Novel Colicin F-Y of Yersinia frederiksenii Inhibits Pathogenic Yersinia Strains via YiuR-Mediated Reception, TonB Import, and Cell Membrane Pore Formation

A novel colicin type, designated colicin F-Y, was found to be encoded and produced by the strain Yersinia frederiksenii Y27601. Colicin F-Y was active against both pathogenic and nonpathogenic strains of the genus Yersinia. Plasmid YF27601 (5,574 bp) of Y. frederiksenii Y27601 was completely sequenced. The colicin F-Y activity gene (cfyA) and the colicin F-Y immunity gene (cfyI) were identified. The deduced amino acid sequence of colicin F-Y was very similar in its C-terminal pore-forming domain to colicin Ib (69% identity in the last 178 amino acid residues), indicating pore forming as its lethal mode of action. Transposon mutagenesis of the colicin F-Y-susceptible strain Yersinia kristensenii Y276 revealed the yiuR gene (ykris001_4440), which encodes the YiuR outer membrane protein with unknown function, as the colicin F-Y receptor molecule. Introduction of the yiuR gene into the colicin F-Y-resistant strain Y. kristensenii Y104 restored its susceptibility to colicin F-Y. In contrast, the colicin F-Y-resistant strain Escherichia coli TOP10F' acquired susceptibility to colicin F-Y only when both the yiuR and tonB genes from Y. kristensenii Y276 were introduced. Similarities between colicins F-Y and Ib, similarities between the Cir and YiuR receptors, and the detected partial cross-immunity of colicin F-Y and colicin Ib producers suggest a common evolutionary origin of the colicin F-Y-YiuR and colicin Ib-Cir systems

The NlpD Lipoprotein Is a Novel Yersinia pestis Virulence Factor Essential for the Development of Plague

Yersinia pestis is the causative agent of plague. Previously we have isolated an attenuated Y. pestis transposon insertion mutant in which the pcm gene was disrupted. In the present study, we investigated the expression and the role of pcm locus genes in Y. pestis pathogenesis using a set of isogenic surE, pcm, nlpD and rpoS mutants of the fully virulent Kimberley53 strain. We show that in Y. pestis, nlpD expression is controlled from elements residing within the upstream genes surE and pcm. The NlpD lipoprotein is the only factor encoded from the pcm locus that is essential for Y. pestis virulence. A chromosomal deletion of the nlpD gene sequence resulted in a drastic reduction in virulence to an LD50 of at least 107 cfu for subcutaneous and airway routes of infection. The mutant was unable to colonize mouse organs following infection. The filamented morphology of the nlpD mutant indicates that NlpD is involved in cell separation; however, deletion of nlpD did not affect in vitro growth rate. Trans-complementation experiments with the Y. pestis nlpD gene restored virulence and all other phenotypic defects. Finally, we demonstrated that subcutaneous administration of the nlpD mutant could protect animals against bubonic and primary pneumonic plague. Taken together, these results demonstrate that Y. pestis NlpD is a novel virulence factor essential for the development of bubonic and pneumonic plague. Further, the nlpD mutant is superior to the EV76 prototype live vaccine strain in immunogenicity and in conferring effective protective immunity. Thus it could serve as a basis for a very potent live vaccine against bubonic and pneumonic plague

Some psychosocial and cultural factors in the Arab-Israeli conflict: a review of the literature

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/66497/2/10.1177_002200277201600210.pd

A comparative study of three-dimensional printing directions: The degradation and toxicological profile of a PLA/PHA blend

The use of biobased plastics is of great importance for many applications. Blending thermoplastic polylactide (PLA) with polyhydroxyalkanoate (PHA) enables the formulation of a more mechanically powerful material and this enables tailored biodegradation properties. In this study we demonstrate the 3D printing of a PLA/PHA blend as a potential candidate for biocompatible material applications. The filament for 3D printing consisted of PHA, which contains predominantly 3-hydroxybutyrate units and a small amount of 3-hydroxyvalerate units, as revealed by multistage mass spectrometry (ESI-MSn). This research found that the properties of 3D printed species before and during abiotic degradation are dependent on printing orientation. Furthermore, the 3D printed specimens exhibited good biocompatibility with HEK293 cells, indicating real promise as biological scaffolds for tissue engineering applications

The anurans and squamates assemblage from Final Natufian Eynan

Excel sheet with the database of anurans, lizards, and snakes studied by Biton et al from the archaeological site of Eynan (Ain Mallaha

Study of two dimensional systems using nuclear resonance scattering of 4 MEV Bremsstrahlung Final scientific report

This report summarizes the progress carried out by personnel from Ben-Gurion University in collaboration with Prof. Kneissl and his research group from the University of Stuttgart in Germany. In this work, a new technique was tested and found to be successful, for measuring the tilt angle of adsorbed molecules on surfaces, using the resonance scattering of bremsstrahlung from nuclear levels in "1"3C. The preparations for the joint experiments were carried out both at Ben-Gurion University and in Stuttgart while the actual accelerator measurements were carried out using the Dynamitron accelerator of the University of Stuttgart. We constructed a new experimental facility for carrying out the research program. During the first few months of the beginning of this research (which started on January 1997), there were many experimental difficulties which could not be anticipated. These had to do with the Accelerating Tube of the Dynamitron Accelerator of the University of Stuttgart which suffered some damage and had to be replaced. This was a major project which delayed all the scheduled runs on the Dynamitron. In addition, we encountered many more technical problems related to the Dynamitron during our first two runs, during March and August 1997, causing a considerable loss of running time. These, combined with the fact that there is an increasing number of external users of the Dynamitron made it impossible to finish the planned research program within one year which was the funding period for this proposal. It was thus necessary to apply for extending the termination date of the research by seven months, i.e., until 31 July 1998, hoping to finish the planned research during this period. (orig.)SIGLEAvailable from TIB Hannover: DtF QN1(78,5) / FIZ - Fachinformationszzentrum Karlsruhe / TIB - Technische InformationsbibliothekGerman-Israeli Foundation for Scientific Research and Development (GIF), Oberschleissheim (Germany)DEGerman