Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “FECES”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 19 recordsLinked to original sources

Isolation of human immunodeficiency virus type 1 (HIV-1) RNA from feces by a simple method and difference between HIV-1 subpopulations in feces and serum.

A simple method for the isolation and subsequent detection of human immunodeficiency virus type 1 (HIV-1) RNA from feces is described. Viral RNA was isolated by the method developed by Boom et al. (R. Boom, C.J.A. Sol, M.M.M. Salimans, C.L. Jansen, P.M.E. Wertheim-van Dillen, and J. van der Noordaa, J. Clin. Microbiol. 28:495-503, 1990), which was adapted for feces. HIV-1 RNA was detected by reverse transcription (RT) followed by a nested PCR encompassing the V3 region. Reconstruction experiments revealed that the efficiencies of the extraction technique and the subsequent RT-PCR were not considerably affected by the varied composition of feces. The method was applied on fecal specimens from 18 HIV-1-infected individuals, among which were samples that had been stored for 9 years. It appeared that HIV-1 RNA was detectable in the feces of 12 persons (67%). Viral RNA was present in the feces of persons who fulfilled the criteria for CDC class II and CDC class III HIV infection as well as in patients who were diagnosed with AIDS (CDC class IV). Direct sequencing of amplimers obtained from paired fecal and serum specimens showed that differences in sequence heterogeneity existed. In one patient a remarkable difference in the HIV-1 sequences between isolates from feces and serum was observed. In conclusion, HIV-1 RNA is frequently present in the feces of HIV-1-infected individuals, and in some cases the HIV-1 subpopulation in feces differs from the HIV-1 subpopulation in serum.

Amino Acid Sequence↗

Behavioral response of Stomoxys calcitrans (Diptera: Muscidae) to conspecific feces and feces extracts.

The attraction response of Stomoxys calcitrans (L.) to its own feces was evaluated in a triple cage olfactometer. Both time- and concentration-response relationships were obtained for female S. calcitrans exposed to cellulose sponges impregnated with fresh fly feces or filter papers treated with chloroform:methanol extracts of fresh fly feces in 6-min tests. Attraction to feces collected on cellulose sponges decreased as the air flow increased. Feces collected on cellulose sponges and held for 28-31 retained attractive activity. More female flies were attracted than males to feces on sponges or to polar solvent extracts of feces-contaminated cages. The activity of feces extract on filter paper decreased rapidly. Chemical identification of the active compounds present could lead to useful baits for traps.

Animals↗

Description of a medium for isolating Anaerobiospirillum spp., a possible cause of zoonotic disease, from diarrheal feces and blood of humans and use of the medium in a survey of human, canine, and feline feces.

Anaerobiospirillum spp., motile, spiral anaerobic bacteria, have been implicated as a cause of diarrhea and bacteremia in humans. Anaerobiospirillumlike organisms and Anaerobiospirillum succiniciproducens were reported from 17 cases of diarrhea. Sixteen of the patients did not have any underlying disorders and recovered from the infection; the other one, who had a heart defect, did not. The formulation of a selective medium for Anaerobiospirillum spp. has enabled a survey of human, cat, and dog feces as possible sources for these anaerobic bacteria. Anaerobiospirillum spp. were not isolated from 527 "normal" human feces but were found in both cat and dog feces. We also describe biochemical tests and API ZYM results of A. succiniciproducens and anaerobiospirillumlike organisms.

Adult↗

[Alkaline phosphatases in human feces, intestinal mucosa and bile, and the occurrence of 5'-nucleotidase in feces (author's transl)].

Alkaline phosphatase (EC 3.1.3.1) in extracts of human feces resembles alkaline phosphatase in extracts of duodenal mucosa, except for its electrophoretic mobility in starch gel. It is very probable that the normal feces alkaline phosphatase derives from intestinal mucosa. Gall bladder alkaline phosphatase, which is markedly different, has not been found in normal feces. Some patients with acute viral hepatitis or protozoasis excrete an alkaline phosphatase which resembles gall bladder alkaline phosphatase and has the characteristics of 5'-nucleotidase (EC 3.1.3.5). The appearance of this enzyme correlates with low total alkaline phosphatase activity of the excreta.

Adult↗

Anaerobiospirillum thomasii sp. nov., an anaerobic spiral bacterium isolated from the feces of cats and dogs and from diarrheal feces of humans, and emendation of the genus Anaerobiospirillum.

Thirty-seven similar strains isolated from feces of cats and dogs and from human diarrheal feces had characteristics of the genus Anaerobiospirillum. These organisms were distinguished from the only previously described Anaerobiospirillum species, Anaerobiospirillum succiniciproducens, by producing acid from adonitol but not from fructose, raffinose, or sucrose and by the lack of alpha-glucosidase. The G + C contents of the DNAs of the new strains were 39 to 42 mol%. The results of morphological, physiological, DNA G + C content, and DNA homology studies support the proposal that the description of the genus Anaerobiospirillum should be emended so that a new species can be included in the genus. The new species Anaerobiospirillum thomasii is proposed, with strain A273/88 (= NCTC 12467) as the type strain.

Animals↗

[Botanical composition of food of domestic ruminants feeding from Senegalese farming fields using a histologic analysis of the feces: effect of the technique of preservation and centrifugation of feces].

During a microhistological study of feces from domestic ruminants (cattle, sheep, goats), centrifugation was used to increase from 11 (classic method) to 93% the rate of dicotyledon epidermis in the total particles of the suspension. Regardless of the conservation method used (drying or addition of salt, formol or ethanol), a better analysis of the dicotyledon part of the diet was obtained.

Animal Feed↗