A Real-Time PCR Screening Assay for Rapid Detection of Listeria Monocytogenes Outbreak Strains

被引:10
|
作者
Torresi, Marina [1 ]
Ruolo, Anna [1 ]
Acciari, Vicdalia Aniela [1 ]
Ancora, Massimo [1 ]
Blasi, Giuliana [2 ]
Camma, Cesare [1 ]
Centorame, Patrizia [1 ]
Centorotola, Gabriella [1 ]
Curini, Valentina [1 ]
Guidi, Fabrizia [2 ]
Marcacci, Maurilia [1 ]
Orsini, Massimiliano [3 ]
Pomilio, Francesco [1 ]
Di Domenico, Marco [1 ]
机构
[1] Ist Zooprofilatt Sperimentale Abruzzo & Molise G, Via Campo Boario, I-64100 Teramo Te, Italy
[2] Ist Zooprofilatt Sperimentale Umbria & Marche Tog, Via Gaetano Salvemini 1, I-06126 Perugia Pg, Italy
[3] Ist Zooprofilatt Sperimentale Venezie, Viale Univ 10, I-35020 Legnaro Pd, Italy
关键词
Listeria monocytogenes; outbreak; molecular methods; real-time PCR; screening; GENOME; CONTAMINATION;
D O I
10.3390/foods9010067
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
From January 2015 to March 2016, an outbreak of 23 human cases of listeriosis in the Marche region and one human case in the Umbria region of Italy was caused by Listeria monocytogenes strains showing a new pulsotype never described before in Italy. A total of 37 clinical strains isolated from patients exhibiting listeriosis symptoms and 1374 strains correlated to the outbreak were received by the Italian National Reference Laboratory for L. monocytogenes (It NRL Lm) of Istituto Zooprofilattico Sperimentale dell'Abruzzo e del Molise (IZSAM) for outbreak investigation. A real-time PCR assay was purposely designed for a rapid screening of the strains related to the outbreak. PCR-positive strains were successively typed through molecular serogrouping, pulsed field gel electrophoresis (PFGE), and Next Generation Sequencing (NGS). Applying the described strategy, based on real-time PCR screening, we were able to considerably reduce time and costs during the outbreak investigation activities.
引用
收藏
页数:9
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