Table of Contents Table of Contents
Previous Page  403 / 596 Next Page
Information
Show Menu
Previous Page 403 / 596 Next Page
Page Background

A Comparative Evaluation of the 3M

Molecular Detection Assay 2 (MDA 2) -

Listeria

for

1

the Detection of

Listeria

species in a Variety of Foods and Environmental Surfaces

2

3

AOAC

Performance Tested Methods

SM

111501

4

5

Abstract

6

7

The 3M

Molecular Detection Assay 2 (MDA2) -

Listeria

for the detection of

Listeria

species

8

(

L. monocytogenes, L. seeligeri, L. ivanovii, L. innocua, L. grayi, L. welshimeri, L. fleishmanii

9

subsp

.

coloradensis

, L. marthii

,

L. grandensis, L. cornellensis

L. aquatic, L. newyorkensis, L.

10

weihenstephanesis, L. baoriae, L. fleishmanii

subsp. fleishmanii,

L. ivanovii

subsp. londoniensis

11

and

L. riparia)

was evaluated following the 2012 AOAC Research Institute

Performance Tested

12

Methods

SM

program guidelines. The evaluation included inclusivity/exclusivity, lot-to-

13

lot/stability, robustness and matrix studies. The 3M MDA 2 -

Listeria

was compared to various

14

reference methods for raw chicken, bagged raw spinach, cold smoked salmon, deli turkey, whole

15

melons, vanilla ice cream, queso fresco, 4% milk fat cottage cheese, beef hot dogs, stainless

16

steel, sealed concrete and plastic in the matrix study. Twenty replicates of each food matrix were

17

analyzed at a low inoculum level of 0.2-2 colony forming units (CFU)/standard test portion, five

18

replicates were analyzed at a high level of 2-5 CFU/test portion, and five control replicates were

19

analyzed at 0 CFU/standard test portion with the exception of naturally contaminated raw

20

chicken (leg pieces) analyzed at the independent laboratory. Naturally contaminated raw chicken

21

(leg pieces), analyzed at the independent laboratory, were evaluated using two separate lots

22

consisting of twenty replicates for each lot. All environmental surfaces were analyzed using

23

twenty replicates at a low inoculum level of ~ 50 CFU/standard area, five replicates were

24

analyzed at a high level of ~ 100 CFU/standard area, and five control replicates were analyzed at

25

0 CFU/standard test area. Based on the probability of detection statistical model, there were no

26

statistically significant differences between the number of presumptive and confirmed positive

27

samples or between the candidate and reference method. There were no unexpected results in the

28

lot-to-lot/stability, robustness studies. In the inclusivity/exclusivity study, 55 target organisms

29

and 30 non-target organisms were tested following the 3M MDA 2 -

Listeria

method with all

30

target organisms detected and none of the non-target organisms detected. The results of this

31

evaluation demonstrate the specificity and sensitivity of the 3M MDA 2 -

Listeria

and its ability

32

to accurately detect

Listeria

species in select food matrixes (beef hot dogs, queso fresco, vanilla

33

ice cream, 4% milk fat cottage cheese, 3% whole milk, bagged raw spinach, cold smoked

34

salmon, raw chicken parts, deli turkey, whole cantaloupe) and environmental surfaces (stainless

35

steel, sealed concrete, plastic), 24-30 hours post enrichment.

36

37

Authors

38

Lisa Monteroso and DeAnn Benesh, 3M Food Safety Division

39

Ben Bastin, Jonathan Flannery, Erin Crowley, Patrick Bird, M. Joseph Benzinger, Jr., James

40

Agin, David Goins, Q Laboratories, Inc.

41

42

Submitting Company

43

3M Company

44

Food Safety Department

45

3M Center, Bldg. 275-5W-05

46

Formatted:

Font: Not Italic