Campbell, Colin
- Institutionen för mark och miljö, Sveriges lantbruksuniversitet
- The James Hutton Institute
Forskningsartikel2012Vetenskapligt granskadÖppen tillgång
Elliott, Geoffrey N; Nadine, Thomas; MacRae, Marion; Campbell, Colin; Ogden, Iain D.; Singh, Brajesh K.
A multiplex T-RFLP test was developed to detect and identify Salmonella enterica and all six species of Listeria inoculated into milk at minimal levels. Extensive in silico analysis was used to design a fifteen-primer, six-amplimer methodology and in vitro application showed target organism DNA, when amplified individually, yielded the predicted terminal restriction fragments (TRFs) following digestion. Non-target organisms were either not-amplified or yielded TRFs which did not interfere with target identification. Multiple target DNA analysis gave over 86% detection of total TRFs predicted, and this was improved to over 90% detection of total TRFs predicted when only two target DNA extracts were combined analysed. Co-inoculation of milk with five strains each of the target species of S. enterica and L. monocytogenes, along with five strains of the non-target species E. coli was followed by enrichment in SEL medium for M-TRFLP analysis. This allowed for detection of both target species in all samples, with detection of one S. enterica and two Listeria TRFs in all cases, and detection of a second S. enterica TRF in 91% of cases. This was from an initial inoculum of <5 cfu per 25 ml milk with a background of competing E. coli present, and gave a result from sampling of under 20 hours. The ability to increase target species number without loss of sensitivity means that extensive screening can be performed at reduced cost due to a reduction in the number of tests required.
PLoS ONE
2012, Volym: 7, nummer: 8, artikelnummer: e43672
Utgivare: PUBLIC LIBRARY SCIENCE 1160 BATTERY STREET, STE 100, SAN FRANCISCO, CA 94111 USA
Mikrobiologi
DOI: https://doi.org/10.1371/journal.pone.0043672
https://res.slu.se/id/publ/38799