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Table

4.

Results

by agar medium

BGS = brilliant green sulfa

agar;

BS = bismuth sulfite agar;

DMLIA = douþle-modified lysine iron

agar;

HE = Hektoen enteric agar

TSA

=

tryptic soy agar; XLD =

xylose

lysine deoxycholate agar;

XLT-4 = xylose lysine terg¡tol agar.

vulgaris

produced

colonies on

XLl--4

agar.

'lhe

remaining

cases

of'no

grorvth

appeared

to

be

random

rvith

respecl

to

strain

and

medium,

A

total

of

691

analyses

ri'ere pelfbrnred on

exclusive

strains.

Collaboralor

l6

r'eported

positive

results

on six

of

seven

plates

sh'eaked

wifh

the

E.

cloacae

cultule.'rhe

renraining

agar.

1'SA,

rvas reported

to

have

no

growth. Collaboratol

16

leporled that the

six

pìates

all

contained

growth rvith

colonies

of

a

Salnonel/a-like

appearance.

It

is

concluded

that

this

culture

becarne

contaminated at some

point during

preparation

or

analysis and therefore

these

data rvere eliminated

from

the

statistical analysis. Otl

685

remainìng

analyses,

661

produced

negative results fbr'¿ìccuracy

rvith exclusive

strains

of

96.5%.

A surnrlarl,

ollesults

b¡'agar

mediunr

is

shorvn

in

Table

4.

The

pÈr'centage

of correct lesults

rvas

very similar fbr all

seven

media,

ranging

liorr

97.6 to

98.99'o.

Discussion

ln

this multilaboralory

evaluation

of

the

ANSR

Salmonella

îcst

lor

iclentilìoation

of

presunrplive

S¿tlntonella

spp.

isolates

lì'om

agar media,

the

method

exhibited

exceptional

accuracy

u'ith

inclusive

strains and

a

high

degree

ofexclusivity

rvith non-

salmonellac.

Of the

l8

laboratories

parlicipating

in

the

study,

l5

reporlcd

results

rvith

overall accuracy

of

99

to

100%.'lhere

ilas

orrll'

a

single

fàlse-negative

result out

of

756 Salntonella

spp, colonie

s

testecl.

L}cluding

dtrta

generated

fiom

a

suspected

contarninaled slant

cultur-e,

thele

rvere

24 lalse-positive

results

on non-S.a/äronella

spp.

colonies out of 685 colonies

tested.

All

lÌtt

scven

ofthese

aberr'¿¡nt

|esr¡]ts

occurred

in

thlce

laboratories.

[-alroralory

l6

ieported

six

faìse-positive

lcsults

in

addition

to

those

linked

to

the

contaminated

slant culture.

No

fìrrther

inlbrmation is available

fbr

these

sanrples,

cxcept

that

all

six

ANSR

lìuorescenoe

cì,ìrves

\vele

vcr'\'

strong,

t¡'pical

o1'true

positive

results.

I-aboratory

2

repolted six fàlse-positive

results;

MOZ-OLA

81.

,AT,,:

JOUIìNAI, OF,AOAC] INTTJIìN^IIONAL

VOL. 97'

NO. 3.

20I4

835

fbur

olthesc

occurred in

a

single

ANSIì

assa¡'

run

ol'

I

5

sarnples.

All

but one

ofthc

lalsc-positive lesults

shorvcd

at¡"pical,

rveak

lìuorescence

culves, suggestive

of

cross-contarlination drrling

pelfbrurarrce

ol

thc

ANSR

assay.

l-aboratory

l3

reported

fìr'e

fälse-positive

results.

Again. all but

one

ofthese

results

shorved

atypical, u'eak

fluorescence

curves.

Additionally,

rau'

data

received

from this laboratoly

indicated that

one assay

run

was

lepeated

in

total

due

to

extreme aberlant results

(i.e., invalid

assays), suggesting

that the

technician

was

experiencing

dif1ìcult¡, in pcrforming

tlie

assay

correctly.

lncluding

data

fionl

all l8

laboratories

(rvith the

exclusion

of

the

six

suspected contaminated samples

from

laboratory

l6),

accuracy

on inclusive

and

exclusive

stlains

rvas

99.9 and96.5Vô,

respectively. Considering

only

data

fi'om

the

l5

laboratories

rvithout

clusters

of

aben'anl

resr¡lts,

accurac)' on exclusive strains

rvas 98.87ir,

Recommendations

'l'he

ANSR

Salmonella test was

adopted

as

Official

First

Action

status

for

use as a

rapid.

accut'¿ìtc

ad.iunct

or altemative

to

biochenical

testing

for

identification

of

presumptive

Salnonella

spp. isolates.

Acknowledgments

We thank the

folloiving

collaborators

lor

their

paÍicipation

in

this study:

Dorn

Clalk

and l-londo Dammann, Marshfield

lrood

Salèt.v

(Marshlìeld,

Wl)

Jessica

Dyszel and

Matlherv Vross.

Iìichter

International

(Colunrbus.

OIì)

Nicole

Cuthbert and

Brian Kupski, Silliker

(Crete,

Il-)

Joe

Benzinger,

ñlegan

Lìoyle,

and

Jonathan

lìlannera.

Q Laboratories

(Cincinnati, OH)

Eric

S.

Adanls,

John

B.

Barrett.

Mark

E,.

llerang,

Douglas

E.

Cosby,

Nelson

A.

Cox,

Jonathan

G.

Frye,

l,ari

M.

I-liotl.

Charlene

R.

Jackson, Steven

W. Knapp,

and Luanne

L.

Rigsby,

U.S.

Deparlrnent

of

Agriculture,

Agricultural

Research

Set'r,ice

(Athens,

GA)

Robert

Fuller

and Jan'od Van

Brunt,'lyson

Foods (Springdale,

AI{)

[{arroud Alnughaymishi

and

Andrerv Scollon.

I\4ichigan

State

University.

l)epartment

ol

lìood

Science

¿rnd

Human

Nutrition

(East

l.ansing.

MI)

Mr:ìanir:

Corebello and

Erika

Sai.

Iinilever tl.S.

(Fìnglewood

Clifls,

NJ)

[.isa Kuepfer

and

Jill

Stepnitz, Covance

(Ilattle

Creek,

Ml)

Michael

Iìudgens

and

Waltel

Jones.

NPAnal¡'tical

L"abolatories

(St.

Louis,

MO)

Douglas Waltman

and Selena

York, Georgia Poultry

Laboratory

(Oakrvood,

CA)

Jake Cannon.

Benjamin

l-lorvard, and

Neil

lìognran.

Clertifìed

Laboratories

of

the

Midrvest (Bolingbrook,

lL)

Chad

Pidgeon

and

Amy

Quenneville.

Ben

&

Jelry's

(Burlington. V'l-)

Vikas

Gill

and

l-lua \\¡ang. United

States

l--ood

and

Drug

Adrninistration.

Center

lbr

lrood

Safety and

Applied Nutrition

(College

Park,

MD)

Cori

F'lores

and

Priyanivacla

Kulkarni,

Ilenningsen

Foods

(Onaha.

NE)

Medium"

Correct

lvl¡sidentified

Totaf

BGS

lnclusive

Exclusìve

lnclus¡ve

Exclus¡ve

lnclus¡ve

Exclusive

lnclusive

Exclusive

lnclusìve

Exclusive

lnclus¡ve

Exclusive

lnclusive

Exclu

sive

lnclus¡ve

Exclusive

BS

DMLIA

HE

TSA

XLD

XLT-4

Total

108

98

108

99

108

93

107

100

108

101

108

101

108

69

661

0

5

0

4

0

3

1

4

0

3

0

3

0

2

1

24

108

103

108

103

108

'108

'104

108

104

108

104

108

71

756

685