Effect of feeding hydrolyzed feather meal and rumen-protected lysine on milk protein and energy utilization in late-lactation Jersey cows.

Hydrolyzed feather meal (HFM) is a feed that is high in rumen undegradable protein; however, it is low in Lys compared with other high rumen undegradable protein sources. Additionally, processing methods differ by facility, which affects AA composition and protein digestibility. The objective of this study was to use lactating dairy cows to determine the effects of feeding 2 sources of HFM that differed by the amount of blood they contained and also to study the effects of supplementing rumen-protected (RP) Lys when these sources of HFM are fed. In this study, 12 multiparous Jersey cows were enrolled in a triplicated 4 × 4 Latin square with 4 periods 28 d in length. Cows were fed 2 total mixed rations that differed by source of HFM. The HFM was included at 4.5% of the diet dry matter, and one source was produced with the addition of poultry blood. Cows were randomly assigned to 1 of 4 treatment sequences. Treatments were as follows: HFM without added blood and no RP-Lys, HFM with added blood and no RP-Lys, HFM without blood and with RP-Lys (22 g of digestible Lys), and HFM with added blood and RP-Lys. The source of HFM containing blood tended to increase dry matter intake (18.3 vs. 17.3 ± 0.72 kg/d), and increased milk yield (20.5 vs. 18.4 ± 1.31 kg/d) and protein yield (0.788 vs. 0.694 ± 0.040 kg/d). The inclusion of RP-Lys did not affect milk or protein yield. In cows fed HFM containing blood, plasma concentration of Lys (82.1 vs. 70.8 ± 4.06 µM) and His (27.8 vs. 17.9 ± 3.15 µM) was higher. The addition of RP-Lys had no effect on the concentration of either plasma Lys or His. Gross energy intake tended to increase for HFM containing more blood (81.4 vs. 77.3 ± 3.29 Mcal/d); however, no difference was observed for intake of digestible energy (52.0 ± 2.20 Mcal/d) or metabolizable energy (46.4 ± 2.02 Mcal/d). Similar to dry matter intake, N intake increased with the inclusion of HFM containing blood, but crude protein digestibility decreased (61.6 vs. 66.0%). Results of this study highlight that source of HFM can be a factor that affects milk production and that this in part is due to differences in the profile of AA. Additionally, the observation that plasma His and milk protein increased with the consumption of HFM containing more blood suggests that His may have played a role in increasing milk and milk protein yield.

Effectiveness of exercise versus normal activity on acute low back pain: an integrative synthesis and meta-analysis.

There are a variety of protocols used to treat acute low back pain in adults. Therapies currently prescribed include bed rest, normal activity, and exercise therapy. The effectiveness of each of these treatments is controversial. The purpose of this study is to compare the effectiveness of exercise therapy with normal activity in the treatment of employed adults with acute low back pain through an integrative synthesis and meta-analysis of published research. The integrative synthesis and meta-analytical results support the hypothesis that employed adults diagnosed with acute low back pain will have fewer number of days absent from work after exercise therapy when compared to number of days absent from work after normal activity. This study's weighted P is 0.0000003109. The weighted effect size D is 0.4785 and this is a strong effect of exercise on number of days absent from work. This study concluded that exercise therapy should be prescribed for the treatment of adults with acute low back pain to expedite recovery. The results of this study allow the health care provider to confidently prescribe exercise therapy for acute low back pain. This study can be used to support exercise therapy as an evidence based care protocol for health care providers.

Ectopic expression of Hox-2.3 induces craniofacial and skeletal malformations in transgenic mice.

To better understand the role of the Hox-2.3 murine homeobox gene during development, a dominant gain-of-function mutation was generated. The developmental malformations that resulted when the chicken beta-actin promoter was used to direct widespread expression of the Hox-2.3 gene in transgenic mice included early postnatal death as well as craniofacial abnormalities, including open eyes and cleft palate. Ventricular septal defects were also observed in the hearts of three transgenic mice. Skeletal malformations were seen in the bones of the craniocervical transition, with the occipital, basisphenoid, and atlas bones deficient or misshapen. Interestingly, one mutant exhibited an extra pair of ribs as well as alterations in cervical vertebrae identities. Some of the malformations observed in Hox-2.3 gain-of-function mutants overlap with those seen in Hox-1.1 and Hox-2.2 misexpression mutants which suggests functional similarities between paralogous homeobox genes. The results of these experiments are consistent with a role for Hox-2.3 in specifying positional information during development.

A functional c-myb gene is required for normal murine fetal hepatic hematopoiesis.

The c-myb proto-oncogene encodes a sequence-specific DNA-binding protein. To better understand its normal biological function, we have altered the c-myb gene by homologous recombination in mouse embryonic stem cells. Resulting homozygous c-myb mutant mice displayed an interesting phenotype. At day 13 of gestation these mice appeared normal, suggesting that c-myb is not essential for early development. By day 15, however, the mutant mice were severely anemic. Analysis indicated that embryonic erythropoiesis, which occurs in the yolk sac, was not impaired by the c-myb alteration. Adult-type erythropoiesis, which first takes place in the fetal liver, was greatly diminished in c-myb mutants, however. Additional hematopoietic lineages were similarly affected. These results are compatible with a role for c-myb in maintaining the proliferative state of hematopoietic progenitor cells.

Demonstration of Epstein-Barr virus in immunoblastic sarcoma of B-cells arising in a child with primary immunodeficiency disease.

The subject of this investigation was an 11-month-old infant girl who presented with a pathological fracture of the right femur due to a metastasis from an abdominal immunoblastic sarcoma. Her past history included recurrent, intractable bacterial and fungal infections. Investigations of her immune status revealed low numbers of T-lymphocytes, a reversed T-helper (TH)/T-suppressor (TS) cell ratio, no response of her peripheral blood lymphocytes to pokeweed mitogen, phytohemagglutinin, concanavalin A, and Candida albicans, and an inability of her cells to react in a mixed lymphocyte culture. Serum levels of IgG, IgM, and IgA were all below normal. No thymic shadow was visible on the chest radiograph. There was no evidence of adenosine deaminase or nucleoside phosphorylase deficiencies. The tumor cells exhibited both surface IgM and IgG, and many of the cells contained large amounts of cytoplasmic IgM. Light chain specificity was restricted to lambda chain for both surface and cytoplasmic immunoglobulin. Ultrastructural study of the tumor cells revealed the presence of both intranuclear and cytoplasmic virions in roughly 1% of the tumor cells. These viral particles strongly resembled herpes viruses. DNA-hybridization studies on the neoplasm revealed the presence of 7-10 genome equivalents of Epstein-Barr virus-DNA per tumor cell.