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At least 523 records · Page 29Linked to original sources

Extracting protostrongylid nematode larvae from ungulate feces.

A major weakness of the Baermann funnel technique for extracting nematode larvae from feces is the funnel. As many as 67% of Parelaphostrongylus tenuis first-stage larvae lodged on the sloping surface of glass Baermann funnels. The number of larvae collected after 24 hr was not significantly correlated with total numbers in the samples, whether feces were supported over tissue paper or over window screening. Instead, we collected about 8 times as many larvae and achieved a significant relationship between larvae collected and the total numbers present when pelleted fecal material was submerged over screening in vertical-sided beakers. The methodology of this more efficient and more accurate way of estimating numbers of protostrongylid larvae is described. Most larvae were located on and in the mucous layer covering fecal pellets and readily left fresh pellets emersed in water; 72% of these larvae left after 6 min and only 11% remained after 1 hr. Larvae in water at room temperature sank as fast as 6 cm/min, but those close to a vertical glass surface sank more slowly (97% sank 18.5 cm in 105 min).

Animals↗

Use of microwave digestion and atomic absorption spectrophotometry to determine chromic oxide as a digestibility marker in feed, feces, and ileal content.

Most conventional digestion procedures, such as dry ashing and wet ashing, are tedious and labor intensive. Microwave digestion is a good alternative, because microwave dissolution is faster, safer, and simpler, and provides more controlled reproducible conditions than conventional methods. The purpose of this study was to develop a microwave digestion method for mineralizing meat and bone meal diets, feces, and ileal contents. Each sample was heated on a hot plate for 10 min, dry ashed at 65 degrees C for 4 h, and transferred into microwave vessels. Then, 10 mL 70% HNO3 was added. Samples were digested for 7, 10, and 20 min at 95, 90, and 85% power, respectively. After the heating cycle, 6 mL 30% H2O2 was added, and samples were returned to the microwave for a second heating cycle of 1 and 7 min at 95% and 90% power, respectively. Finally, chromium concentration was determined by flame atomic absorption spectrophotometry. The digestion method was validated by using a standard reference material, SRM domestic sludge 2781, with a certified chromium value of 195 +/- 9 micrograms/g. The value obtained in this study was 178 +/- 11 micrograms/g, for a difference of 17 micrograms/g. Spike recovery experiments resulted in 103.16 and 100.35% recoveries of chromium from diet and feces samples, respectively. Coefficients of variation were 10.8 and 7.8%, respectively.

Animal Feed↗

[Utilization of a solid nutrient medium for the serological method of detecting the causative agent of typhoid in patients' feces].

The causative agent of typhoid fever can be revealed in feces of patients not only by the bacteriological, but also by the serological method, if the material is preliminarily grown on hard nutrient media; Ploskirev's medium proved to be the optimal. It is suggested that microbial cultures left on the ager in Petri dishes after the bacteriological study should be used for bacteriological analysis. In a number of cases it was possible to reveal the causative agent of typhoid fever in feces by the serological method, although no coproculture was isolated bacteriologically.

Antigens, Bacterial↗

[Composition and role of short chain fatty acids in feces and peripheral blood serum of patients with cholelithiasis].

Gas-liquid chromatography was used to estimate content of short-chain fatty acids (SCFA) in 25 patients with cholelithiasis, 32 patients with irritable colon syndrome and constipation (ICS) and 35 healthy subjects. It was found that SCFA absolute and relative concentration in the feces of cholelithiasis patients is abnormal indicating disturbance of microbiocenosis as shown by changes in functional activity of some anaerobes of the intestinal microflora participating in enterohepatic circulation of bile acids. Alterations of SCFA content in the serum of cholelithiasis patients may be related to steroids disbolism. The study of SCFA in the feces and peripheral blood serum from cholelithiasis patients is of diagnostic value.

Cholelithiasis↗

Extraction of human nuclear DNA from feces samples using the QIAamp DNA Stool Mini Kit.

The use of a QIAamp DNA Stool Mini Kit (QIAGEN) for extracting human nuclear DNA from feces samples is reported. This method employs a stool lysis buffer and a unique matrix (InhibitEX tablet) to remove PCR inhibitory substances specific to feces samples. DNA extracted from various amounts of stool and from stool samples exposed to different environmental impacts was successfully amplified and typed using the Profiler Plus Amplification Kit and ABI PRISM 310 Genetic Analyser.

Adult↗

[Influence of intestinal microflora on the amino acid composition of lamb feces].

6 conventional and 5 germfree male lambs were fed ad libitum a UHT sterilized cow milk. Body weight and food intake were recorded. Whole feces were collected for 5 consecutive days. Growth rate reached 259 g/d for the germfree. Daily fecal excretion of dry matter and nitrogenous compounds are not found different in the two groups of animals. The influence of intestinal microflora appears on the biochemical composition of the feces. As compared to the conventional fecal proteins from germfree lambs are very high in threonine and serine and low in lysine. Moreover the difference of amino acid composition between these two groups come not only from the histidine alanine and arginine composition of bacteries; it also involves the high levels of threonine serine cystine and tyrosine of the endogenous digestive proteins.

Amino Acids↗

Development of monoclonal antibody ELISA for simultaneous detection of bovine coronavirus, rotavirus serogroup A, and Escherichia coli K99 antigen in feces of calves.

A rapid ELISA was developed for simultaneous detection of bovine coronavirus (BCV), rotavirus (RV) serogroup A, and Escherichia coli K99 antigen in feces of calves. A mixture of 3 monoclonal antibodies specific for BCV, RV, or K99 was used successfully to capture the antigens; the same antibodies labeled with peroxidase were used to detect BCV, RV, or K99. The triple ELISA was compared with standard reference diagnostic methods by examining feces from experimentally and naturally infected and healthy calves. All the components of the test were highly specific (greater than 90%) and sensitive (BCV, 77%; K99, 93%; RV, 100%) when used in a format requiring short incubation steps at 20 C and visual recording of results.

Animals↗

[Evaluation of an immunoenzyme technique for the detection in feces of the Giardia intestinalis antigen].

An evaluation is made of the utility for the diagnosis of giardiasis of an enzyme immunoassay (EIA) that detects the GSA65 specific antigen in feces, as compared with the formalin-ether sedimentation test. Within the context of a longitudinal study on intestinal parasitization, 147 fecal samples from children attending 7 day care centres in the city of Salamanca were studied. The feces were examined a few hours after collection by the sedimentation technique and conserved in 10% formol. They were later studied by the EIA method. G. intestinalis was detected by microscopy and/or EIA in 26 of the 147 fecal samples (17.7%). Both assays were positive in 22 of the 26 cases detected (84.6%) and the remaining 4 cases were positive only by EIA (4/26; 15.4%). The EIA assay, using visual reading and very simple to implement, showed sensitivity, specificity, positive predictive and negative predictive values of 100, 96.9, 84.6 and 100%, respectively.

Animals↗

[Genetic determinants of Escherichia coli pathogenicity isolated from urine and feces of children with different clinical variants of urinary system infection].

In the process of examination of 156 children of different age groups 176 E. coli cultures were isolated; of these, 98 cultures were isolated from acute cystitis and pyelonephritis patients, 28--from urine in cases of aysmptomatic bacteriuria, 30--from feces in cases of asymtomatc bacteriuria and intestinal dysbacteriosis, while 20 cultures--from feces of healthy children. In these bacteria the presence of genes associated with pathogenicity islets (PI) hlyA, hlyB, cnf-1, papC, sfaG and gene irp-2 (iron-regulated protein) was established with PCR. The detection rate of PI determinants in uropathogenic E. coli (UPEC) was shown to depend on the variants of the clinical manifestation of urinary tract infection. The total detection rate of PI gene fragments in UPEC cultures of different origin was indicative of their definitely less frequent occurrence in asymptomatic bacteriuria, observed simultaneously with intestinal dysbacteriosis, in comparison with acute urological infection. Practically the same detection rate of PI determinants in E. coli, isolated in asymptomatic bacteriuria in children, reflected high probability of genetic exchange in the above-mentioned fragments and made it possible to presume the existence of DNA sites, characteristic mainly of pathogenic clones. The established heterogeneity of the detection rate of PI determinants in E. coli clinical isolates requires further study.

Acute Disease↗

[An in vitro study of cholesterol-lowering properties of probiotics isolated from the human feces].

21 strains of Lactobacillus and Bifidobacterium, isolated from feces of healthy youth and children feces and identified by molecular biological methods, together with 6 strains of probiotics preserved in Onlly lab were studied in the experiments, including removal cholesterol from media, bile-tolerance and acid-tolerance. The results demonstrated that all strains could remove cholesterol from media and removal rates of 5 strains were more than 40%. Meanwhile these 5 strains had high removal effectiveness. The bile-tolerance and acid-tolerance were varied from strain to strain. Among 27 strains, Bm26 demonstrated higher ability of removal cholesterol, bile-tolerance and bile-tolerance than other strains.

Adolescent↗

[How much does partially hydrolyzed guar gum affect the weight, moisture and hardness of feces?].

OBJECTIVE: The ministry of Health, Labor and Welfare recommends Japanese people to intake a certain amount of dietary fiber, believing that incorporating more dietary fiber into our diet can reduce the risk of colorectal cancer. The present study aimed to demonstrate and confirm the theory's validity by applying it to reality-to what extent is the intake of partially hydrolyzed guar gum (PHGG) useful in promoting bowel movements, and what problems are involved? We therefore investigated to what extent PHGG affects the weight, moisture and hardness of feces when healthy female students consumed PHGG as a supplement. METHOD: During two fourteen-day sessions in spring and autumn, 9 healthy female students took the same diets. During the first session, the students were provided a strict dietary formula, while during the second session, they were administered an amount of 12.5 g/day PHGG (purity 80%, equivalent to 10 g of dietary fiber) dissolved in adequate amount of water at the end of each meal. Feces of the subjects were collected and weighted just after defection. A moisture meter was used to measure fecal moisture and a rheometer was used to measure fecal hardness. Fecal conditions and intestinal motility were also examined. RESULTS: (1) Due to the PHGG intake, the fecal bulk increased in 4 subjects and decreased in 2 subjects, significantly, out of 9. (2) Due to the PHGG intake, the fecal condition softened in 3 subjects while significantly hardening in 4 subjects. (3) The PHGG intake induced an increased of fecal moisture in 5 subjects, while moisture decreased in 2 subjects. (4) Fecal hardness measured more than 150 g/cm when it is classified as "frozen hard". (5) A significant inverse correlation could be seen between fecal hardness and fecal bulk, and between fecal hardness and its moisture. When PHGG was administered a significant inverse correlation could be seen between fecal hardness and its moisture. CONCLUSION: The conclusion is that the PHGG intake resulted in increase of the fecal bulk for 4 subjects and fecal moisture for 5 out of 9 subjects, but decrease of fecal hardness in 3 subjects; the benefit of bowel movements provided by the PHGG intake, however, varied greatly among the subjects.

Adult↗

[Study on methods for isolation and purification of Cryptosporidium parvum oocysts from mouse feces].

OBJECTIVE: To explore an applicable method for isolation and purification of Cryptosporidium parvum oocysts with high purity, recovery and vigor from mouse feces. METHODS: Four techniques were used for isolating and purifying C. parvum oocysts from mouse feces: modified saturated saline flotation, percoll gradient centrifugation, CsCl gradient centrifugation and the classical discontinuous sucrose gradient centrifugation. Oocysts received from the methods were used respectively to infect in vitro bovine fallopian tube epithelial cells (BFTE) and the development of the oocysts was examined under microscope after 48 h and 72 h cultivation. RESULTS: The number of oocysts received by the classical discontinuous sucrose gradient centrifugation [(2.86 +/- 0.08) x 10(7)] was significantly higher than that of percoll gradient centrifugation [(1.52 +/- 0.08) x 10(7)] (P<0.01) and CsCl gradient centrifugation [(2.46 +/- 0.13) x 10(7)] (P<0.05), but similar to that of the modified saturated saline flotation [(2.88 +/- 0.15) x 10(7)]. No significant difference was found on the number of oocysts by BFTE cultivation at 48 and 72 hours post-inoculation(P>0.05). Oocysts received from CsCl gradient centrifugation showed higher purity than those by discontinuous sucrose gradient centrifugation. CONCLUSION: In comparison to the classical discontinuous sucrose gradient centrifugation, operation of the modified saturated saline flotation is easier and faster, and the purity of oocysts isolated by CsCl gradient centrifugation is higher.

Animals↗

[Determination of sialic acids in the urine and feces of children].

Hess's method for measurement of the blood serum sialic acids has been adapted to measurements thereof in the urine and feces. The modification is based on ethanol sedimentation of urinary and fecal proteins. Sialic acids are measured in the protein precipitate by the unified Hess's procedure. The examinations have revealed differences in the levels and excretion of sialic acids with feces in healthy infants and those suffering from acute intestinal infections.

Acute Disease↗

[Importance of the results of a virological examination of sewage. A comparison of the series of enteroviruses isolated from sewage and from the feces of virus excreters].

Simultaneous examinations for the presence of enteroviruses were carried out on sewage of the central aeration station, periferal collectors of the most populous institutions, preschool children's institutions as well as feces of children attending these institutions in a community of urban type. A high degree of coincidence of spectra of enteroviruses isolated from sewage of the central station, periferal collectors, sewage of children's institutions, and from the feces of most virus excretors was demonstrated. No enteroviruses found in occasional virus excretors were detected in sewage. Enteroviruses were regularly found in sewage of periferal collectors if approximately 10% of children excreted a certain virus type simultaneously.

Carrier State↗

[Determination of Shigella antigens in the feces of people, immunized with enteral vaccine prepared from S. flexneri antigen].

The dynamic determination of the presence of the specific antigen and its activity in the excreta of humans subjected to enteral immunization with vaccine prepared from S. flexneri antigen was made in the agglutination test and neutralization test with the use of, respectively, antibody and antigenic erythrocyte diagnosticums. In the feces and urine of the vaccinees antibodies occurred less commonly and, as a rule, they were less active than those detected in dysentery patients at the corresponding time from the beginning of the disease. The occurrence of Shigella antigens in the feces of the vaccinees was greater than in their urine at the corresponding time. Similarities and differences in the dynamics of the isolation of Shigella antigen from dysentery patients and from the vaccinees receiving enteral vaccine prepared from S. flexneri antigens were established.

Adolescent↗

[Presence of Cryptosporidium sp. in diarrheic feces of a population of children].

Searching for Cryptosporidium sp., we examined (throughout a year) 300 samples of feces belonging to 210 diarrheic children assisted at the Hospital Provincial del Centenario. Their ages ranged from a week to thirteen years, though most of them were not older than three years. Feces were collected in 10% formol, enriched by the formol-ether method and stained with safranine 1% and modified Ziehl Neelsen permanent techniques. Cryptosporidium oocysts were detected in 16 out of the 210 children examined (7.6%). The number of oocysts in positive samples was from moderate to abundant, with the exception of one child who showed a very low number of oocysts. Additional samples of only 5 out of these 16 children were obtained. In 3 of them the sample became negative. In none of the positive patients, trophozoites, cysts, sporocysts, eggs or any other enteroparasite larvae were simultaneously detected. The search for Cryptosporidium sp. in diarrheic children should be considered a parasitological routine for a differential etiological diagnosis.

Adolescent↗

[Study on metabolism of pyridonecarboxylic acid II. Determination of metabolites of (+-)-7-(3-amino-1-pyrrolidinyl)-6-fluoro-1-(2,4-difluorophenyl)- 1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid p-toluenesulfonate hydrate (T-3262) in blood, urine, bile, and feces].

The fate of (+-)-7-(3-amino-1-pyrrolidinyl)-6-fluoro-1-(2,4-difluorophenyl-1,4- dihyro-4-oxo-1,8-naphthyridine-3-carboxylic acid p-toluenesulfonate hydrate (T-3262) was studied using T-3262 and 14C-T-3262 in various animals. 1. Metabolites in serum and urine were assayed for mouse, rat, rabbit, dog and monkey following oral administration of T-3262. In serum, besides unchanged T-3262 base, T-3262A (N-acetylated) was detected in rat, rabbit and monkey; T-3262B (deamino-hydroxylated) was detected in monkey. In urine, unchanged T-3262 base was excreted mainly. But a few of metabolites (T-3262A, T-3262B, T-3262 glucuronide, T-3262A glucuronide, T-3262B glucuronide, and unknown compound M-1) were detected, and species difference existed in types of metabolites. 2. Metabolites in bile and feces were assayed for mouse and rat following oral administration of T-3262 and 14C-T-3262. Metabolites in bile were similar to the urine, but the volume of T-3262A and T-3262A glucuronide was larger than in urine. In feces, the excreted compounds mainly consisted of unchanged T-3262 base. 3. p-Toluenesulfonic acid, which is the counter acid for T-3262 base, was absorbed following the oral administration of T-3262, and excreted in urine in the unchanged form.

4-Quinolones↗