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SUBMITTED 050113
Results and Discussion
Results are presented in Tables 1 and 2. All 113
Salmonella
spp. strains tested produced
positiveresults(“
Salmonella
spp.”) from all 7 selective/differential agar media with a singleexception.
The known non-inclusive strain of
S
. Weslaco produced negative results from all agar media tested.A
second strain of
S
. Weslaco produced positive results from all agar media. Overall inclusivity of the
ANSR confirmation method was 99.1%. Excluding the single non-inclusive strain, all 784 tests performed
on inclusivity strains produced positive results, for accuracy of 100%.
Of the 266 plates streaked with exclusivity strains, there were 15 cases of no growth and no ANSR test
performed (see Table 2). Of251 ANSR tests performed on exclusivity strains, 248produced negative
results (“not
Salmonella
spp.”)for overall accuracy on exclusivity strains of 98.8%. A colony of
Enterobacter intermedia
from DMLIA agar, and a colony of
Escherichia hermanii
from XLT4 agar
produced weakly positive, atypical ANSR fluorescence curves. A colony of
Edwardsiella tarda
from XLD
agar produced a strong positive ANSR curve. Re-tests of these strain/colony combinations all produced
negative results. The cause of the two atypical curves is not known. The aberrant strong positive curve
suggests a cross-contamination event or a sample handling or pipetting error.
Considering the total of 784 results on inclusivity stains (non-inclusive
S
. Weslaco strain excluded) and
251 results on exclusivity strains, overall accuracy of the ANSR confirmation method in initial testing was
99.7%.
Example assay curves for positive and negative results are shown in Fig. 1. Almost without exception,
assay curves generated for
Salmonella
spp. were very robust and of the type shown in the example.
Recommendations
Based on results of this pre-collaborative study, it is recommended that the ANSR
Salmonella
test
application for identification of
Salmonella
spp. from colony picks be subjected to inter-laboratory
collaborative study.
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