Risk of Infection with Leishmania spp. in the Canine Population in the Netherlands

The dog is the main reservoir of Leishmania infantum, the causative agent of visceral leishmaniasis (VL) in humans in Southern Europe. In order to identify the risk of dogs from a Leishmania non-endemic area traveling to a Leishmania -endemic area becoming infected and the risk of transmitting infection to humans in non-endemic areas an investigation was performed, in which the results of a questionnaire were combined with the results of a serologic survey.     

Zinc efficiency of oilseed rape (t Brassica napus and t B. juncea) genotypes

Twenty five genotypes of oilseed rape (canola and mustard) were tested under varied supply of Zn (+Zn: 2 mg kg^–1 soil, -Zn: no Zn added) in two pot experiments in soil culture to determine the genotypic variation in tolerance to the Zn-deficient conditions, that is, to identify the Zn-efficient genotypes. On the basis of performance of genotypes in pot experiments, ten genotypes were tested in 1995 for their performance under varied supply of Zn (+Zn: 3.5 kg ha^–1, -Zn: no Zn added) on a Zn-deficient field in South Australia.Zn efficiency (ratio of shoot dry matter in -Zn to shoot dry matter in +Zn treatment and expressed in percentage) in pot Experiment 1 varied from 35% for 92-13 to 74% for Siren. Narendra, Dunkeld, Barossa, Oscar and Xinza 2 performed well under -Zn treatment. Zn efficiency in Experiment 2 varied from 32% for Wuyou 1 to 62% for Pusa Bold. Pusa Bold and CSIRO-1(mustard genotypes) were the most efficient in terms of dry matter production among all the oilseed rape genotypes tested. Root dry matter accumulation was significantly higher in Zn-efficient genotypes. Zn efficiency (ratio of seed yield in -Zn to seed yield in +Zn and expressed in percentage) in field experiment varied from 62% for Huashang 2 to 76% for Dunkeld. With few exceptions, the ranking of genotypes in pot and field experiments indicates similarity in their response to Zn deficiency. There looks to be genetic control over Zn concentration in tissues. Zn-efficient genotypes had lower Zn concentration in roots and higher Zn concentration in youngest fully opened leaf blades, indicating a better transport of Zn. This, together with a higher Zn uptake, appears to be the basis of expression of Zn efficiency.     

NMR solution structures of the apo and peptide-inhibited human rhinovirus 3C protease (Serotype 14): structural and dynamic comparison

The human rhinovirus (HRV) is a positive sense RNA virus responsible for about 30% of "common colds". It relies on a 182 residue cysteine protease (3C) to proteolytically process its single gene product. Inhibition of this enzyme in vitro and in vivo has consistently demonstrated cessation of viral replication. This suggests that 3C protease inhibitors could serve as good drug candidates. However, significant proteolytic substrate diversity exists within the 110+ known rhinovirus serotypes. To investigate this variability we used NMR to solve the structure of the rhinovirus serotype 14 3C protease (subgenus B) covalently bound to a peptide (acetyl-LEALFQ-ethylpropionate) inhibitor. The inhibitor-bound structure was determined to an overall rmsd of 0.82 A (backbone atoms) and 1.49 A (all heavy atoms). Comparison with the X-ray structure of the serotype 2 HRV 3C protease from subgenus A (51% sequence identity) bound to the inhibitor ruprintrivir allowed the identification of conserved intermolecular interactions involved in proximal substrate binding as well as subgenus differences that might account for the variability observed in SAR studies. To better characterize the 3C protease and investigate the structural and dynamic differences between the apo and bound states we also solved the solution structure of the apo form. The apo structure has an overall rmsd of 1.07 +/- 0.17 A over backbone atoms, which is greater by 0.25 A than what is seen for the inhibited enzyme (2B0F.pdb). This increase is localized to the enzyme's C-terminal beta-barrel domain, which is responsible for recognizing and binding proteolytic substrates. Amide hydrogen exchange dynamics revealed dramatic differences between the two enzyme states. Furthermore, a number of residues exhibited exchange-broadened amide NMR signals in the apo state compared to the inhibited state. The majority of these residues are associated with proteolytic substrate interaction.