scholarly journals 259 Screening of Lespedeza germplasm for forage quality and bioactivity

2019 ◽  
Vol 97 (Supplement_3) ◽  
pp. 90-90
Author(s):  
Thomas H Terrill ◽  
Breyanna Morning ◽  
Erica Courson ◽  
Bradley Morris ◽  
Harley Naumann ◽  
...  

Abstract Interest in the condensed tannin-containing legume sericea lespedeza (Lespedeza cuneata) as a nutraceutical (bioactive) forage for livestock has been increasing in the United States but other Lespedeza species have not been adequately evaluated. A study was completed to determine the nutritional and bioactivity potential of Lespedeza species obtained from the USDA Plant Genetic Resources Conservation Unit in Griffin, GA. Accessions from 15 Lespedeza species were planted in small plots at Fort Valley State University in Fort Valley, GA. After establishment, forage was harvested, freeze-dried, ground and analyzed for neutral detergent fiber (NDF), acid detergent fiber (ADF), in vitro true digestibility (IVTD), total phenolics (TP), and protein precipitable phenolics (PPP). Species differences were significant (P < 0.01) for all parameters measured. Lespedeza cuneata accessions, including “AUGrazer,” the cultivar most commonly used as an anti-parasitic crop in the United States had NDF, ADF, and IVTD values of 35.7±0.4%, 26.8±0.4%, and 74.3±1.2%, while L. virginica, a native species, had 34.9±3.0%, 26.0±2.5%, and 74.9±4.2%, respectively. The L. cuneata accessions averaged 179.6±4.3 and 133.6±3.5 mg/g of forage material for TP and PPP, while L. virginica averaged 564.2±24.6 and 306.5±19.9 mg/g, respectively. Other species varied from 30.5±3.0 to 47.4±4.2% NDF, 22.9±1.6 to 36.4±3.6% ADF, 55.2±5.9 to 81.6±3.4% IVTD, and 107.7±17.4 to 283.5±34.7 and 55.2±14.0 to 139.4±28.1 mg/g of forage for TP and PPP, respectively. Based upon these results, Lespedeza species tested in this study, particularly L. virginica, have potential as nutraceutical forages for livestock production systems. As L. cuneata accessions established and grew much better than other Lespedeza species in this study, agronomic testing of this germplasm collection in other environments is warranted. In addition, determining potential anti-parasitic properties of these species using in vitro and in vivo testing would be beneficial.

1984 ◽  
Vol 64 (3) ◽  
pp. 637-642 ◽  
Author(s):  
S. L. FALES

A normal and a low-tannin sericea lespedeza (Lespedeza cuneata (Dumont) G. Don.) cultivar were grown in controlled environments under a warm (32/24 °C) or cool (22/17 °C) temperature regime. Both cultivars accumulated more dry matter at the higher temperature. The normal-tannin sericea contained a higher concentration of tannin, and lower concentrations of crude protein and neutral detergent fiber (NDF than the low-tannin sericea. Tannin concentration in the leaves of the normal-tannin cultivar was 10 percentage units greater and crude protein and NDF were each 3 units lower at 32/24 °C than at 22/17 °C. Tannin concentration in the leaves of the low-tannin cultivar was 2 percentage units higher, crude protein was 3 units lower, and NDF was 3 units higher at 32/24 °C than at 22/17 °C. In vitro dry matter disappearance (IVDMD) of the normal-tannin leaves was approximately 20 percentage units less than that of the low-tannin leaves, and was not influenced by temperature. Stems were more digestible than the leaves in both cultivars, but normal-tannin stems were slightly less digestible than the low-tannin stems. The IVDMD of low-tannin stems was 6 units lower at 32/24 °C than at 22/17 °C. Future breeding efforts with low-tannin sericea should place emphasis on lower tannin and NDF concentrations because both these components tend to increase with temperature and bear negative associations with IVDMD.Key words: Lespedeza cuneata, neutral detergent fiber, crude protein, forage quality


Author(s):  
A. Hakam ◽  
J.T. Gau ◽  
M.L. Grove ◽  
B.A. Evans ◽  
M. Shuman ◽  
...  

Prostate adenocarcinoma is the most common malignant tumor of men in the United States and is the third leading cause of death in men. Despite attempts at early detection, there will be 244,000 new cases and 44,000 deaths from the disease in the United States in 1995. Therapeutic progress against this disease is hindered by an incomplete understanding of prostate epithelial cell biology, the availability of human tissues for in vitro experimentation, slow dissemination of information between prostate cancer research teams and the increasing pressure to “ stretch” research dollars at the same time staff reductions are occurring.To meet these challenges, we have used the correlative microscopy (CM) and client/server (C/S) computing to increase productivity while decreasing costs. Critical elements of our program are as follows:1) Establishing the Western Pennsylvania Genitourinary (GU) Tissue Bank which includes >100 prostates from patients with prostate adenocarcinoma as well as >20 normal prostates from transplant organ donors.


Crop Science ◽  
1994 ◽  
Vol 34 (1) ◽  
pp. 279-285 ◽  
Author(s):  
Noa Diwan ◽  
Gary R. Bauchan ◽  
Marla S. McIntosh

2019 ◽  
Vol 109 (12) ◽  
pp. 2055-2063 ◽  
Author(s):  
Francesca Dennert ◽  
Joana Beatrice Meyer ◽  
Daniel Rigling ◽  
Simone Prospero

Intraspecific cryptic invasions may occur when new strains of an invasive species are introduced into an area where this species had already been introduced previously. In plant pathogens, such invasions are not well studied, even if, potentially, they can have severe consequences. Here, we investigated the effects of a potential intraspecific invasion in Europe of Cryphonectria parasitica, the causal agent of chestnut blight. Specifically, we tested the hypotheses that (i) non-European strains are more virulent on Castanea sativa than those already present in Europe because they have never encountered this new host, and (ii) the variation in virulence among strains is higher within native than within introduced populations. In a greenhouse, 2-year-old C. sativa seedlings were inoculated with Cryphonectria parasitica strains from South Korea, the United States, and Switzerland, and lesion development and seedling mortality were recorded weekly. Additionally, growth and sporulation of the strains were measured in vitro on agar medium at 15 and 24°C. Although lesion growth was similar for all strains, seedlings inoculated with strains from South Korea and Switzerland died faster than seedlings inoculated with strains from the United States. Moreover, in vitro strains from South Korea grew faster and produced more spores at both temperatures than the strains from the other two countries. In conclusion, our results did not support the two hypotheses. All strains, regardless of their origin, were found to be highly virulent on the inoculated chestnut seedlings. Nevertheless, current phytosanitary measures to avoid the introduction of new genotypes of C. parasitica into Europe should be further implemented.


2005 ◽  
Vol 79 (17) ◽  
pp. 11412-11421 ◽  
Author(s):  
Chang-Won Lee ◽  
David E. Swayne ◽  
Jose A. Linares ◽  
Dennis A. Senne ◽  
David L. Suarez

ABSTRACT In early 2004, an H5N2 avian influenza virus (AIV) that met the molecular criteria for classification as a highly pathogenic AIV was isolated from chickens in the state of Texas in the United States. However, clinical manifestations in the affected flock were consistent with avian influenza caused by a low-pathogenicity AIV and the representative virus (A/chicken/Texas/298313/04 [TX/04]) was not virulent for experimentally inoculated chickens. The hemagglutinin (HA) gene of the TX/04 isolate was similar in sequence to A/chicken/Texas/167280-4/02 (TX/02), a low-pathogenicity AIV isolate recovered from chickens in Texas in 2002. However, the TX/04 isolate had one additional basic amino acid at the HA cleavage site, which could be attributed to a single point mutation. The TX/04 isolate was similar in sequence to TX/02 isolate in several internal genes (NP, M, and NS), but some genes (PA, PB1, and PB2) had sequence of a clearly different origin. The TX/04 isolate also had a stalk deletion in the NA gene, characteristic of a chicken-adapted AIV. By analyzing viruses constructed by in vitro mutagenesis followed by reverse genetics, we found that the pathogenicity of the TX/04 virus could be increased in vitro and in vivo by the insertion of an additional basic amino acid at the HA cleavage site and not by the loss of a glycosylation site near the cleavage site. Our study provides the genetic and biologic characteristics of the TX/04 isolate, which highlight the complexity of the polygenic nature of the virulence of influenza viruses.


1999 ◽  
Vol 123 (4) ◽  
pp. 285-289 ◽  
Author(s):  
Gary V. Doern ◽  
Angela B. Brueggemann ◽  
Michael A. Pfaller ◽  
Ronald N. Jones

Abstract Objective.—To assess the performance of clinical microbiology laboratories in the United States when conducting in vitro susceptibility tests with Streptococcus pneumoniae. Methods.—The results of a nationwide College of American Pathologists Proficiency Survey test sample, in which susceptibility testing of an isolate of S pneumoniae was performed, were assessed with respect to precision and accuracy. Results.—Wide variability was noted among participating laboratories with both minimum inhibitory concentration procedures and disk diffusion susceptibility tests when both methods were applied to S pneumoniae. Despite this high degree of variation, categorical interpretive errors were uncommon. Numerous laboratories reported results for antimicrobial agents that are not recommended by the National Committee for Clinical Laboratory Standards for tests with S pneumoniae. Conclusions.—Current susceptibility testing practices with S pneumoniae in the United States indicate limited precision and a tendency for laboratories to test and report results obtained with antimicrobial agents of questionable therapeutic value against this organism. Continued efforts to standardize susceptibility testing of S pneumoniae in the United States are warranted. In addition, modifications of existing interpretive criteria may be necessary.


1970 ◽  
Vol 8 (1) ◽  
pp. 78-81
Author(s):  
Shubham Prajapati ◽  
Sanjay Saha ◽  
B Shambulingappa ◽  
Dilip Kumar Ch. ◽  
Bikash Sahoo

Generic Nebulized aerosol is often perceived as inferior to their branded counterparts; however, they are safe and effective if they can meet the regulatory requirements. International regulatory agencies have developed recommendations and guidance for bioequivalence approaches of orally inhaled drug products (OIDPs) for local action. The objective of this article is to discuss the approaches can be used for to show bioequivalence requirement for Food and Drug Administration (FDA) in the United States of America (USA) with reference product. This review endorsed that inhalation solutions and suspensions undertaken to determine the drug substance delivery rate, total drug substance delivered and Aerodynamic assessment of nebulized aerosols [aerodynamic particle size distribution (APSD)/droplet size distribution (DSD)].These are the most important parameters in characterization, evaluation and bioequivalence studies of nebulizers. These devices operate continuously; once loaded and require little or no co-ordination on the part of user they proved that these devices suitable for weak, pediatric or geriatric patients. The regulatory agencies declared that; there is no specific requirements testing in case of nebulizers like Metered dose inhalers (MDI) and Dry powder inhalers (DPIs). In United States of America (USA) regulation falls under the auspices of centre for devices and radiological health (CDRH), and new devices require 510(k) premarket notification. This review outlines all the bioequivalence test parameter.  


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