Characteristics of water soluble markers for measuring rumen liquid volume and dilution rate

The utility of five water soluble markers (WSM) for measuring rumen liquid volume and dilution rate was examined in nine in vitro and in vivo experiments. The WSM tested included polyethylene glycol (PEG) and ethylenediaminetetraacetic acid (EDTA) complexes of Cr, Co, Fe and Yb. Feedstuffs incubated in vitro absorbed variable amounts of distilled H2O and autoclaved rumen fluid with roughages imbibing greater (P less than .05) amounts of fluid than feeds higher in starch. Liquid present in the feeds tested reached equilibrium with added WSM in about 20 min. Corn grain in the whole or ground form appeared to exclude 4 to 16% of the WSM while imbibing water. Cottonseed hulls reduced detectable PEG due to some water soluble substance present. The WSM tested did not produce different estimates of dilution rate (P = .65) and volume (p = .29) of steers fed either 80% whole shelled corn, 90% chopped alfalfa hay or 90% prairie hay diets. Ruminal liquid measured by hand removal was about 4% greater than volume estimated by WSM. The percentage of total ruminal water associated with solids varied from 27 to 86% among steers. Compared with steers fed an 80% whole shelled corn diet, steers fed equal dry matter from alfalfa hay had 15% more dry matter in the rumen, 21% larger liquid volume, 80% greater ruminal liquid dilution rate and 116% greater rate of liquid flow from the rumen. Dilution rate of ruminal liquid during feeding was examined with six steers fed a 90% chopped alfalfa hay diet once daily at 1.8% of body weight. Dilution rate estimated with Co EDTA increased by 166% during the 4 h after feeding. The WSM did not influence (P greater than .10) digestibility of dry matter with steers fed a 90% roughage or a 90% concentrate ration. Recovery of WSM administered via a rumen cannula ranged from 96.8 to 99.7% in feces and 1.2 to 3.4% in urine. All WSM examined appeared suitable for estimating rumen liquid volume and dilution rate for diets not containing cottonseed hulls.     

Reaction of potato varieties toPotato mop-top virus infection in the andes

The unexpected detection ofPotato mop-top virus (PMTV) in potatoes growing at several locations in the U.S.A. and Canada in 2002 has led to the realization that this soil-borne virus may be widespread throughout the potato-producing regions of both countries. A lack of information concerning the response of U.S. cultivars to PMTV infection caused us to examine the effects of PMTV on field-grown plants at three locations in the Peruvian Andes where the virus and its fungal vector,Spongospora subterranea, are endemic. All 21 U.S. cultivars tested proved susceptible to PMTV infection, especially at La Victoria where the overall incidence of both PMTV and powdery scab was high. Symptom expression in the foliage proved to be an unreliable indicator of virus infection, and thus, more reliable serological (NCM-ELISA) and nucleic acid-based techniques (NASH and RT-PCR) were used to monitor tuber tissue for the presence of PMTV. As much as 25% of field-grown tubers of cvs Kennebec, Monona, and Norland were infected with PMTV, but no correlation between virus infection and either the incidence or severity of powdery scab for any variety was apparent. Although PMTV infection did not result in the appearance of spraing or other internal necrotic reactions resembling those reported from many North American and European locations, a disproportionate proportion of infected tubers did exhibit a reticulate surface cracking. In hydroponic culture, the proportion of cracked tubers increased dramatically when the nutrient solution was seeded with virus-infestedS. subterranea. Comparatively few tubers of cvs Monona and Russet Burbank exhibited this surface cracking, suggesting that these two varieties may be somewhat tolerant to PMTV infection.     

Compositional analysis of tubers from insect and virus resistant potato plants

Genetically modified potato plants that are resistant to the Colorado potato beetle, plus either the potato leaf roll virus or potato virus Y, have recently been commercialized. As part of the safety assessment for plants produced by modern biotechnology, the composition of the food/feed must be compared to that of the food/feed produced by an equivalent plant variety from a conventional source. The composition of important nutritional and antinutritional factors in tubers produced by virus- and insect-resistant potato plants were compared to tubers produced by conventional potato plants. Key nutritional, quality, and antinutritional components measured were total solids, vitamin C, dextrose, sucrose, soluble protein, and glycoalkaloids. Proximate analyses included fat, ash, calories, total protein, and crude fiber. Minor nutrients measured were vitamin B6, niacin, copper, magnesium, potassium, and amino acids. The results from these analyses confirm that tubers produced by insect- and virus-protected varieties are substantially equivalent to tubers produced by conventional potato varieties.     

Effect of Physiologically Relevant Heat Shock on Development,Apoptosis and Expression of Some Genes in Buffalo (Bubalus bubalis) Embryos Produced In Vitro

For investigating the effects of physiologically relevant heat shock, buffalo oocytes/embryos were cultured at 38.5°C (control) or were exposed to 39.5°C (Group II) or 40.5°C (Group III) for 2 h once every day throughout in vitro maturation (IVM), fertilization (IVF) and culture (IVC). Percentage of oocytes that developed to 8‐cell, 16‐cell or blastocyst stage was lower (p < 0.05) and the number of apoptotic nuclei was higher (p < 0.05) for Group III > Group II > controls. At both 8–16‐cell and blastocyst stages, relative mRNA abundance of stress‐related genes HSP 70.1 and HSP 70.2 and pro‐apoptotic genes CASPASE‐3, BID and BAX was higher (p < 0.05) in Groups III and II than that in controls with the exception of stress‐related gene HSF1. Expression level of anti‐apoptotic genes BCL‐XL and MCL‐1 was also higher (p < 0.05) in Groups III and II than that in controls at both 8–16‐cell and blastocyst stages. Among the genes related to embryonic development, at 8–16‐cell stage, the expression level of GDF9 was higher (p < 0.05) in Group III than that in controls, whereas that of GLUT1, ZAR1 and BMP15 was not significantly different among the three groups. At the blastocyst stage, relative mRNA abundance of GLUT1 and GDF9 was higher (p < 0.05) in Group II than that in controls, whereas that of ZAR‐1 and BMP15 was not affected. The results of this study demonstrate that exposure of buffalo oocytes and embryos to elevated temperatures for duration of time that is physiologically relevant severely compromises their developmental competence, increases apoptosis and affects stress‐, apoptosis‐ and development‐related genes.     

Buffalo (Bubalus bubalis) ES Cell–Like Cells are Capable of In Vitro Skeletal Myogenic Differentiation

When buffalo embryonic stem (ES) cell–like cells that expressed surface markers SSEA‐4, TRA‐1‐60, TRA‐1‐81, CD9 and CD90 and intracellular markers OCT4, SOX2 and FOXD3, as shown by immunofluorescence, and that expressed REX‐1 and NUCLEOSTEMIN as confirmed by RT‐PCR, were subjected to suspension culture in hanging drops in absence of LIF and buffalo foetal fibroblast feeder layer support, they differentiated to form three‐dimensional embryoid bodies (EBs). Of 231 EBs examined on Day 3 of suspension culture, 141 (61.3 ± 3.09%) were of compact type, whereas 90 (38.4 ± 3.12%) were of cystic type. The cells obtained from EBs were found to express NF‐68 and NESTIN (ectodermal lineage), BMP‐4 and α‐skeletal actin (mesodermal lineage), and α‐fetoprotein, GATA‐4 and HNF‐4 (endodermal lineage). When these EBs were cultured on gelatin‐coated dishes, they spontaneously differentiated to several cell types such as epithelial‐ and neuron‐like cells. When EBs were cultured in the presence of 1 or 2% DMSO or 10^?8 m or 10^?7 m retinoic acid for 25 days, ES cells could be directed to form muscle cell–like cells, the identity of which was confirmed by expression of α‐actinin by immunofluorescence and of MYF‐5, MYOD and MYOGENIN genes by RT‐PCR. MYOD was first detected on Day 10 in both treatment groups and on Day 15 in controls, whereas MYOGENIN was first detected on Day 10, Day 15 and Day 25 in the presence of retinoic acid, in the presence of DMSO and in controls, respectively. The present study demonstrates the ability of buffalo ES cell–like cells to undergo directed differentiation to cells of skeletal myogenic lineage.     

Analysis of reports of human exposure to Micotil 300 (tilmicosin injection)

OBJECTIVE: To identify clinical signs associated with and outcome of human exposure to Micotil 300 (tilmicosin injection). DESIGN: Retrospective case series. STUDY POPULATION: Reports of 3,168 human exposures to Micotil 300. PROCEDURES: Reports of human exposure to Micotil 300 submitted to the Elanco Animal Health Pharmacovigilance Unit between March 1992 and March 2005 were reviewed. RESULTS: At least 1 clinical sign was described in 1,404 (44%) reports, whereas the remaining 1,764 (56%) exposures were presumably asymptomatic. Eighty percent of exposures involved males; mean age was 38 years. Sixty-one percent of exposures were a result of accidental injection, with injection site pain, bleeding, swelling, or inflammation being the most common signs, followed by nausea, tachycardia, dizziness, anxiety, an abnormal taste, headache, lightheadedness, limb pain, paresthesia, chest pain, and soreness. Only 156 (5%) reports involved serious adverse effects (ie, tachycardia, bradycardia, hypertension, hypotension, heart disorder, chest pain, tachypnea, or death). There were reports of 13 deaths following tilmicosin exposure, but only 2 of those deaths were related to accidental exposure. Time to onset of clinical signs was < or = 60 minutes in 63 of the 156 (40%) reports involving serious adverse effects. CONCLUSIONS AND CLINICAL RELEVANCE: Results suggest that the overall risk of accidental human exposure to tilmicosin resulting in serious adverse effects is low (approx 2 people for every 1 million doses administered). Nevertheless, safe handling and proper use should be emphasized.     

Radiographic assessment of pulmonary fluid clearance and lung aeration in newborn calves delivered by elective Caesarean section

The aim of this study was to develop a radiographic standard for the assessment of pulmonary fluid clearance and lung aeration in newborn calves. Caesarean‐delivered mature calves (n = 9) underwent lung assessment by thoracic radiography as well as arterial and venous blood gas analysis within the first 30 min, 1, 2, 3, 6, 12 and 24 hr after birth. The results indicated that newborn calves delivered by elective Caesarean section suffered from a physiological combined respiratory and metabolic acidosis with the dominance of respiratory acidosis, and an improvement in these conditions was recorded within 24 hr after birth. Concerning the radiographic results, clear lung fields, improvement in lung expansion, air content of the lung and absence of lung opacification occurred within 24 hr of birth. Furthermore, the ventral lung quadrant showed an improvement in radiographic opacification and lung expansion earlier than the dorsal lung regions. The findings of this study support the potential role of thoracic radiography in the assessment of pulmonary fluid clearance and lung aeration in newborn calves.