Scanning electron microscope study of Sendai virus fusion between HeLa cells and chick erythrocytes.

Chick erythrocytes were fused with HeLa cells by Sendai virus and preparations examined by scanning electron microscopy at different times after fusion. Heterokaryons were usually formed by fusion of erythrocyte ghosts with HeLa cells. Occasionally whole erythrocytes were engulfed but there was no evidence that free nuclei fused. Initial inter-cell attachments were usually, and possibly always, made at the site of an attached virus particle. This study helps to correlate topographical findings with previous two-dimensional studies with the transmission electron microscope and may also provide a model system for the fusion of parasitised erythrocytes with eukaryotic cells.     

Spermatic and oxidative profile of domestic cat (Felis catus) epididymal sperm subjected to different cooling times (24, 48 and 72 hours)

Cooling stored epididymal samples for several days allows facilities to transport and process genetic material post‐mortem. Improvements to this practice allow the preservation of sperm from domestic cats, which are the ideal study model for wild felids. However, the modifications in spermatic features and the oxidative profile are not fully understood in cats. This information is necessary for the development of biotechniques, such as new extenders for cryopreservation. Therefore, the purpose of this study was to evaluate the spermatic and oxidative profile in samples from the epididymal cauda of domestic cats cooled at 5°C for 24, 48 and 72 hr. Spermatozoa were collected from the epididymis cauda. Evaluations consisted of computer‐assisted sperm analysis (CASA), plasma membrane integrity (eosin/nigrosin), acrosome integrity (fast green/rose bengal), sperm morphology, sperm DNA integrity (toluidine blue), mitochondrial activity (3′3 diaminobenzidine), activity of the antioxidant enzymes glutathione peroxidase (GPx) and superoxide dismutase (SOD), measurement of lipid peroxidation (TBARS) and protein oxidation. A decrease in sperm motility parameters was observed after 72 hr of cooling (i.e. total and progressive) with a higher percentage of minor (37.7 ± 6.3%) and total defects (53.4 ± 6.3%). Additionally, a decrease in high mitochondrial activity (Class I: 16.6 ± 2.2%) occurred after 72 hr. The decrease in motility rates after a long cooling time probably was caused by the increase in sperm abnormalities. A long cooling time causes cold shock and mitochondrial exhaustion, but there was no observed change with the oxidative stress condition. Therefore, cat epididymal sperm stored at 5°C appear to maintain a high quality for up to 48 hr of cooling time.     

In-row tillage methods for subsoil amendment and starter fertilizer application to conservation-tilled grain sorghum

Acid subsoils and tillage pans limit crop yields on sandy soils of the Southern Coastal Plain of the United States. Studies were conducted for 3 years on two soils with acid subsoils and tillage pans to determine the effect of starter fertilizer (22 kg N, 10 kg P ha⁻¹ and fluid lime (1350 kg ha⁻¹) placement with in-row tillage methods on growth and yield of grain sorghum (Sorghum bicolor (L.) Moench) grown in a conservation-tillage system. Fertilizer and lime were applied in factorial combinations in the in-row subsoil channel, in a narrow (4-mm) slit 18 cm below the tillage pan (slit-tillage), or 7 cm to the side of the row incorporated 7 cm deep. Slit-tillage was as effective as subsoiling in two of the four tests where plant growth and grain yield responded to deep tillage. Of the other two tests where there was a response to deep tillage, slit-tillage resulted in a 6% decrease in grain yield compared to subsoiling in one test, and an 8% yield increase in the other. Starter fertilizer placement was not critical, but response to starter fertilizer occurred only when deep tillage, either in-row subsoiling or slit-tillage, was used in conjunction with the fertilizer. Starter fertilizer consistently increased early-season plant growth; however, yield response to starter fertilizer was highly dependent on rainfall. Starter fertilizer application increased yield in only one of five tests. There was no benefit from injecting lime.     

商陆(Phytolacca acinosa Roxb.)的锰耐性和超积累

超积累植物的确证对成功实施重金属污染环境植物修复是必不可少的。通过野外调查和营养液培养试验 ,研究超积累植物商陆 (PhytolaccaacinosaRoxb )的锰富集特性 ,结果表明 ,商陆对生长介质中的Mn具有很强的耐性和累积能力。商陆在锰含量高达 114× 10 3 mgkg-1的尾矿废弃地上依然生长良好 ,叶锰含量最高达 19 3× 10 3 mgkg-1。温室培养条件下 ,当生长介质中Mn浓度为 8 0 0 0mmolL-1时 ,虽然其生物量与对照相比有所降低 ,但植株仍能生长。随着生长介质中Mn浓度的升高 ,商陆叶和茎的Mn含量逐渐增加 ,生物富集系数则逐渐降低 ,但是地上部分锰积累量则先增加后减少。当Mn浓度为 5 0 0 0mmolL-1时 ,商陆地上部分锰积累量达到最大值 2 5 8 2mgplant-1;当Mn浓度为 12 0 0 0mmolL-1时 ,商陆仍能完成整个生命周期 ,叶锰含量达到最大值 36 4× 10 3 mgkg-1,生物富集系数为 5 5。不同锰供应水平下 ,商陆吸收的锰有87%～ 95 %被转移到地上部分。这进一步验证商陆的锰超积累特性 ,为利用超积累植物对大面积污染土壤实施植物修复提供了有力证据 ,对锰污染土壤和水体实施植物修复具有很大的应用前景     

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.     

Within-farm variability in number of females mated per week during a one-year period and breeding herd productivity on swine farms

OBJECTIVE: To determine the effect of within-farm variability in the number of females mated per week during a 1-year period on annual breeding herd productivity in swine breeding herds and to apply statistical process control charts to measures of within-farm variability. DESIGN: Longitudinal study. SAMPLE POPULATION: 84 swine farms with a female inventory of 390 to 1,491 sows and gilts (mean, 761 females). PROCEDURE: As a measure of within-farm variability in a breeding herd, SD for the number of females mated per week during a 1-year period was evaluated. Two types of production records for 84 farms were evaluated. One file contained within-farm variability (SD) in mated females for each farm, and the second included annual productivity 19 weeks after week of mating. We also defined forewarning limits as mean +/- 2 SD, using a statistical process control chart. RESULTS: Larger within-farm variability in number of mated females was associated with lower annual measurements, such as fewer pigs weaned per mated female per year and lower farrowing rate. In addition, farms that did not have any weeks outside the forewarning limits for number of mated females produced more pigs weaned per mated female per year than those with 1 or more weeks of over- or underproduction. Furthermore, the number of weeks outside of forewarning limits was positively associated with within-farm variability in number of mated females. CLINICAL IMPLICATIONS: We recommend that farm managers determine a target range for the number of females mated per week to prevent large week-to-week variations in breeding herd operations.     

Technical note: recombinant LHRH fusion protein suppresses estrus in heifers

A recombinant luteinizing hormone-releasing hormone (LHRH) fusion protein was evaluated for its effectiveness in suppression of estrus in heifers. Eight heifers were randomly assigned to two equal treatment groups. Treatments consisted of recombinant ovalbumin-LHRH-7 or recombinant ovalbumin (control). This recombinant chimeric fusion protein consisted of ovalbumin with seven LHRH peptides (ovalbumin-LHRH-7). The plasmid for this protein was expressed in E. coli and was collected and purified as an insoluble protein. One milligram of the respective proteins was suspended in 2 mL of Z-Max adjuvant and administered by intramammary injection three times at 7-wk intervals. Luteinizing hormone-releasing hormone antibody binding was elevated in heifers treated with ovalbumin-LHRH-7 compared to ovalbumin-treated heifers (P < .05). Serum progesterone concentrations (< 1 ng/mL) indicate that the estrous cycle of the four heifers treated with ovalbumin-LHRH-7 was suppressed for a time period ranging from 60 to 238 d, which was different from control heifers (P < .01). Serum progesterone for the control heifers continued to exhibit cyclic profiles over the experimental period. This preliminary study in heifers demonstrated that a chimeric LHRH fusion protein induced elevated concentrations of circulating LHRH antibodies that suppressed estrus for an average of 122 +/- 41 d.     

Active immunization of beef heifers against luteinizing hormone: I. Evaluation of protein carriers and adjuvants on antigenicity of LH

Two experiments were conducted to evaluate two carrier proteins and nine adjuvants in promoting antibody production in heifers immunized against LH. The anti-LH antibody response was evaluated in heifers immunized against LH conjugated to either ovalbumin or keyhole limpet hemocyanin (KLH) (Exp. 1). In Exp. 2, an LH-ovalbumin conjugate was used to evaluate effectiveness of nine different adjuvants in antibody production. Weekly blood samples were collected from all heifers throughout the 23-wk study to determine LH antibody binding activity. In Exp. 1, heifers immunized with the LH-ovalbumin (LH-oval) conjugate had greater LH antibody binding activities (P less than .001) than those immunized with the LH-KLH conjugate. In Exp. 2, nine groups of heifers were immunized with LH-oval suspended in one of nine adjuvants; a 10th group was immunized against ovalbumin alone (control). Only adjuvants that contained at least 40% oil resulted in LH antibody binding activity that differed (P less than .01) from control. These results show that ovalbumin was a superior carrier protein to KLH in enhancing antibody production; adjuvants with greater than 50% oil were superior to those with less oil in promoting LH antibody production.