scholarly journals Comparison of Culture Methods for Detection of Salmonella in Dried Active Yeast

1974 ◽  
Vol 57 (3) ◽  
pp. 696-700
Author(s):  
Clyde R Wilson ◽  
Paul L Poelma ◽  
Wallace H Andrews

Abstract An improved procedure has been developed for the isolation of Salmonella from dried active yeast. Examination is presently made with a procedure employing pre-enrichment in 1% tryptone broth using a sample-broth ratio of 1:5, with subsequent transfers to selenite cystine (SC) broth and tetrathionate (TT) broth before streaking onto selective agars. The new method employs trypticase soy broth as the pre-enrichment medium using a samplebroth ratio of 1: 10, and subsequent transfers to lauryl sulfate tryptose (LST) broth and TT broth before streaking onto selective agars. The most significant points of change are samplebroth ratio and substitution of LST broth for SC broth. After a 24 hr pre-enrichment period, most probable numbers of the 5 Salmonella serotypes tested with the present procedure ranged from 13 × 103 to 7 × 105/ml compared with 13 × 106 to 49 × 107/ml using the new procedure. An incompatibility between active yeast and SC broth resulted in marked inhibition of 4 of the 5 Salmonella serotypes tested. LST broth was found to be highly productive for Salmonella growth and can be used in place of SC broth because of the absence of a large bacterial flora in dried active yeast. TT broth is retained as one of the selective broths in the event gross contamination is encountered and Salmonella becomes overgrown by non-salmonellae in the LST broth.

The Lancet ◽  
1957 ◽  
Vol 270 (6991) ◽  
pp. 370-372 ◽  
Author(s):  
R.H. Gorrill ◽  
E.J.K. Penikett
Keyword(s):  

1983 ◽  
Vol 46 (7) ◽  
pp. 618-621 ◽  
Author(s):  
V. KALAPOTHAKI ◽  
P. VASSILIADIS ◽  
CH. MAVROMMATI ◽  
D. TRICHOPOULOS

The effectiveness of Rappaport-Vassiliadis enrichment medium (RV medium) and Difco's tetrathionate brilliant green broth (TBG) for detection of Salmonella in 553 samples of meat products was compared. All samples were preenriched for 20 h in buffered peptone water. Then 0.1 ml of the preenrichment was inoculated into 10 ml of RV medium, 1 ml was added to 9 ml of TBG broth, and 1 ml was inoculated into 10 ml of Muller-Kauffman (MK) tetrathionate broth. All enrichments were incubated at 43°C for 24 h, except for MK broth which was incubated for 48 h, and all were subcultured onto brilliant green deoxycholate agar and bismuth sulfite agar. The Rappaport-Vassiliadis medium was superior to Difco's tetrathionate brilliant green broth, being considerably more sensitive and more specific. The superiority of RV medium concerned the number of positive samples (36% and 28%, respectively), and also the number of Salmonella serotypes and strains. The RV medium inhibited the lactose- and sucrose-negative competing organisms much more than the Difco's tetrathionate broth. The performance of Difco and Muller-Kauffman tetrathionate brilliant green broths was similar. Addition of the brilliant green solution after boiling the tetrathionate broth slightly increased its efficacy. The effectiveness of brilliant green deoxycholate agar and bismuth sulfite agar was similar, whether after enrichment in RV medium or in any of the studied tetrathionate brilliant green broths.


1968 ◽  
Vol 127 (1) ◽  
pp. 67-76 ◽  
Author(s):  
Dwayne C. Savage ◽  
René Dubos ◽  
Russell W. Schaedler

Colonization of the gastrointestinal tract by bacteria of the normal flora was followed by bacteriological and special histological techniques in mice from several colonies. These histological techniques were designed to preserve the intimate associations that become established between particular strains of microorganisms and the epithelium of the mucosa of certain areas of the gut. The findings were as follows: 1. The various strains of bacteria of the normal flora became established in the different areas of the guts of infant mice according to a definite time sequence. 2. The first types of bacteria that could be cultured from the gut were lactobacilli and Group N streptococci. Within the first day after birth, these bacteria colonized the entire digestive tract and formed layers on the stratified squamous epithelium of the nonsecreting portion of the stomach and of the distal esophagus. 3. The bacterial types that appeared next were coliforms and enterococci. From about the 9th to the 18th day after birth, these bacteria could be cultured in extremely high numbers from the cecum and the colon. Histological sections of those organs taken during the first 2 or 3 days of that interval revealed microcolonies of Gram-positive cocci in pairs and tiny Gram-negative rods embedded in the mucous layer of the epithelium. The microcolonies were well separated from the mixture of digesta and bacteria that occupied the center of the lumen; they may have consisted of the coliforms and enterococci mentioned above; but this possibility remains to be proved. 4. Histological sections also revealed that, at about the 12th day after birth, long, thin Gram-variable rods with tapering ends were present, side by side, with the small Gram-negative rods and Gram-positive cocci in the mucous layer. By the 15th day after birth, the fusiform bacteria formed thick layers in the mucus, and seemed to be the only bacteria remaining in that location. It has not yet been possible to enumerate these tapered rods by culture methods, but as judged by visual appearances in the histological sections, they seemed to outnumber all other bacteria in the cecum and the colon by a factor of as much as 1000. It must be stressed that these bacterial layers are readily disrupted and even washed away by conventional histological techniques; their discovery was largely due to the use of the special histological techniques described in the text. The bacteriological and histological findings described here constitute further evidence for the hypothesis that symbiotic associations exist between microorganisms and animals, and that a very large percentage of the bacteria in the gastrointestinal tract constitutes a true autochthonous flora. The constant occurrence of several distinct associations of bacteria with the special histological structures of the animal host renders obsolete the notion that the intestine constitutes a chemostat in which the bacterial populations are randomly mixed. For a full understanding of the ecology of the normal microflora, it is necessary to think of body surfaces as distinct microenvironments in which virtually pure cultures of a few species of microorganisms interact with their host and the adjacent microbial populations. Experiments based on this hypothesis are admittedly difficult to design, but on the other hand studies based on the assumption that microorganisms exist as mixtures in the gastrointestinal tract will be only of limited value and may often be misleading.


1982 ◽  
Vol 15 (2) ◽  
pp. 83-88 ◽  
Author(s):  
Iwao Oshiro ◽  
Toru Takenaka ◽  
Jiro Maeda

1953 ◽  
Vol 10 (2) ◽  
pp. 62-63 ◽  
Author(s):  
Leo Margolis

Sixteen bullheads (Ameiurus nebulosus) and three speckled trout (Salvelinus fontinalis) were kept in complete starvation for periods of time varying from one to two months and seven to ten days respectively. They were then examined, by culture methods, for the presence of bacteria in the intestine. Fifteen bullheads and the three trout did not yield bacteria. A Pseudomonad was obtained, in small numbers, from the intestine of one bullhead. Three bullheads and two trout examined two hours after the last feeding yielded intestinal bacteria in large numbers. In non-feeding fish, bacteria are usually absent from the intestine.


Author(s):  
Aki Takase ◽  
Akihiro Hamuro ◽  
Megumi Ashimura ◽  
Natusko Yokoi ◽  
Takuya Misugi ◽  
...  

Among surgical procedures of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome, the laparoscopic Davydov's technique seems to offer the most feasible and effective approach for creating a neovagina. Several reports have pointed at the necessity for mobilization of the peritoneum to obtain a longer neovagina and have reported a modified laparoscopic Davydov’s method. A new method was performed for a 24- and an 18-year-old patient. The most significant method in present procedure was to leave the thickened tissue that connects both rudimentary uteruses. The advantages of present procedure are physiological, creating a longer neovagina. Furthermore, this approach may help prevent prolapse of pelvic organs by leaving the thickened tissue as a ceiling.


Blood ◽  
1959 ◽  
Vol 14 (11) ◽  
pp. 1194-1212 ◽  
Author(s):  
LAWRENCE BERMAN ◽  
EDWARD R. POWSNER ◽  
Mary L. Davis ◽  
Marie Fly

Abstract Characteristics of various tissue and cell culture methods for studying maturation of human erythroblasts were reviewed and the basic assumptions required in their use were examined. The relationship of maturation and proliferation of erythroblasts in different types of cultures was considered. Criteria for selection of an in vitro model for studying maturation were established. A new clot-free culture system in roller tubes was found to be superior to those previously described because of convenience, replicability and adaptability to studies of proliferation. The results of challenging the new culture system with various types of cell-plasma relationships indicated that it was effective in distinguishing among erythroblasts and plasmas of iron deficiency anemia, thalassemia, azotemia and erythrocytosis, and that the deductions arrived at were similar to those derived from the use of less convenient in vitro systems in which different parameters of maturation were used. Experience with the new method suggests that it may be useful in the study of humoral factors affecting maturation of human erythroblasts. The chief limitation of the proposed method, as for other in vitro methods, is that only direct effects of humoral agents on erythroblasts can be studied.


2005 ◽  
Vol 68 (8) ◽  
pp. 1606-1612 ◽  
Author(s):  
B. R. WARREN ◽  
M. E. PARISH ◽  
K. R. SCHNEIDER

Detection of Shigella boydii UI02 and Shigella sonnei UI05 artificially inoculated onto tomatoes was evaluated using enrichment protocols of the U.S. Food and Drug Administration's Bacteriological Analytical Manual (BAM) and the American Public Health Association's Compendium of Methods for the Microbiological Examination of Food (CMMEF), enrichment in Enterobacteriaceae enrichment (EE) broth supplemented with 1.0 μg/ml novobiocin and incubated at 42°C, and FTA filtration–nested PCR. To assess the effect of natural tomato microflora on recovery, conventional culture enrichments were repeated using rifampin-adapted inocula and enrichment medium supplemented with 50 μg/ml rifampin. The lowest detection levels for S. boydii UI02 were >5.3 × 105 (BAM, CMMEF, and EE broth) and 6.2 CFU per tomato (FTA filtration–nested PCR). For S. sonnei UI05, the lowest detection levels were 1.9 × 101 (BAM), 1.5 × 103 (CMMEF), 1.1 × 101 (EE broth), and 7.4 CFU per tomato (FTA filtration–nested PCR). Natural tomato microflora had a large impact on recovery of S. sonnei UI05 and completely inhibited recovery of S. boydii UI02. EE broth was inhibitory to S. boydii UI02. FTA filtration–nested PCR provided superior detection (P < 0.05) compared with the conventional culture enrichment protocols.


1979 ◽  
Vol 62 (2) ◽  
pp. 276-277
Author(s):  
Dwight B West

Abstract The American Society of Brewing Chemists (ASBS) has released one new procedure and one change in a present procedure. A new method for calculating the carbohydrate content of malt beverages, after determining the specific gravity, real extract, protein, and ash contents by AOAC methods, is presented. The method is applicable to either weight or volume amounts of malt beverages. Two changes are presented in method 10.027, caloric content of malt beverages: (1) the calorie factor for grams of ethanol is changed from 7.0 to 6.9, and (2) the ash content of the malt beverage is subtracted from the real extract before calculating the calories of the extract. The 2 changes are needed to make the caloric calculation more precise.


1977 ◽  
Vol 23 (5) ◽  
pp. 563-566
Author(s):  
C. E. Park ◽  
M. K. Rayman ◽  
Z. K. Stankiewicz

A previously described procedure for the selective enrichment of Shigella in competition with E. coli has been modified and tested with a total of 48 strains of the four Shigella species. The new enrichment medium consists of 1.5-strength trypticase soy broth, 1 mM 4-chloro-2-cyclopentylphenyl β-D-galactopyranoside (CPPG), 0.25% lactose, and 0.1 M citrate buffer (pH 6.2). In competition with a 1000-fold higher population of E. coli than Shigella, 42 of 48 strains from the four species of Shigella were selectively enriched by the new method. Different lots of CPPG did not appear to affect the performance of the medium.


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