Health advantages of transition to batch management system in farrow-to-finish pig herds

Sow batch management systems have become more popular due to advantages in labour planning, piglet batch sizes, all-in all-out practices and health management. The present study investigated the potential health advantages of 10 selected farrow-to-finish pig herds before and after transition from a one week batch management system to a four or five week batch management system. Five different animal categories (gilts, sows, piglets, growers and finishers) were sampled at three time points (T0, T1 and T2) before and after transition to a four or five week batch management system. Different matrices of the animals were collected: blood, nasal swabs and faeces. Several economically important diseases were monitored through serology: Lawsonia intracellularis, Porcine Reproductive and Respiratory Syndrome virus (PRRSv), Mycoplasma hyopneumoniae, Actinobacillus pleuropneurnoniae; and PCR-testing: Pasteurella multocida dermonecrotic toxin (DNT) and Brachyspira species, especially the major pathogenic Brachyspira hyodysenteriae. Following serological analysis, the percentage of positive animals per category and sampling occasion were calculated. Health improvement based on serology was defined as the reduction in the percentage of positive animals for a specific disease in a specified animal category. All samples were negative for P. multocida DNT and B. hyodysenteriae. Little to no improvement could be observed for PRRSv. For L. intracellularis an improvement could be observed in piglets (71%) and growers (56%; P < 0.05). For both of the respiratory pathogens, M. hyopneumoniae and A. pleuropneumoniae, significant improvement was observed in finishers (34 and 24%, respectively). In growers, only M. hyopneumoniae showed a significant improvement (34%). In conclusion, the transition from a one week batch management system to a four or five week batch management system in the present herds resulted in a reduction of the percentage of seropositive animals for three of the monitored economically important diseases: L. intracellularis, M. hyopneumoniae and A. pleuropneumoniae

The role of HLA-DP mismatches and donor specific HLA-DP antibodies in kidney transplantation : a case series

BACKGROUND: The impact of HLA-DP mismatches on renal allograft outcome is still poorly understood and is suggested to be less than that of the other HLA loci. The common association of HLA-DP donor-specific antibodies (DSA) with other DSA obviates the evaluation of the actual effect of HLA-DP DSA. METHODS: From a large multicenter data collection, we retrospectively evaluated the significance of HLA-DP DSA on transplant outcome and the immunogenicity of HLA-DP eplet mismatches with respect to the induction of HLA-DP DSA. Furthermore, we evaluated the association between the MFI of HLA-DP antibodies detected in Luminex assays and the outcome of flowcytometric/complement-dependent cytotoxicity (CDC) crossmatches. RESULTS: In patients with isolated pretransplant HLA-DP antibodies (N = 13), 6 experienced antibody-mediated rejection (AMR) and 3 patients lost their graft. In HLAMatchmaker analysis of HLA-DP mismatches (N = 72), HLA-DP DSA developed after cessation of immunosuppression in all cases with 84DEAV (N = 14), in 86% of cases with 85GPM (N = 6/7), in 50% of cases with 56E (N = 6/12) and in 40% of cases with 56A mismatch (N = 2/5). Correlation analysis between isolated HLA-DP DSA MFI and crossmatches (N = 90) showed negative crossmatch results with HLA-DP DSA MFI <2000 (N = 14). Below an MFI of 10,000 CDC crossmatches were also negative (N = 33). Above these MFI values both positive (N = 35) and negative (N = 16) crossmatch results were generated. CONCLUSIONS: Isolated HLA-DP DSA are rare, yet constitute a significant risk for AMR. We identified high-risk eplet mismatches that can lead to HLA-DP DSA formation. We therefore recommend HLA-DP typing to perform HLA-DP DSA analysis before transplantation. HLA-DP DSA with high MFI were not always correlated with positive crossmatch results

Effects of General Incidence and Polymer Joining on Nucleated Polymerization in a Model of Prion Proliferation

Two processes are incorporated into a new model for transmissible prion diseases. These are general incidence for the lengthening process of infectious polymers attaching to and converting noninfectious monomers, and the joining of two polymers to form one longer polymer. The model gives rise to a system of three ordinary differential equations, which is shown to exhibit threshold behavior dependent on the value of the parameter combination giving the basic reproduction number R0. For R00 \u3e1, the system is locally asymptotic to a positive disease equilibrium. The effect of both general incidence and joining is to decrease the equilibrium value of infectious polymers and to increase the equilibrium value of normal monomers. Since the onset of disease symptoms appears to be related to the number of infectious polymers, both processes may significantly inhibit the course of the disease. With general incidence, the equilibrium distribution of polymer lengths is obtained and shows a sharp decrease in comparison to the distribution resulting from mass action incidence. Qualitative global results on the disease free and disease equilibria are proved analytically. Numerical simulations using parameter values from experiments on mice (reported in the literature) provide quantitative demonstration of the effects of these two processes

Eigenvalue location for nonnegative and Z-matrices

AbstractLet Lk0 denote the class of n × n Z-matrices A = tl − B with B ⩾ 0 and ϱk(B) ⩽ t < ϱk + 1(B), where ϱk(B) denotes the maximum spectral radius of k × k principal submatrices of B. Bounds are determined on the number of eigenvalues with positive real parts for A ϵ Lk0, where k satisfies, ⌊n2⌋ ⩽ k ⩽ n − 1. For these classes, when k = n − 1 and n − 2, wedges are identified that contain only the unqiue negative eigenvalue of A. These results lead to new eigenvalue location regions for nonnegative matrices

Impact of travel between patches for spatial spread of disease

A multipatch model is proposed to study the impact of travel on the spatial spread of disease between patches with different level of disease prevalence. The basic reproduction number for the ith patch in isolation is obtained along with the basic reproduction number of the system of patches, R(0). Inequalities describing the relationship between these numbers are also given. For a two-patch model with one high prevalence patch and one low prevalence patch, results pertaining to the dependence of R(0) on the travel rates between the two patches are obtained. For parameter values relevant for influenza, these results show that, while banning travel of infectives from the low to the high prevalence patch always contributes to disease control, banning travel of symptomatic travelers only from the high to the low prevalence patch could adversely affect the containment of the outbreak under certain ranges of parameter values. Moreover, banning all travel of infected individuals from the high to the low prevalence patch could result in the low prevalence patch becoming diseasefree, while the high prevalence patch becomes even more disease-prevalent, with the resulting number of infectives in this patch alone exceeding the combined number of infectives in both patches without border control. Under the set of parameter values used, our results demonstrate that if border control is properly implemented, then it could contribute to stopping the spatial spread of disease between patches

Intracranial oligodendroglioma with optic nerve infiltration in a Labrador retriever

A seven-year-old neutered male Labrador retriever was presented with behavioral changes and reduced vision. Neurological examination revealed blindness of the left eye with a positive pupillary light reflex and a decreased mental status. Blood and cerebrospinal fluid analyses showed no abnormalities. MRI revealed a deviant area located in the thalamic, hypothalamic and caudate nuclear regions. Invasion of the left optic nerve was also observed. The dog was euthanized after 38 days of palliative treatment. Necropsy showed a non-encapsulated extruding white lardaceous mass, with a diameter of 2 cm, in the white matter, located in the ventral thalamic region near the chiasma opticum, which extended along the left optic nerve. Histologically, neoplastic cells had a “fried egg” appearance. Immunolabelling for glial fibrillary acidic protein demonstrated the presence of numerous reactive astrocytes. The tumor was diagnosed as a low grade (II) intracranial oligodendroglioma with infiltration of the optic nerve.</jats:p

Not just fractal surfaces, but surface fractal aggregates: Derivation of the expression for the structure factor and its applications

Densely packed surface fractal aggregates form in systems with high local volume fractions of particles with very short diffusion lengths, which effectively means that particles have little space to move. However, there are no prior mathematical models, which would describe scattering from such surface fractal aggregates and which would allow the subdivision between inter- and intraparticle interferences of such aggregates. Here, we show that by including a form factor function of the primary particles building the aggregate, a finite size of the surface fractal interfacial sub-surfaces can be derived from a structure factor term. This formalism allows us to define both a finite specific surface area for fractal aggregates and the fraction of particle interfacial sub-surfaces at the perimeter of an aggregate. The derived surface fractal model is validated by comparing it with an ab initio approach that involves the generation of a "brick-in-a-wall" von Koch type contour fractals. Moreover, we show that this approach explains observed scattering intensities from in situ experiments that followed gypsum (CaSO4 · 2H2O) precipitation from highly supersaturated solutions. Our model of densely packed "brick-in-a-wall" surface fractal aggregates may well be the key precursor step in the formation of several types of mosaic- and meso-crystals