Evaluation of new culture media for rapid detection and isolation of salmonellae in foods

Conventional methods for Salmonella detection in foods can require up to 6 and at least 4 days. We have observed that the total analysis time can be reduced to 48 h by using Salmosyst broth as a liquid medium for both preenrichment and selective enrichment and Rambach agar (RA), a new selective plat...

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Veröffentlicht in:Applied and Environmental Microbiology 1995-05, Vol.61 (5), p.1996-1999
Hauptverfasser: Pignato, S. (Universita di Catania, Catania, Italy.), Marino, A.M, Emanuele, M.C, Iannotta, V, Caracappa, S, Giammanco, G
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container_end_page 1999
container_issue 5
container_start_page 1996
container_title Applied and Environmental Microbiology
container_volume 61
creator Pignato, S. (Universita di Catania, Catania, Italy.)
Marino, A.M
Emanuele, M.C
Iannotta, V
Caracappa, S
Giammanco, G
description Conventional methods for Salmonella detection in foods can require up to 6 and at least 4 days. We have observed that the total analysis time can be reduced to 48 h by using Salmosyst broth as a liquid medium for both preenrichment and selective enrichment and Rambach agar (RA), a new selective plate medium. In samples of artificially contaminated ground beef Salmonella enteritidis was detected at a concentration of 0.4 CFU/g (10 CFU/25 g) by both a conventional method and the new method. Of 519 samples of foods for sale, 38 were Salmonella positive by both methods while 471 were negative. Nine samples which were negative by the conventional method were positive by the Salmosyst-RA method, while one sample positive by the first method was negative by the last. Therefore, the Salmosyst-RA method showed 97.9% sensitivity compared with the 81.2% sensitivity of the conventional method. The new method was also highly specific (98% specificity) in presumptive identification of Salmonella colonies. Furthermore, a 6-h preenrichment in Salmosyst broth has been proved sufficient for the repair of heat-injured Salmonella cells and for subsequent recovery by selective enrichment. In conclusion, the Salmosyst-RA method shows several advantages over both conventional and rapid noncultural methods: (i) only two media are required instead of the five media for conventional methods; (ii) in real time it is comparable to other rapid noncultural methods, which require 30 to 31 h; (iii) it is highly sensitive and specific; and (iv) it allows the isolation of Salmonella strains which can be characterized by appropriate phenotypic and genotypic typing methods for epidemiological investigations
doi_str_mv 10.1128/aem.61.5.1996-1999.1995
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(Universita di Catania, Catania, Italy.) ; Marino, A.M ; Emanuele, M.C ; Iannotta, V ; Caracappa, S ; Giammanco, G</creator><creatorcontrib>Pignato, S. (Universita di Catania, Catania, Italy.) ; Marino, A.M ; Emanuele, M.C ; Iannotta, V ; Caracappa, S ; Giammanco, G</creatorcontrib><description>Conventional methods for Salmonella detection in foods can require up to 6 and at least 4 days. We have observed that the total analysis time can be reduced to 48 h by using Salmosyst broth as a liquid medium for both preenrichment and selective enrichment and Rambach agar (RA), a new selective plate medium. In samples of artificially contaminated ground beef Salmonella enteritidis was detected at a concentration of 0.4 CFU/g (10 CFU/25 g) by both a conventional method and the new method. Of 519 samples of foods for sale, 38 were Salmonella positive by both methods while 471 were negative. Nine samples which were negative by the conventional method were positive by the Salmosyst-RA method, while one sample positive by the first method was negative by the last. Therefore, the Salmosyst-RA method showed 97.9% sensitivity compared with the 81.2% sensitivity of the conventional method. The new method was also highly specific (98% specificity) in presumptive identification of Salmonella colonies. Furthermore, a 6-h preenrichment in Salmosyst broth has been proved sufficient for the repair of heat-injured Salmonella cells and for subsequent recovery by selective enrichment. 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(Universita di Catania, Catania, Italy.)</creatorcontrib><creatorcontrib>Marino, A.M</creatorcontrib><creatorcontrib>Emanuele, M.C</creatorcontrib><creatorcontrib>Iannotta, V</creatorcontrib><creatorcontrib>Caracappa, S</creatorcontrib><creatorcontrib>Giammanco, G</creatorcontrib><title>Evaluation of new culture media for rapid detection and isolation of salmonellae in foods</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>Conventional methods for Salmonella detection in foods can require up to 6 and at least 4 days. We have observed that the total analysis time can be reduced to 48 h by using Salmosyst broth as a liquid medium for both preenrichment and selective enrichment and Rambach agar (RA), a new selective plate medium. In samples of artificially contaminated ground beef Salmonella enteritidis was detected at a concentration of 0.4 CFU/g (10 CFU/25 g) by both a conventional method and the new method. 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In samples of artificially contaminated ground beef Salmonella enteritidis was detected at a concentration of 0.4 CFU/g (10 CFU/25 g) by both a conventional method and the new method. Of 519 samples of foods for sale, 38 were Salmonella positive by both methods while 471 were negative. Nine samples which were negative by the conventional method were positive by the Salmosyst-RA method, while one sample positive by the first method was negative by the last. Therefore, the Salmosyst-RA method showed 97.9% sensitivity compared with the 81.2% sensitivity of the conventional method. The new method was also highly specific (98% specificity) in presumptive identification of Salmonella colonies. Furthermore, a 6-h preenrichment in Salmosyst broth has been proved sufficient for the repair of heat-injured Salmonella cells and for subsequent recovery by selective enrichment. In conclusion, the Salmosyst-RA method shows several advantages over both conventional and rapid noncultural methods: (i) only two media are required instead of the five media for conventional methods; (ii) in real time it is comparable to other rapid noncultural methods, which require 30 to 31 h; (iii) it is highly sensitive and specific; and (iv) it allows the isolation of Salmonella strains which can be characterized by appropriate phenotypic and genotypic typing methods for epidemiological investigations</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>7646035</pmid><doi>10.1128/aem.61.5.1996-1999.1995</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record>
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subjects ALIMENTOS
Animals
Bacteria
BIODEGRADACION
BIODEGRADATION
Biological and medical sciences
Biology
CARNE DE CABALLO
CARNE DE CERDO
CARNE DE POLLO
CARNE DE RES
Cattle
CONTAMINACION
CONTAMINATION
Culture Media
Eggs - microbiology
Food Contamination
Food contamination & poisoning
Food industries
Food Microbiology
Fundamental and applied biological sciences. Psychology
Horses
HUEVOS
INFECCION
INFECTION
Meat - microbiology
MEDIO DE CULTIVO
MILIEU DE CULTURE
OEUF
Poultry - microbiology
PRODUIT ALIMENTAIRE
SALMONELLA
Salmonella - growth & development
Salmonella - isolation & purification
SALMONELLA ENTERITIDIS
Swine
Time Factors
VIANDE BOVINE
VIANDE CHEVALINE
VIANDE DE POULET
VIANDE PORCINE
title Evaluation of new culture media for rapid detection and isolation of salmonellae in foods
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