Methods used for the detection and subtyping of Listeria monocytogenes

被引:152
作者
Jadhav, Snehal [1 ]
Bhave, Mrinal [1 ]
Palombo, Enzo A. [1 ]
机构
[1] Swinburne Univ Technol, Environm & Biotechnol Ctr, Fac Life & Social Sci, Hawthorn, Vic 3122, Australia
关键词
Listeria monocytogenes; Detection; Subtyping; REAL-TIME PCR; DESORPTION IONIZATION-TIME; FIELD GEL-ELECTROPHORESIS; FLIGHT MASS-SPECTROMETRY; TANDEM-REPEAT ANALYSIS; LOCUS VARIABLE-NUMBER; SEQUENCE-BASED PCR; MULTILOCUS ENZYME ELECTROPHORESIS; TRANSFORM INFRARED-SPECTROSCOPY; ESCHERICHIA-COLI;
D O I
10.1016/j.mimet.2012.01.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Listeria monocytogenes is an important foodborne pathogen responsible for non-invasive and invasive diseases in the elderly, pregnant women, neonates and immunocompromised populations. This bacterium has many similarities with other non-pathogenic Listeria species which makes its detection from food and environmental samples challenging. Subtyping of L monocytogenes strains can prove to be crucial in epidemiological investigations, source tracking contamination from food processing plants and determining evolutionary relationships between different strains. In recent years there has been a shift towards the use of molecular subtyping. This has led to the development of new subtyping techniques such as multi-locus variable number tandem repeat analysis (MLVA) and multi-locus sequence based typing (MLST). This review focuses on the available methods for Listeria detection including immuno-based techniques and the more recently developed molecular methods and analytical techniques such as matrix-assisted laser desorption/ionisation time-of-flight based mass spectrometry (MALDI-TOF MS). It also includes a comparison and critical analysis of the available phenotypic and genotypic subtyping techniques that have been investigated for L. monocytogenes. (C) 2012 Elsevier E.V. All rights reserved.
引用
收藏
页码:327 / 341
页数:15
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