Variation in the salivary proteomes of differentially virulent greenbug (Schizaphis graminum Rondani) biotypes

被引:51
作者
Nicholson, Scott J. [1 ]
Puterka, Gary J. [1 ]
机构
[1] USDA ARS, PSRL, Stillwater, OK 74074 USA
关键词
Greenbug; Phytotoxicity; Saliva; Proteome; Virulence; Plant-insect interactions; GENE-EXPRESSION; RUSSIAN WHEAT; STATISTICAL-MODEL; RESISTANCE GENES; PLANT DEFENSE; GENTISIC ACID; WINTER-WHEAT; PROTEINS; APHID; HOMOPTERA;
D O I
10.1016/j.jprot.2013.12.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Greenbug (Schizaphis graminum Rondani) biotypes are classified by their differential virulence to wheat, barley, and sorghum varieties possessing greenbug resistance genes. Virulent greenbug biotypes exert phytotoxic effects upon their hosts during feeding, directly inducing physiological and metabolic alterations and accompanying foliar damage. Comparative analyses of the salivary proteomes of four differentially virulent greenbug biotypes C, E, G, and H showed significant proteomic divergence between biotypes. Thirty-two proteins were identified by LC-MS/MS; the most prevalent of which were three glucose dehydrogenase paralogs (GDH), lipophorin, complementary sex determiner, three proteins of unknown function, carbonic anhydrase, fibroblast growth factor receptor, and abnormal oocyte (ABO). Seven nucleotide-binding proteins were identified, including ABO which is involved in mRNA splicing. Quantitative variation among greenbug biotypes was detected in six proteins; two GDH paralogs, carbonic anhydrase, ABO, and two proteins of unknown function. Our findings reveal that the greenbug salivary proteome differs according to biotype and diverges substantially from those reported for other aphids. The proteomic profiles of greenbug biotypes suggest that interactions between aphid salivary proteins and the plant host result in suppression of plant defenses and cellular transport, and may manipulate transcriptional regulation in the plant host, ultimately allowing the aphid to maintain phloem ingestion. Biological significance Greenbug (Schizaphis graminum Rondani, GB) is a major phytotoxic aphid pest of wheat, sorghum, and barley. Unlike non-phytotoxic aphids, GB directly damages its host, causing uniformly characteristic symptoms leading to host death. As saliva is the primary interface between the aphid and its plant host, saliva is also the primary aphid biotypic determinant, and differences in biotypic virulence are the result of biotypic variations in salivary content. This study analyzed the exuded saliva of four distinct Greenbug biotypes with a range of virulence to crop lines containing greenbug resistance traits in order to identify differences between salivary proteins of the examined biotypes. Our analyses confirmed that the salivary proteomes of the examined greenbug biotypes differ widely, identified 32 proteins of the greenbug salivary proteome, and found significant proteomic variation between six identified salivary proteins. The proteomic variation identified herein is likely the basis of biotypic virulence, and the proteins identified can serve as the basis for functional studies into both greenbug-induced phytotoxic damage and into the molecular basis of virulence in specific GB biotypes. This article is part of a Special Issue entitled: Si: Proteomics of non-model organisms. Published by Elsevier B.V.
引用
收藏
页码:186 / 203
页数:18
相关论文
共 84 条
[1]   Mixed lineage leukemia: roles in gene expression, hormone signaling and mRNA processing [J].
Ansari, Khairul I. ;
Mandal, Subhrangsu S. .
FEBS JOURNAL, 2010, 277 (08) :1790-1804
[2]   Caterpillar herbivory and salivary enzymes decrease transcript levels of Medicago truncatula genes encoding early enzymes in terpenoid biosynthesis [J].
Bede, JC ;
Musser, RO ;
Felton, GW ;
Korth, KL .
PLANT MOLECULAR BIOLOGY, 2006, 60 (04) :519-531
[3]   Accumulation of gentisic acid as associated with systemic infections but not with the hypersensitive response in plant-pathogen interactions [J].
Bellés, JM ;
Garro, R ;
Pallás, V ;
Fayos, J ;
Rodrigo, I ;
Conejero, V .
PLANTA, 2006, 223 (03) :500-511
[4]   The maternal effect gene, abnormal oocyte (abo), of Drosophila melanogaster encodes a specific negative regulator of histones [J].
Berloco, M ;
Fanti, L ;
Breiling, A ;
Orlando, V ;
Pimpinelli, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (21) :12126-12131
[5]   The gene csd is the primary signal for sexual development in the honeybee and encodes an SR-type protein [J].
Beye, M ;
Hasselmann, M ;
Fondrk, MK ;
Page, RE ;
Omholt, SW .
CELL, 2003, 114 (04) :419-429
[6]   Transcriptome analysis of trichothecene-induced gene expression in barley [J].
Boddu, Jayanand ;
Cho, Seungho ;
Muehlbauer, Gary J. .
MOLECULAR PLANT-MICROBE INTERACTIONS, 2007, 20 (11) :1364-1375
[7]  
Boyko EV, 2006, J ECON ENTOMOL, V99, P1430, DOI 10.1603/0022-0493-99.4.1430
[8]   Posterior migration of the salivary gland requires an intact visceral mesoderm and integrin function [J].
Bradley, PL ;
Myat, MM ;
Comeaux, CA ;
Andrew, DJ .
DEVELOPMENTAL BIOLOGY, 2003, 257 (02) :249-262
[9]   Biotypic diversity in Greenbug (Hemiptera: Aphididae):: Characterizing new virulence and host associations [J].
Burd, JD ;
Porter, DR .
JOURNAL OF ECONOMIC ENTOMOLOGY, 2006, 99 (03) :959-965
[10]   Physiological modification of the host feeding site by cereal aphids (Homoptera:Aphididae) [J].
Burd, JD .
JOURNAL OF ECONOMIC ENTOMOLOGY, 2002, 95 (02) :463-468