A rapid method for detecting prfA and hly toxin genes of Listeria monocytogenes using double nucleic acid colloidal gold strips.
10.12122/j.issn.1673-4254.2025.02.20
- Author:
Yan LIU
1
;
Jianyu YANG
1
;
Yujiao ZHOU
1
;
Wenbo DING
1
;
Xianyu ZHANG
1
;
Linran GAO
1
;
Beizhen PAN
1
;
Jifei YANG
1
;
Yundong ZHAO
1
Author Information
1. Department of Clinical Biochemistry and Molecular Biology, School of Medical Technology, Beihua University, Jilin 132013, China.
- Publication Type:Journal Article
- Keywords:
Listeria monocytogenes;
double nucleic acid test strip;
hly;
prfA
- MeSH:
Listeria monocytogenes/isolation & purification*;
Gold Colloid;
Bacterial Toxins/genetics*;
Polymerase Chain Reaction/methods*;
Hemolysin Proteins/genetics*;
Bacterial Proteins/genetics*;
DNA, Bacterial/genetics*;
Food Microbiology;
Heat-Shock Proteins
- From:
Journal of Southern Medical University
2025;45(2):387-394
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVES:To detect prfA and hly toxin genes of Listeria monocytogenes using polymerase chain reaction (PCR) and colloidal gold technology.
METHODS:L. monocytogenes DNA was extracted by boiling method. With prfA and hly of L. monocytogenes as the target genes, the 5' ends of upstream and downstream primers of prfA gene were labeled with 6-FAM and biotin, and the 5' ends of upstream and downstream primers of hly gene were labeled with digoxin and biotin, respectively, to establish the toxin gene detection method. Using cloning transformation, sequencing analysis, cloning of positive control products, the detection kid was developed and its specificity, sensitivity, reproducibility and stability were tested, followed by verification with sample testing.
RESULTS:The concentration of L. monocytogenes DNA extracted by boiling method was 148.81±0.97 ng/μL, and the A260/A280 ratio ranged from 1.8 to 2.0. The PCR products showed a 100% homology with the gene sequences in GenBank database after cloning, transformation and sequencing. The colloidal gold strip yielded positive results only for L. monocytogenes samples without cross-reactions with Staphylococcus aureus, Escherichia coli or Bacillus cereus, and its minimum detection limit was 10-2 ng/μL, demonstrating a 10-fold greater sensitivity of the test than agarose gel electrophoresis. The test also showed good reproducibility of the results when performed by different operators with good stability of the test strips after storage for 6 to 12 months. The test results showed that this kit could accurately and quickly detect L.monocytogenes in the test samples.
CONCLUSIONS:The detection kit developed in this study can simultaneously detect prfA and hly toxin genes of L. monocytogenes with good specificity, sensitivity, reproducibility and stability for use in food safety inspection.
