A General Approach to L(h, k)-Label Interconnection Networks

Given two non-negative integers h and k,an L(h,k)-labeling of a graph G=(V,E) is a function from the set V to a set of colors,such that adjacent nodes take colors at distance at least h,and nodes at distance 2 take colors at distance at least k.The aim of the L(h,k)-labeling problem is to minimize the greatest used color.Since the decisional version of this problem is NP-complete,it is important to investigate particular classes of graphs for which the problem can be efficiently solved.It is well known that the most common interconnection topologies,such as Butterfly-like,Bene(?),CCC,Trivalent Cayley networks,are all characterized by a similar structure:they have nodes organized as a matrix and connections are divided into layers.So we naturally introduce a new class of graphs,called (1×n)-multistage graphs,containing the most common interconnection topologies,on which we study the L(h,k)-labeling.A general algorithm for L(h,k)-labeling these graphs is presented,and from this method an efficient L(2,1)-labeling for Butterfly and CCC networks is derived.Finally we describe a possible generalization of our approach.     

Rheological behavior and morphology of poly(lactic acid)/low-density polyethylene blends based on virgin and recycled polymers: Compatibilization with natural surfactants

Blends based on poly(lactic acid) and low-density polyethylene were compatibilized exploiting an innovative strategy involving the introduction of different mixtures of two sustainable liquid surfactants characterized by dissimilar hydrophilic–lipophilic ratios. The compatibilization method was first applied on blends made of virgin polymers, aiming at assessing the surfactant mixture inducing a more significant morphology refinement. Besides, to verify the effectiveness of the selected compatibilizers on recycled materials, the same process was carried out on blends based on reprocessed polymers. Interestingly, the compatibilization caused a significant microstructure modification, with a decrease of 54% of the mean size of the dispersed particles, in the case of virgin polymers-based blends, with a consequent increase of 19% of the dynamic elastic modulus. On the other hand, in the case of reprocessed polymers-based blends, a different compatibilizer efficiency was observed, as the noncompatibilized blend showed amore regular microstructure compared to the compatibilized counterpart.     

Pediatric Celiac Disease Patients Show Alterations of Dendritic Cell Shape and Actin Rearrangement

Celiac disease (CD) is a frequent intestinal inflammatory disease occurring in genetically susceptible individuals upon gluten ingestion. Recent studies point to a role in CD for genes involved in cell shape, adhesion and actin rearrangements, including a Rho family regulator, Rho GTPase-activating protein 31 (ARHGAP31). In this study, we investigated the morphology and actin cytoskeletons of peripheral monocyte-derived dendritic cells (DCs) from children with CD and controls when in contact with a physiological substrate, fibronectin. DCs were generated from peripheral blood monocytes of pediatric CD patients and controls. After adhesion on fibronectin, DCs showed a higher number of protrusions and a more elongated shape in CD patients compared with controls, as assessed by immunofluorescence actin staining, transmitted light staining and video time-lapse microscopy. These alterations did not depend on active intestinal inflammation associated with gluten consumption and were specific to CD, since they were not found in subjects affected by other intestinal inflammatory conditions. The elongated morphology was not a result of differences in DC activation or maturation status, and did not depend on the human leukocyte antigen (HLA)-DQ2 haplotype. Notably, we found that ARH-GAP31 mRNA levels were decreased while RhoA-GTP activity was increased in CD DCs, pointing to an impairment of the Rho pathway in CD cells. Accordingly, Rho inhibition was able to prevent the cytoskeleton rearrangements leading to the elongated morphology of celiac DCs upon adhesion on fibronectin, confirming the role of this pathway in the observed phenotype. In conclusion, adhesion on fibronectin discriminated CD from the controls’ DCs, revealing a gluten-independent CD-specific cellular phenotype related to DC shape and regulated by RhoA activity.     

Genotoxicity and Epigenotoxicity of Carbazole-Derived Molecules on MCF-7 Breast Cancer Cells

The carbazole compounds PK9320 (1-(9-ethyl-7-(furan-2-yl)-9H-carbazol-3-yl)-N-methylmethanamine) and PK9323 (1-(9-ethyl-7-(thiazol-4-yl)-9H-carbazol-3-yl)-N-methylmethanamine), second-generation analogues of PK083 (1-(9-ethyl-9H-carbazol-3-yl)-N-methylmethanamine), restore p53 signaling in Y220C p53-mutated cancer cells by binding to a mutation-induced surface crevice and acting as molecular chaperones. In the present paper, these three molecules have been tested for mutant p53-independent genotoxic and epigenomic effects on wild-type p53 MCF-7 breast adenocarcinoma cells, employing a combination of Western blot for phospho-γH2AX histone, Comet assay and methylation-sensitive arbitrarily primed PCR to analyze their intrinsic DNA damage-inducing and DNA methylation-changing abilities. We demonstrate that small modifications in the substitution patterns of carbazoles can have profound effects on their intrinsic genotoxic and epigenetic properties, with PK9320 and PK9323 being eligible candidates as “anticancer compounds” and “anticancer epi-compounds” and PK083 a “damage-corrective” compound on human breast adenocarcinoma cells. Such different properties may be exploited for their use as anticancer agents and chemical probes.     

Detection of Escherichia coli O157 in bovine meat products in northern Italy

Tests for Escherichia coli and E. coli O157 were carried out on meat samples collected from randomly chosen stores throughout the city of Bologna and suburban areas. The samples consisted of 25 g of loose minced beef, sometimes already shaped into meatballs or hamburgers, some of which were mixed with vegetables. The meat was purchased from retail outlets, open market stalls, and supermarket chains during 25 sampling visits from October 2000 to December 2001. For E. coli detection, Tryptone soya broth (TSB) supplemented with novobiocin and C-EC agar were used. Immunomagnetic separation with SMAC-BCIG-CT agar and chromogenic E. coli O 157 agar, API 20E system and agglutination latex test were used to detect E. coli O157; Vero cell assay and polymerase chain reaction (PCR) were used to assess toxin production and the presence of virulence genes.

E. coli were detected in 45 (30.2%) of the 149 samples examined, mainly in the hamburger samples mixed with vegetables and in the loose minced beef. E. coli O157 was found in one sample of hamburger and two samples of hamburger mixed with vegetables (2%) collected from three different butcher's stores between July and October. All the strains of E. coli O157 and most cases of E. coli were found in meat from small retailers.

The three strains of E. coli O157 were positive for verocytotoxin production. PCR analysis revealed genes coding for vt2 and one strain possessed the gene for eae A. Chromogenic E. coli O157 agar was found to be more selective and differential, allowing easier identification of suspected colonies with mixed flora and producing less false-positive colonies.     

Dolichol levels in younger and older rat hearts heterotopically transplanted in younger recipients

Dolichol (D) levels increase dramatically in older tissue. An understanding of the exchangeability of D between tissues may be essential in order to understand the mechanism of the abnormal accumulation associated with aging. The question was investigated by the use of organ transplantation. D-poor hearts donated by 3-mon-old and D-rich by 22-mon-old male Lewis rats were transplanted heterotopically in 3-mon-old syngenic recipients, whose peripheral tissues and liver were poor in D. Native and transplanted hearts were taken 7 and 21 d after surgery. Native hearts of 3-mon- and 22-mon-old male Lewis rats served as control. D concentration and quantity were higher in older than in younger native hearts as expected. In the transplanted hearts, the quantity of D was unchanged, irrespective of the age of the donor and of the time of transplantation, whereas D concentration increased because of the remarkable disuse atrophy. No changes in D were observed in recipients’ tissues. It is concluded that dolichol is not redistributed via circulation from the transplanted heart to the tissues and liver of the younger recipient.     

Investigations on the migration mode method (MMM) for reactor calculations

Current calculation codes for reactor analysis are based on the multi-group method to evaluate energy distribution of neutron flux. Usually a two energy group diffusion equation is adopted. This choice is adequate for PWRs associated to cross sections libraries tabulated versus fuel exposure and other state parameters as moderator density, fuel temperature, boron concentration. An improvement of this approach is represented by the migration mode method (MMM) by which the neutron spectrum is expanded in terms of base functions corresponding to the different modes of migration of the neutrons in the energy dimension. For a thermal reactor, three such functions may be easily identified: the Maxwellian distribution of the neutrons at thermal equilibrium with the moderator, the 1/E slowing down distribution (corrected to take into account resonance absorption effects) and the fission neutron spectrum. The (space-dependent) coefficients of the expansion are calculated by solving a differential equation which results having a structure similar to the one relevant to multi-group theory. The method can therefore be easily implemented adopting existing diffusion theory codes.     

Strategies to Tackle Antimicrobial Resistance: The Example of Escherichia coli and Pseudomonas aeruginosa

Traditional antimicrobial treatments consist of drugs which target different essential functions in pathogens. Nevertheless, bacteria continue to evolve new mechanisms to evade this drug-mediated killing with surprising speed on the deployment of each new drug and antibiotic worldwide, a phenomenon called antimicrobial resistance (AMR). Nowadays, AMR represents a critical health threat, for which new medical interventions are urgently needed. By 2050, it is estimated that the leading cause of death will be through untreatable AMR pathogens. Although antibiotics remain a first-line treatment, non-antibiotic therapies such as prophylactic vaccines and therapeutic monoclonal antibodies (mAbs) are increasingly interesting alternatives to limit the spread of such antibiotic resistant microorganisms. For the discovery of new vaccines and mAbs, the search for effective antigens that are able to raise protective immune responses is a challenging undertaking. In this context, outer membrane vesicles (OMV) represent a promising approach, as they recapitulate the complete antigen repertoire that occurs on the surface of Gram-negative bacteria. In this review, we present Escherichia coli and Pseudomonas aeruginosa as specific examples of key AMR threats caused by Gram-negative bacteria and we discuss the current status of mAbs and vaccine approaches under development as well as how knowledge on OMV could benefit antigen discovery strategies.