Donggen Zhou
Research Subjects
Donggen Zhou has a total of 13 co-authors. Here are the top co-authors by number of shared publications:
- Hengyi Xu
State Key Laboratory of Food Science and Resources, Nanchang University, Nanchang 330047, China
2 shared publications - Bei Gan
Institute for Testing of Industrial Products of Jiangxi General Institute of Testing and Certification, Nanchang 330047, China
1 shared publication Dan Mu
State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang, 330047, PR China
1 shared publicationGuoyang Xie
State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang, 330047, PR China
1 shared publication- Guoyang Xie
State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang 330047, China
1 shared publication Hengyi Xu
State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang, People's Republic of China
1 shared publication
Latest Publications
- Open Access
A Combination of Novel Nucleic Acid Cross-Linking Dye and Recombinase-Aided Amplification for the Rapid Detection of Viable Salmonella in Milk
Salmonella, as an important foodborne pathogen, can cause various diseases, such as severe enteritis. In recent years, various types of nucleicacid-intercalating dyes have been utilized to detect viable Salmonella. However, in principle, the performance of existing nucleic acid dyes is limited because they depend on the integrity of cell membrane. Herein, based on the metabolic activity of bacteria, a novel DNA dye called thiazole orange monoazide (TOMA) was introduced to block the DNA from dead bacteria. Recombinase-aided amplification (RAA) was then performed to detect viable Salmonella in samples. In this study, the permeability of TOMA to the cell membrane of Salmonella was evaluated via confocal laser scanning microscopy and fluorescence emission spectrometry. The limit of detection (LOD) of the TOMA–RAA method was 2.0 × 104 CFU/mL in pure culture. The feasibility of the TOMA–RAA method in detecting Salmonella was assessed in spiked milk. The LOD for Salmonella was 3.5 × 102 CFU/mL after 3 h of enrichment and 3.5 × 100 CFU/mL after 5 h of enrichment. The proposed TOMA–RAA assay has great potential to be applied to accurately detect and monitor foodborne pathogens in milk and its byproducts.
Open AccessA Combination of Novel Nucleic Acid Cross-Linking Dye and Recombinase-Aided Amplification for the Rapid Detection of Viable Salmonella in Milk
Salmonella, as an important foodborne pathogen, can cause various diseases, such as severe enteritis. In recent years, various types of nucleicacid-intercalating dyes have been utilized to detect viable Salmonella. However, in principle, the performance of existing nucleic acid dyes is limited because they depend on the integrity of cell membrane. Herein, based on the metabolic activity of bacteria, a novel DNA dye called thiazole orange monoazide (TOMA) was introduced to block the DNA from dead bacteria. Recombinase-aided amplification (RAA) was then performed to detect viable Salmonella in samples. In this study, the permeability of TOMA to the cell membrane of Salmonella was evaluated via confocal laser scanning microscopy and fluorescence emission spectrometry. The limit of detection (LOD) of the TOMA–RAA method was 2.0 × 104 CFU/mL in pure culture. The feasibility of the TOMA–RAA method in detecting Salmonella was assessed in spiked milk. The LOD for Salmonella was 3.5 × 102 CFU/mL after 3 h of enrichment and 3.5 × 100 CFU/mL after 5 h of enrichment. The proposed TOMA–RAA assay has great potential to be applied to accurately detect and monitor foodborne pathogens in milk and its byproducts.
- 1 December 2021
- Published by Elsevier in Molecular and Cellular Probes
- Vol. 60, 101777
The fluorescent probe-based recombinase-aided amplification for rapid detection of Escherichia coli O157:H7
- 1 December 2021
- Published by Elsevier in Molecular and Cellular Probes
- Vol. 60, 101777
The fluorescent probe-based recombinase-aided amplification for rapid detection of Escherichia coli O157:H7
- Open Access
- 1 February 2021
- Published by Elsevier in International Journal of Infectious Diseases
- Vol. 103, 517-524
Simultaneous detection and differentiation of SARS-CoV-2, influenza A virus and influenza B virus by one-step quadruplex real-time RT-PCR in patients with clinical manifestations
- 1 February 2021
- Published by Elsevier in International Journal of Infectious Diseases
- Vol. 103, 517-524
Open AccessSimultaneous detection and differentiation of SARS-CoV-2, influenza A virus and influenza B virus by one-step quadruplex real-time RT-PCR in patients with clinical manifestations