Identifi cation of Salmonella spp and serovars Typhimurium, Enteritidis by qPCR

This article presents the results of the identifi cation of the Salmonella genus as well as serovars Enteritidis and Typhimurium by a real-time polymerase chain reaction. We constructed three pairs of primers and fl uorescent probes to simultaneously identify the Salmonella genus, serovars Enteritidis...

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Main Author: Rublenko N.
Format: Article
Language:English
Published: Bila Tserkva National Agrarian University 2020-05-01
Series:Науковий вісник ветеринарної медицини
Subjects:
Online Access:http://nvvm.btsau.edu.ua/sites/all/modules/pubdlcnt/pubdlcnt.php?fid=1001
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author Rublenko N.
author_facet Rublenko N.
author_sort Rublenko N.
collection DOAJ
description This article presents the results of the identifi cation of the Salmonella genus as well as serovars Enteritidis and Typhimurium by a real-time polymerase chain reaction. We constructed three pairs of primers and fl uorescent probes to simultaneously identify the Salmonella genus, serovars Enteritidis and Typhimurium in a qPCR. The specifi city of the primers was evaluated on Salmonella strains of diff erent serovars from the National Center for Strains of Microorganisms (UNCMS) strains of the State Scientifi c Control Institute of Biotechnology and Strains of Microorganisms (SSCIBSM) and 46 Salmonella strains isolated from poultry. E. coli ATCC 25922, Bacillus cereus ATCC 11778, Listeria monocytogenes ATCC 19112 from UNCMS collection were used to check the specifi city of the primers as heterologous samples. Bacterial DNA was extracted using a DNA Sorb B (Amplisens) kit, and realtime PCR was accomplished with the "Real-time PCR kit" (Syntol) on Bio-rad CFX. A series of 10-fold S. Typhimurium and S. Enteritidis DNA dilutions were studied to evaluate the sensitivity of the primers: 10-1-10-5. The analytical sensitivity of primers for detection of the genus Salmonella is: for S. Typhimurium - 0.25 ng/sample (Typhimurium) and S. Enteritidis - 0.27 ng/ sample (Enteritidis). The results of the studies confi rmed the specifi city of the primer set and the high sensitivity. No hybridization of primers with DNA samples of other bacteria found, in particular, the nonspecifi c reaction products were absent. The primer sets for the detection of DNA of Enteritidis and Typhimurium serovars also has high specifi city. If necessary, this set of primers can be used to perform a multiplex qPCR, that can simultaneously identify bacteria of the Salmonella genus and diff erentiate Enteritidis and Typhimurium serovars.
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spelling doaj.art-55e19b83652040769c1c1efb026cf0782022-12-21T21:20:23ZengBila Tserkva National Agrarian UniversityНауковий вісник ветеринарної медицини2310-49022415-75892020-05-011213110.33245/2310-4902-2020-154-1-21-31Identifi cation of Salmonella spp and serovars Typhimurium, Enteritidis by qPCRRublenko N.0https://orcid.org/0000-0002-2179-4781State Research and Control Institute of Biotechnology and Strains of MicroorganismsThis article presents the results of the identifi cation of the Salmonella genus as well as serovars Enteritidis and Typhimurium by a real-time polymerase chain reaction. We constructed three pairs of primers and fl uorescent probes to simultaneously identify the Salmonella genus, serovars Enteritidis and Typhimurium in a qPCR. The specifi city of the primers was evaluated on Salmonella strains of diff erent serovars from the National Center for Strains of Microorganisms (UNCMS) strains of the State Scientifi c Control Institute of Biotechnology and Strains of Microorganisms (SSCIBSM) and 46 Salmonella strains isolated from poultry. E. coli ATCC 25922, Bacillus cereus ATCC 11778, Listeria monocytogenes ATCC 19112 from UNCMS collection were used to check the specifi city of the primers as heterologous samples. Bacterial DNA was extracted using a DNA Sorb B (Amplisens) kit, and realtime PCR was accomplished with the "Real-time PCR kit" (Syntol) on Bio-rad CFX. A series of 10-fold S. Typhimurium and S. Enteritidis DNA dilutions were studied to evaluate the sensitivity of the primers: 10-1-10-5. The analytical sensitivity of primers for detection of the genus Salmonella is: for S. Typhimurium - 0.25 ng/sample (Typhimurium) and S. Enteritidis - 0.27 ng/ sample (Enteritidis). The results of the studies confi rmed the specifi city of the primer set and the high sensitivity. No hybridization of primers with DNA samples of other bacteria found, in particular, the nonspecifi c reaction products were absent. The primer sets for the detection of DNA of Enteritidis and Typhimurium serovars also has high specifi city. If necessary, this set of primers can be used to perform a multiplex qPCR, that can simultaneously identify bacteria of the Salmonella genus and diff erentiate Enteritidis and Typhimurium serovars.http://nvvm.btsau.edu.ua/sites/all/modules/pubdlcnt/pubdlcnt.php?fid=1001salmonellabacteriapolymerasechainreactiondnaqpcr
spellingShingle Rublenko N.
Identifi cation of Salmonella spp and serovars Typhimurium, Enteritidis by qPCR
Науковий вісник ветеринарної медицини
salmonella
bacteria
polymerasechainreaction
dna
qpcr
title Identifi cation of Salmonella spp and serovars Typhimurium, Enteritidis by qPCR
title_full Identifi cation of Salmonella spp and serovars Typhimurium, Enteritidis by qPCR
title_fullStr Identifi cation of Salmonella spp and serovars Typhimurium, Enteritidis by qPCR
title_full_unstemmed Identifi cation of Salmonella spp and serovars Typhimurium, Enteritidis by qPCR
title_short Identifi cation of Salmonella spp and serovars Typhimurium, Enteritidis by qPCR
title_sort identifi cation of salmonella spp and serovars typhimurium enteritidis by qpcr
topic salmonella
bacteria
polymerasechainreaction
dna
qpcr
url http://nvvm.btsau.edu.ua/sites/all/modules/pubdlcnt/pubdlcnt.php?fid=1001
work_keys_str_mv AT rublenkon identificationofsalmonellasppandserovarstyphimuriumenteritidisbyqpcr