AAFP and ISFM feline-friendly nursing care guidelines

NURSING CARE: The term nursing care means different things to different people. The authors of these AAFP and ISFM Feline-Friendly Nursing Care Guidelines define nursing care as any interaction between the cat and the veterinary team (veterinarian, technician or nurse, receptionist or other support staff) in the clinic, or between the cat and its owner at home, that promotes wellness or recovery from illness or injury and addresses the patient's physical and emotional wellbeing. Nursing care also helps the sick or convalescing cat engage in activities that it would be unable to perform without help. GUIDELINES RATIONALE: The purpose of the Guidelines is to help all members of the veterinary team understand the basic concepts of nursing care, both in the clinic and at home. This includes methods for keeping the patient warm, comfortable, well nourished, clean and groomed. The Guidelines provide numerous practical tips gleaned from the authors' many years of clinical experience and encourage veterinary team members to look at feline nursing care in ways they previously may not have considered. OVERARCHING GOAL: The primary goal of feline-friendly nursing care is to make the cat feel safe and secure throughout its medical experience.     

A predator unmasked: life cycle of Bdellovibrio bacteriovorus from a genomic perspective

Predatory bacteria remain molecularly enigmatic, despite their presence in many microbial communities. Here we report the complete genome of Bdellovibrio bacteriovorus HD100, a predatory Gram-negative bacterium that invades and consumes other Gram-negative bacteria. Its surprisingly large genome shows no evidence of recent gene transfer from its prey. A plethora of paralogous gene families coding for enzymes, such as hydrolases and transporters, are used throughout the life cycle of B. bacteriovorus for prey entry, prey killing, and the uptake of complex molecules.     

Effect of soil drying on mucilage exudation and its water repellency: a new method to collect mucilage

Despite the importance of mucilage for soil–plant relations, little is known about the effect of soil drying on mucilage exudation. We introduce a method to collect mucilage from maize growing in wet and dry soils. Mucilage was collected from brace roots. The amount of mucilage exuded did not change with soil water content and transpiration rate. Mucilage exuded in dry soils had a higher degree of hydrophobicity, suggesting that the wetting properties of mucilage change in response to soil drying.     

Mycorrhizal communities in relation to biomass production and nutrient use efficiency in two varieties of Douglas fir (Pseudotsuga menziesii var. menziesii and var. glauca) in different forest soils

To investigate the role of arbuscular and ectomycorrhizas for growth and nutrition, Douglas fir (Pseudotsuga menziesii), a species capable of establishing both types of symbioses, was used. Seedlings of two varieties of Douglas fir, var. menziesii (DFM) and var. glauca (DFG), differing in biomass production under non-mycorrhizal conditions, were planted in two soils of different nutrient status without preceding Douglas fir cultivation. After 2 years, the abundance of ectomycorrhizas was significantly higher on DFM than on DFG roots and higher in nutrient rich than in poor soil. Independent of the abundance of ectomycorrhiza colonization, roots of both Douglas fir varieties contained in most cases a minimum of six to nine different fungal species identified by ITS sequencing, which displayed both soil- and seed origin-specific patterns. Rhizopogon vinicolor was associated with DFM, whereas Cadophora finlandia, Sebacinaceous sp., Tricholoma sp. and a Tuber sp. were more frequently found on DFG roots. Ectendomycorrhizas were also identified and included under ectomycorrhiza for determination of nutrient relations. Net primary productivity and nitrogen-use efficiency were positively correlated with the degree of ectomycorrhiza colonization of Douglas fir seedlings suggesting that nitrogen accumulation did not keep pace with biomass production despite increased ectomycorrhizal colonization. Phosphorus-use efficiency was negatively correlated with the abundance of arbuscular mycorrhizas, suggesting higher efficiency of these fungi than of ectomycorrhizas for phosphorus supply to the host. DFM, which had higher inherited growth capacities than DFG, displayed higher ectomycorrhizal colonization than DFG. In our experimental design the physiology of the host tree and soil properties, but not the diversity of fungi present on roots, were decisive factors for formation and abundance of ectomycorrhiza.     

Intensity of browsing on trees and shrubs under experimental variation of cattle stocking densities in southern Bolivia

Mountain forests are traditionally used for cattle grazing during the dry season in southern Bolivia. To evaluate browsing intensity and damage to young trees and shrubs, a forest grazing area was monitored for about 3 months in both 2006 and 2007. Three similar paddocks of about 3 ha each, consisting of grassland and forest in a ratio of about 1:3 were stocked with 0.9, 1.6 and 2.6 tropical livestock units per ha (equivalents of 250 kg of body weight), reflecting low, medium and high stocking densities. Six 5 m × 5 m plots were mapped out within each paddock in 2006. Three additional plots per paddock were added in 2007. Within plots, the individuals of 18 woody species were coded and evaluated weekly for intensity of browsing. Intensity was quantified using five-scale categories reflecting the proportions of plant tissue removed (0 = no browsing, 1 = 1–25%, 2 = 26–50%, 3 = 51–75% and 4 = 76–100%). Across all plant species, the average category of browsing intensity, as determined in the post-grazing evaluation, was affected (P < 0.001) by stocking density. Browsing intensity increased in an approximately linear manner from 1.58 to 2.18 and 2.77 with low, medium and high stocking density, respectively. There was no significant difference between years. Most woody species followed the same general response pattern to stocking density, although some species were only noticeably browsed at high stocking density while a few others were intensively browsed at all stocking densities. The onset of browsing on woody species was observed only after some weeks had passed, indicating that herbaceous plants were preferred as a forage resource. The proportion of fatally damaged individuals, as assessed about 8 months after grazing in 2006, were 10.6%, 8.6% and 11.4% for low, medium and high stocking density, respectively. The percentage of completely browsed individuals increased with stocking density, but 80% of those plant individuals recovered following a resting period of 8 months. However, although most woody species recovered from browsing and fatal damage was infrequent, long-term changes in woody plant species composition and structure caused by grazing cannot be excluded. High stocking density in particular may reduce the vigour of heavily browsed species.     

A New Cell Wall Located N-rich Protein is Strongly Induced During the Hypersensitive Response in Glycine Max L.

Soybean (Glycine max (L.) Merill, cv. Williams 82) plants and cell cultures respond to avirulent pathogens with a hypersensitive reaction. After inoculation of soybean with Pseudomonas syringae pv. glycinea, carrying the avirulence gene avrA, or zoospores from the fungus Phytophthora sojae Race 1, a resistance-gene-dependent cell death programme is activated. A new gene was identified by differential display of mRNAs that is specifically activated during the early phase of incompatible pathogen-soybean interactions but does not respond to compatible pathogens. The gene is strongly induced within 2h after addition of P. sojae zoospores. A similar kinetic pattern was observed for P. syringae (avrA) inoculated soybean cell cultures. The gene encodes a deduced protein of 368 amino acids with a very high content of asparagine and was therefore termed N-rich protein (NRP). The protein is composed of two distinct domains, of which only the C-terminal domain has striking homology to proteins of unknown function from other plants. An antibody raised against the recombinant NRP recognizes a protein of 42kDa. The protein is located in the cell wall as indicated by cell fractionation studies. Comparison of the genomic DNA-sequence with the cDNA, identified two introns within the open reading frame. The NRP-gene is not directly induced by salicylic acid or hydrogen peroxide, indicating a distinct and specific signal transduction pathway which is only activated during programmed cell death. The NRP-gene appears to be a new marker in soybean activated early in plant disease resistance.     

Growth and accumulation of caffeic acid derivatives in Echinacea angustifolia DC. var. angustifolia grown in hydroponic culture

In separate experiments conducted in 2007 and 2008, growth and accumulation of selected caffeic acid derivatives (CADs; i.e., caftaric acid, chlorogenic acid, echinacoside, caffeic acid, cynarin, p-coumaric acid, ferulic acid and cichoric acid) were determined in Echinacea angustifolia DC. var. angustifolia seedlings grown in hydroponic culture (floating raft system) at a density of 122 plant m⁻² (at planting). Plants were harvested 11 (2007) or 16 (2008) weeks after transplanting (i.e., 15 or 20 weeks after sowing). In both years, plants grew vigorously and at harvest approximately half of the plants under observation had developed one to three inflorescences. In 2008, the root yield (2940 kg ha⁻¹) harvested in nearly eight months from two consecutive hydroponic cultures was within the yield reported in the literature for field cultivations lasting two to four years. None of the selected CADs was found in the leaves, while the inflorescences (stem and capitulum) contained only caftaric acid and echinacoside at concentrations higher than the detection limits (0.05 mg g⁻¹ dry weight). Echinacoside, cynarin and chlorogenic acid were found in root tissues at concentrations ranging from 0.36 to 5.25 mg g⁻¹ dry weight. In all plant samples, echinacoside, which is the marker compound for E. angustifolia material, did not reach the minimum quality standard (10 mg g⁻¹ dry weight) for the production of standardized extract. We concluded that short-cycle, high-density greenhouse hydroponic culture stimulates plant growth and root production in E. angustifolia, but it does not ensure sufficient CADs accumulation in dried roots.     

Aerosol transmission of arthropathic and amyloidogenic Enterococcus faecalis.

One-day-old brown layer chicks were exposed to an aerosol of an arthropathic and amyloidogenic Enterococcus faecalis strain alone or after being subjected to treatment with formaldehyde gas (100-200 ppm). Four-day-old chicks were also treated with the same aerosol but after treatment with a Newcastle disease vaccine virus (NDVV) aerosol or intramuscular injection with methylprednisolon at day 1. The same E. faecalis strain was inoculated intramuscularly in day-old chicks as positive control. Bacteremia with time showed that 24 hr after the aerosol the day-old exposed chicks had the highest rate of positive blood cultures (70%-80%). Lower numbers of bacteremic birds at this point in time were found in the chicks treated with E. faecalis aerosol at day 4 (3/10 in the methylprednisolon-treated group and 0/10 in the NDVV-treated group) and the E. faecalis intramuscular-injected group at day 1 (2/10). Formaldehyde gas treatment did not favor the occurrence of bacteremia. NDVV aerosol exposure or injection with corticosteroids did not favor the occurrence of bacteremia 24 hr after E. faecalis aerosol exposure at day 4 either, although 66 days after aerosol, one bird (1/14) treated with NDVV showed bacteremia. A few bacteremic birds were found 10 days after aerosol in the NDVV- and methylprednisolon-treated groups, whereas at 14 days after aerosol, one bacteremic bird was seen in the group subjected to E. faecalis aerosol at day 1, indicating the occurrence of chronic bacteremia. In contrast to the E. faecalis intramuscular-inoculated birds, no joint pathology was seen in the aerosol-exposed groups in spite of the occurrence of chronic bacteremia.     

Meniscal Mineralization in Domestic Cats

Objective: To (1) determine prevalence of radiographically detectable meniscal mineralization in domestic cats and (2) to evaluate the association between meniscal mineralization and degenerative joint disease (DJD). Study Design: Prospective study. Animals: Client‐owned cats (n=100) and 30 feline cadavers. Methods: Randomly selected client‐owned cats were used to determine the prevalence of meniscal mineralization. Stifles from feline cadavers were used to evaluate the relationship between meniscal mineralization (using high‐resolution X‐ray), radiographic DJD, and cartilage damage. Menisci were evaluated histologically. Results: Forty‐six percent of the client‐owned cats had meniscal mineralization detected in 1 or both stifles. Pain scores were not significantly different between stifles with meniscal mineralization and those with no radiographic pathology (P=.38). Thirty‐four of 57 cadaver stifles had meniscal mineralization, which was always located in the cranial horn of the medial meniscus. Percentage mineralization of the menisci was significantly correlated with the cartilage damage score of the medial femoral (r²=0.6; P<.0001) and tibial (r²=0.5; P<.0001) condyles as well as with the total joint cartilage damage (r²=0.36; P<.0001) score and DJD score (r²=0.8; P<.0001). Conclusion: Meniscal mineralization is a common condition in domestic cats and seems to indicate medial compartment DJD. Clinical Relevance: Clinical significance of meniscal mineralization is uncertain. Further work is needed to determine if the meniscal mineralization is a cause, or a consequence of joint degeneration.