A Numerical Investigation of Blast Loading and Clearing on Small Targets

When a blast wave strikes a finite target, diffraction of the blast wave around the free edge causes a rarefaction clearing wave to propagate along the loaded face and relieve the pressure acting at any point it passes over. For small targets, the time taken for this clearing wave to traverse the loaded face will be small in relation to the duration of loading. Previous studies have not shown what happens in the late-time stages of clearing relief, nor the mechanism by which the cleared reflected pressure decays to approach the incident pressure. Current design guidance assumes a series of interacting clearing waves propagate over the target face - this assumption is tested in this article by using numerical analysis to evaluate the blast pressure acting on small targets subjected to blast loads. It is shown that repeat propagations of the rarefaction waves do not occur and new model is proposed, based on an over-expanded region of air in front of the loaded face of the target

Lipopolysaccharide Diversity Evolving in Helicobacter pylori Communities through Genetic Modifications in Fucosyltransferases

Helicobacter pylori persistently colonizes the gastric mucosa of half the human population. It is one of the most genetically diverse bacterial organisms and subvariants are continuously emerging within an H. pylori population. In this study we characterized a number of single-colony isolates from H. pylori communities in various environmental settings, namely persistent human gastric infection, in vitro bacterial subcultures on agar medium, and experimental in vivo infection in mice. The lipopolysaccharide (LPS) O-antigen chain revealed considerable phenotypic diversity between individual cells in the studied bacterial communities, as demonstrated by size variable O-antigen chains and different levels of Lewis glycosylation. Absence of high-molecular-weight O-antigen chains was notable in a number of experimentally passaged isolates in vitro and in vivo. This phenotype was not evident in bacteria obtained from a human gastric biopsy, where all cells expressed high-molecular-weight O-antigen chains, which thus may be the preferred phenotype for H. pylori colonizing human gastric mucosa. Genotypic variability was monitored in the two genes encoding α1,3-fucosyltransferases, futA and futB, that are involved in Lewis antigen expression. Genetic modifications that could be attributable to recombination events within and between the two genes were commonly detected and created a diversity, which together with phase variation, contributed to divergent LPS expression. Our data suggest that the surrounding environment imposes a selective pressure on H. pylori to express certain LPS phenotypes. Thus, the milieu in a host will select for bacterial variants with particular characteristics that facilitate adaptation and survival in the gastric mucosa of that individual, and will shape the bacterial community structure