In utero infection of swine fetuses with infectious bovine rhinotracheitis virus (bovine herpesvirus-1)

The pathogenesis of infectious bovine rhinotracheitis (IBR) virus (bovine herpesvirus-1) was studied in porcine fetuses after in utero inoculation. Laparotomies were performed on 8 seronegative pregnant sows at 34 to 86 days of gestation, and all fetuses in 1 uterine horn of each sow were exposed to IBR virus via inoculation into the amniotic sacs. Fetuses in the other horn served as controls. Clinical signs of infection were not observed in the sows, except for 2 sows that aborted at postinoculation days (PID) 11 and 15. Fetuses of the remaining 6 sows were collected at slaughter on PID 15 to 28. Fetuses were examined for gross abnormalities, presence of IBR virus in tissues, and the formation of neutralizing antibodies to IBR virus. Of 33 inoculated fetuses from 6 sows, 10 were mummified, 11 were hemorrhagic and/or edematous, and 12 were alive. Necrotic lesions were observed on the skin and in the liver of dead and live fetuses. Virus was recovered from 29 of 33 inoculated fetuses. Infectious bovine rhinotracheitis virus was isolated from fetal skin, liver, lungs, kidney, spleen, stomach contents, brain, amniotic fluid, and placenta. Virus was isolated from 4 of 11 fetuses recovered from 1 aborting sow. Antibodies to IBR virus were not detected in sera from the sows. However, antibodies were detected in 6 of 15 fetuses inoculated at 63 to 86 days of gestation and collected at slaughter at 86 to 112 days of gestation. The youngest fetus with detectable IBR antibody was estimated to be 74 days of gestation by measuring crown-rump length of the fetus.     

The influence of premating feed intake on the reproductive performance of gilts.

In an attempt to improve the reproductive performance of gilts mated at puberty, 70 Yorkshire x Landrace gilts were allocated at 120 d of age and 60 kg body weight to one of two treatments. Restricted gilts were fed 2.0 kg d-1 of a diet formulated to provide 18% crude protein and 14.5 MJ DE kg-1 from selection until mated at their first estrus (n = 35). Flushed gilts were fed 2.0 kg d-1 of the same diet from 120 to 150 d of age, but then had their feed intake increased to 3.5 kg d-1 until mated at their first estrus (n = 35). An additional group of gilts (control fed; n = 33) were fed 3.0 kg d-1 from selection until they were bred at their third estrus in order to investigate the influence of feed restriction on the onset of puberty. During gestation all gilts were fed 1.8 to 2.2 kg d-1 of a 16.8% crude protein diet having 13.7 MJ DE kg-1. Control fed gilts were younger (p less than 0.05) at puberty (150 d) than restricted (165 d) or flushed gilts (165 d). There was no difference in subsequent litter size between the restricted and flushed gilts (7.7 and 8.0, respectively). It is concluded that the institution of a flushing nutritional regime in the prepubertal period will not enhance piglet production from gilts mated at puberty.     

Development of a computerized systems model for health management decision support in growing hogs

A study was designed to provide decision support for health management in growing hogs. A dynamic, stochastic systems model for a confinement, continuous production hog growing enterprise (including nursery, grower and finisher phases) was developed to simulate the economic effects of disease, available floor space and feed additives using farm- specific data. Modeling techniques included: discrete and distributed (continuous) delays; triangular probability density functions; autocorrelation; table look-up functions; an alpha-beta tracker; non-linear, constrained optimization. The model was designed to be initialized with the system's current status, using an accompanying production/financial database to achieve individual-farm specificity. Initialization of rate variables required ‘reverse optimization’ of historical system performance. Model predictions are based on an adjustment approach, where changes in current performance are dictated by changes in disease rates, available floor space and feed additive use. These effects vary randomly, but are autocorrelated between production phases, between similar diseases and over time.     

Antigen-specific proliferation and activation of peripheral blood mononuclear cells from Mycobacterium bovis-infected reindeer

To evaluate antigen-specific proliferative and activation-associated responses from Mycobacterium bovis-infected reindeer, blood mononuclear cells from M. bovis- (n = 10) and non-infected reindeer (n = 4) were stimulated with a recombinant early secretory antigenic target-6 and culture filtrate protein-10 fusion protein (rESAT6:CFP10), M. bovis purified protein derivative, pokeweed mitogen, or medium alone and evaluated by flow cytometry using dye tracker analysis and cell surface marker staining. gammadelta TCR+ and CD8+ cells, but not CD4+ cells, from M. bovis-infected reindeer proliferated in response to specific antigen stimulation. Expression (i.e., mean fluorescence intensity) of CD44 was increased and CD62L decreased on proliferative as compared to non-proliferative fractions in antigen- and mitogen-stimulated cultures. In response rESAT6:CFP10 stimulation, MHC II fluorescence intensity was increased on CD4+, gammadelta TCR+, CD172a+, and IgM+ cells from infected reindeer as compared to that of non-stimulated cells from the same reindeer. Recombinant ESAT6:CFP10 stimulation also induced expansion of a CD172a+, MHC II+ population within mononuclear cell cultures from M. bovis-infected reindeer. Despite a moderate challenge dose and extended duration of incubation, experimental infection of reindeer was generally limited to lymph nodes draining the inoculation site, suggestive of host resistance to progressive disease. Present in vitro findings, therefore, may be predictive of host responses by reindeer that limit progression to disseminated disease.     

Characterization of turkey coronavirus from turkey poults with acute enteritis.

The present study was to characterize turkey coronavirus associated with turkey poult enteritis and mortality. Intestinal contents or intestines from affected turkey poults and inoculated turkey embryos contained coronaviruses as revealed by electron microscopy or were positive for turkey coronavirus by immunofluorescent antibody assay. Sucrose density gradient ultracentrifugation of the virus-containing intestinal homogenate yielded two opalescent bands corresponding to the buoyant densities of 1.14-1.15 and 1.18-1.20 g/ml, respectively. Coronaviral particles from intestinal contents or the sucrose density gradient preparation were mainly spherical in shape and had envelope and central depression. They were surrounded by a fringe of regularly spaced petal-shaped projections attached to the particles by a short stalk. Purified viruses hemagglutinated rabbit erythrocytes with a titer of 16. Major protein bands of purified viruses analyzed by SDS-PAGE were located at 200, 100-110, 50-60, and 30-35 kDa. The patterns of protein bands were consistent with those of Minnesota or Quebec turkey coronavirus isolates. A 568 bp nucleotide fragment of turkey coronavirus spike protein gene was amplified from RNA of inoculated turkey embryo intestine or purified virus. Sequence analysis of the 568 bp PCR product revealed high degree of identity with the corresponding spike protein gene sequence of human and bovine coronaviruses. The results indicated that turkey coronavirus was associated with turkey poults with acute enteritis.     

不同方法控制PRRS病毒的实践经验

上期回顾：为了在 PRRS疫情爆发期间更好地控制猪群临床疾病,上期从传播途径和保护免疫力方面,详细介绍了PRRS循环爆发的观点及猪场控制的方法。     

Influence of Land-Use Legacies Following Shrub Reduction and Seeding of Big Sagebrush Sites

Big sagebrush (Artemisia tridentata Nutt.) plant communities often require management to reduce shrub density and rehabilitate understory vegetation. We studied vegetation responses to a two-way chain harrow treatment and broadcast seeding of 12 herbaceous species at eight Wyoming big sagebrush (A. tridentata Nutt. subsp. wyomingensis Beetle & Young) sites. These sites differed in land-use history; five were cultivated for dryland wheat production during the 1950 ? 1980s and then seeded with introduced forage grasses (C-S), while three had not been exposed to this land-use legacy (non C-S). Our objective was to evaluate whether the C-S legacy influences the magnitude of vegetation change following contemporary treatment. Before treatment, C-S sites had lower sagebrush cover, higher dead sagebrush cover, and higher broom snakeweed (Gutierrezia sarothrae [Pursh] Britton & Rusby) cover than adjacent non C-S sites. Plant community change 3 years after treatment, determined with multivariate ordination analysis of species composition, varied between site histories, and response to treatment was most strongly correlated with reductions in sagebrush cover, increases in perennial grasses, and increases in 10 other herbaceous species—including some undesirable species and four that were seeded in 2010. Five years after treatment, mature sagebrush cover remained reduced for both land-use histories, yet density of sagebrush seedlings and broom snakeweed increased in C-S sites during the second and third years after treatment. In addition, perennial forb cover increased for C-S sites, while perennial grass biomass increased for non C-S sites. Our results emphasize that broad variability in plant community responses to sagebrush reduction and seeding is possible within the same ecological site classification and that legacy effects due to the combination of past cultivation and seeding should be considered when planning restoration projects, including the consideration that seeding may not always be necessary on C-S sites.     

Swine diseases transmissible with artificial insemination

The transport of fresh and frozen semen to be used for artificial insemination creates a mode of disease transmission between farms. Normally, semen contains a number of nonpathogenic bacterial contaminants; however, excessive bacterial contamination can result in infertile matings. Contamination with a known pathogen, eg, Brucella suis, could initiate a serious outbreak of disease in a recipient herd. Methods to minimize bacterial contamination of semen include sanitary collecting and processing of semen, isolation of boards from certain pathogens, and the addition of appropriate broad spectrum or combination antibiotics to the semen. Mycoplasmas also have been isolated from semen, although transmission by this route is unlikely. The addition of an appropriate antimycoplasmal antibiotic to semen may be warranted in some situations. Numerous viruses have been detected in semen. Their exclusion from semen is especially critical because of their ability to survive in frozen semen. These viruses include pseudorabies virus, porcine parvovirus, enterovirus, adenovirus, vesicular disease virus, and African swine fever virus. The likelihood of disease transmission is greater with the introduction of a boar into a herd than through the use of fresh or frozen semen. We believe that artificial insemination allows for the introduction of new genetics into a breeding program, with minimal risk of disease transmission.