Resistance to nematode parasites in Merino sheep: Correlation with production traits

Merino sheep representing a range of bloodlines in resource flocks located across Australia were tested for resistance to gastro-intestinal nematodes. These flocks included the JB Pye Flock (Camden, NSW), Katanning Base Flock (Katanning, WA), Turretfield Merino Resource Flock (Rosedale, SA), and the CSIRO Finewool Flock (Armidale, NSW) and included a total of 328 sire groups. Resistance to nematodes was measured by faecal egg count (FEC). Data were also available for greasy and clean fleece weight (GFW and CFW, respectively), fibre diameter (FD), and body weight (BW) at a range of ages from weaning to 21 months. Variance components were estimated by restricted maximum likelihood, fitting an animal model and estimating covariances in a series of bivariate analyses. Phenotypic correlations between FEC0·33 and production traits were all close to zero ( –0·09–0·02). Genetic correlations between FEC0·33 and production traits were –0·20, –0·18, and –0·26 for weaning weight, 10-month BW, and 16-month BW, respectively; 0·21, –0·06, and 0·21 for 10-month GFW, 16-month GFW, and 21-month GFW; 0·21, –0·05, and 0·07 for 10-month CFW, 16-month CFW, and 21-month CFW; and –0·09, –0·12, and 0·04 for 10-month FD, 16-month FD, and 21-month FD. When estimates were pooled for all fleece traits and all BW traits, the genetic correlations between FEC0·33 and GFW, CFW, FD, and BW were 0·15, 0·10, –0·06, and –0·21, respectively. Using pooled estimates for CFW, FD, and BW, selection for a breeding objective based on production traits alone would lead to an unfavourable correlated response in FEC0·33 of approximately 1% per year

Resistance to nematode parasites in Merino sheep: Sources of genetic variation

Merino sheep representing a range of bloodlines in resource flocks located across Australia were tested for resistance to gastro-intestinal nematodes. These flocks included the JB Pye Flock (Camden, NSW), Katanning Base Flock (Katanning, WA), Turretfield Merino Resource Flock (Rosedale, SA), CSIRO Finewool Flock (Armidale, NSW), and the Trangie D Flock (Trangie, NSW). Faecal egg count (FEC) was used to measure relative resistance of sheep to nematode parasites after either natural or artificial infection with Haemonchus contortus and Trichostrongylus colubriformis. Differences in FEC 0' 33 between strains and between and within bloodlines were examined and the heritability of this trait was estimated. A low proportion of the total variation in parasite resistance could be attributed to strain and bloodline effects (1 and 3.5%, respectively) after either natural or artificial infection. The major source of genetic variation was found within bloodlines (22.2% of total variation), with individual sires showing a wide range in parasite resistance. Paternal half-sib heritability estimates for FEC 0' 33 were significant (P < 0.05) in 9 of the 11 analyses and ranged from 0.07 to 0.42, with a weighted average of 0.22. The influence of the environmental effects of sex, age of dam, birth-rearing rank, and day of birth were also investigated, and were found to be only occasionally significant, accounting for a small proportion (0.3-2.2%) of variation. Management group effects both prior to and at the time of measurement were often significant, and accounted for 2.2-19.4% of variation in FEC. Correction of FEC for effects other than management group would seem to add little to precision of selection. These results have demonstrated that significant genetic variation for nematode parasite resistance exists within a wide range of Merino bloodlines, and within-flock selection of resistant sires appears to be an effective method of improving this trait in Merino sheep

A novel S = 3/2 EPR signal associated with native Fe-proteins of nitrogenase

In addition to their g = 1.94 EPR signal, nitrogenase Fe-proteins from Azotobacter vinelandii, Azotobacter chroococcum and Klebsiella pneumoniae exhibit a weak EPR signal with g [congruent with]5. Temperature dependence of the signal was consistent with an S = 3/2 system with negative zero-field splitting, d = -5 +/- 0.7 cm-1. The ms, = +/- 3/2 ground state doublet gives rise to a transition with geff = 5.90 and the transition within the excited ms = +/- 1/2 doublet has a split geff = 4.8, 3.4. Quantitation gave 0.6 to 0.8 spin mol-1 which summed with the spin intensity of the S = 1/2 G = 1.94 line to roughly 1 spin/mol. MgATP and MgADP decreased the intensity of the s = 3/2 signal with no concomitant changes in intensity of the s = 1/2 signal.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/25566/1/0000108.pd

Correction for creatine interference with the direct indophenol measurement of NH3 in steady-state nitrogenase assays

Creatine was identified as a major source of interference with the direct phenol/hypochlorite colorimetric determination of ammonia in nitrogenase reaction mixtures. A method is described for removing other compounds which inhibit color development and for compensating for the interference produced by creatine. This method avoids time-consuming microdiffusion and also routinely makes available the efficiency of ATP hydrolysis coupled to substrate reduction (View the MathML source ratio) with N2 as a reducible substrate. Using this method we determined values for this ratio at 30°C of 4.87 ± 0.03 during the reduction of protons to H2 and 7.16 ± 0.14 during the reduction of N2 by the vanadium-containing nitrogenase of Azotobacter chroococcum

Possible role of a short extra loop of the long-chain flavodoxin from Azotobacter chroococcum in electron transfer to nitrogenase: Complete H-1, N-15 and C-13 backbone assignments and secondary solution structure of the flavodoxin

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