Affiliation:
1. Department of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, Alabama
Abstract
ABSTRACT
We investigated the acquisition and prevalence of
Chlamydophila
sp. infection in calves. Specimens were collected at weekly intervals from birth to week 12 postpartum from 40 female Holstein calf-dam pairs in a dairy herd. Real-time PCR detected, quantified, and differentiated
Chlamydophila
23S rRNA gene DNA from vaginal cytobrush swabs and milk samples. Chemiluminescence enzyme-linked immunosorbent assay with lysed
Chlamydophila abortus
or
Chlamydophila pecorum
elementary body antigens quantified antibodies against
Chlamydophila
spp. in sera.
Chlamydophila
sp. DNA was found in 61% of calves and 20% of dams in at least one positive quantitative PCR. In calves, clinically inapparent
C. pecorum
infection with low organism loads was fivefold more prevalent than
C. abortus
infection and was most frequently detected by vaginal swabs compared to rectal or nasal swabs. In dams,
C. abortus
dominated in milk and
C. pecorum
dominated in the vagina. The group size of calves correlated positively (
P
< 0.01) with
Chlamydophila
infection in quadratic, but not linear, regression. Thus, a doubling of the group size was associated with a fourfold increase in frequency and intensity of
Chlamydophila
infection. For groups of 14 or 28 calves, respectively, logistic regression predicted a 9 or 52% probability of infection of an individual calf and a 52 or 99.99% probability of infection of the group. Anti-
Chlamydophila
immunoglobulin M antibodies in
Chlamydophila
PCR-positive calves and dams and in dams that gave birth to calves that later became positive were significantly higher than in PCR-negative animals (
P
≤ 0.02). Collectively, crowding strongly enhances the frequency and intensity of highly prevalent
Chlamydophila
infections in cattle.
Publisher
American Society for Microbiology
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