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Method Article

Detecting Virus and Salivary Proteins of a Leafhopper Vector in the Plant Host

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DOI:

10.3791/63020

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September 14th, 2021

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In This Article

Summary

This protocol demonstrates how to use the plant host to detect salivary proteins of leafhopper and plant viral proteins released by leafhopper vectors.

Abstract

Insect vectors horizontally transmit many plant viruses of agricultural importance. More than one-half of plant viruses are transmitted by hemipteran insects that have piercing-sucking mouthparts. During viral transmission, the insect saliva bridges the virus-vector-host because the saliva vectors viruses, and the insect proteins, trigger or suppress the immune response of plants from insects into plant hosts. The identification and functional analyses of salivary proteins are becoming a new area of focus in the research field of arbovirus-host interactions. This protocol provides a system to detect proteins in the saliva of leafhoppers using the plant host. The leafhopper vector Nephotettix cincticeps infected with rice dwarf virus (RDV) serves as an example. The vitellogenin and major outer capsid protein P8 of RDV vectored by the saliva of N. cincticeps can be detected simultaneously in the rice plant that N. cincticeps feeds on. This method is applicable for testing the salivary proteins that are transiently retained in the plant host after insect feeding. It is believed that this system of detection will benefit the study of hemipteran-virus-plant or hemipteran-plant interactions.

Introduction

The vector-host transmission mode of arboviruses, a fundamental problem, is at the frontier of biological science. Many plant viruses of agricultural importance are horizontally transmitted by insect vectors1. More than one-half of plant viruses are vectored by hemipteran insects, including aphids, whiteflies, leafhoppers, planthoppers, and thrips. These insects have distinct features that enable them to efficiently transmit plant viruses1. They possess piercing-sucking mouthparts and feed on the sap from phloem and xylem, and secrete their saliva1,2,<....

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Protocol

The non-viruliferous adult leafhoppers were propagated in the Vector-borne Virus Research Center in Fujian Agriculture and Forestry University, China.

1. Nonviruliferous insect rearing

  1. Rear the adults on rice seedlings in a cube cage that is 40 cm x 35 cm x 20 cm (length x width x height). Keep one side of the cage covered with an insect-proof net for ventilation.
    1. Keep the cages with leafhoppers in an incubator that contains an in-built humidity controller at 26 °C with a relative humidity of 60-75% under a photoperiod of 16 h light and 8 h dark.
  2. Use an aspirator to gently transfer all th....

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Results

Figure 1 illustrates all of the steps in this protocol: insect rearing, virus acquisition, the collection of salivary proteins via rice feeding, and the western blot. The western blots results showed that specific and expected bands of approximately 220 kDa were observed in the samples of feeding rice and salivary glands of insects on the membrane incubated with antibodies against Vg. In contrast, no band was observed in the non-feeding rice sample. The result in

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Discussion

The saliva directly secreted by the salivary glands of the piercing-sucking insects plays a pivotal role because it predigests and detoxifies the host tissues and vectors' cross-kingdom biological factors into the hosts1,3,4. The cross-kingdom biological factors, including elicitors, effectors, and small RNA, are critical for insect-host communication14,15,

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Disclosures

The authors have nothing to disclose.

Acknowledgements

This work was supported by grants from the National Natural Science Foundation of China (31772124 and 31972239) and Fujian Agriculture and Forestry University (Grant KSYLX014).

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Reagents
Tris baseRocheD609K69032For 5×Tris-glycine buffer and 10×TBS buffer preparation
glycineSigma-AldrichWXBD0677VFor 5×Tris-glycine buffer preparation
SDSSigma-AldrichSLCB4394For 5×Tris-glycine buffer preparation
NaClSinopharm Chemical Reagent Co., Ltd10019318For 10×TBS buffer preparation
KClSinopharm Chemical Reagent Co., Ltd10016318For 10×TBS buffer preparation
ß-mercaptoethanolXiya ReagentB14492For 4× protein sample buffer preparation
bromophenol blueSigma-AldrichSHBL3668For 4× protein sample buffer preparation
glycerolSinopharm Chemical Reagent Co., Ltd10010618For 4× protein sample buffer preparation
methanolSinopharm Chemical Reagent Co., Ltd10014118For transfer buffer preparation
Tween 20Coolaber SCIENCE&TeCHNoLoGYCT30111220For TBST preparation
non-fat dry milkBecton.Dickinso and company252038For membrane blocking, antibodies dilution
goat anti-rabbit IgGSangon BiotechD110058-0001Recognization of the primary andtibody
ECL Western kitThermoFisher Scientific32209Chemiluminescent substrate
nitrocellulose membranePall Corporation25312915For proteins transfer
Buffers and Solutions
BufferCompositionComments/Description
 5×Tris-glycine buffer15.1 g Tris base
94 g glycine
 5 g SDS in 1 L sterile water
 Stock solution
1×Tris-glycine buffer200 mL of 5×Tris-glycine buffer
800 mL sterile water
Work solution, for SDS-PAGE
10×Tris-buffered saline (TBS) buffer80 g NaCl
30 g Tris base
2 g KCl
in 1 L sterile water
Stock solution
TBS with Tween 20 (TBST) solution100 mL 10×TBS solution
3 mL Tween 20
900 mL sterile water
Work solution
4× protein sample buffer8 g SDS
4 mL ß-mercaptoethanol
0.02 g bromophenol blue
40 mL glycerol
in 40 mL 0.1 M Tris-HCl (pH 6.8)
For protein extraction
Transfer buffer800 mL Tris-glycine buffer
200 mL methanol
For protein transfer
Instruments
Bromophenol blueSigma-AldrichSHBL3668For 4x protein sample buffer preparation
Constant temperature incubatorNingbo Saifu Experimental Instrument Co., Ltd.PRX-1200BFor rearing leafhoppers
ElectrophoresisTanon Science & Technology Co.,Ltd.Tanon EP300For SDS-PAGE
Electrophoretic transfer core moduleBIO-RAD1703935For SDS-PAGE
glycerolSinopharm Chemical Reagent Co., Ltd10010618For 4x protein sample buffer preparation
glycineSigma-AldrichWXBD0677VFor 5x Tris-glycine buffer preparation
goat anti-rabbit IgGSangon BiotechD110058-0001Recognization of the primary andtibody
High-pass tissue grinding instrumentShanghai Jingxin Industrial Development Co., Ltd.JXFSIPRP-24For grinding plant tissues
KClSinopharm Chemical Reagent Co., Ltd10016318For 10x TBS buffer preparation
methanolSinopharm Chemical Reagent Co., Ltd10014118For transfer buffer preparation
Mini wet heat transfer troughBIO-RAD1703930For SDS-PAGE
NaClSinopharm Chemical Reagent Co., Ltd10019318For 10x TBS buffer preparation
nitrocellulose membranePall Corporation25312915For proteins transfer
non-fat dry milkBecton.Dickinso and company252038For membrane blocking, antibodies dilution
Pierce ECL Western kitThermoFisher Scientific32209Chemiluminescent substrate
Protein color instrumentGE Healthcare bio-sciences ABAmersham lmager 600For detecting proteins
SDSSigma-AldrichSLCB4394For 5x Tris-glycine buffer preparation
Tris baseRocheD609K69032For 5x Tris-glycine buffer and 10×TBS buffer preparation
Tween 20Coolaber SCIENCE&TeCHNoLoGYCT30111220For TBST preparation
Vertical plate electrophoresis tankBIO-RAD1658001For SDS-PAGE
Water bathShanghai Jinghong Experimental equipment Co., Ltd.XMTD-8222For boil the protein samples
β-mercaptoethanolXiya ReagentB14492For 4x protein sample buffer preparation

References

  1. Hogenhout, S. A., Ammar el, D., Whitfield, A. E., Redinbaugh, M. G. Insect vector interactions with persistently transmitted viruses. Annual Review of Phytopathology. 46, 327-359 (2008).
  2. Cranston, P. S., Gullan, P. J. Phylogeny of insects. Encyclopedia of Insects. Resh, V. H., Carde, R. T. , Academic. Amste....

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