scholarly journals Natural Occurrence of Ochratoxin A in Blood and Milk Samples from Jennies and Their Foals after Delivery

Toxins ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 758
Author(s):  
Vincenzo Lippolis ◽  
Shafaq Asif ◽  
Michelangelo Pascale ◽  
Salvatore Cervellieri ◽  
Erminia Mancini ◽  
...  
Keyword(s):  
Incidence Rate ◽  
Ochratoxin A ◽  
Reference Method ◽  
Seasonal Effect ◽  
Official Method ◽  
Natural Occurrence ◽  
Blood Samples ◽  
Milk Samples ◽  
Aoac Official ◽  
Feed Samples

An assessment of the natural ochratoxin A (OTA) exposure of seven Martina Franca jennies was carried out by analyzing blood and milk samples collected close to and after delivery. A total of 41 and 34 blood samples were collected from jennies and foals, respectively, and analyzed by ELISA. A total of 33 milk samples were collected from jennies and analyzed by the HPLC/FLD method based on IAC clean-up. Furthermore, 53 feed samples were collected from January to September and analyzed by a reference method (AOAC Official Method No. 2000.03) for OTA content. Feed samples showed OTA levels up to 2.7 ng/g with an incidence of 32%, while the OTA incidence rate in jennies’ blood samples was 73%, with a median value of 97 ng/L and concentrations ranging from <LOD to 6000 ng/L. A seasonal effect on OTA levels in positive blood samples was observed, with increases in the 53% of the positive ones from April to June. Concerning foals, the incidence rate of blood samples was 50%, with a median value of 52 ng/L, and concentrations ranged from <LOD to 4034 ng/L. The incidence of milk samples was 36%, with levels ranging from <LOD to 82 ng/L. In conclusion, the results showed a natural exposure of jennies and foals to OTA, and its presence in jenny milk could pose a risk for human newborns, considering its well-known nutritional and health properties.

Enumeration of β-Glucuronidase-Positive Escherichia coli in Foods by Using the ISO-GRID Method with SD-39 Agar

1998 ◽  
Vol 61 (7) ◽  
pp. 913-916 ◽  
Author(s):  
PHYLLIS ENTIS ◽  
IRINA LERNER
Keyword(s):  
Escherichia Coli ◽  
Membrane Filter ◽  
Reference Method ◽  
Grid Method ◽  
Test Method ◽  
Cottage Cheese ◽  
Filter Method ◽  
Official Method ◽  
Membrane Filter Method ◽  
Aoac Official

A study was undertaken to compare β-glucuronidase-positive Escherichia coli counts produced by the ISO-GRID hydrophobic grid membrane filter method using SD-39 agar (test method) with those produced by AOAC Official Method 990.11, an existing ISO-GRID method using lactose monensin glucuronate agar and buffered MUG agar (reference method). The methods were evaluated using 21 food products, with three independent lots of five replicate samples analyzed per product by both methods. The test and reference methods were statistically equivalent for 19 of the 21 products; frozen, raw ground lamb produced significantly higher counts using the reference method, whereas counts obtained from cottage cheese were significantly higher using the SD-39 agar-based method.

scholarly journals Fungal contamination and natural occurrence of ochratoxin A (OTA) in poultry feed

2014 ◽  
Vol 30 (3) ◽  
pp. 481-488 ◽  
Author(s):  
V. Krnjaja ◽  
Z. Pavlovski ◽  
M. Lukic ◽  
Z. Skrbic ◽  
Lj. Stojanovic ◽  
...  
Keyword(s):  
Ochratoxin A ◽  
Laying Hens ◽  
Enzymatic Assay ◽  
Poultry Feed ◽  
Natural Occurrence ◽  
Fungal Contamination ◽  
Penicillium Species ◽  
Toxigenic Fungi ◽  
Feed Samples

Total fungal count, the presence of potentially toxigenic fungi and natural occurrence of ochratoxin A (OTA) were studied in 30 poultry feed samples (14 samples of feed for chickens and 16 samples of feed for laying hens), which were collected from different farms in Serbia at the beginning of year 2014. The total number of fungi was determined by the method of dilution and OTA was detected using the imunoadsorption enzymatic assay (ELISA). In most of the samples of chickens feed (50%) the total number of fungi was 1 - 3 x 102 CFU g-1, and in feed for laying hens the highest number of samples (37.50%) had the total fungal count from 1.4 to 4.8 x 104 CFU g -1. The species of genera Aspergillus and Penicillium were identified as producers of OTA in 21.43% and 42.86% of chickens feed samples and in 68.75% and 25% of samples of feed for laying hens. The presence of OTA was detected in 100% of samples of feed for chickens and laying hens, with average concentrations of 34.40 ?g kg-1 (feed for chickens) and 43.89 ?g kg-1 (feed for laying hens). The total fungal count and content of OTA were not above the maximum allowed quantities, even though the presence of Aspergillus and Penicillium species was found in a large number of samples (up to 68.75%). These results indicate that the tested samples of poultry feed were mycologically and mycotoxicologically correct.

Ochratoxin A in Cow’s Milk and in Human Milk with Corresponding Human Blood Samples

1993 ◽  
Vol 76 (4) ◽  
pp. 842-846 ◽  
Author(s):  
Anna Breitholtz-Emanuelsson ◽  
Monica Olsen ◽  
Agneta Oskarsson ◽  
Ira Palminger ◽  
Karl Hult
Keyword(s):  
Human Milk ◽  
Ochratoxin A ◽  
Human Blood ◽  
Cow’S Milk ◽  
Blood Samples ◽  
Cow's Milk ◽  
Milk Samples ◽  
Quantitation Limit ◽  
Extraction Step ◽  
Human Blood Samples

Abstract A method for determining ochratoxin A in milk has been elaborated in which the sample was subjected to a liquid-liquid extraction step and then purified on a silica gel column packed in a Pasteur pipet. The purified samples were analyzed by ion-pair liquid chromatography with fluorescence detection. The detection and quantitation limits for determination of ochratoxin A in cow’s milk were 10 and 40 ng ochratoxin A/L milk, respectively. The same limits were valid for the analysis of human milk. A total of 36 cow’s milk and 40 human milk samples were analyzed. All samples were collected in Sweden. Ochratoxin A was found in 5 (14%) of the cow’s milk samples (range 10-40 ng/mL) and in 23 (58%) of the human milk samples (range 10-40 ng/L). Blood samples were collected from the mothers who gave milk samples. A total of 39 samples were analyzed. All blood samples contained ochratoxin A in concentrations exceeding the quantitation limit (60 ng/L blood). The mean concentration of ochratoxin A in the samples was 167 ng/L blood (range 90-940 ng/L). The concentration of ochratoxin A in human milk was ≤0.1 of that in the human blood.

scholarly journals Modification of Babcock Method to Eliminate Fat Testing Bias Between Babcock and Ether Extraction Methods (Modification of AOAC Official Methods 989.04 and 995.18): Collaborative Study

1997 ◽  
Vol 80 (4) ◽  
pp. 845-859 ◽  
Author(s):  
Joanna M Lynch ◽  
David M Barbano ◽  
J Richard Fleming
Keyword(s):  
Standard Deviation ◽  
Collaborative Study ◽  
Reference Method ◽  
Official Method ◽  
Test Results ◽  
Testing Bias ◽  
Ether Extraction ◽  
Relative Standard ◽  
Aoac Official ◽  
Aoac Official Method

Abstract The Babcock test for determining fat in milk (AOAC Official Method 989.04) and in cream (AOAC Official Method 995.18) gives consistently higher test results than does the modified Mojonnier ether extraction reference method (AOAC Official Methods 989.05 and 995.19). To decrease the density of material in Babcock columns and thus lower test results, the Babcock method was modified by lowering the temperatures used at various points in the method, from about 57.5° to 48°C. Using the AOAC collaborative study format, 9 laboratories tested 9 pairs of blind duplicate raw milk samples (fat range 2.5–5.7%) and 9 pairs of blind duplicate heat-treated cream samples (fat range 30–45%) using the temperature modified (TM) Babcock method. The ether extraction test was conducted as the reference method. The statistical performance (invalid and outlier data removed) of the TM Babcock method was, for milk: percent fat value of 4.110, repeatability standard deviation (sr) value of 0.037, reproducibility standard deviation (sR) value of 0.047, repeatability relative standard deviation (RSDr) value of 0.901% and reproducibility relative standard deviation (RSDR) value of 1.147%; and for cream: percent fat value of 37.555, sr value of 0.258, sR value of 0.353, RSDr value of 0.687% and RSDR value of 0.940%. The TM Babcock method performance was acceptable but not as good as that achieved in previous studies of the unmodified method. For the TM Babcock and ether methods, respectively, average percentages fat were 4.110 and 4.114 for milk, and 37.555 and 37.485 for cream. Temperature modification statistically eliminated the testing bias between methods. The tem-perature modifications of the Babcock methods for determination of fat in milk and cream (989.04 and 995.18) have been adopted revised first action by AOAC INTERNATIONAL.

AOAC Official MethodSM Matrix Extension Validation Study of Assurance GDSTM for the Detection of Salmonella in Selected Spices

2015 ◽  
Vol 98 (4) ◽  
pp. 930-938
Author(s):  
Philip Feldsine ◽  
Mandeep Kaur ◽  
Khyati Shah ◽  
Amy Immerman ◽  
Markus Jucker ◽  
...  
Keyword(s):  
Animal Feed ◽  
Reference Method ◽  
High Sensitivity ◽  
Official Method ◽  
Culture Methods ◽  
Environmental Surfaces ◽  
Microbiological Methods ◽  
Chili Powder ◽  
Aoac Official ◽  
Matrix Extension

Abstract Assurance GDSTM for Salmonella Tq has been validated according to the AOAC INTERNATIONAL Methods Committee Guidelines for Validation of Microbiological Methods for Food and Environmental Surfaces for the detection of selected foods and environmental surfaces (Official Method of AnalysisSM 2009.03, Performance Tested MethodSM No. 050602). The method also completed AFNOR validation (following the ISO 16140 standard) compared to the reference method EN ISO 6579. For AFNOR, GDS was given a scope covering all human food, animal feed stuff, and environmental surfaces (Certificate No. TRA02/12-01/09). Results showed that Assurance GDS for Salmonella (GDS) has high sensitivity and is equivalent to the reference culture methods for the detection of motile and non-motile Salmonella. As part of the aforementioned validations, inclusivity and exclusivity studies, stability, and ruggedness studies were also conducted. Assurance GDS has 100% inclusivity and exclusivity among the 100 Salmonella serovars and 35 non-Salmonella organisms analyzed. To add to the scope of the Assurance GDS for Salmonella method, a matrix extension study was conducted, following the AOAC guidelines, to validate the application of the method for selected spices, specifically curry powder, cumin powder, and chili powder, for the detection of Salmonella.

Effect of Concentration of Trisodium Citrate Anticoagulant on Calculation of the International Normalised Ratio and the International Sensitivity Index of Thromboplastin

1994 ◽  
Vol 72 (01) ◽  
pp. 084-088 ◽  
Author(s):  
E M Duncan ◽  
C R Casey ◽  
B M Duncan ◽  
J V Lloyd
Keyword(s):  
Reference Material ◽  
Oral Anticoagulants ◽  
Reference Method ◽  
Trisodium Citrate ◽  
Sensitivity Index ◽  
Blood Samples ◽  
Orthogonal Regression ◽  
Significant Difference ◽  
International Normalised Ratio ◽  
International Sensitivity Index

SummaryThe aim of this study was to determine whether the concentration of trisodium citrate used to anticoagulate blood has an effect on the INR of the sample and the ISI of the thromboplastin. Five thromboplastins including and Australian reference material were used to measure the prothrombin time of normal and patient samples collected into two concentrations of trisodium citrate - 109 mM and 129 mM. There was no effect of citrate concentration on the INRs determined with the reference material. However for the other four thromboplastins there was a significant difference between INRs for the two citrate groups. The prothrombin times of the samples collected into 129 mM were longer than those collected into 109 mM. This difference was only slight in normal plasma but more marked in patients receiving oral anticoagulants, causing the INRs for patient plasmas collected into 129 mM citrate to be higher then the corresponding samples collected into 109 mM citrate.From orthogonal regression of log prothrombin times by the reference method against each thromboplastin, we found that the ISI for each thromboplastin was approximately 10% lower when determined with samples collected into 129 mM citrate than with samples collected into 109 mM. These results suggest that the concentration of trisodium citrate used for collection of blood samples can affect the calculation of the INR and the calibration of the ISI of thromboplastin. This was found both for commercial thromboplastins prepared by tissue extraction and for a recombinant tissue factor.

Adaptation of the AOAC Fluorine Method for Determining Fluoride in Fish Protein Concentrate

1970 ◽  
Vol 53 (1) ◽  
pp. 3-6
Author(s):  
R. Bruce Klemm ◽  
Mary E. Ambrose Klemm
Keyword(s):  
Steam Distillation ◽  
Silica Sand ◽  
Official Method ◽  
Protein Concentrate ◽  
Fish Protein ◽  
Direct Titration ◽  
Modified Method ◽  
Aoac Official ◽  
Aoac Official Method

Abstract The AOAC official method, 24.029–24.035, for the determination of fluorine in foods was modified slightly to o btain quantitative recoveries of fluorine from samples of fish protein concentrate (FPC). The most important alterations include the use of steam distillation, the addition of finely ground silica sand in the distillation, a decrease in the distillation temperature, and the utilization of direct titration. Recoveries of fluoride added to FPC before ashing, using this modified method, averaged 96.0 ± 3.0%. Our results are in agreement with those of several other analysts who used a variety of methods.

scholarly journals Apicomplexan Protozoa Responsible for Reproductive Disorders: Occurrence of DNA in Blood and Milk of Donkeys (Equus asinus) and Minireview of the Related Literature

Pathogens ◽  
2021 ◽  
Vol 10 (2) ◽  
pp. 111
Author(s):  
Stefania Perrucci ◽  
Lisa Guardone ◽  
Iolanda Altomonte ◽  
Federica Salari ◽  
Simona Nardoni ◽  
...  
Keyword(s):  
Animal Species ◽  
Neospora Caninum ◽  
Reproductive Disorders ◽  
Theileria Equi ◽  
Blood Samples ◽  
Related Literature ◽  
Milk Samples ◽  
Equus Asinus ◽  
Time Periods ◽  
Blood Specimens

Donkeys may be susceptible to many pathological agents and may act as carriers of pathogens for other animal species and humans. This study evaluated the occurrence of potentially abortifacient apicomplexan protozoa DNA in blood and milk samples collected at different time periods during lactation (1, 6, and 10 months) from 33 healthy dairy jennies. A total of 73 blood and 73 milk samples were used for DNA extraction and analysis. Blood specimens from 11/33 (33%) jennies scored positive for Theileria equi, while milk samples scored negative. Blood and milk of 3/33 jennies yielded DNA of Toxoplasma gondii at 6 months (n. 1) and 10 months (n. 2) after parturition. Neospora caninum DNA was found in four milk and in five blood samples only at one month after parturition. This study is the first report about the presence of N. caninum DNA in milk of naturally infected jennies. Moreover, the excretion of N. caninum DNA in some of these jennies at 30 days from the parturition may suggest a possible occurrence of an endogenous cycle, while the presence of T. gondii DNA in the milk collected at 6 and 10 months after parturition may be suggestive of a discontinuous excretion.

scholarly journals Evaluation of the performance of sysmex XN-3100 automated hematology analyzer regarding the sysmex XE-2100 and microscopic examination

2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Said Incir ◽  
Kerim Erhan Palaoglu
Keyword(s):  
Comparative Method ◽  
Reference Method ◽  
Turnaround Time ◽  
Analytical Sensitivity ◽  
Biological Variability ◽  
Comparison Analysis ◽  
Blood Samples ◽  
Hematology Analyzer ◽  
Quality Control Materials ◽  
Automated Hematology Analyzer

AbstractObjectivesWe performed a verification study of the Sysmex XN-3100 hematology analyzer in comparison with the XE-2100 according to the guidelines of the Clinical and Laboratory Standards Institute (CLSI) and the International Council for Standardization in Hematology (ICSH).Materials and methodsBlood samples and quality control materials were used for precision. For comparison, we used the current XE-2100 as the comparative method and analyzed 540 blood samples. The Passing-Bablok and Bland-Altman tests were performed according to the CLSI EP09-A3 and a carryover study was performed according to the CLSI H26-A2 guidelines. The flagging performance of the two analyzers was compared, using two experienced laboratory technicians as the reference method.ResultsThe Sysmex XN-3100 demonstrated high levels of precision for most parameters. For the comparison analysis, all parameters, except for MCHC, monocytes and basophils were within the systematic error limits of desirable biological variability criterion (SeDBV). The carryover was less than 0.4% for all parameters. The flagging performance of the XN-3100 was satisfactory and the overall efficiency was high.ConclusionsThe XN-3100 not only showed a strong correlation and agreement with the XE-2100 but also displayed a comparable analytical sensitivity, and increased specificity, which may result in an improved turnaround time and throughpu.

Sign in / Sign up

Export Citation Format

Share Document