Detecting Tomato Leaf Curl New Delhi Virus Causing Ridge Gourd Yellow Mosaic Disease, and Other Begomoviruses by Antibody-Based Methods

• Published in: Plants (Basel) Vol. 12; no. 3; p. 490
• Main Authors: Naganur, Priya, Shankarappa, Kodegandlu Subbanna, Mesta, Raghavendra K, Rao, Chilakalapudi Durga, Venkataravanappa, Venkataravanappa, Maruthi, Midatharahally Narasegowda, Reddy, Lakshminarayana Reddy C Narasimha
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.01.2023; MDPI
• Subjects: Analysis; Antibodies; Antigens; Assaying; Begomovirus; Cloning; Coat protein; Cucurbita; Diseases and pests; ELISA; Enzyme-linked immunosorbent assay; Epidemiology; Geminiviridae; Gene amplification; Gourds; Immunoassay; immunocapture assays; Leaf-curl; Methods; Mosaic disease; Outbreaks; Plant diseases; Plant viruses; Polyclonal antibodies; Polymerase chain reaction; Proteins; ridge gourd; Serology; Sorbents; Strategic planning (Business); Tomatoes; Viral antibodies; Viruses; Western blotting; India; ridge gourd; begomovirus; immunocapture assays; Geminiviridae; tomato leaf curl New Delhi virus (ToLCNDV); ELISA; coat protein
• ISSN: 2223-7747; 2223-7747
• DOI: 10.3390/plants12030490

The incidence and severity of begomovirus diseases have been increasing around the world recently, and the ridge gourd [ (Roxb.) L.] is the latest example of a crop that has become highly susceptible to the outbreak of the tomato leaf curl New Delhi virus (ToLCNDV, genus ) in India. Accurate diagnosis of causal agents is important in designing disease management strategies. In this study the coat protein (CP) gene from a ToLCNDV-Rg ridge gourd isolate was used to produce polyclonal antibodies (ToLCNDV-Rg-CP-PAb) in a rabbit. The antibodies successfully detected a 30.5 kDa ToLCNDV-Rg-CP in extracts of symptomatic ridge gourd leaf samples by several assays, such as Western Blotting (WB), Dot Immuno Binding Assay (DIBA), Direct Antigen Coating Enzyme Linked Immuno Sorbent Assay (DAC-ELISA), Immuno Capture Polymerase Chain Reaction (IC-PCR), and Immuno Capture Loop-Mediated Isothermal Amplification (IC-LAMP) assays. However, none of the negative samples tested positive in either of the detection methods. Among all the methods tested, the immunocapture assay, IC-LAMP, was the most sensitive in detecting ToLCNDV-Rg. Furthermore, antibodies generated in this study also detected other commonly occurring begomoviruses in South India, such as tomato leaf curl Palampur virus and squash leaf curl China virus in cucurbits. Together, ToLCNDV-Rg-CP-PAb can be used for detecting at least three species of begomoviruses infecting cucurbits. The obtained antibodies will contribute to monitoring disease outbreaks in multiple crops.