Desaibeyer0191

Salmonella Indiana has emerged in recent years as an important zoonotic pathogen, but its pathogenicity has not been fully elucidated. In this study, using in vivo and in vitro animal and cellular experimental model systems, we evaluated the pathogenicity of Salmonella Indiana (S. Indiana) compared with three other serotypes of Salmonella, S. Enteritidis, S. Typhimurium and S. Thompson. The animal experiments included observations of clinical symptoms, pathological changes and determination of median lethal dose in mice. The adhesion and invasiveness and intracellular proliferative capacity of Salmonella in vitro were measured with the murine macrophage-like cell line RAW264.7 cells and the human colon adenocarcinoma cell line Caco-2 cells. The results of animal experiments showed that S. Indiana, S. Enteritidis, S. Typhimurium and S. Thompson caused histopathological changes in most organs to varying degrees, primarily in the liver and intestine of mice. The gross lesions included white necrotic foci on the teritidis, and was similar to that of S. Thompson.Members of the Mycobacterium tuberculosis complex (MTBC) are responsible for tuberculosis in several mammals. In this complex, Mycobacterium tuberculosis and Mycobacterium bovis, which are closely related, show host preference for humans and cattle, respectively. Although human and bovine tuberculosis are clinically similar, M. tuberculosis mostly causes latent infection in humans, whereas M. bovis frequently leads to an acute infection in cattle. This review attempts to connect the pathology in experimental animal models as well as the cellular responses to M. bovis and M. tuberculosis regarding the differences in protein expression and regulatory mechanisms of both pathogens that could explain their apparent divergent latency behaviour. The occurrence of latent bovine tuberculosis (bTB) would represent a serious complication for the eradication of the disease in cattle, with the risk of onward transmission to humans. Thus, understanding the physiological events that may lead to the state of latency in bTB could assist in the development of appropriate prevention and control tools.The primary objective of this study was to determine the distribution of major pathogens causing mastitis and analyze the association of the main pathogens with the type of milk milk samples collected from cows with mastitis of different severities, which consisted of subclinical mastitis (Lanzhou Mastitis Test weak positive, positive, and strong positive) and clinical mastitis, region, season, bedding material, parity and lactation stage on large dairy farms. Fifteen large dairy farms in twelve major milk-producing provinces of China were enrolled in the study for approximately one year; 1,153 mastitis milk samples were collected and processed. The most frequently isolated pathogens were Staphylococcus spp. (39.03 %), Streptococcus spp. RGT-018 concentration (11.01 %), Bacillus spp. (8.24 %), Aerococcus viridans (6.76 %), and Acinetobacter spp. (3.38 %), and most of these pathogens were environmental bacteria (67.53 %). Contagious pathogens (Staphylococcus aureus and Streptococcus agalactiae) were more prevalent in milk samples from bovine clinical mastitis cases than in milk samples from bovine subclinical mastitis cases. The percentages of Staphylococcus spp. and Bacillus spp. might be higher in northeastern farms than in farms located in other regions. A higher percentage of Staphylococcus spp. was observed in summer, while a lower proportion of Streptococcus spp. was detected in fall. Streptococcus agalactiae and Streptococcus uberis were more frequently isolated in farms using sand bedding, whereas Staphylococcus aureus, Staphylococcus haemolyticus and Bacillus licheniformis were more prevalent in farms using organic bedding. No obvious associations were found between the main mastitis pathogens and parity or lactation stage. Based on these findings, the dominant pathogens, types of milk, regions, seasons and bedding materials should be considered when designing mastitis prevention and control programs at large Chinese dairy farms.Porcine circovirus type 3 (PCV3) infection causes substantial economic losses in pig populations since its discovery in 2016. However, PCV3 molecular epidemiology remains need further study. In order to assess the prevalence of PCV3 infection in China, 4094 clinical samples from 271 pig farms in 10 provinces of China were evaluated by PCR. It was shown that the overall prevalence of PCV3 infection was 29.3 % (1200/4094) and 74.2 % (201/271) at sample and farm levels respectively, suggesting that PCV3 infection is prevalent in China. Furthermore, a statistical analysis showed PCV3 might exacerbate PCV2 and PRRSV infection rate and have a potential association with pig clinical disease. In addition, we sequenced the entire genome of 57 PCV3 strains; homology analysis showed that PCV3 strains have more than 96 % similarities at the nucleotide level, and PCV3 shares less than 60 % similarities with other circoviruses. By comparing the total 673 PCV3 strains from the NCBI GenBank, we found the major of amino acid mutations are located in predicted epitope regions and the mutations ratio changed during PCV3 evolution. Phylogenetic analysis revealed that all isolates belonged to PCV3a and PCV3b, and increasing PCV3a and decreasing PCV3b trends were observed during PCV3 evolution. Overall, this study provides important insights for understanding PCV3 prevalence, pathogenesis, and evolution and will guide future efforts to develop effective preventive and control measures.In piglets, Clostridioides (C.) difficile infection presents mostly subclinical manifestation. As this agent became important in veterinary medicine due to a hypothesis of zoonosis, the objective of this study was to evaluate the transmission of C. difficile by nose-to-nose contact in young piglets. Six 20-day-old piglets were separated into three groups (infected, sentinel and control), and distributed in different isolation cabinets which allowed nose-to-nose contact only between infected and sentinel groups. The challenged group received an inoculum 106 CFU/mL of C. difficile 096 by oropharyngeal route. Rectal swab samples were daily collected for microbiological and molecular analysis. Euthanasia of all piglets was performed 18 days after challenge to evaluate anatomical, histological and microbiological lesions of the organs of these animals. The challenged and sentinel groups showed clinical signs of infection and genes encoding TcdB were detected by conventional PCR in both groups, confirming the transmission of the pathogen from the challenged to the sentinel piglets.