Allelic composition and associated quality traits of the <Emphasis Type="Italic">Glu-1</Emphasis> and <Emphasis Type="Italic">Glu-3</Emphasis> loci in selected modern Ethiopian durum wheat varieties

Gluten protein determines the processing quality of both durum wheat and bread wheat. The glutenin subunits compositions and associated quality traits of 20 Ethiopian durum wheat varieties were systematically analyzed using SDS-PAGE and Payne numbers. A total of 16 glutenin patterns were identified. At the Glu-A1 locus, all varieties scored the null allele. The predominant glutenin alleles at the Glu-B1 locus were Glu-B1b (7+8) and Glu-B1e (20). In Glu-3, the most abundant glutenin subunits were Glu-A3a and Glu-B3c. Based on the Payne scores, the varieties Yerer, Ginchi, Candate, and Foka were identified to have allelic composition suitable for pasta making. The cluster analysis using agglomerative hierarchical clustering (AHC) method classified the varieties into four similarity classes. Based on the findings of this experiment, suggestions were made for allelic composition improvement through introgression of superior alleles from known Glu-1 and Glu-3 sources.     

Identification and validation of cold responsive microRNAs of <Emphasis Type="Italic">Hevea brasiliensis</Emphasis> using high throughput sequencing

Cold stress is one of the major abiotic factors that influence the productivity and geographical distribution of many agriculturally important crops like Hevea brasiliensis. Cultivation of H. brasiliensis in India is being extended to northeastern regions, where low temperature during winter adversely affects its survival, growth, and productivity. Developing cold-tolerant genotypes is a primary requisite to maximize the productivity under such challenging environmental conditions. However, lack of methods for early evaluation of cold tolerance in the newly developed clones and the extensive time required for assessing their tolerance in the field are major constraints for clonal selection. The present study was initiated with an objective to identify and characterize cold stress responsive miRNAs from H. brasiliensis that show stronger association with cold tolerance. Next generation sequencing using Illumina HiSeq method revealed the expression of 21 and 29 conserved miRNA (from clone RRIM 600) families in cold-stressed and control samples, respectively. Forty-two novel miRNAs were identified from this study. Upon differential expression analysis, eight conserved miRNAs were found commonly expressed in both the samples. When expression analyses were performed subsequently with six selected miRNAs in two Hevea clones (viz. RRII 105 and RRIM 600), miR169 showed a strong association with cold tolerance. miRNAs such as miR482 and miR159 also exhibited association with cold tolerance. This study suggests the possibility of employing these miRNAs as markers for cold tolerance after validation in more number of genotypes with varying levels of cold tolerance.     

Zu Prekler’s „rationellem Baldwirth“

Ohne Zusammenfassung f. f?chf. Dberforftmeifter. f. bahr. Regierungs- und Forftrath von Mürzburg. f. preuk. Dberforftmeifter aus Breslau. f. f?chf. Dberforftmeifter. f. bahr. Regierungs- und Forftrath von Augsburg. f. bahr. Regierungs- und Forftrath aus Regensburg. Dberj?germeifter von Braunfchweig. f. bahr. Regierungs- und Forftrath aus München. f. f?chf. Dberf?rfter. f. f?chf. Dberforftmeifter. f. f?chf. Dberforftrath. herz. braunfchweig. Forftmeifter von Blanfenburg. Direftor der fürftlich Cfterhazh’fchen Herrfchaft Spoly Parsto. fürftl. fondershauf. Dberfortmeifter. f. bahr. Redierf?rfter don Schmarzenbach. f. preuk. Dberf?rfter. f. f. Forftrath aus Brekburg. f. preuk. Dberf?rfter von Altruppin. f. hann?v. Forftmeifter von Rienburg. Forftmeifter in preuk. Schleften. f. preuk. Dberforftmeifter von Berlin. herz. aftenburg. Dberfortmeifter. f. preuk. Dberf?rfter. f. f?chf. Dberf?rfter. f. ruff. Forftfomiff?r aus Marfchau. f. preuk. Forftinfpeftor. f. f?chf. Forftinfpeftor. grokh. meimar. Forftinfpeftor von Martfuhl. f. mürttb. Dberf?rfter und Brofeffor aus Hohenheim. f. hannov. Forftmeifter aus Hammeln. Dberforftmeifter aus Sotha. herz. altenburg. Dberf?rfter aus Hummelshain. herz. altenburg. Revierf?rfter aus Milchwig. herz. altenburg. geheimer Finanzrath und Dberforftmeifter. herz. altenb. Dberforftmeifter aus Hummelshain. grokh. f?chf. geheimer Dberforftrath aus Qifenach. herz. naffau. Dberforftrath aus Miesbaden. grokh. heff. Dberforftfefret?r aus Darmftadt. f. f?chf. Dberforftmeifter.     

Die Geminnung des Stockholzes

Ohne Zusammenfassung     

Adenohypophyseal receptors for LHRH, pituitary content of gonadotropins and plasma concentrations of LH in cyclic, pregnant and postpartum beef cows

Adenohypophyseal concentrations of LHRH receptors, pituitary content of LH and FSH, and plasma concentrations of LH were determined in thirty Hereford, Angus or Hereford-Angus heifers that were randomly assigned by breed and weight to five periods including day 3 of the estrous cycle (CY), pregnant day 120 (P120), 200 (P200), 275 (P275), or day 2 postpartum (PP). Jugular blood samples were collected at 10-min intervals for 8 hr from all cows. Within 2 hr after completion of blood sampling, animals were slaughtered and the pituitary gland frozen at −196 C. LH pulse frequency/8 hr was reduced (P<.05) during gestation (.5, .2, and 1.5 ± .5/8 hr, for P120, P200, and P275, respectively) and PP (.5 ± .5/8 hr) compared to CY (7.8 ± .5/8 hr). Frequency of LH pulses/8 hr was not different (P>.1) among P120, P200 or PP periods but was different (P<.05) between P200 and P275. There were no differences in LH pulse height (P>.1) among periods; however, pulse amplitude was greatest (P<.05) at P120 (1.3 ± .2 ng/ml) and lowest between P200 and PP (.6 to .8 ± .2 ng/ml). Baseline concentrations of plasma LH did not differ (P>.1) among P and PP periods (.3 ± .1 ng/ml), but were lower (P<.05) than in CY animals (.7 ± .1 ng/ml). Concentration of adenohypophyseal LHRH receptors was approximately two-fold greater (P<.05) at P120 (25.85 ± 2.2 fmol/mg) than at all other periods (9.5 to 14.9 ± 2.2 fmol/mg). Pituitary content of LH was greatest at P120 (1.56 ± .11 ug/mg) and lowest (P<.05) at P275 and PP (0.46 to 0.52 ± .11 ug/mg). Pituitary content of FSH was greatest (P<.05) in P (12.7 to 17.0 ± 1.4 ug/mg) and PP (18.3 ± 1.4 ug/mg) vs CY (5.0 ± 1.4 ug/mg) cows and increased from P120 to PP (P<.05). Results indicate that physiological changes occurring during gestation may have an effect on subsequent function of the adenohypophysis in beef cows.     

The non-specific stimulation of avian peripheral blood lymphocytes from uninfected chickens by paramyxoviruses and influenza viruses

Avian paramyxovirus-3 was mitogenic to peripheral blood lymphocytes (PBL) from about half the normal birds sampled from 3 inbred flocks. Eight other myxoviruses including Newcastle disease virus, Sendai virus and influenza virus were also irregularly mitogenic. This could complicate in vitro assays for specific immunity.     

A radial immunodiffusion enzyme assay for detection of antibody to equine rhinopneumonitis virus (EHV-1) in horse serum

A radial immunodiffusion enzyme assay (RIDEA) was developed for detection and quantitation of antibodies to equine herpes virus-1 (EHV-1) in horse sera. The detection and quantitation of EHV-1 antibody levels were based on the diameter of the radial diffusion zone of specific antibody in each serum sample reacting with EHV-1 antigen. The circular zone was made visible using peroxidase-conjugated rabbit anti-horse immunoglobulin G and a substrate containing hydrogen peroxide. The results of the RIDEA were compared with those of virus neutralization (VN) and enzyme-linked immunosorbent assay (ELISA) and found to be highly correlated. The relative sensitivity and specificity (percentage of agreement with VN test) were found to be 98.2 and 92.5%, respectively. Because the test procedure is relatively easy to perform, the RIDEA could be used as a field test to detect antibodies to EHV-1 in horses.     

Isolation of anaerobic mollicutes from the intestine of swine

Anaerobic mollicutes were isolated from the intestinal content and the epithelium of the caecum and colon of 4 of 8 swine. All of the isolates belonged to the same species. This species was resistant to digitonin and polyanethol sulfonate and was able to ferment glucose, hemolyse erythrocytes and lyse horse serum. For testing the cholesterol requirement the strain 4 A 11 was selected which was independent of cholesterol. The agent was different in the immunofluorescence test from the mollicutes reported previously in swine and quite different in its nutritional requirements from cholesterol-independent mollicutes isolated from the rumen of cattle and sheep. Thus the isolated mollicutes seem to represent a new species.