Serosurvey of three virus infections in reindeer in northern Norway and Svalbard

Sera from 326 Norwegian reindeer (NR) and from 40 Svalbard reindeer (SR) were examined for antibodies to reindeer herpesvirus (RHV), bovine viral diarrhoea virus (BVDV) and parainfulenza type 3 virus (PIV-3). No antibodies to any of these three viruses were detected in sera from SR. Sixty-three percent of sera from 101 adult NR (> 12 months old) and 15% of 225 NR calves (6 months old) had antibodies to RHV; corresponding values for BVDV were 41% and 6%, respectively. Twenty-seven percent of adult NR and 1% of NR calves had antibodies to both viruses. No antibodies to PIV-3 were detected in any NR sera

Reduced Lentivirus Susceptibility in Sheep with TMEM154 Mutations

Visna/Maedi, or ovine progressive pneumonia (OPP) as it is known in the United States, is an incurable slow-acting disease of sheep caused by persistent lentivirus infection. This disease affects multiple tissues, including those of the respiratory and central nervous systems. Our aim was to identify ovine genetic risk factors for lentivirus infection. Sixty-nine matched pairs of infected cases and uninfected controls were identified among 736 naturally exposed sheep older than five years of age. These pairs were used in a genome-wide association study with 50,614 markers. A single SNP was identified in the ovine transmembrane protein (TMEM154) that exceeded genome-wide significance (unadjusted p-value 3×10−9). Sanger sequencing of the ovine TMEM154 coding region identified six missense and two frameshift deletion mutations in the predicted signal peptide and extracellular domain. Two TMEM154 haplotypes encoding glutamate (E) at position 35 were associated with infection while a third haplotype with lysine (K) at position 35 was not. Haplotypes encoding full-length E35 isoforms were analyzed together as genetic risk factors in a multi-breed, matched case-control design, with 61 pairs of 4-year-old ewes. The odds of infection for ewes with one copy of a full-length TMEM154 E35 allele were 28 times greater than the odds for those without (p-value<0.0001, 95% CI 5–1,100). In a combined analysis of nine cohorts with 2,705 sheep from Nebraska, Idaho, and Iowa, the relative risk of infection was 2.85 times greater for sheep with a full-length TMEM154 E35 allele (p-value<0.0001, 95% CI 2.36–3.43). Although rare, some sheep were homozygous for TMEM154 deletion mutations and remained uninfected despite a lifetime of significant exposure. Together, these findings indicate that TMEM154 may play a central role in ovine lentivirus infection and removing sheep with the most susceptible genotypes may help eradicate OPP and protect flocks from reinfection

Serosurvey of three virus infections in reindeer in northern Norway and Svalbard

Sera from 326 Norwegian reindeer (NR) and from 40 Svalbard reindeer (SR) were examined for antibodies to reindeer herpesvirus (RHV), bovine viral diarrhoea virus (BVDV) and parainfulenza type 3 virus (PIV-3). No antibodies to any of these three viruses were detected in sera from SR. Sixty-three percent of sera from 101 adult NR (> 12 months old) and 15% of 225 NR calves (6 months old) had antibodies to RHV; corresponding values for BVDV were 41% and 6%, respectively. Twenty-seven percent of adult NR and 1% of NR calves had antibodies to both viruses. No antibodies to PIV-3 were detected in any NR sera

Hydrogenation of aryldiazenido complexes. Synthesis and structure of trans-hydrido(acetonephenylhydrazone)bis(triphenylphosphine)platinum(II) tetrafluoroborate

Pt(BF4)(N:NAr)(PPh3)2 (Ar = C6H5, p-FC6H4) can be hydrogenated in a variety of solvents under mild conditions using no addnl. catalyst. In ethanol the hydrazine complex [PtH(H2NNHAr)(PPh3)2][BF4] is formed, while in the presence of acetone the corresponding hydrazone complex results. The ready availability of a coordination site on the Pt(N:NAr)(PPh3)2 unit must play a key role in the easy activation of mol. H which leads to these hydrazine derivs. The crystal structure of trans-[PtH(PhHNNC3H6)(PPh3)2][BF4]•C6H6 was detd. The coordination geometry about the Pt atom is square planar with trans phosphine groups. The hydrazone group is bound to the Pt atom through the sp2- hydridized N atom

Proline transport and osmotic stress response in Escherichia coli K-12.

Proline is accumulated in Escherichia coli via two active transport systems, proline porter I (PPI) and PPII. In our experiments, PPI was insensitive to catabolite repression and was reduced in activity twofold when bacteria were subjected to amino acid-limited growth. PPII, which has a lower affinity for proline than PPI, was induced by tryptophan-limited growth. PPII activity was elevated in bacteria that were subjected to osmotic stress during growth or the transport measurement. Neither PPI nor uptake of serine or glutamine was affected by osmotic stress. Mutation proU205, which was similar in genetic map location and phenotype to other proU mutations isolated in E. coli and Salmonella typhimurium, influenced the sensitivity of the bacteria to the toxic proline analogs azetidine-2-carboxylate and 3,4-dehydroproline, the proline requirements of auxotrophs, and the osmoprotective effect of proline. This mutation did not influence proline uptake via PPI or PPII. A very low uptake activity (6% of the PPII activity) observed in osmotically stressed bacteria lacking PPI and PPII was not observed when the proU205 lesion was introduced