scholarly journals Аналіз мікробної контамінації туш свиней в процесі забою та первинної обробки

2017 ◽  
Vol 19 (77) ◽  
pp. 194-199
Author(s):  
V.B. Kusturov ◽  
V.V. Kasyanchuk ◽  
A.M. Bergievich

The article presents the results of studies on the еxploring of microbial contamination of pigs' carcasses in the pork slaughter and primary processing with microorganisms such as general mesophilic bacteria, Enterobacteriaceae coliforms and E.coli. The carcass surfaces were examined in six technological operations: after bleeding (1) after scalding and removing bristles and hair (2) after singeing and polishing (3); аfter the nutration (4); аt the final point after a veterinary examination (5); аfter cooling down to a temperature of 4–5 °C (6). Sampling swabs was carried out during 2015–2016 years, 530 samples were selected from 260 carcasses accordance with ISO Standard 17604 Microbiology of food and animal feeding stuffs-Carcass sampling for microbiological analysis. Swabs sampling from carcass sites taken from thigh and outer and inner surfaces of the chest and abdominal wall. It was found that the high level of contamination of surfaces carcasses with general mesophilic bacteria, Enterobacteriaceae. They were exceeded after bleeding the microbiological criteria an average of 2.2–2.4 Log CFU/cm2 and 2.5-2.7 Log CFU/cm2, respectively. Each subsequent technological operation reduced the level of contamination of carcass surfaces: the amount of general mesophilic bacteria, Enterobacteriaceae after scalding, removing bristles and hair on the carcass surface, significantly decreased compared to levels that were after bleeding, but were above the standard values by an average of 0.7 Log CFU/Cm2 and by 0.35 Log CFU/cm2, respectively. The number of coliform forms and E. coli on the carcass surface after singeing and polishing was less than after bleeding by an average of 1.8 Log CFU/cm2 and 1.23 Log CFU/cm2, respectively. The intestinal tract is also the an important pathway for contamination of pigs' carcasses. Enterobacteriaceae and E. coli testing demonstrate the effectiveness of slaughter process control procedures and is the indicator for fecal contamination. After cooling of the carcasses, on their surfaces the amount of microorganisms studied was within the permissible levels.

Author(s):  
Anderson Gomes Nascimento Santana ◽  
Cecilia Nahomi Kawagoe Suda ◽  
Jairo Rodrigues Santana Nascimento ◽  
Gannabathula Sree Vani

The quality of groundwater from Imperatriz (MA) is little known. This work investigated microbiological contaminants (total coliforms and Escherichia coli) and the levels of 10 physicochemical parameters in 10 wells located in the urban periphery of the municipality of Imperatriz. The counts of E. coli and total coliforms were ≥ 1600 CFU mL-1 in all the wells. Levels of chloride, sulfate, hardness and turbidity levels were below the maximum allowed for drinking water. However, levels of iron (0.46 – 1.75 mg L-1) and pH (5.02 – 5.92) were not in compliance with drinking water standards in all the wells investigated. The same was observed in relation to oil and grease in water (0.0 – 6.8 mg L-1), which were detected in 40% of the wells. Levels of nitrite (0.71 – 3.84 mg L-1), nitrate (4.16 – 13.52 mg L-1) and total dissolved solids (810 – 2060 mg L-1) were above the highest limit in 50%, 60% and 70% of wells, respectively. The acidic pH observed in all the wells makes them also unsuitable for animal intake and irrigation. The acidity and the high level of iron in all wells suggest that they are natural characteristics of the soil and the groundwater of the region. Contamination with nitrite and nitrate in some wells, as well as high counts of coliforms, may be related to deficiencies in basic sanitation in the area. The origin of oil and grease in the wells should be better investigated to avoid contamination of the water table.


2009 ◽  
Vol 72 (2) ◽  
pp. 428-430 ◽  
Author(s):  
STEVEN C. INGHAM ◽  
RYAN J. ALGINO ◽  
BARBARA H. INGHAM ◽  
JOHN R. RUBY

The U.S. Department of Agriculture (USDA) requires beef abattoir operators to periodically analyze beef carcass sponge samples for levels of Escherichia coli. Additional beef carcass sponge sampling is commonly used by processors to evaluate the efficacy of beef abattoir antimicrobial intervention systems. The USDA sample preparation procedure requires that beef carcass sponge samples be mechanically stomached for 2 min before the sample fluid is squeezed out for analysis. When a large number of sponge samples must be analyzed, the stomaching step can limit throughput. In this study, we compared the USDA sample preparation procedure with repeatedly squeezing the sponge during a 10-s interval to expel the sample fluid. Separate sponge samples were obtained from each half of 100 chilled postintervention beef carcasses from a large-volume abattoir during a 4-month period. The USDA and squeezing treatments were randomly assigned to the halves of each carcass. All sponge samples were analyzed for E. coli, coliforms, Enterobacteriaceae, and aerobic mesophilic bacteria using Petrifilm methods. The sample preparation method had no significant effect (signed rank value > 0.05) on the results of any analytical test, although aerobic mesophilic bacteria counts tended to be higher after the USDA method than after manual squeezing alone. These results suggest that manual squeezing may be a simple and rapid alternative sample preparation method when gram-negative bacteria such as E. coli, coliforms, or Enterobacteriaceae are being enumerated from beef carcass sponge samples used to monitor operational abattoir hygiene.


Author(s):  
Kouassi Kra Athanase ◽  
Ouina Toualy Serge Thibaut ◽  
Voko Bi Rosin Don Rodrigue ◽  
Kouassi Kouassi Clément ◽  
Coulibaly Ibourahema ◽  
...  

The objective of this study is to assess the presence of harmful microorganisms and to characterize some physicochemical parameters in the soya flour sold in Daloa. To carry out the work, sixty (60) samples of soybean flour were collected by purchase in PMI (20), supermarkets (20) and in certain markets (20) made up of grains that will be transformed into flour according to the defined conditions. by ourselves. His samples will be transferred to the microbiology laboratory for analysis. A count to assess the microbiological quality was carried out. The assay of some chemical parameters and the determination of some physical parameters were performed. The different pH values ​​obtained are all alkaline. Microbiological analysis revealed compliance of average microbial loads of fungi (yeasts and molds) below 103 CFU / g and aerobic mesophilic bacteria below 105 CFU / g. On the other hand, the average microbial loads of total coliforms do not comply with the defined microbiological criteria. Furthermore, with regard to the potentially pathogenic germs in Bacillus cereus occurrences, there is no conformity of the average loads of the three types of flour. The defined criterion being 10 CFU / g. As for E. coli and S. aureus, only F1 flour complies with microbiological criteria. There is a presence of Salmonella in 60% of the samples of the F1 flour. Good practices should be observed in the processing of grains into flour in order to avoid possible contamination of the flour.


2019 ◽  
Vol 35 (6) ◽  
pp. 67-72 ◽  
Author(s):  
I.V. Manukhov ◽  
L.S. Yaguzhinsky ◽  
M.V. Bermeshev ◽  
M.A. Zisman ◽  
V.G. Pevgov ◽  
...  

Toxic effect of 2-ethylnorbornane (2-ethyl(bicyclo[2.2.1]heptane) (EBH)) on bacteria has been studied using the E. coli pRecA-lux and E. coli pKatG- lux cells as lux-biosensors. It was shown that the addition of EBH to the incubation medium leads to death and growth retardation, high level oxidative stress and DNA damage in E. coli cells. It is assumed that the oxidation of EBH with atmospheric oxygen causes the formation of reactive oxygen species in the medium, which makes a major contribution to the toxicity of this substance. biosensor, luciferase, bioluminescence, inducible promoter, PrecA, PkatG The authors are grateful to Stanislav Filippovich Chalkin for the development of interdisciplinary ties in the scientific community. The work was financially supported by the Ministry of Higher Education and Science of Russia (Project Unique Identifier RFMEFI60417X0181, Agreement No. 14.604.21.0181 of 26.09.2017).


2006 ◽  
Vol 13 (2) ◽  
pp. 155-161 ◽  
Author(s):  
Haiqin Chen ◽  
Zhinan Xu ◽  
Naizheng Xu ◽  
Peilin Cen

2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Kayhan Ilbeigi ◽  
Mahdi Askari Badouei ◽  
Hossein Vaezi ◽  
Hassan Zaheri ◽  
Sina Aghasharif ◽  
...  

Abstract Objectives The emergence of colistin-resistant Enterobacteriaceae from human and animal sources is one of the major public health concerns as colistin is the last-resort antibiotic for treating infections caused by multidrug-resistant Gram-negative bacteria. We aimed to determine the prevalence of the prototype widespread colistin resistance genes (mcr-1 and mcr-2) among commensal and pathogenic Escherichia coli strains isolated from food-producing and companion animals in Iran. Results A total of 607 E. coli isolates which were previously collected from different animal sources between 2008 and 2016 used to uncover the possible presence of plasmid-mediated colistin resistance genes (mcr-1 and mcr-2) by PCR. Overall, our results could not confirm the presence of any mcr-1 or mcr-2 positive E. coli among the studied isolates. It is concluded that despite the important role of food-producing animals in transferring the antibiotic resistance, they were not the main source for carriage of mcr-1 and mcr-2 in Iran until 2016. This study suggests that the other mcr variants (mcr-3 to mcr-9) might be responsible for conferring colistin resistance in animal isolates in Iran. The possible linkage between pig farming industry and high level of mcr carriage in some countries needs to be clarified in future prospective studies.


1995 ◽  
Vol 58 (1) ◽  
pp. 13-18 ◽  
Author(s):  
ERROL V. RAGHUBEER ◽  
JIM S. KE ◽  
MICHAEL L. CAMPBELL ◽  
RICHARD S. MEYER

Commercial mayonnaise and refrigerated ranch salad dressing were inoculated at two levels with two strains of Escherichia coli O157:H7, a non-pathogenic E. coli, and the non-fecal coliform Enterobacter aerogenes. Results showed that at the high inoculation level (>106 colony forming units [CFU]/g) in mayonnaise stored at room temperature (ca. 22°C) both strains of O157:H7 were undetected at 96 h. At the high inoculation level, all strains of coliform bacteria tested survived longer in salad dressing stored at 4°C than in mayonnaise stored at 22°C. The O157:H7 strains were still present at low levels after 17 days. The survival time in the low-level inoculum (104CFU/g) study decreased, but the survival pattern in the two products was similar to that observed in the high-level inoculum study. Slight differences in survival among strains were observed. The greater antimicrobial effect of mayonnaise may be attributable to differences in pH, water activity (aw), nutrients, storage temperature, and the presence of lysozyme in the whole eggs used in the production of commercial mayonnaise. Coliform bacteria survived longer in refrigerated salad dressing than in mayonnaise particularly at the high-level inoculum. Both mayonnaise (pH 3.91) and salad dressing (pH 4.51) did not support the growth of any of the microorganisms even though survival was observed.


1996 ◽  
Vol 40 (10) ◽  
pp. 2380-2386 ◽  
Author(s):  
M J Everett ◽  
Y F Jin ◽  
V Ricci ◽  
L J Piddock

Twenty-eight human isolates of Escherichia coli from Argentina and Spain and eight veterinary isolates received from the Ministry of Agriculture Fisheries and Foods in the United Kingdom required 2 to > 128 micrograms of ciprofloxacin per ml for inhibition. Fragments of gyrA and parC encompassing the quinolone resistance-determining region were amplified by PCR, and the DNA sequences of the fragments were determined. All isolates contained a mutation in gyrA of a serine at position 83 (Ser83) to an Leu, and 26 isolates also contained a mutation of Asp87 to one of four amino acids: Asn (n = 14), Tyr (n = 6), Gly (n = 5), or His (n = 1). Twenty-four isolates contained a single mutation in parC, either a Ser80 to Ile (n = 17) or Arg (n = 2) or a Glu84 to Lys (n = 3). The role of a mutation in gyrB was investigated by introducing wild-type gyrB (pBP548) into all isolates; for three transformants MICs of ciprofloxacin were reduced; however, sequencing of PCR-derived fragments containing the gyrB quinolone resistance-determining region revealed no changes. The analogous region of parE was analyzed in 34 of 36 isolates by single-strand conformational polymorphism analysis and sequencing; however, no amino acid substitutions were discovered. The outer membrane protein and lipopolysaccharide profiles of all isolates were compared with those of reference strains, and the concentration of ciprofloxacin accumulated (with or without 100 microM carbony cyanide m-chlorophenylhydrazone [CCCP] was determined. Twenty-two isolates accumulated significantly lower concentrations of ciprofloxacin than the wild-type E. coli isolate; nine isolates accumulated less then half the concentration. The addition of CCCP increased the concentration of ciprofloxacin accumulated, and in all but one isolate the percent increase was greater than that in the control strains. The data indicate that high-level fluoroquinolone resistance in E. coli involves the acquisition of mutations at multiple loci.


Sign in / Sign up

Export Citation Format

Share Document