Search Results (3)

Chronic non-specific contamination of the reproductive tract in animals is a major issue during early postpartum, natural coitus, or artificial insemination. Uterine infection is one of the major concerns reducing fertility, production loss, and early culling of the animals. Therefore, the aim of this study was to identify any novel bacterium if present in the uterine environment of Bubalus bubalis causing infections. A strictly anaerobic bacterial strain designated as Paraclostridium bifermentans GBRC was isolated and characterized. Bacterium was found to be Gram positive moderate rod with motility. The optimum growth was observed at 40 ± 2 °C. The pathogenic characteristics of the GBRC strain, such as hemolysis, gelatin hydrolysis, and the production of volatile sulfur compounds, were similar to those seen in the epithelial layer invading pathogenic strains. Assembled genome size was 3.6 MB, with 78 contigs, and a G + C content of 28.10%. Furthermore, the whole genome sequence analysis confirmed the presence of genes encoding virulence factors and provided genomic insights on adaptation of the strain in the uterine environment. Based on the phenotypic and genetic differences with phylogenetic relatives, strain GBRC is proposed to represent a first reported species of the genus Paraclostridium with potential pathogenic character, from the buffalo uterine environment. This study analysis of the GBRC strain serves as a key reference point for the investigation of potential pathogenic strains that may cause endometritis and metritis in bovine. Full article

Conventional practice is to breed sows by artificial insemination (AI) at least twice using approximately three billion sperm per insemination upon estrus at standing heat. This research explored the use of combined technologies, including fixed-time insemination (FTAI) and an alternative catheter design that reportedly reduces semen backflow, in order to reduce the number of inseminations and the semen dosage and maintain reproductive efficiency. The FTAI technique used in this study was to inject I.M. 600 IU equine chorionic gonadotropin (eCG) at weaning and 5 mg porcine luteinizing hormone (pLH) to stimulate ovulation 80 h later, followed by a single insemination 36 h after the pLH injection. The two catheters used in this study were a conventional foam-tipped insemination catheter and a Gedis catheter. The Gedis catheter is designed to be completely inserted into the vagina. The semen is enclosed along the length of the rod and held in place by a gel cap that melts when inserted into the cervix. Sows were assigned to the following treatments: Group 1 (n = 135), bred twice with a conventional catheter and a standard semen dose of approximately three billion sperm in 80 mL; Group 2 (n = 123), FTAI with conventional catheter and a standard semen dose; Group 3 (n = 127), FTAI with Gedis catheter and a standard semen dose; Group 4 (n = 126), FTAI with Gedis catheter and a reduced semen dose with one billion sperm. The farrowing rates were 81.6%, 77.7%, 74.0%, and 62.7% for Groups 1 to 4, respectively. The likelihood of farrowing was lower for Group 3 and Group 4 compared to Group 1 (odds ratio (OR) = 0.57; p = 0.08 and OR = 0.35; p = 0.001, respectively). Likewise, litter size of Group 3 and Group 4 was smaller than Group 1 (p = 0.006 and p = 0.04, respectively). Overall, the combination of Gedis catheter and FTAI resulted in decreased reproductive performance that outweighed the value of using less semen. Full article

The Glossina hytrosavirus (family Hytrosaviridae) is a double-stranded DNA virus with rod-shaped, enveloped virions. Its 190 kbp genome encodes 160 putative open reading frames. The virus replicates in the nucleus, and acquires a fragile envelope in the cell cytoplasm. Glossina hytrosavirus was first isolated from hypertrophied salivary glands of the tsetse fly, Glossina pallidipes Austen (Diptera; Glossinidae) collected in Kenya in 1986. A certain proportion of laboratory G. pallidipes flies infected by Glossina hytrosavirus develop hypertrophied salivary glands and midgut epithelial cells, gonadal anomalies and distorted sex-ratios associated with reduced insemination rates, fecundity and lifespan. These symptoms are rare in wild tsetse populations. In East Africa, G. pallidipes is one of the most important vectors of African trypanosomosis, a debilitating zoonotic disease that afflicts 37 sub-Saharan African countries. There is a large arsenal of control tactics available to manage tsetse flies and the disease they transmit. The sterile insect technique (SIT) is a robust control tactic that has shown to be effective in eradicating tsetse populations when integrated with other control tactics in an area-wide integrated approach. The SIT requires production of sterile male flies in large production facilities. To supply sufficient numbers of sterile males for the SIT component against G. pallidipes, strategies have to be developed that enable the management of the Glossina hytrosavirus in the colonies. This review provides a historic chronology of the emergence and biogeography of Glossina hytrosavirus, and includes researches on the infectomics (defined here as the functional and structural genomics and proteomics) and pathobiology of the virus. Standard operation procedures for viral management in tsetse mass-rearing facilities are proposed and a future outlook is sketched. Full article