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Extracting Protostrongylus spp. larvae from bighorn sheep feces.

First-stage larvae of Protostrongylus spp. were more numerous in the core of bighorn sheep (Ovis canadiensis canadiensis) pellets than near the surface. As a result, only 22% could be extracted from whole pellets and the numbers collected did not reflect the total number of larvae present in samples. Crushing semi-dried pellets yielded seven times as many larvae and numbers collected were correlated with totals present. The use of tissue, in addition to a screen filter in a beaker extraction method, produced a cleaner sample and did not affect larval collection or the correlation. By comparison, most first-stage larvae of Parelaphostrongylus tenuis from white-tailed deer (Odocoileus virginianus) were near the surface of fecal pellets where they may be removed readily by water.

Animals↗

Quantification of Clostridium botulinum type A toxin and organisms in the feces of a case of infant botulism and examination of other related specimens.

Bacteriological examinations were performed on the first case of infant botulism in Japan (an infant boy aged 79 days at onset of illness). Clostridium botulinum type A toxin and organisms were detected continually in the stools of the infant for at least 31 days and 39 days, respectively. The highest levels of the toxin and of the population of the organisms, 7.8 X 10(4) LD50/g and 1.3 X 10(6) colony forming units (cfu)/g, were detected in the stool specimen taken on the 20th day of illness. Type A organisms were detected also in the honey fed to the infant before onset of illness, teats of his feeding bottle, soil specimens taken at the house entry and the vacuum-cleaner dust. Fecal excretion of the toxin and organisms was no longer detected from the 68th day of illness and he recovered.

Botulinum Toxins↗

[Bile acid concentrations in serum, bile and feces of healthy calves and calves with diarrhea].

On 32 calves (age 3 to 14 days) with spontaneously occurring diarrhoea, the following investigations were carried out: Regular examination of serum bile acid concentrations, collection of the entire faeces with determination of bile acid concentrations, as well as microbiological examinations. Six clinically healthy calves served as control group. In addition, bile acids in bile were determined in 16 other calves of the same age group and in 6 beef bulls. There was no significant influence of daytime or feed intake on serum bile acid concentration in diarrhoeic or healthy calves. Possibly due to the low concentrations of bile acids in the bile of young calves (4.8 +/- 3.7 mmol/l, compared to 57 +/- 13 mmol/l in the bulls), the concentrations in faeces were also rather low (control group 623 +/- 92, calves with diarrhoea 318 +/- 277, after diarrhoea. 794 +/- 935 mumol/kg). Most of it was cholic acid, whereas only traces of desoxycholic acid were found. In spite of the comparatively low concentrations of fecal bile acids, the diarrhoeic calves excreted larger amounts of bile acids than the healthy calves (12.7 +/- 13.5 vs. 1.4 +/- 0.8 mumol/kg), but this was independent of the type of enteropathogen or pathogen combinations which were detected. There were no indications for a direct influence of the diarrhoea by bile acids. However, through enteral bile acid losses, profuse diarrhoea lasting several days can cause a reduction in the total bile acid pool.

Animals↗

[Feasibility of detecting steroid hormones in cattle feces for monitoring ovarian function].

Faecal material from four non pregnant cows was withdrawn in two-day intervalls during a four-week period. At the same time bloodsamples were taken to monitor the ovarian function. Clinical and ultrasonographical examinations were recorded in parallel. To look for the stability of the faecal steroid analogues for P4 (Progesterone) and E2 (Estradiol-17 beta) faecal material was stored at 37 degrees C and samples from that analyzed in two-day intervals. The P4 (Progesterone)-analogues values in the faeces showed good correlation to cycling ovarian functions as monitored by bloodlevels from P4, clinical examination and ultrasonography. In contrast the E2-analogues values showed no cycling pattern. One cow however showed ovarian cysts which was monitored in the P4 values for blood and faeces. Concerning the stability of the steroid analogues it could be demonstrated that the P4-values show a steady decrease with minimum values of 20 ng/g dry material. During the first four days after sampling reliable values for clinical interpretations can be found. The concentrations for E2 are very inconstant and so far not of interest. The investigation shows that the faecal steroid P4 can be used for monitoring ovarian function. It has to be analyzed within four days after sampling when stored at room temperature.

Animals↗

[Use of a fast test to detect rotavirus in feces].

The commercially available immunoassay "OnSite Rotavirus" was used for the detection of animal rotaviruses in 113 faecal samples. The sensitivity of the test was 88% and the specificity 96% compared with reference methods (EIA, EM). This test would detect approximately 4.4 x 10(6) to 1.8 x 10(7) virus particles per ml. The presence of virus could be demonstrated in fresh faecal samples from cattle, horses and pigs within a few minutes. The rotaviruses of group A were identified independently of the virus serotype. Further results and additional problems of using this test kit are described.

Animals↗

[Children hospitalized with acute gastroenteritis. II. No relation between clinical symptoms and causative agents isolated from feces].

OBJECTIVE: To determine if it is possible to predict a bacterial cause in children with gastroenteritis on the basis of clinical features and if the number of stool cultures can be reduced. DESIGN: Retrospective. METHOD: The results of the stool cultures of 227 children admitted with acute gastroenteritis to the department of Paediatrics of Sint Joseph Hospital, Veldhoven, the Netherlands, in the period 1992-1996 were related by review of medical records to clinical symptoms and blood tests. The diagnostic values of the various parameters were calculated. RESULTS: Rotavirus was identified in 40% of the faeces of the children, other viruses in 10% and bacteria in 8%. In 95% the bacterial pathogen was identified in the first stool sample. The diagnostic value of the investigated parameters was low. CONCLUSION: It is not possible on the basis of clinical parameters to predict a bacterial gastroenteritis. The number of stool samples may, however, be reduced if the stools of each child with acute diarrhoea are first investigated for rotavirus. Only if this test is negative are further investigations required. The number of bacterial cultures can be limited to one stool sample.

Acute Disease↗

The prevalence of verotoxins, Escherichia coli O157:H7, and Salmonella in the feces and rumen of cattle at processing.

Fecal samples collected from cattle at processing during a 1-year period were tested for verotoxins (VT1, VT2), Escherichia coli O157:H7, and Salmonella. Verotoxins were detected in 42.6% (95% CI, 39.8% to 45.4%), E. coli O157:H7 in 7.5% (95% CI, 6.1% to 9.1%), and Salmonella in 0.08% (95% CI, 0.004% to 0.5%) of the fecal samples. In yearling cattle, the median within-lot prevalence (percentage of positive samples within a lot) was 40% (range, 0% to 100%) for verotoxins and 0% for E. coli O157:H7 (range, 0% to 100%) and Salmonella (range, 0% to 17%). One or more fecal samples were positive for verotoxins in 80.4% (95% CI, 72.8% to 86.4%) of the lots of yearling cattle, whereas E. coli O157:H7 were detected in 33.6% (95% CI, 26.0% to 42.0%) of the lots. In cull cows, the median within-lot prevalence was 50% (range, 0% to 100%) for verotoxins and 0% (range, 0% to 100%) for E. coli O157:H7 and Salmonella (range, 0% to 0%). Verotoxins were detected in one or more fecal samples from 78.0% (95% CI, 70.4% to 84.2%) of the lots of cull cows, whereas E. coli O157:H7 were detected in only 6.0% (95% CI, 3.0% to 11.4%) of the lots of cull cows. The prevalence of verotoxins in fecal samples was lower in yearling cattle than in cull cows, whereas the prevalence of E. coli O157:H7 in fecal samples was higher in yearling cattle than in cull cows. The prevalence of E. coli O157:H7 in fecal samples was highest in the summer months. Rumen fill, body condition score, sex, type of cattle (dairy, beef), and distance travelled to the plant were not associated with the fecal prevalence of verotoxins or E. coli O157:H7. The prevalence of verotoxins in fecal samples of cull cows was associated with the source of the cattle. It was highest in cows from the auction market (52%) and farm/ranch (47%) and lowest in cows from the feedlot (31%). In rumen samples, the prevalence of verotoxins was 6.4% (95% CI, 4.2% to 9.4%), and it was 0.8% (95% CI, 0.2% to 2.3%) for E. coli O157:H7, and 0.3% (95% CI, 0.007% to 1.5%) for Salmonella.

Abattoirs↗

Estradiol and progesterone metabolite concentration in white-tailed deer (Odocoileus virginianus) feces.

Assays of reproductive hormone metabolites require validation in each animal species. For validation of methodology in white-tailed deer (Odocoileus virginianus), fecal samples were collected from females that had been injected by blowgun with estradiol, progesterone, or a control substance. Analysis by radioimmunoassay revealed that estradiol and pregnanediol were more abundant fecal metabolites of estrogens and progestins than were estrone or progesterone. Peak excretion rates of estradiol and pregnanediol occurred within 12 and 24 hr of injection, respectively. Ovulation time was estimated by measuring the frequency of occurrence of eight behavior patterns, including copulation. Profiles were compiled for three deer over the course of estrus and early pregnancy for estradiol, estrone, progesterone, and pregnanediol using radioimmunoassay. Pregnanediol was excreted at concentrations about 1,000 times higher than those of the other three fecal steroid metabolites, and pregnanediol differed in concentration during estrus, the luteal phase, and early pregnancy. Consequently, a simpler enzyme immunoassay was adapted and used to measure pregnanediol levels over the course of estrus and early pregnancy for seven deer. Measurement of fecal pregnanediol is useful for monitoring reproductive events in female white-tailed deer.

Animals↗