A single method for recovery and concentration of enteric viruses and bacteria from fresh-cut vegetables

被引:54
作者
Sanchez, G.
Elizaquivel, P. [2 ]
Aznar, R. [1 ,2 ]
机构
[1] Spanish Council Sci Res CSIC, Dept Biotecnol, Inst Agroquim & Tecnol Alimentos, Valencia, Spain
[2] Univ Valencia, Dept Microbiol & Ecol, E-46003 Valencia, Spain
关键词
Foodborne pathogens; Vegetables; Real-time PCR; Quantification; REAL-TIME PCR; REVERSE TRANSCRIPTION-PCR; ESCHERICHIA-COLI O157-H7; COMPLETE GENOME SEQUENCE; HEPATITIS-A VIRUS; LISTERIA-MONOCYTOGENES; QUANTITATIVE DETECTION; SALMONELLA-ENTERICA; MATRIX LYSIS; BROAD RANGE;
D O I
10.1016/j.ijfoodmicro.2011.10.002
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Fresh-cut vegetables are prone to be contaminated with foodborne pathogens during growth, harvest, transport and further processing and handling. As most of these products are generally eaten raw or mildly treated, there is an increase in the number of outbreaks caused by viruses and bacteria associated with fresh vegetables. Foodborne pathogens are usually present at very low levels and have to be concentrated (i.e. viruses) or enriched (i.e. bacteria) to enhance their detection. With this aim, a rapid concentration method has been developed for the simultaneous recovery of hepatitis A virus (HAV), norovirus (NV), murine norovinis (MNV) as a surrogate for NV, Escherichia coli O157:H7, Listeria monocytogenes and Salmonella enterica. Initial experiments focused on evaluating the elution conditions suitable for virus release from vegetables. Finally, elution with buffered peptone water (BPW), using a Pulsifier, and concentration by polyethylene glycol (PEG) precipitation were the methods selected for the elution and concentration of both, enteric viruses and bacteria, from three different types of fresh-cut vegetables by quantitative PCR (qPCR) using specific primers. The average recoveries from inoculated parsley, spinach and salad, were ca. 9.2%, 43.5%, and 20.7% for NV, MNV, and HAV, respectively. Detection limits were 132 RT-PCR units (PCRU), 1.5 50% tissue culture infectious dose (TCID50), and 6.6 TCID50 for NV, MNV, and HAV, respectively. This protocol resulted in average recoveries of 57.4%, 64.5% and 64.6% in three vegetables for E. coli O157:H7, L. monocytogenes and Salmonella with corresponding detection limits of 10(3), 10(2) and 10(3) CFU/g, respectively. Based on these results, it can be concluded that the procedure herein is suitable to recover, detect and quantify enteric viruses and foodborne pathogenic bacteria within 5 h and can be applied for the simultaneous detection of both types of foodborne pathogens in fresh-cut vegetables. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:9 / 13
页数:5
相关论文
共 33 条
[1]  
[Anonymous], 2010, EFSA J, P1496
[2]   Evaluation of viral extraction methods on a broad range of Ready-To-Eat foods with conventional and real-time RT-PCR for Norovirus GII detection [J].
Baert, Leen ;
Uyttendaele, Micke ;
Debevere, Johan .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2008, 123 (1-2) :101-108
[3]   Fresh fruit and vegetables as vehicles for the transmission of human pathogens [J].
Berger, Cedric N. ;
Sodha, Samir V. ;
Shaw, Robert K. ;
Griffin, Patricia M. ;
Pink, David ;
Hand, Paul ;
Frankel, Gad .
ENVIRONMENTAL MICROBIOLOGY, 2010, 12 (09) :2385-2397
[4]   Simultaneous recovery of bacteria and viruses from contaminated water and spinach by a filtration method [J].
Brassard, Julie ;
Guevremont, Evelyne ;
Gagne, Marie-Josee ;
Lamoureux, Lisyanne .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2011, 144 (03) :565-568
[5]   Sample Preparation: The Forgotten Beginning [J].
Brehm-Stecher, Byron ;
Young, Crarles ;
Jaykus, Lee-Ann ;
Tortorello, Mary Lou .
JOURNAL OF FOOD PROTECTION, 2009, 72 (08) :1774-1789
[6]   Procedure for rapid concentration and detection of enteric viruses from berries and vegetables [J].
Butot, S. ;
Putallaz, T. ;
Sanchez, G. .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2007, 73 (01) :186-192
[7]   Inactivation of Enteric Viruses in Minimally Processed Berries and Herbs [J].
Butot, S. ;
Putallaz, T. ;
Amoroso, R. ;
Sanchez, G. .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2009, 75 (12) :4155-4161
[8]   Evaluation of various real-time RT-PCR assays for the detection and quantitation of human norovirus [J].
Butot, Sophie ;
Le Guyader, Francoise S. ;
Krol, Joanna ;
Putallaz, Thierry ;
Amoroso, Richard ;
Sanchez, Gloria .
JOURNAL OF VIROLOGICAL METHODS, 2010, 167 (01) :90-94
[9]   Surrogates for the study of norovirus stability and inactivation in the environment:: A comparison of murine norovirus and feline calicivirus [J].
Cannon, Jennifer L. ;
Papafragkou, Efstathia ;
Park, Geunwoo W. ;
Osborne, Jason ;
Jaykus, Lee-Ann ;
Vinje, Jan .
JOURNAL OF FOOD PROTECTION, 2006, 69 (11) :2761-2765
[10]   Concentration Method for the Detection of Enteric Viruses from Large Volumes of Foods [J].
Cheong, Sooryun ;
Lee, Cheonghoon ;
Choi, Weon Cheon ;
Lee, Chan-Hee ;
Kim, Sang-Jong .
JOURNAL OF FOOD PROTECTION, 2009, 72 (09) :2001-2005