No abstract

The objective was to measure rumen fermentation and duodenal flow of amino acids and nonammonia N components in five groups of five ruminally and duodenally cannulated wethers that were fauna-free, or inoculated with the ciliate protozoa genera of Isotricha, Dasytricha, Entodinium, or a normal population (total) of fauna. They were used in two 25-d periods and fed a haycrop-based diet in the first period and a corn silage-based diet in the second period. Feces, duodenal digesta, and rumen contents were sampled in each period and analyzed. The number of Entodinium in wethers containing the Entodinium monofauna was higher than the total protozoa numbers, including Entodinium, in wethers containing total fauna population. The type of diet or fauna did not affect total volatile fatty acid concentrations in rumen fluid. The ammonia N concentration in rumen fluid was higher in wethers containing total fauna (25 mg/100 ml) than in fauna-free wethers fed the two diets (18 and 12 mg/ 100 ml). In comparison with the respective fauna-free wethers, the concentration of ammonia in wethers containing Entodinium was higher when fed the corn silage diet, but not different when fed the haycrop diet. Ruminal presence of total fauna or Entodinium decreased the nonammonia N by 16 and 17%, and total amino acid flows from the stomach by 20 and 19%, respectively. Flow of bacteria N was decreased in wethers fed the two diets when Entodinium or total fauna were present in the rumen. The presence of Isotricha resulted in higher flow of bacteria N in wethers fed the haycrop diet, but the presence of Dasytricha resulted in higher bacteria N flow in wethers fed the corn silage diet. Entodinium was the most detrimental of ciliate protozoa species concerning protein nutrition of the host ruminant.

No abstract

Naturally fauna-free (FF) wethers, equipped with ruminal and duodenal cannulas, were used in two groups of eight (Group A) and seven (Group B) animals in six consecutive experimental periods, each lasting for 28 d. The objective was to measure ruminal fermentation traits, and flows of nonammonia nitrogen (NAN), total amino acid (TAA), and bacterial nitrogen (BN) from the stomach after inoculation with individual ciliate protozoa species in each period. The wethers in both groups were fed a diet based on corn silage, haylage, and soybean meal, and they remained FF during the first period. At the beginning of each other period, the wethers were progressively inoculated intraruminally with one individual major species of ruminal ciliate protozoa or total fauna (TF). Thus, Group A was progressively inoculated (+) with Dasytricha ruminantium (DS), Polyplastron multivesiculatum (PP), Isotricha intestinalis (IS), Entodinium caudatum (EN) and TF-type A. Also, Group B was progressively inoculated (+) with IS, DS, Epidinium ecaudatum (EP), Eudiplodinium maggi (EU), and EN. Duodenal digesta and ruminal fluid were collected and sampled in each period on d 26 and 28, respectively, and subjected to chemical analyses. A significantly higher (P < .05) pH (6.4) in ruminal fluid of the Group A wethers was obtained when each DS, DS+PP, DS-PP-IS+EN, and TF population was present in the rumen than when the wethers were FF (6.2). In the Group B wethers, pH (6.1) was lower (P < .05) for the population of IS-DS-EP+EU than for other populations (6.2 to 6.3). The concentration of total VFA in ruminal fluid was higher (P < .05) in the Group B wethers when IS, IS+DS, or IS-DS+EP populations were present in the rumen than when the wethers were FF. The flow of NAN, TAA, and BN from the stomach to the intestinal tract was generally lower for different protozoa populations than for the FF period. Largest decreases (P < .05) in the flow of NAN, TAA, and BN occurred when EN was added into the rumen of wethers in the A and B groups, which already contained populations of DS-PP+IS and IS-DS-EP+EU, respectively. Holotrich protozoa had very little effect on the protein metabolism in the rumen, but cellulolytic protozoa (PP, EP, and EU) and EN decreased the efficiency of protein utilization by the ruminant host.

No abstract

Neill, L. and Ivan, M. 1996. Comparison of methods for isolation of protozoa from ruminal fluid' can J Anim Sci' 76: 4g l-4g3. Isolation of protozoa from ruminal fluid taken from the same cow on five different days was carried out by three methods based on sedimentation-o, on r,ti.ution r.ing ro l.,rlr..rr't tpr"lg-r0) or 20 pm mesh The content of the cheesecloth was rinsed with 200 mL of 0.85% saline. which was then strained through fresh cheesecloth into the first fraction and the total volume recorded' A portion representing 600 mL of the original ruminal fluid was equaliy divided among nine centrifuge bottles using a 60-mL tyting" while maintaining constant stining' The bottles were ceitrifuged at 500 x g for l0 min at 5oC' The supematant was decanted and the pellet of each bottle resuso*a.a in 200 mL of cold saline' Initially only a small amount of the 200 mL cold saline was used with constant stirring to resuspend the paste-like pellet' The centrifugation and reiuspension were repeated three times' The residue of each bottie was again resuspended in cold saline' The contents of three bottles were combined and transfetred quantitatively into a l-L graduate cylinder' Cold saline was added to each cylinder to ipproximately 800 mL, followed by 135Abbreviations: DAPA, diaminopemelic acid; PMB-10' filtration using l0-pm mesh polyester monofilament bag; PMB-20, filtrition using 20-pm mesh polyester monofila- For personal use only.

No abstract

Pseudomonas aeruginosa is a significant nosocomial pathogen responsible for severe and life threatening infections particularly in immunocompromised patients. This organism is ubiquitous in healthcare environments particularly water systems which act as a reservoir of infection. Recognition of a potential outbreak and having the ability to quickly identify and mitigate sources of exposure is critical for effective infection control. Historically analysis of P. aeruginosa antibiogram profiles represents a convenient and frequently used ‘first line’ indicator of strain relatedness. Reported here is a comparison of P. aeruginosa antibiogram profiles with those obtained using rapid Variable Number Tandem Repeat (VNTR) for patient and environmental isolates in in three separate local nosocomial outbreaks. The results demonstrate that antibiogram profiles from P. aeruginosa should not be employed as presumptive indicators of relatedness, doing so can falsely re-assure clinicians. Use of rapid molecular typing method VNTR allows genotypically identical strains to be unambiguously identified within 48 h.