Topic:Contagious Equine Metritis
Contagious Equine Metritis (CEM) is a venereal disease in horses caused by the bacterium Taylorella equigenitalis. It primarily affects the reproductive tract of mares, leading to inflammation and potentially impacting fertility. Stallions can carry the bacterium asymptomatically, acting as vectors for transmission during breeding. Diagnosis of CEM involves bacterial culture, polymerase chain reaction (PCR) testing, and serological assays. Control measures include quarantine, testing, and treatment of infected animals. This page compiles peer-reviewed research studies and scholarly articles that investigate the epidemiology, pathogenesis, diagnostic methods, and management strategies for Contagious Equine Metritis in equine populations.
Serological response in mares affected by contagious equine metritis 1977. A serum agglutination and antiglobulin test is described for the detection of antibodies to the contagious equine metritis organism. A provisional interpretation of the test is proposed and using this interpretation the results of 66 such tests are discussed.
Contagious equine metritis. An outbreak of contagious equine metritis that occurred on stud farms in the Newmarket area during 1977 is described. A Gram-negative coccobacillus was isolated from field cases and the disease was reproduced experimentally by inoculating a pure culture of the organism through the cervix of clean pony mares. Natural spread of the disease occurred by venereal transmission and following the handling, examination or teasing of infected mares. Bacteriological screening of the genital tract of mares and stallions before covering plus stricter standards of hygiene on the stud farms have been recomme...
Nucleotide sequencing and analysis of 16S rDNA and 16S-23S rDNA internal spacer region (ISR) of Taylorella equigenitalis, as an important pathogen for contagious equine metritis (CEM). The primer set for 16S rDNA amplified an amplicon of about 1500 bp in length for three strains of Taylorella equigenitalis (NCTC11184(T), Kentucky188 and EQ59). Sequence differences of the 16S rDNA among the six sequences, including three reference sequences, occurred at only a few nucleotide positions and thus, an extremely high sequence similarity of the 16S rDNA was first demonstrated among the six sequences. In addition, the primer set for 16S-23S rDNA internal spacer region (ISR) amplified two amplicons about 1300 bp and 1200 bp in length for the three strains. The ISRs were estimated to ...