INHIBITION OF GROWTH OF AIRBORNE COLIFORMS AND OTHER BACTERIA ON SELECTIVE MEDIA1

1972 ◽  
Vol 35 (3) ◽  
pp. 156-162 ◽  
Author(s):  
Attila K. Stersky ◽  
T. I. Hedrick
Keyword(s):  
Methylene Blue ◽  
Skim Milk ◽  
Enterobacter Aerogenes ◽  
Colony Growth ◽  
Coliform Bacteria ◽  
Plate Count ◽  
Pseudomonas Fragi ◽  
Selective Media ◽  
Standard Plate Count ◽  
Plate Count Agar

Coliforms when sampled from air were inhibited or restricted in growth on regular selective media. For trials, growth on Standard Plate Count Agar ( SPC) was used as 100%. The percentage of colony growth of Escherchia coli and Enterobacter aerogenes on modified selective media or with SPC were respectively as follows: violet red bile/violet red bile (VRB/VRB) (overlay on base) <4, 15; desoxycholate/desoxyeholate (DES/DES) < 1, 17; tergitol/tergitol (TER/TER) 23,49; eosine methylene blue/eosine methylene blue (EMB/EMB) 122, 86; endo/endo (END/END) 40, 104; MacConkey/MacConkey (MAC/MAC) <2, 10; SPC/VRB <2, 22; SPC/DES <2, 23; VRB/SPC 54, 60; TER/SPC 72, 119; EMB/SPC 97, 119; END/SPC 95, 90; 1 VRB: 1 SPC, as overlay and base 14, 50. Recovery percentages of Pseudomonas aeruginosa and Pseudomonas fragi on modified selective media were greater than those of the coliform bacteria. Fewer Serratia marcescens colonies grew on DES or SPC/DES and more grew on the other modified selective media than did coliform colonies. Growth of airborne Salmonella newbrumwick ranged from <1% on SS agar to 118% on MAC/SPC. Aerosolization of coliforms with skim milk compared to distilled water resulted in growth of more colonies on selective media. Desoxycholate, Bile Salts No. 3, Tergitol No. 7, and crystal violet in the media definitely limited growth of airborne coliforms.

NON-LETHAL INJURY AND LIMITATIONS OF RECOVERY OF COLIFORM ORGANISMS ON SELECTIVE MEDIA1

1970 ◽  
Vol 33 (10) ◽  
pp. 445-448 ◽  
Author(s):  
R. B. Maxcy
Keyword(s):  
Cell Injury ◽  
Inhibitory Effect ◽  
Selective Medium ◽  
Coliform Bacteria ◽  
Plate Count ◽  
Limiting Factor ◽  
Freezing And Thawing ◽  
Selective Media ◽  
Standard Plate Count ◽  
Plate Count Agar

Cell injury as a factor in the enumeration of coliform bacteria with selective media was evaluated. Non-lethal injury reduced the ability of cells to produce outgrowth. Escherichia coli and Aerobacter aerogenes were equally sensitive. Brilliant green lactose bile broth, desoxycholate lactose agar, and violet red bile agar were similar in inhibitory effect. Cell injury occurred with sub-lethal heat treatments, exposure to chlorine, exposure to sodium chloride, and freezing and thawing cycles. Circumstances to inflict injury are found in common environmental conditions of the food industry. Presence of injured cells may provide a count with a selective medium that is only 10% of the total count obtained with standard plate count agar. The limiting factor for recovery in selective media was associated with the surfactant. An understanding of these limitations in the use of selective media in quality control and public health applications of the tests should contribute to proper interpretation of results.

Pyruvate as an Indicator of Quality in Grading Nonfat Dry Milk1

1982 ◽  
Vol 45 (6) ◽  
pp. 561-565 ◽  
Author(s):  
R. T. MARSHALL ◽  
Y. H. LEE ◽  
B. L. O'BRIEN ◽  
W. A. MOATS
Keyword(s):  
Geometric Mean ◽  
Regression Line ◽  
Skim Milk ◽  
Plate Count ◽  
Department Of Agriculture ◽  
Standard Plate Count ◽  
Geometric Average ◽  
Dry Milk ◽  
Standard Plate ◽  
Microscopic Count

Samples of skim milk and nonfat dry milk (NDM) made from it were collected, paired and tested for pyruvate concentration, [P], and Direct Microscopic count (DMC). The skim milk was tested for Standard Plate Count (SPC) and Psychrotrophic Plate Count (PPC). The geometric average DMC of skim milk was more than three times higher than that of the paired NDM samples. However, [P] of NDM was not significantly different from that of the skim milk. Although [P] of skim milk was poorly correlated with SPC and PPC, r = .31 and .26, respectively, it was relatively well correlated with DMC, r = .64. Data were widely dispersed around the regression line when [P] was ≤ 4.0 mg/L. However, [P] increased rapidly when DMCs were > 106/ml. A limit of 10 mg/L of [P] in NDM reconstituted 1:9 was chosen to represent the current U.S. Department of Agriculture Standard for DMC in NDM. This limit failed to classify about 10% of the samples correctly, assuming that each geometric mean DMC was correct. However, the probability that samples meeting the DMC standard would be rejected by the pyruvate test was quite low and the probability was moderate that samples which would be acceptable by the pyruvate test would be rejected by the DMC. For the latter, 28% of the samples having DMCs of ≥ 107/ml contained < 10 mg/L of pyruvate. No sample having ≥ 10 mg/L of pyruvate had a DMC of ≤ 107/ml. Pyruvate concentration in NDM did not change during storage at 5 or 32°C for 90 days.

Potato-Like Odor of Retail Beef Cuts Associated with Species of Pseudomonas

1986 ◽  
Vol 49 (4) ◽  
pp. 272-273 ◽  
Author(s):  
R. L. DAISE ◽  
E. A. ZOTTOLA ◽  
R. J. EPLEY
Keyword(s):  
Coliform Bacteria ◽  
Plate Count ◽  
Aerobic Bacteria ◽  
Gram Negative ◽  
Consumer Complaints ◽  
Psychrotrophic Bacteria ◽  
Plate Count Agar ◽  
Litmus Milk ◽  
Musty Odor ◽  
Retail Cuts

Retail cuts of beef and hamburger packages from a North Dakota meat processor were examined due to consumer complaints of a strong potato-like or musty odor associated with the meat. Examination for total numbers of aerobic bacteria on plate count agar and for gram-negative psychrotrophic bacteria on crystal violet tetrazolium agar revealed numbers in excess of 108 CFU/g. Numbers of coliform bacteria on violet red bile agar were in excess of 106 CFU/g. Gram-negative rods were isolated and identified. The isolates were characterized by a positive catalase reaction, oxidase production, an oxidative O/F reaction, nonutilization of lactose, liquefication of nutrient gelatin, slight motility, production of acid in litmus milk with decoloration and clotting, nonproduction of indole, and nonreduction of nitrate. The isolate was tentatively identified as a Pseudomonas of undetermined species, probably a variant of either Pseudomonas taetrolens or Pseudomonas perolens.

Behavior of Listeria monocytogenes in Skim Milk during Fermentation with Mesophilic Lactic Starter Cultures

1988 ◽  
Vol 51 (8) ◽  
pp. 600-606 ◽  
Author(s):  
MICHELLE M. SCHAACK ◽  
ELMER H. MARTH
Keyword(s):  
Lactic Acid ◽  
Listeria Monocytogenes ◽  
Lactic Acid Bacteria ◽  
Skim Milk ◽  
Starter Cultures ◽  
Plate Count ◽  
Inoculum Level ◽  
Plate Count Agar ◽  
Streptococcus Lactis ◽  
Streptococcus Cremoris

The ability of Listeria monocytogenes to grow and compete with mesophilic lactic acid bacteria was examined. Autoclaved skim milk was inoculated with 103 cells of L. monocytogenes (strain V7 or Ohio)/ml, and with 5.0, 1.0, 0.5 or 0.1% of a milk culture of either Streptococcus cremoris or Streptococcus lactis. Inoculated milks were fermented for 15 h at 21 or 30°C, followed by refrigeration at 4°C. Samples were plated on McBride Listeria Agar to enumerate L. monocytogenes and on either APT Agar or plate count agar to enumerate lactic acid bacteria. L. monocytogenes survived in all fermentations, and commonly also grew to some extent. Incubation at 30°C with 5% S. lactis as inoculum appeared to be the most inhibitory combination for strain V7, causing 100% inhibition in growth based on maximum population attained. S. cremoris at the 5.0% and 0.1% inoculum levels, was slightly less inhibitory to L. monocytogenes at 37°C, but it was slightly more inhibitory to L. monocytogenes at the 1.0% inoculum level than was S. lactis. In general, S. lactis reduced the pH of fermented milks more than did S. cremoris. The population of L. monocytogenes began to decrease before 15 h in only one test combination, which was use of a 5.0% inoculum of S. cremoris and 30°C incubation. In most instances, growth of the pathogen appeared to be completely inhibited when the pH dropped below 4.75.

Effect of Delayed Heading on Some Quality Attributes of Penaeus Shrimp1

1979 ◽  
Vol 42 (5) ◽  
pp. 407-409 ◽  
Author(s):  
R. J. ALVAREZ ◽  
J. A. KOBURGER
Keyword(s):  
Panel Data ◽  
Storage Period ◽  
Plate Count ◽  
Sensory Panel ◽  
Bacterial Populations ◽  
Standard Plate Count ◽  
Plate Count Agar ◽  
Pseudomonas Species ◽  
Standard Plate ◽  
Plate Counts

To determine the effect of delayed heading on shrimp quality, shrimp were stored on ice with and without heads for 10 days. Some shrimp were delay-headed after 5 days and returned to ice for the remainder of the storage period. Microbiological studies were conducted at 0, 5 and 10 days of storage. Total aerobic plate counts were done using Standard Plate Count agar with an added 0.5% NaCl. Incubation was at 20 C for 5 days. Analyses indicated similar counts on shrimp tails stored with or without heads and those delayed-headed. Counts ranged from 2.4 × 106 bacteria/gram at 0 day to 1.6 × 109 bacteria/gram on the 10th day. Identification of the flora present revealed that the same major groups of organisms predominated on shrimp tails subjected to the different storage treatments and the head did not alter development of the usual flora. Flavobacterium, Pseudomonas, Planococcus, Moraxella and the Vibrio/Aeromonas group were the major genera encountered. A shift in bacterial populations was observed during storage. Flavobacterium species predominated during the first 5 days of storage; however, after the fifth day Pseudomonas species predominated. Sensory panel data revealed no differences in acceptability between shrimp tails stored with or without heads and those delay-headed.

Temperature Equilibration Times of Plate Count Agar and a Comparison of 50 Versus 45 C for Recovery of Raw-Milk Bacteria1

1975 ◽  
Vol 38 (6) ◽  
pp. 319-322 ◽  
Author(s):  
C. N. HUHTANEN ◽  
A. R. BRAZIS ◽  
W. L. ARLEDGE ◽  
C. B. DONNELLY ◽  
R. E. GINN ◽  
...  
Keyword(s):  
Raw Milk ◽  
Plate Count ◽  
Equilibration Time ◽  
Standard Methods ◽  
Standard Plate Count ◽  
Milk Samples ◽  
Plate Count Agar ◽  
Standard Plate ◽  
Time Required ◽  
Tempering Time

Sixty raw milk samples were plated using “Standard Methods” agar tempered to 45 or 50 ± 1 C. The standard plate count was significantly lower with the agar at 50 C. Tempering time (to 44–46 C) of a flask of agar in a water bath was about 5–10 min longer than that of a comparable flask of water. Time required to reach the desired temperature depended upon the volume of agar in the flasks, the number of flasks, and the volume of the water in the bath. Up to an hour of equilibration time may be necessary for newly autoclaved agar to reach the recommended temperature (44–46 C). Insufficient tempering time might cause an excessively high plating agar temperature which might cause a reduction in bacterial counts, especially of a heat sensitive psychrotrophic bacterium.

THE MICROFLORA OF RAW BULK TANK MILK

1966 ◽  
Vol 12 (3) ◽  
pp. 429-432 ◽  
Author(s):  
H. Jackson ◽  
L. F. L. Clegg
Keyword(s):  
Colony Count ◽  
Plate Count ◽  
Staining Reaction ◽  
Dominant Group ◽  
Standard Plate Count ◽  
Plate Count Agar ◽  
Gram Staining ◽  
Lactose Fermentation ◽  
Standard Plate ◽  
Bulk Tank

Milk samples from 141 farms were plated on standard plate count agar and the colony count determined after incubation for 48 hours at 32 °C. Twenty colonies were picked at random from plates containing between 30 and 300 colonies. The isolates were inoculated into litmus milk and subsequently characterized on the basis of shape, Gram-staining reaction, catalase production, lactose fermentation, and the ability to form spores.Certain general trends in the flora were observed. In milk of a colony count less than 2 × 104 per ml, micrococci were the dominant group of organisms, and as the colony count of the milk increased the percentage of micrococci decreased and the percentage of Gram-negative rods and streptococci usually increased. In spite of these general trends a study of the flora of individual samples showed that quite marked variations did occur.

scholarly journals Multiregional Evaluation of the SimPlate Heterotrophic Plate Count Method Compared to the Standard Plate Count Agar Pour Plate Method in Water

2000 ◽  
Vol 66 (1) ◽  
pp. 453-454 ◽  
Author(s):  
R. Wayne Jackson ◽  
Karen Osborne ◽  
Gary Barnes ◽  
Carol Jolliff ◽  
Dianna Zamani ◽  
...  
Keyword(s):  
Regression Analysis ◽  
Water Samples ◽  
Plate Count ◽  
Heterotrophic Plate Count ◽  
Plate Method ◽  
Standard Plate Count ◽  
Plate Count Agar ◽  
Count Method ◽  
Standard Plate ◽  
Plate Count Method

ABSTRACT A new SimPlate heterotrophic plate count (HPC) method (IDEXX Laboratories, Westbrook, Maine) was compared with the pour plate method at 35°C for 48 h. Six laboratories tested a total of 632 water samples. The SimPlate HPC method was found to be equivalent to the pour plate method by regression analysis (r = 0.95;y = 0.99X + 0.06).

A New Medium for Determining the Total Plate Count in Food

1999 ◽  
Vol 62 (12) ◽  
pp. 1404-1410 ◽  
Author(s):  
C. F. SMITH ◽  
D. E. TOWNSEND
Keyword(s):  
Linear Regression Analysis ◽  
Alternative Methods ◽  
Plate Count ◽  
Most Probable Number ◽  
Suitable Alternative ◽  
Probable Number ◽  
Standard Plate Count ◽  
Plate Count Agar ◽  
Total Plate Count ◽  
Standard Plate

SimPlate for Total Plate Count–Color Indicator (TPC-CI, IDEXX Laboratories, Inc., Westbrook, Me.) is a new medium that incorporates the redox dye resazurin to detect and quantify bacteria in food. Enumeration is achieved by the most probable number method using a SimPlate device. Viable bacteria are detected in each well of the SimPlate device by the biochemical reduction of resazurin, which is blue, to the pink resorufin or the clear dihydroresorufin indicators. Results after 24 h of incubation for TPC-CI are highly correlated with standard plate count agar after 48 h of incubation. Correlation coefficients from studies conducted at five laboratories ranged from 0.94 to 0.98 in side-by-side comparisons against standard plate count agar. Four additional test sites, using alternative methods for determining the aerobic plate count in food, reported similar results in comparison studies (r = 0.91 to 0.97). The slopes from linear regression analysis at all sites ranged from 0.91 to 0.98, with y intercepts ranging from 0.11 to 0.84. Samples used for the validation of TPC-CI included raw food products (i.e., liver and grains), which may contain natural enzymes that interfere with enzyme-based detection methods. No interference was seen from the foods tested. These results suggest that TPC-CI is a suitable alternative to existing plate count methods and has reduced incubation time.

Destruction de Microbacterium lacticum, Escherichia coli et Staphylococcus aureus au cours du séchage du lait par atomisation. I. Dénombrement sélectif des bactéries survivantes

1977 ◽  
Vol 23 (6) ◽  
pp. 716-720
Author(s):  
A. Chopin ◽  
G. Mocquot ◽  
Y. Le Graet
Keyword(s):  
Escherichia Coli ◽  
Staphylococcus Aureus ◽  
Spray Drying ◽  
Skim Milk ◽  
Resistant Mutant ◽  
Plate Count ◽  
Mannitol Salt Agar ◽  
E Coli ◽  
Plate Count Agar ◽  
Plate Counts

In this paper a method which allows the measure of microbial death rate during spray-drying by means of a streptomycin-resistant mutant that can be grown on a streptomycin-containing agar is described. Plate counts of Microbacterium lacticum, Escherichia coli, and Staphylococcus aureus recovered from skim milk powders were done on plate count agar in the presence and absence of streptomycin and on various selective media. The powders were produced from evaporated milk previously inoculated with those organisms.Our results showed that the proposed method allows the recovery of 78% of M. lacticum, 61% of E. coli, and 100% of S. aureus that survived spray-drying. Recoveries of surviving E. coli on violet bile agar and brilliant green bile 2% were 34% and 29% respectively. Baird-Parker and mannitol salt agar media allow the recovery of all surviving S. aureus, thus showing that S. aureus cells did not lose their ability to grow in media containing 7.5% NaCl. Our results show that physiological injury of the cells during spray-drying differs from injury due to heating only. [Traduit par le journal]

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