Microbial enrichment and multiplexed microfiltration for accelerated detection of Salmonella in spinach

被引:9
作者
Ku, Seockmo [1 ,6 ]
Ximenes, Eduardo [1 ,2 ]
Kreke, Thomas [1 ,7 ]
Foster, Kirk [3 ]
Couetil, Justin L. [1 ]
Zuponcic, Jessica [1 ,2 ]
Zhao, Xiaojun [4 ]
Hoagland, Lori [4 ]
Deering, Amanda J. [5 ]
Ladisch, Michael R. [1 ,2 ,3 ]
机构
[1] Purdue Univ, Renewable Resources Engn Lab, 500 Cent Dr, W Lafayette, IN 47907 USA
[2] Purdue Univ, Dept Agr & Biol Engn, W Lafayette, IN 47907 USA
[3] Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
[4] Purdue Univ, Dept Hort & Landscape Architecture, W Lafayette, IN 47907 USA
[5] Purdue Univ, Dept Food Sci, Smith Hall, W Lafayette, IN 47907 USA
[6] Middle Tennessee State Univ, Fermentat Sci Program, Sch Agr, Coll Basic & Appl Sci, 1301 East Main St, Murfreesboro, TN 37132 USA
[7] Indiana Dept Environm Management, 100 North Senate Ave, Indianapolis, IN 46204 USA
关键词
detection; microbial enrichment; multiplexed microfiltration; Salmonella; spinach; REAL-TIME PCR; BORDETELLA-PERTUSSIS; BACTERIAL ADHESION; BIOFILM FORMATION; PATHOGENS; TYPHIMURIUM; MEMBRANE; ULTRAFILTRATION; BEHAVIOR; LIPOPOLYSACCHARIDE;
D O I
10.1002/btpr.2874
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To attain Salmonella detection thresholds in spinach suspensions using enrichment media requires at least 24 hr. Separation and concentration of selected microorganisms via microfiltration and microfugation reduce time for sample preparation, especially when working with large volumes of vegetable suspensions. This facilitates accelerated detection of Salmonella in spinach suspensions, and may contribute to effectively monitoring this pathogen before it reaches the consumer. We report a microfiltration-based protocol for accelerated sample preparation to concentrate and recover =1 colony forming unit (CFU) Salmonella/g pathogen-free spinach. Storebought samples of spinach and a spinach plant subjected to two environmental conditions (temperature and light exposure) during its production were tested. The overall procedure involves extraction with buffer, a short enrichment step, prefiltration using a nylon filter, crossflow hollow fiber microfiltration, and retentate centrifugation to bring microbial cells to detection levels. Based on 1 CFU Salmonella/g frozen spinach, and a Poisson distribution statistical analyses with 99% probability, we calculated that 3 hr of incubation, when followed by microfiltration, is sufficient to reach the 2 log concentration required for Salmonella detection within 7 hr. Longer enrichment times (5 hr or more) is needed for concentrations lower than 1 CFU Salmonella/g of ready to eat spinach. The recovered microbial cells were identified and confirmed as Salmonella using both polymerase chain reaction (PCR) and plating methods. Different environmental conditions tested during production did not affect Salmonella viability; this demonstrated the broad adaptability of Salmonella and emphasized the need for methods that enable efficient monitoring of production for the presence of this pathogen.
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页数:10
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