Affiliation:
1. Saitama Institute of Public Health, Saitama 338-0824
2. Division of Microbiology, National Institute of Health Sciences, Setagaya-ku, Tokyo 158-8501, Japan
Abstract
ABSTRACT
Loop-mediated isothermal amplification (LAMP) assay was effective in detecting
Salmonella enterica
in naturally contaminated liquid egg samples.
Salmonella
was detected in 110 samples taken from four egg-breaking plants. The egg samples were pre-enriched in buffered peptone water (BPW) at 37°C for 20 h. The selective enrichment was done in Rappaport-Vassiliadis or tetrathionate broth and plated onto xylose lysine deoxycholate agar and brilliant green agar, modified. In addition, the PCR assay was used to detect
Salmonella
after pre-enrichment in BPW at 37°C for 20 h. The culture method and PCR assay were compared to the LAMP assay, which was also performed after pre-enrichment in BPW. PCR failed to detect
Salmonella
in 10% of 110 samples, whereas the culture method and LAMP assay successfully identified
Salmonella
in all samples. However, the LAMP assay was found to be much more rapid than the culture method and as sensitive in detecting
Salmonella
from liquid eggs. In all of the egg-breaking plants studied,
Salmonella
was isolated on most tested days. The positive samples showed that more than 75% of the
Salmonella
strains had identical genetic patterns when analyzed by pulsed-field gel electrophoresis. This suggests that the same
Salmonella
strains having survived long periods of time in the plants were contaminating the production line. The LAMP assay is rapid, specific, and sensitive for
Salmonella
detection in liquid eggs and is able to monitor
Salmonella
contamination in egg-handling plants more reliably.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
131 articles.
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