Molecular epidemiology of Salmonella spp. isolates from gulls, fish-meal factories, feed factories, animals and humans in Norway based on pulsed-field gel electrophoresis

The molecular epidemiology of 98 isolates of Salmonella serovar Agona (n=27), S. Montevideo (n=42) and S. Senftenberg (n=29) from wild-living gulls, fish-meal factories, feed factories, humans and domestic animals was investigated using pulsed-field gel electrophoresis (PFGE) and computerized numeri...

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Published in:Epidemiology and infection 2005-02, Vol.133 (1), p.53-58
Main Authors: NESSE, L. L., REFSUM, T., HEIR, E., NORDBY, K., VARDUND, T., HOLSTAD, G.
Format: Article
Language:English
Subjects:
Animal Feed - microbiology
Animals
Bacterial Typing Techniques
Bacteriology
Biological and medical sciences
Birds
Birds - microbiology
Domesticated animals
Electrophoresis
Electrophoresis, Gel, Pulsed-Field
Epidemiology
Factories
Feeds
Fishes
Food Microbiology
Fundamental and applied biological sciences. Psychology
Gels
Herring
Humans
Investigations
Laboratories
Microbiology
Miscellaneous
Molecular Epidemiology
Norway - epidemiology
Poultry
Poultry farms
Public health
Salmonella
Salmonella - isolation & purification
Salmonella Infections - epidemiology
Salmonella Infections, Animal - epidemiology
Sea birds
Serotyping
Wild birds
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container_issue 1
container_start_page 53
container_title Epidemiology and infection
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creator NESSE, L. L.
REFSUM, T.
HEIR, E.
NORDBY, K.
VARDUND, T.
HOLSTAD, G.
description The molecular epidemiology of 98 isolates of Salmonella serovar Agona (n=27), S. Montevideo (n=42) and S. Senftenberg (n=29) from wild-living gulls, fish-meal factories, feed factories, humans and domestic animals was investigated using pulsed-field gel electrophoresis (PFGE) and computerized numerical analysis. Two of the S. Agona profiles were identified both in gulls and in two of the factories. In addition, one of these profiles was detected in two infected poultry farms. Two of the S. Montevideo profiles were also identified both in gulls and in two of the factories, and one of these profiles was observed in a human isolate. Four factories shared an identical S. Senftenberg profile. The S. Senftenberg profile found in gulls was not identified in any other source investigated. The presence of isolates with identical PFGE profiles indicates potential epidemiological links between different factories, as well as between gulls and factories.
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L.</creatorcontrib><creatorcontrib>REFSUM, T.</creatorcontrib><creatorcontrib>HEIR, E.</creatorcontrib><creatorcontrib>NORDBY, K.</creatorcontrib><creatorcontrib>VARDUND, T.</creatorcontrib><creatorcontrib>HOLSTAD, G.</creatorcontrib><title>Molecular epidemiology of Salmonella spp. isolates from gulls, fish-meal factories, feed factories, animals and humans in Norway based on pulsed-field gel electrophoresis</title><title>Epidemiology and infection</title><addtitle>Epidemiol. Infect</addtitle><description>The molecular epidemiology of 98 isolates of Salmonella serovar Agona (n=27), S. Montevideo (n=42) and S. Senftenberg (n=29) from wild-living gulls, fish-meal factories, feed factories, humans and domestic animals was investigated using pulsed-field gel electrophoresis (PFGE) and computerized numerical analysis. Two of the S. Agona profiles were identified both in gulls and in two of the factories. In addition, one of these profiles was detected in two infected poultry farms. 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L.</au><au>REFSUM, T.</au><au>HEIR, E.</au><au>NORDBY, K.</au><au>VARDUND, T.</au><au>HOLSTAD, G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular epidemiology of Salmonella spp. isolates from gulls, fish-meal factories, feed factories, animals and humans in Norway based on pulsed-field gel electrophoresis</atitle><jtitle>Epidemiology and infection</jtitle><addtitle>Epidemiol. Infect</addtitle><date>2005-02-01</date><risdate>2005</risdate><volume>133</volume><issue>1</issue><spage>53</spage><epage>58</epage><pages>53-58</pages><issn>0950-2688</issn><eissn>1469-4409</eissn><coden>EPINEU</coden><abstract>The molecular epidemiology of 98 isolates of Salmonella serovar Agona (n=27), S. Montevideo (n=42) and S. Senftenberg (n=29) from wild-living gulls, fish-meal factories, feed factories, humans and domestic animals was investigated using pulsed-field gel electrophoresis (PFGE) and computerized numerical analysis. Two of the S. Agona profiles were identified both in gulls and in two of the factories. In addition, one of these profiles was detected in two infected poultry farms. Two of the S. Montevideo profiles were also identified both in gulls and in two of the factories, and one of these profiles was observed in a human isolate. Four factories shared an identical S. Senftenberg profile. The S. Senftenberg profile found in gulls was not identified in any other source investigated. The presence of isolates with identical PFGE profiles indicates potential epidemiological links between different factories, as well as between gulls and factories.</abstract><cop>Cambridge, UK</cop><pub>Cambridge University Press</pub><pmid>15724711</pmid><doi>10.1017/S0950268804003279</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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1469-4409
language eng
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source Cambridge Journals Online; JSTOR Archival Journals and Primary Sources Collection; PubMed Central
subjects Animal Feed - microbiology
Animals
Bacterial Typing Techniques
Bacteriology
Biological and medical sciences
Birds
Birds - microbiology
Domesticated animals
Electrophoresis
Electrophoresis, Gel, Pulsed-Field
Epidemiology
Factories
Feeds
Fishes
Food Microbiology
Fundamental and applied biological sciences. Psychology
Gels
Herring
Humans
Investigations
Laboratories
Microbiology
Miscellaneous
Molecular Epidemiology
Norway - epidemiology
Poultry
Poultry farms
Public health
Salmonella
Salmonella - isolation & purification
Salmonella Infections - epidemiology
Salmonella Infections, Animal - epidemiology
Sea birds
Serotyping
Wild birds
title Molecular epidemiology of Salmonella spp. isolates from gulls, fish-meal factories, feed factories, animals and humans in Norway based on pulsed-field gel electrophoresis
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