Seropositivity to Toxoplasma infection in sheep samples submitted to Animal and Plant Health Agency laboratories between 2005 and 2012.

Ovine serum samples submitted to Animal and Plant Health Agency (APHA) (formerly the Animal Health and Veterinary Laboratories Agency) - Weybridge regional laboratories in England and Wales for diagnostic and monitoring purposes between 2005 and 2012 were investigated for possible spatial and temporal variations in seropositivity to Toxoplasma gondii infection. Of the 4354 samples tested by latex agglutination, 2361 (54.2 per cent) were seropositive. No correlation between seropositivity and climatic conditions was identified by mixed-effects modelling using meteorological data summaries. The proportion of seropositive samples collected during November was found to be significantly lower than those collected during other months and samples from the North West England and North Wales Regions had significantly lower odds of being positive. Spatial cluster analysis identified a significantly higher proportion of seropositive animals in East Anglia and the South, East and Midlands of England. Spatio-temporal cluster analysis detected a single significant cluster of seropositive animals dating from January 2006 to January 2011, which covered a large proportion of the farm locations. As well as confirming high overall levels of infection within the national flock, these findings also indicate possible temporal and regional variations in exposure of sheep to T. gondii.

Cross-sectional survey of antibiotic resistance in Escherichia coli isolated from diseased farm livestock in England and Wales.

Between 2005 and 2007, E. coli obtained from clinical diagnostic submissions from cattle, goats, pigs and sheep to government laboratories in England and Wales were tested for sensitivity to 16 antimicrobials. Resistance was most commonly observed against ampicillin, streptomycin, sulphonamides and tetracyclines. Resistance levels varied significantly between species, with isolates from cattle frequently showing the highest levels. Verocytotoxigenic E. coli (VTEC) expressed less resistance than non-VTEC. Only 19·3% of non-VTEC and 43·5% of VTEC were susceptible to all antimicrobials, while 47·1% and 30·4%, respectively, were resistant to ⩾5 antimicrobials. The resistance phenotype SSuT was commonly observed, and isolates resistant to third-generation cephalosporins were also identified. We recommend judicious antimicrobial usage in the livestock industry in order to preserve efficacy.

Survey to determine the seroprevalence of Toxoplasma gondii infection in British sheep flocks.

A serological survey of Toxoplasma gondii infection in adult breeding sheep in Great Britain was conducted using surplus sera taken during a seroprevalence study of Brucella melitensis in 2009. Of the 3539 sera collected from 227 flocks, 2619 (74 per cent) were found to be positive for T gondii specific antibody when tested using latex agglutination. Multilevel logistic modelling suggested that the likelihood of infection increased with age and this effect appeared to be amplified in animals vaccinated against T gondii. The model also indicated that the odds of sheep being seropositive were increased on premises where cattle were also kept. These results suggest a high level of Toxoplasma infection in breeding sheep in Great Britain and provide further evidence to suggest that postnatal infection is more common than congenital infection in sheep.

Verocytotoxin-producing and attaching and effacing activity of Escherichia coli isolated from diseased farm livestock.

Between May 2005 and June 2008, strategically selected isolates of Escherichia coli obtained from clinical submissions to Veterinary Laboratories Agency (VLA) regional laboratories in England and Wales were serogrouped and examined by PCR for verocytotoxin (VT) production and attaching and effacing (eae) genes, both of which are zoonotic determinants. VT-encoding genes were detected in 54 (5.3 per cent) of the 1022 isolates examined. Only one isolate (0.1 per cent) was identified as verocytotoxigenic E coli (VTEC) O157. Non-O157 VTECs were present in 4.7 per cent of isolates from cattle, compared with 7.9 per cent in pigs, 2.3 per cent in sheep and 6.7 per cent in goats. The predominant serogroup identified in cattle was O26 and the predominant serogroup in pigs was O2. Attaching and effacing activity was attributed to 69 (6.8 per cent) of all isolates.

Mechanism of nucleotide release from Rho by the GDP dissociation stimulator protein.

Guanine nucleotide dissociation stimulator (GDS) promotes the release of tightly bound GDP from various Ras superfamily proteins, including RhoA, Rac1, K-Ras, Rap1A, and Rap1B. It displays no significant sequence homology to other known exchange factors for small G-proteins. Studies are reported here of the mechanism of GDS-mediated nucleotide release from RhoA using a combination of equilibrium and stopped-flow kinetic measurements, employing fluorescent N-methylanthraniloyl (mant) derivatives of GDP and 2'-deoxyGDP. It is proposed that GDS operates by an associative displacement mechanism where stimulated nucleotide release from the Rho.mantGDP complex occurs via a transiently populated ternary complex (Rho.GDS.mantGDP). In kinetic experiments where excess GDS was mixed with the Rho.mantGDP complex, stimulated mantGDP dissociation rates of 1 s(-)(1) were measured during a single turnover, representing a 5000-fold enhancement over the intrinsic rate of mantGDP dissociation from Rho. The stable, nucleotide-free binary complex Rho.GDS was isolated. When the Rho.GDS complex was mixed with excess mantGDP, a biphasic increase in fluorescence occurred, the observed rate constants of which both reached saturating values at high mantGDP concentrations. This is compelling evidence that an isomerization of the Rho.GDS.mantGDP ternary complex is an important feature of the mechanism of nucleotide release.

Secondary structure forming propensity coupled with amphiphilicity is an optimal motif in a peptide or protein for association with chaperonin 60 (GroEL).

The interactions of GroEL with six dansyl peptides were investigated by means of our previously established fluorescence binding assay [Hutchinson, J. P., Oldham, T. C., El-Thaher, T. S. H., and Miller, A. D. (1997) J. Chem. Soc., Perkin Trans. 2, 279-288]. Three peptides (AMPH series) were constructed with a hierarchy of alpha-helix-forming propensities and amphiphilic characteristics. The remaining three peptides (NON-AMPH series) were prepared with a reordered amino acid sequence designed to form peptides of differing non-amphiphilic alpha-helix-forming propensity. Of these six peptides, two (AMPH(+) and NON-AMPH(+)) were N-capped with an S-form alpha-helix-inducing template (Ro 47-1615, Hoffmann-La Roche), two (AMPH(-) and NON-AMPH(-)) were N-capped with an R-form non-inducing template (Ro 47-1614, Hoffmann-La Roche), and two (AMPH(R) and NON-AMPH(R)) were without N-cap modification. This paper describes how the known strength of interaction of an unfolded protein substrate with the molecular chaperone GroEL (K(d) micromolar to nanomolar) may be emulated with a single peptide (AMPH(+)) (apparent K(d) 5 nM) which has a high propensity to form an amphiphilic alpha-helical structure in solution. Secondary structure forming propensity is not, in and of itself, an important contributor to the strength of interaction with GroEL. However, secondary structure forming propensity coupled with amphiphilicity may be sufficient to account for most, if not all, of the interaction strength between GroEL and an unfolded peptide or protein substrate.

Refolding and recognition of mitochondrial malate dehydrogenase by Escherichia coli chaperonins cpn 60 (groEL) and cpn10 (groES).

In vitro refolding of pig mitochondrial malate dehydrogenase is investigated in the presence of Escherichia coli chaperonins cpn60 (groEL) and cpn10 (groES). When the enzyme is initially denatured with 3 M guanidinium chloride, chaperonin-assisted refolding is 100% efficient. C.d. spectroscopy reveals that malate dehydrogenase is almost unfolded in 3 M guanidinium chloride, suggesting that a state with little or no residual secondary structure is the optimal 'substrate' for chaperonin-assisted refolding. Malate dehydrogenase denatured to more highly structured states proves to refold less efficiently with chaperonin assistance. The enzyme is shown not to aggregate under the refolding conditions, so that losses in refolding efficiency result from irreversible misfolding. Evidence is advanced to suggest that the chaperonins are unable to rescue irreversibly misfolded malate dehydrogenase. A novel use is made of 100 K Centricon concentrators to study the binding of [14C]acetyl-labelled malate dehydrogenase to groEL by an ultrafiltration binding assay. Analysis of the data by Scatchard plot shows that acetyl-malate dehydrogenase, which has previously been extensively unfolded with guanidinium chloride, binds to groEL at a specific binding site(s). At saturation, one acetyl-malate dehydrogenase homodimer (two polypeptides) is shown to bind to each groEL homooligomer with a binding constant of approx. 10 nM.

Eulerian graphs and polynomial identities for sets of matrices.

Let the standard identity of degree m be given by [Formula: see text] Then the minimum standard identity is determined for the set of all n x n skew-symmetric matrices over a field of characteristic 0.