1999
DOI: 10.1016/s0168-1605(99)00081-1
|View full text |Cite
|
Sign up to set email alerts
|

Methodology for detection and typing of foodborne microorganisms

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
153
0
4

Year Published

2006
2006
2013
2013

Publication Types

Select...
6
2
1

Relationship

0
9

Authors

Journals

citations
Cited by 340 publications
(159 citation statements)
references
References 38 publications
0
153
0
4
Order By: Relevance
“…Reference laboratories are also able to further type isolates using techniques such a phage typing (Anderson and Williams 1956;Callow 1959;Anderson 1964;Anderson et al 1977), antibiotic susceptibility (Bauer et al 1966), pulsed-field gel electrophoresis (PFGE), or other emerging genetic typing technologies such Multiple-Locus Variable Number Tandem Repeat Analysis (MLVA) and Multilocus sequence typing (MLST) (Kruy et al 2011). Although standard culture methods are excessively time-consuming, there is potential for further improvements, and thus many attempts have been made to maximize their efficiency by introducing new technologies, making reliability of detection more convenient, user friendly, as well as by reducing the costs of materials and labour (de Boer and Beumer 1999;Weenk, 1992). For example, biochemical confirmatory tests may be easily replaced by commercial identification kits such as the API 20E (BioMérieux) or other commercially available bacterial identification kits.…”
Section: Culture Methodsmentioning
confidence: 99%
“…Reference laboratories are also able to further type isolates using techniques such a phage typing (Anderson and Williams 1956;Callow 1959;Anderson 1964;Anderson et al 1977), antibiotic susceptibility (Bauer et al 1966), pulsed-field gel electrophoresis (PFGE), or other emerging genetic typing technologies such Multiple-Locus Variable Number Tandem Repeat Analysis (MLVA) and Multilocus sequence typing (MLST) (Kruy et al 2011). Although standard culture methods are excessively time-consuming, there is potential for further improvements, and thus many attempts have been made to maximize their efficiency by introducing new technologies, making reliability of detection more convenient, user friendly, as well as by reducing the costs of materials and labour (de Boer and Beumer 1999;Weenk, 1992). For example, biochemical confirmatory tests may be easily replaced by commercial identification kits such as the API 20E (BioMérieux) or other commercially available bacterial identification kits.…”
Section: Culture Methodsmentioning
confidence: 99%
“…The sensitivities of conventional culture (ISO) and immunomagnetic separation (IMS) method, which are used to detect Salmonella bacteria, are calculated by using the formula described in Boer and Beumer [22] :…”
Section: Determination Of Sensitivities Of Conventional Culture and Imentioning
confidence: 99%
“…After enrichment, samples are grown on selective media in order to isolate individual bacterial colonies. Additional biochemical or immunological characterization of individual bacterial clones is usually necessary to identify the pathogen [2]. Similarly, in microbial toxin testing, extraction and concentration steps are used prior to detection by serological or animal assays [3].…”
Section: Introductionmentioning
confidence: 99%