The efficacy of the Statens Serum Institut (SSI) enteric medium for isolation and direct identification of enteric pathogens was evaluated. Six different biochemical reactions can be read by using the SSI enteric medium, allowing direct identification of a range of enteric pathogens. All 248 gram-negative bacterial species that were tested grew on the SSI enteric medium. Only 10 of 248 bacteria (4%) showed discrepant results in the biochemical reactions, and none of these were enteric pathogens. Forty-three of 47 enteric pathogens (92%) produced identical rates of semiquantitative growth on the SSI enteric medium and 5% blood agar, whereas three Vibrio spp. and oneAeromonas spp. showed reduced growth. Gram-positive bacteria did not grow on the SSI enteric medium. Most enteric pathogens had a detection limit of 50 bacteria per ml of feces, but higher numbers of Vibrio spp. and some Shigella spp. were required for detection. The growth rates of 125 enteric pathogens and 12 Yersinia spp. on the SSI enteric medium, xylose lysine deoxycholate (XLD), Hektoen enteric (HE),Salmonella-Shigella (SS), and cefsulodin-irgasan-novobiocin (CIN) agar were compared. Detection rates after application of 200 CFU were 99% for SSI enteric medium, 92% for XLD, 88% for HE, and 82% for SS agar. The 12 Yersinia spp. grew excellently on both the SSI enteric medium and CIN agar. We conclude that the performance of the SSI enteric medium compares favorably to those of other media tested. Its ability to detect Yersinia spp. may limit the number of media needed in the typical laboratory. The direct identification of enteric pathogens on the medium may also provide a more rapid diagnosis.
Plasmid profiles of 674 Salmonella berta strains isolated in the period 1985–1989 from 674 cases of human infections were recorded. Five hundred and eighty‐nine of the strains examined (87.4%) contained plasmids and the mean number of plasmids was 1.8 per strain. Sixteen different plasmid sizes were recognized, 13 of which had also been reported from S. berta of poultry origin. The plasmids formed 90 different profiles. Forty‐five of these profiles, comprising 90.7% of isolates, had previously been recorded among poultry strains. Only 12 human isolates (1.8%) carried plasmids which were not demonstrated among isolates obtained from broilers. The prevalences of the 20 most commonly demonstrated profiles were not significantly different among isolates obtained from humans and broilers. The average difference between the prevalences of individual plasmid profiles was 2.1, with a standard deviation of 4.2. Based on the results, indications are that broilers represent the main reservoir for human S. berta infections in Denmark.
Heat‐stable antigens from Helicobacter pylori were investigated for the detection of serum IgG, IgA and IgM antibodies against H. pylori by an ELISA technique. Antibody titers against H. pylori were measured in 167 dyspeptic patients, of whom 96 were H. pylori positive confirmed by culture or microscopy, and in 482 controls (0–98 years). Increased IgG antibody titers were found significantly more often in dyspeptic patients with active chronic gastritis than in patients with normal morphology, as well as in H. pylori‐positive patients as compared to H. pylori‐negative patients, independent of the endoscopic findings. The heat‐stable antigens were compared with acid glycine‐extracted antigens and a high degree of concordance was found in the results obtained with the two antigen preparations. The differences in the IgA antibody titers against H. pylori between H. pylori‐positive and H. pylori‐negative dyspeptic patients were significant and may be useful to confirm a borderline IgG result. No differences were found in IgM antibody titer between H. pylori‐positive and ‐negative patients. The greatest age‐dependent increase in IgG and IgA antibody titers was found in children, and if a lower cut‐off level is used for children than for adults, as has been proposed, the proportion of people with increased antibody titers against H. pylori would be almost constant from the age of between five and 10 years until the time between 61 and 80 years. Comparison of H. pylori IgG antibodies with IgG antibodies against Campylobacter jejuni and total antibodies against cytomegalovirus (CMV) showed a greater similarity between H. pylori and C. jejuni (R = 0.51) than between H. pylori and CMV (R = 0.22). This may possibly be caused by cross‐reactions between H. pylori and C. jejuni. The H. pylori heat‐stabile antigen seems not to be very different from other crude H. pylori antigens like acid glycine‐extracted antigens, but purification and characterization of the antigens are needed to improve antibody assays.
The food and water hygiene in two Liberian communities was studied in a house-to-house diarrhoea survey. The level of contamination with enterobacteria of drinking water stored in the households was significantly higher than at the water sources. Food hygiene standards were low, particularly in the urban slum where storage of cooked food for long periods led to bacterial multiplication at high levels. Infant foods were particularly heavily contaminated. It is concluded that when water supply programmes are planned, the presence of other risk factors for water-related diseases should be investigated. To ensure maximum health benefits, water projects should as a rule be accompanied by other interventions.
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