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Development of Rapid Detection and Genetic Characterization of Salmonella in Poultry Breeder Feeds
Salmonella is a leading cause of foodborne illness in the United States, with poultry and poultry products being a primary source of infection to humans. Poultry may carry some Salmonella serovars without any signs or symptoms of disease and without causing any adverse effects to the health of the b...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3274138/ https://www.ncbi.nlm.nih.gov/pubmed/22346699 http://dx.doi.org/10.3390/s90705308 |
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author | Jarquin, Robin Hanning, Irene Ahn, Soohyoun Ricke, Steven C. |
author_facet | Jarquin, Robin Hanning, Irene Ahn, Soohyoun Ricke, Steven C. |
author_sort | Jarquin, Robin |
collection | PubMed |
description | Salmonella is a leading cause of foodborne illness in the United States, with poultry and poultry products being a primary source of infection to humans. Poultry may carry some Salmonella serovars without any signs or symptoms of disease and without causing any adverse effects to the health of the bird. Salmonella may be introduced to a flock by multiple environmental sources, but poultry feed is suspected to be a leading source. Detecting Salmonella in feed can be challenging because low levels of the bacteria may not be recovered using traditional culturing techniques. Numerous detection methodologies have been examined over the years for quantifying Salmonella in feeds and many have proven to be effective for Salmonella isolation and detection in a variety of feeds. However, given the potential need for increased detection sensitivity, molecular detection technologies may the best candidate for developing rapid sensitive methods for identifying small numbers of Salmonella in the background of large volumes of feed. Several studies have been done using polymerase chain reaction (PCR) assays and commercial kits to detect Salmonella spp. in a wide variety of feed sources. In addition, DNA array technology has recently been utilized to track the dissemination of a specific Salmonella serotype in feed mills. This review will discuss the processing of feeds and potential points in the process that may introduce Salmonella contamination to the feed. Detection methods currently used and the need for advances in these methods also will be discussed. Finally, implementation of rapid detection for optimizing control methods to prevent and remove any Salmonella contamination of feeds will be considered. |
format | Online Article Text |
id | pubmed-3274138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-32741382012-02-15 Development of Rapid Detection and Genetic Characterization of Salmonella in Poultry Breeder Feeds Jarquin, Robin Hanning, Irene Ahn, Soohyoun Ricke, Steven C. Sensors (Basel) Review Salmonella is a leading cause of foodborne illness in the United States, with poultry and poultry products being a primary source of infection to humans. Poultry may carry some Salmonella serovars without any signs or symptoms of disease and without causing any adverse effects to the health of the bird. Salmonella may be introduced to a flock by multiple environmental sources, but poultry feed is suspected to be a leading source. Detecting Salmonella in feed can be challenging because low levels of the bacteria may not be recovered using traditional culturing techniques. Numerous detection methodologies have been examined over the years for quantifying Salmonella in feeds and many have proven to be effective for Salmonella isolation and detection in a variety of feeds. However, given the potential need for increased detection sensitivity, molecular detection technologies may the best candidate for developing rapid sensitive methods for identifying small numbers of Salmonella in the background of large volumes of feed. Several studies have been done using polymerase chain reaction (PCR) assays and commercial kits to detect Salmonella spp. in a wide variety of feed sources. In addition, DNA array technology has recently been utilized to track the dissemination of a specific Salmonella serotype in feed mills. This review will discuss the processing of feeds and potential points in the process that may introduce Salmonella contamination to the feed. Detection methods currently used and the need for advances in these methods also will be discussed. Finally, implementation of rapid detection for optimizing control methods to prevent and remove any Salmonella contamination of feeds will be considered. Molecular Diversity Preservation International (MDPI) 2009-07-06 /pmc/articles/PMC3274138/ /pubmed/22346699 http://dx.doi.org/10.3390/s90705308 Text en © 2009 by the authors; licensee MDPI, Basel, Switzerland This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Jarquin, Robin Hanning, Irene Ahn, Soohyoun Ricke, Steven C. Development of Rapid Detection and Genetic Characterization of Salmonella in Poultry Breeder Feeds |
title | Development of Rapid Detection and Genetic Characterization of Salmonella in Poultry Breeder Feeds |
title_full | Development of Rapid Detection and Genetic Characterization of Salmonella in Poultry Breeder Feeds |
title_fullStr | Development of Rapid Detection and Genetic Characterization of Salmonella in Poultry Breeder Feeds |
title_full_unstemmed | Development of Rapid Detection and Genetic Characterization of Salmonella in Poultry Breeder Feeds |
title_short | Development of Rapid Detection and Genetic Characterization of Salmonella in Poultry Breeder Feeds |
title_sort | development of rapid detection and genetic characterization of salmonella in poultry breeder feeds |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3274138/ https://www.ncbi.nlm.nih.gov/pubmed/22346699 http://dx.doi.org/10.3390/s90705308 |
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