Highly sensitive time‐resolved fluoroimmunoassay for the quantitative onsite detection of Alternaria longipes in tobacco

Abstract

Aims: Alternaria longipes is a causal agent of brown spot of tobacco, which remains a serious threat to tobacco production. Herein, we established a detection method for A. longipes in tobacco samples based on the principle of time-resolved fluoroimmunoassay, in order to fulfil the requirement of rapid, sensitive and accurate detection in situ. Methods and Results:A monoclonal antibody against A. longipes was generated, and its purity and titration were assessed using western blot and ELISA. The size of europium (III) nanospheres was measured to confirm successful antibody conjugation. The method described here can detect A. longipes protein lysates as low as 0.78 ng ml −1 , with recovery rates ranging from 85.96% to 99.67% in spiked tobacco.The specificity was also confirmed using a panel of microorganisms. Conclusions:The fluorescent strips allow rapid and sensitive onsite detection of A.longipes in tobacco samples, with high accuracy, specificity, and repeatability.Significance and Impact of the Study: This novel detection method provides convenience of using crude samples without complex procedures, and therefore allows rapid onsite detection by end users and quick responses towards A. longipes, which is critical for disease control and elimination of phytopathogens.

Detection of trh+Vibrio parahaemolyticus in seafood by lac dye coloration‐based label‐free lateral flow immunoassay strip

“…LFIS assay specificity depends on the quality of antibodies, but determining the pairing of two antibodies can be challenging. Most studies of LFIS assays focused on developing novel antibody labelling materials, including colloidal gold (Wu et al, 2021a), quantum dots (Kim et al, 2021), colloidal carbon (Xu et al, 2019) and europium nanospheres (Ji et al, 2021). Although these newly developed materials can be used to label antibodies efficiently and yield reliable experimental results, obtaining a homogeneous preparation of labelling materials can be challenging.…”