Development of a rapid detection method for real-time fluorescent quantitative PCR of Salmonella spp. and Salmonella Enteritidis in ready-to-eat fruits and vegetables

LWT ◽  
2021 ◽  
pp. 111837
Author(s):  
Jiajia Wan ◽  
Liping Zheng ◽  
Liangyu Kong ◽  
Zhaoxin Lu ◽  
Yang Tao ◽  
...  
2021 ◽  
Vol 251 ◽  
pp. 02027
Author(s):  
Lina Sui ◽  
Jishun Li ◽  
Jindong Hu ◽  
Yan Wang

We have established a real-time fluorescent quantitative PCR system that can detect wheat crown rot rapidly and accurately quantify fungi, Fusarium species and Fusarium pseudograminearum in the rhizosphere soil of infected wheat through the standard curve produced, with a view to the early stage of wheat Provide help in predicting the occurrence of wheat crown rot.


The Analyst ◽  
2013 ◽  
Vol 138 (19) ◽  
pp. 5745 ◽  
Author(s):  
Yu Qing Du ◽  
Peng Fei Gao ◽  
Wei Wang ◽  
Ting Ting Wang ◽  
Yong Chang ◽  
...  

PLoS ONE ◽  
2018 ◽  
Vol 13 (10) ◽  
pp. e0206316 ◽  
Author(s):  
Raymond Heymans ◽  
Amir Vila ◽  
Caroliene A. M. van Heerwaarden ◽  
Claudia C. C. Jansen ◽  
Greetje A. A. Castelijn ◽  
...  

2006 ◽  
Vol 69 (3) ◽  
pp. 639-643 ◽  
Author(s):  
K. H. SEO ◽  
I. E. VALENTIN-BON ◽  
R. E. BRACKETT

Salmonellosis caused by Salmonella Enteritidis (SE) is a significant cause of foodborne illnesses in the United States. Consumption of undercooked eggs and egg-containing products has been the primary risk factor for the disease. The importance of the bacterial enumeration technique has been enormously stressed because of the quantitative risk analysis of SE in shell eggs. Traditional enumeration methods mainly depend on slow and tedious most-probable-number (MPN) methods. Therefore, specific, sensitive, and rapid methods for SE quantitation are needed to collect sufficient data for risk assessment and food safety policy development. We previously developed a real-time quantitative PCR assay for the direct detection and enumeration of SE and, in this study, applied it to naturally contaminated ice cream samples with and without enrichment. The detection limit of the real-time PCR assay was determined with artificially inoculated ice cream. When applied to the direct detection and quantification of SE in ice cream, the real-time PCR assay was as sensitive as the conventional plate count method in frequency of detection. However, populations of SE derived from real-time quantitative PCR were approximately 1 log higher than provided by MPN and CFU values obtained by conventional culture methods. The detection and enumeration of SE in naturally contaminated ice cream can be completed in 3 h by this real-time PCR method, whereas the cultural enrichment method requires 5 to 7 days. A commercial immunoassay for the specific detection of SE was also included in the study. The real-time PCR assay proved to be a valuable tool that may be useful to the food industry in monitoring its processes to improve product quality and safety.


2016 ◽  
Vol 31 (2) ◽  
pp. 121
Author(s):  
Sang-Hyun Min ◽  
Jee-Hee Wang ◽  
Su-Jin Lim ◽  
Chil-Woo Lee ◽  
Byoung-Su Yoon

2018 ◽  
Vol 33 (1) ◽  
pp. 50-57
Author(s):  
Seok Hwan Kim ◽  
Yu-Si Lee ◽  
In-Sun Joo ◽  
Hyo Sun Kwak ◽  
Gyung Tae Chung ◽  
...  

2014 ◽  
Vol 184 ◽  
pp. 113-120 ◽  
Author(s):  
David Rodriguez-Lazaro ◽  
Patricia Gonzalez-García ◽  
Elisabetta Delibato ◽  
Dario De Medici ◽  
Rosa Maria García-Gimeno ◽  
...  

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