Establishing the Median Infectious Dose (ID₅₀) and Characterizing the Clinical Manifestations of Mouse, Rat, Cow, and HumanCorynebacterium bovisIsolates in Select Immunocompromised Mouse Strains

Corynebacterium bovis(Cb), the etiology of hyperkeratotic dermatitis in various immunocompromised mouse strains, significantly impacts research in which infected mice are used. Although Cb has been isolated from a variety of species, including mice, rats, cows, and humans, little is known about the differences in the infectivity and clinical disease in mice associated with unique isolates. The infectious dose yielding colonization of 50% of the exposed population (ID50) and any associated clinical disease was determined for mouse (n=3), rat (n=1), cow (n=1), and human (n=2) Cb isolates in athymic nude mice (Hsd:Athymic Nude-Foxn1nu). The same investigations were undertaken comparing 2 of these murine isolates in 2 furred immunocompromised mouse strains (NSG [NOD.Cg-PrkdcscidIl2rgtm1Wjl/Sz] and NSG-S [NOD.Cg-PrkdcscidIl2rgtm1WjlTg(CMV-IL3,CSF2,KITLG)1Eav/MloySzJ]). To determine the ID50, mice (n=6/dose; 3 of each sex) were inoculated topically with 1 to 108bacteria (10-fold increments) of each Cb isolate. Mice were scored (0 to 5) daily based on the severity of clinical signs for 14 days. On day 7 and 14 post-inoculation (PI), buccal and dorsal skin swabs were evaluated by aerobic culture to determine infection status. The mouse isolates yielded a lower ID50(58 to 1,000 bacteria) as compared to the bovine (6,460 to 7,498 bacteria) and rat (10,000 bacteria) Cb isolates. Mice were not colonized and disease did not result when inoculated with human isolates. Mouse isolates produced varying clinical disease severity in nude mice (max score/isolate: 0 to 5). Despite significant immunodeficiency, furred NSG and NSG-S mice required a considerably higher (1,000- to 3,000-fold) inoculum to become colonized as compared to athymic nude mice. Once colonized, clinically detectable hyperkeratosis did not develop in these strains until 18 to 22 days PI. In contrast, in athymic nude mice that developed clinically detectable disease, hyperkeratosis was observed 6 to 14 days PI. In conclusion, there are significant differences in Cb’s ID50, disease course, and severity between Cb isolates and among immunodeficient mouse strains.