Literature DB >> 14572237

Methods for rapid separation and concentration of bacteria in food that bypass time-consuming cultural enrichment.

Patrick W Benoit1, Darrell W Donahue.   

Abstract

The rapid detection of pathogenic organisms that cause foodborne illnesses is needed to insure food safety. Conventional methods for the detection of pathogens in foods are time-consuming and labor-intensive. New advanced rapid methods (i.e., polymerase chain reaction, DNA probes) are more sensitive and selective than conventional techniques, but many of these tests are inhibited by food components, rendering them dependent on slow cultural enrichment. The need for alternative methods that will rapidly separate and concentrate bacteria directly from food samples, thereby reducing the time required for these new rapid detection techniques, is evident. Separation and concentration methods extract target bacteria from interfering food components and/or concentrate bacteria to detectable levels. This review describes several methods used to separate and/or concentrate bacteria in food samples. Several methods discussed here, including centrifugation and immunomagnetic separation, have been successfully used, individually and in combination, to rapidly separate and/or concentrate bacteria from food samples in less time than is required for cultural enrichment.

Entities:  

Mesh:

Year:  2003        PMID: 14572237     DOI: 10.4315/0362-028x-66.10.1935

Source DB:  PubMed          Journal:  J Food Prot        ISSN: 0362-028X            Impact factor:   2.077


  9 in total

Review 1.  Current and developing technologies for monitoring agents of bioterrorism and biowarfare.

Authors:  Daniel V Lim; Joyce M Simpson; Elizabeth A Kearns; Marianne F Kramer
Journal:  Clin Microbiol Rev       Date:  2005-10       Impact factor: 26.132

2.  Immobilization and detection of Listeria monocytogenes.

Authors:  B D Schindler; L A Shelef
Journal:  Appl Environ Microbiol       Date:  2006-06       Impact factor: 4.792

3.  Rapid separation and concentration of food-borne pathogens in food samples prior to quantification by viable-cell counting and real-time PCR.

Authors:  Hiroshi Fukushima; Kazunori Katsube; Yukiko Hata; Ryoko Kishi; Satomi Fujiwara
Journal:  Appl Environ Microbiol       Date:  2006-10-20       Impact factor: 4.792

4.  Novel genomic tools for specific and real-time detection of biothreat and frequently encountered foodborne pathogens.

Authors:  Abdela Woubit; Teshome Yehualaeshet; Tsegaye Habtemariam; Temesgen Samuel
Journal:  J Food Prot       Date:  2012-04       Impact factor: 2.077

5.  Plastic-adherent DNA aptamer-magnetic bead and quantum dot sandwich assay for Campylobacter detection.

Authors:  John G Bruno; Taylor Phillips; Maria P Carrillo; Randy Crowell
Journal:  J Fluoresc       Date:  2008-12-04       Impact factor: 2.217

6.  Surface plasmon resonance detection using antibody-linked magnetic nanoparticles for analyte capture, purification, concentration, and signal amplification.

Authors:  Scott D Soelberg; Richard C Stevens; Ajit P Limaye; Clement E Furlong
Journal:  Anal Chem       Date:  2009-03-15       Impact factor: 6.986

7.  Comparison of subtypes of Listeria monocytogenes isolates from naturally contaminated watershed samples with and without a selective secondary enrichment.

Authors:  Lisa Gorski; Samarpita Walker; Anita S Liang; Kimberly M Nguyen; Jessica Govoni; Diana Carychao; Michael B Cooley; Robert E Mandrell
Journal:  PLoS One       Date:  2014-03-20       Impact factor: 3.240

Review 8.  Current Methods for Extraction and Concentration of Foodborne Bacteria with Glycan-Coated Magnetic Nanoparticles: A Review.

Authors:  Emma Dester; Evangelyn Alocilja
Journal:  Biosensors (Basel)       Date:  2022-02-11

9.  Direct Detection of Escherichia coli, Staphylococcus aureus, and Salmonella spp. in Animal-derived Foods Using a Magnetic Bead-based Immunoassay.

Authors:  Jong-Hui Kim; Jae Gyu Yoo; Jun-Sang Ham; Mi-Hwa Oh
Journal:  Korean J Food Sci Anim Resour       Date:  2018-09-30       Impact factor: 2.622

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.