Lixian Cui
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Lixian Cui has a total of 11 co-authors. Here are the top co-authors by number of shared publications:
- Bixia Qin
Plant Protection Research Institute, Guangxi Academy of Agricultural Sciences, Nanning 530007, China
2 shared publications - Cuiping Mo
Plant Protection Research Institute, Guangxi Academy of Agricultural Sciences, Nanning 530007, China
2 shared publications - Jianhe Cai
Plant Protection Research Institute, Guangxi Academy of Agricultural Sciences, Nanning 530007, China
2 shared publications - Zhanbiao Li
Plant Protection Research Institute, Guangxi Academy of Agricultural Sciences, Nanning 530007, China
2 shared publications - Huiting Xie
State Key Laboratory for Agricultural and Forestry Biosecurity, College of Plant Protection, Fujian Agriculture and Forestry University , Fuzhou 350002
1 shared publication - Huiting Xie
Plant Protection Research Institute, Guangxi Academy of Agricultural Sciences, Nanning 530007, China
1 shared publication
Latest Publications
- Open Access
In Situ Visual Detection of TelMV, EAPV, and PaMoV in Passionfruit Using Reverse Transcription-Recombinase-Aided Amplification and CRISPR/Cas12a
As a tropical fruit of considerable economic importance, passionfruit (Passiflora edulis Sims) is extensively cultivated in the tropical and subtropical regions of China; however, the widespread incidence of viral diseases has significantly hampered the safety of its production. Rapid, sensitive, and visual detection of plant viruses is essential to effectively prevent and manage these viral diseases. In this study, we developed a visual detection system (displaying under blue light or UV) utilizing reverse transcription recombinase-aided amplification (RT-RAA) in conjunction with CRISPR/Cas12a to detect three viruses harmful to passionfruit production: telosma mosaic virus (TelMV), East Asian passiflora virus (EAPV), and passiflora mottle virus (PaMoV). Within this system, the optimal primer concentration for the RT-RAA reaction was determined to be 0.4 μM for all three viruses, with an optimal reaction temperature of 37 °C. The optimal reaction times were established as 20 min for TelMV, 15 min for EAPV, and 30 min for PaMoV. The entire detection process could be completed within 30 min without the need for sophisticated equipment or instruments. For TelMV and EAPV, the detection system demonstrated the capability to detect samples at a dilution of 106, representing an approximately 104-fold improvement over RT-PCR, while for PaMoV, it could identify samples at a dilution of 106, representing an approximately 102-fold improvement over traditional RT-PCR methods. These results confirm the successful development of the CRISPR/Cas12a-based detection systems. Subsequently, the system was applied for in situ detection of the three target viruses in field settings, yielding results that were fully consistent with laboratory-based RT-PCR assays, a consistency which underscores the system’s strong potential for field application in detecting important crop viruses.
Open AccessIn Situ Visual Detection of TelMV, EAPV, and PaMoV in Passionfruit Using Reverse Transcription-Recombinase-Aided Amplification and CRISPR/Cas12a
As a tropical fruit of considerable economic importance, passionfruit (Passiflora edulis Sims) is extensively cultivated in the tropical and subtropical regions of China; however, the widespread incidence of viral diseases has significantly hampered the safety of its production. Rapid, sensitive, and visual detection of plant viruses is essential to effectively prevent and manage these viral diseases. In this study, we developed a visual detection system (displaying under blue light or UV) utilizing reverse transcription recombinase-aided amplification (RT-RAA) in conjunction with CRISPR/Cas12a to detect three viruses harmful to passionfruit production: telosma mosaic virus (TelMV), East Asian passiflora virus (EAPV), and passiflora mottle virus (PaMoV). Within this system, the optimal primer concentration for the RT-RAA reaction was determined to be 0.4 μM for all three viruses, with an optimal reaction temperature of 37 °C. The optimal reaction times were established as 20 min for TelMV, 15 min for EAPV, and 30 min for PaMoV. The entire detection process could be completed within 30 min without the need for sophisticated equipment or instruments. For TelMV and EAPV, the detection system demonstrated the capability to detect samples at a dilution of 106, representing an approximately 104-fold improvement over RT-PCR, while for PaMoV, it could identify samples at a dilution of 106, representing an approximately 102-fold improvement over traditional RT-PCR methods. These results confirm the successful development of the CRISPR/Cas12a-based detection systems. Subsequently, the system was applied for in situ detection of the three target viruses in field settings, yielding results that were fully consistent with laboratory-based RT-PCR assays, a consistency which underscores the system’s strong potential for field application in detecting important crop viruses.
- 2 October 2023
- Published by Scientific Societies in Plant Disease
- Vol. 107 (10) , 2944-2948
Characteristics of the Complete Genome of Ageratum Yellow Vein China Virus Infecting Sonchus oleraceus
Sonchus (Sonchus oleraceus) was originated from Europe and now is cultivated worldwide. The wild resources of sonchus are very abundant, it has rich nutritional value and medicinal value. In this s...
- 2 October 2023
- Published by Scientific Societies in Plant Disease
- Vol. 107 (10) , 2944-2948
Characteristics of the Complete Genome of Ageratum Yellow Vein China Virus Infecting Sonchus oleraceus
Sonchus (Sonchus oleraceus) was originated from Europe and now is cultivated worldwide. The wild resources of sonchus are very abundant, it has rich nutritional value and medicinal value. In this s...