Next Article in Journal
Mass Spectrometric Detection of Bacterial Protein Toxins and Their Enzymatic Activity
Next Article in Special Issue
Aflatoxin B1 Detection Using a Highly-Sensitive Molecularly-Imprinted Electrochemical Sensor Based on an Electropolymerized Metal Organic Framework
Previous Article in Journal
Effects of Dietary Exposure to Zearalenone (ZEN) on Carp (Cyprinus carpio L.)
Open AccessArticle

Development of a Monoclonal Antibody-Based icELISA for the Detection of Ustiloxin B in Rice False Smut Balls and Rice Grains

1
College of Agronomy and Biotechnology, China Agricultural University, Beijing 100193, China
2
Institute of Agro-Products Processing Science and Technology, Chinese Academy of Agricultural Sciences, Beijing 100193, China
3
Department of Molecular Biosciences and Bioengineering, University of Hawaii at Manoa, Honolulu, HI 96822, USA
*
Authors to whom correspondence should be addressed.
Academic Editor: Maria C. DeRosa
Toxins 2015, 7(9), 3481-3496; https://doi.org/10.3390/toxins7093481
Received: 4 July 2015 / Revised: 14 August 2015 / Accepted: 18 August 2015 / Published: 28 August 2015
(This article belongs to the Collection Biorecognition Assays for Mycotoxins)
Rice false smut is an emerging and economically-important rice disease caused by infection by the fungal pathogen Villosiclava virens. Ustiloxin B is an antimitotic cyclopeptide mycotoxin isolated from the rice false smut balls that formed in the pathogen-infected rice spikelets. A monoclonal antibody (mAb) designated as mAb 1B5A10 was generated with ustiloxin B—ovalbumin conjugate. A highly-sensitive and specific indirect competitive enzyme-linked immunosorbent assay (icELISA) was then developed. The median inhibitory concentration (IC50) of the icELISA was 18.0 ng/mL for the detection of ustiloxin B; the limit of detection was 0.6 ng/mL, and the calibration range was from 2.5 to 107.4 ng/mL. The LOD/LOQ values of the developed ELISA used for the determination of ustiloxin B in rice false smut balls and rice grains were 12/50 μg/g and 30/125 ng/g, respectively. The mAb 1B5A10 cross-reacted with ustiloxin A at 13.9% relative to ustiloxin B. Average recoveries of ustiloxin B ranged from 91.3% to 105.1% for rice false smut balls at spiking levels of 0.2 to 3.2 mg/g and from 92.6% to 103.5% for rice grains at spiking levels of 100 to 5000 ng/g. Comparison of ustiloxin B content in rice false smut balls and rice grains detected by both icELISA and high performance liquid chromatography (HPLC) demonstrated that the developed icELISA can be employed as an effective and accurate method for the detection of ustiloxin B in rice false smut balls, as well as rice food and feed samples. View Full-Text
Keywords: ustiloxin B; ELISA; mycotoxin; phytotoxin; rice false smut; Villosiclava virens ustiloxin B; ELISA; mycotoxin; phytotoxin; rice false smut; Villosiclava virens
Show Figures

Graphical abstract

MDPI and ACS Style

Fu, X.; Wang, A.; Wang, X.; Lin, F.; He, L.; Lai, D.; Liu, Y.; Li, Q.X.; Zhou, L.; Wang, B. Development of a Monoclonal Antibody-Based icELISA for the Detection of Ustiloxin B in Rice False Smut Balls and Rice Grains. Toxins 2015, 7, 3481-3496. https://doi.org/10.3390/toxins7093481

AMA Style

Fu X, Wang A, Wang X, Lin F, He L, Lai D, Liu Y, Li QX, Zhou L, Wang B. Development of a Monoclonal Antibody-Based icELISA for the Detection of Ustiloxin B in Rice False Smut Balls and Rice Grains. Toxins. 2015; 7(9):3481-3496. https://doi.org/10.3390/toxins7093481

Chicago/Turabian Style

Fu, Xiaoxiang; Wang, Ali; Wang, Xiaohan; Lin, Fengke; He, Lishan; Lai, Daowan; Liu, Yang; Li, Qing X.; Zhou, Ligang; Wang, Baoming. 2015. "Development of a Monoclonal Antibody-Based icELISA for the Detection of Ustiloxin B in Rice False Smut Balls and Rice Grains" Toxins 7, no. 9: 3481-3496. https://doi.org/10.3390/toxins7093481

Find Other Styles

Article Access Map by Country/Region

1
Only visits after 24 November 2015 are recorded.
Search more from Scilit
 
Search
Back to TopTop