Corynebacterium-Associated Hyperkeratosis

• Published in: Journal of the American Association for Laboratory Animal Science 2025-01, p.1-9
• Main Authors: Michelson, Abigail, Cheleuitte-Nieves, Christopher, Miranda, Ileana C, Ricart Arbona, Rodolfo, Dobtsis, Irina, Wipf, Juliette, Lipman, Neil S
• Format: Article
• Language: English
• ISSN: 1559-6109
• DOI: 10.30802/AALAS-JAALAS-24-100

Corynebacterium bovis (Cb), the etiologic agent of Corynebacterium -associated hyperkeratosis (CAH) in nude mice, may impact research outcomes. Little is known about the differences in the course and severity of CAH in different outbred athymic nude mice stocks. Three genetic stocks (designated A, B, and C), 1 of which was obtained from 2 geographically separate colonies with distinct microbiota (A1 and A2), were inoculated topically with 1 × 10 8 cfu of a pathogenic Cb field isolate (no. 7894; n = 6/stock) or sterile media ( n = 2/stock; controls). Clinical signs were assessed daily and scored 0 to 5 based on lesion severity. Mice were euthanized at 14 (A1, A2, B, and C) or 28 (B) days postinoculation (dpi), macroscopic changes were documented, and 6 skin samples per mouse were obtained and histologically scored 0 to 4 based on the presence and severity of hyperkeratosis, acanthosis, inflammation, and bacterial colonies. No stock A1 or control mice developed clinical disease; 1 of 6 stock B mice developed mild CAH (mean peak clinical score [MPCS]: 0.33) at 14 dpi (14-d group); 2 of 6 stock B (28-d group) developed mild CAH at 15 dpi (MPCS: 0.33); and all stock C and A2 mice developed significant clinical signs at 5 dpi (MPCS: 2.5 and 3, respectively), which resolved by 11 dpi. Despite differences in clinical presentation, all Cb-infected mice had hyperkeratosis and/or acanthosis with associated bacterial colonies. Stocks A1 and B, which had minimal or no clinical signs, were colonized with Corynebacterium amycolatum (Ca). In contrast, stocks C and A2 were not colonized with Ca, raising the possibility that Ca and/or other components of the skin microbiota may mitigate clinical signs but not necessarily all histopathologic changes associated with infection. These findings suggest host genetics and/or the skin microbiota can markedly influence the presentation of CAH in nude mice.