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14

test portions evaluated by the USDA/FSIS MLG reference method, 60 out of 132 test portions

1

produced positive results. A dLPOD

C

value of 0.04 with 95% confidence intervals of

2

(-0.08, 0.17) was obtained between the candidate and reference method, indicating

the difference

3

between methods was not statistically significant at the 0.05 probability levelno statistical

4

significant difference between the two methods.

A dLPOD

CP

value of 0.02 with 95% confidence

5

intervals of (-0.11, 0.14) was obtained between presumptive and confirmed results indicating

the

6

difference between presumptive and confirmed results was not statistically significant at the 0.05

7

probability

level.no

statistically significant difference between the presumptive and confirmed

8

results.

9

For the high inoculum level, 132 out of 132 test portions (POD

CP

of 1.00) were reported as

10

presumptive positive by the 3M MDA 2 –

Listeria

method with 132out of 132 test portions

11

(POD

CC

of 1.00) confirming positive.For samples that produced presumptive positive results on

12

the 3M MDA 2 –

Listeria

method, 132out of 132 samples confirmed positive (POD

C

of 1.00). For

13

test portions evaluated by the USDA/FSISMLG reference method, 132 out of 132 test portions

14

produced positive results. A dLPOD

C

value of 0.00 with 95% confidence intervals of (-0.03,

15

0.03) was obtained between the candidate and reference method, indicating

the difference

16

between methods was not statistically significant at the 0.05 probability level. no statistical

17

significant difference between the two methods.

A dLPOD

CP

value of 0.00 with 95% confidence

18

intervals of (-0.03, 0.03) was obtained between presumptive and confirmed results indicating

the

19

difference between presumptive and confirmed results was not statistically significant at the 0.05

20

probability

level.no

statistically significant difference between the presumptive and confirmed

21

results.

22

For the un-inoculated controls, 0 out of 132 samples (POD

CP

of 0.00) produced a presumptive

23

positive result by the 3M MDA 2 -

Listeria

method with 0out of 132 test portions (POD

CC

of

24

0.00) confirming positive.For samples that produced presumptive positive results on the 3M

25

MDA 2 –

Listeria

method, 0out of 132 samples confirmed positive (POD

C

of 0.00). For test

26

portions evaluated by the USDA/FSIS MLG reference method, 0 out of 132 test portions

27

produced positive results. A dLPOD

C

value of 0.00 with 95% confidence intervals of (-0.03,

28

0.03) was obtained between the candidate and reference method, indicating

the difference

29

between methods was not statistically significant at the 0.05 probability

level.no

statistical

30

significant difference between the two methods.

A dLPOD

CP

value of 0.00 with 95% confidence

31

intervals of (-0.03, 0.00) was obtained between presumptive and confirmed results indicating

the

32

difference between presumptive and confirmed results was not statistically significant at the 0.05

33

probability

level.no

statistically significant difference between the presumptive and confirmed

34

results.

35

36

Detailed results of the POD statistical analysis are presented in Table 2016.2A and Figures 1A-

37

1B.

38

39

Raw Chicken Breast Fillet (25 g Test Portions)

40

41

Raw chicken breast fillet test portions were inoculated at a low and high inoculum level and were

42

analyzed for the detection of

Listeria

spp. Un-inoculated controls were included in each

43