Identification of a Novel Aminopeptidase P-Like Gene (OnAPP) Possibly Involved in Bt Toxicity and Resistance in a Major Corn Pest (Ostrinia nubilalis)

被引:26
作者
Khajuria, Chitvan [1 ]
Buschman, Lawrent L. [1 ]
Chen, Ming-Shun [1 ,2 ]
Siegfried, Blair D. [3 ]
Zhu, Kun Yan [1 ]
机构
[1] Kansas State Univ, Dept Entomol, Manhattan, KS 66506 USA
[2] Kansas State Univ, USDA ARS, Hard Winter Wheat Genet Res Unit, Manhattan, KS 66506 USA
[3] Univ Nebraska, Dept Entomol, Lincoln, NE 68583 USA
来源
PLOS ONE | 2011年 / 6卷 / 08期
关键词
BACILLUS-THURINGIENSIS TOXIN; BORER LEPIDOPTERA; DELTA-ENDOTOXIN; HELICOVERPA-ARMIGERA; INSECT RESISTANCE; MOLECULAR-CLONING; CANDIDATE GENES; FAT-BODY; MIDGUT; BINDING;
D O I
10.1371/journal.pone.0023983
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Studies to understand the Bacillus thuringiensis (Bt) resistance mechanism in European corn borer (ECB, Ostrinia nubilalis) suggest that resistance may be due to changes in the midgut-specific Bt toxin receptor. In this study, we identified 10 aminopeptidase-like genes, which have previously been identified as putative Bt toxin receptors in other insects and examined their expression in relation to Cry1Ab toxicity and resistance. Expression analysis for the 10 aminopeptidase-like genes revealed that most of these genes were expressed predominantly in the larval midgut, but there was no difference in the expression of these genes in Cry1Ab resistant and susceptible strains. This suggested that altered expression of these genes was unlikely to be responsible for resistance in these ECB strains. However, we found that there were changes in two amino acid residues of the aminopeptidase-P like gene (OnAPP) involving Glu(305) to Lys(305) and Arg(307) to Leu(307) in the two Cry1Ab-resistant strains as compared with three Cry1Ab-susceptible strains. The mature OnAPP contains 682 amino acid residues and has a putative signal peptide at the N-terminus, a predicted glycosylphosphatidyl-inositol (GPI)-anchor signal at the C-terminal, three predicted N-glycosylation sites at residues N178, N278 and N417, and an O-glycosylation site at residue T653. We used a feeding based-RNA interference assay to examine the role of the OnAPP gene in Cry1Ab toxicity and resistance. Bioassays of Cry1Ab in larvae fed diet containing OnAPP dsRNA resulted in a 38% reduction in the transcript level of OnAPP and a 25% reduction in the susceptibility to Cry1Ab as compared with larvae fed GFP dsRNA or water. These results strongly suggest that the OnAPP gene could be involved in binding the Cry1Ab toxin in the ECB larval midgut and that mutations in this gene may be associated with Bt resistance in these two ECB strains.
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页数:10
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共 60 条
[1]   Inheritance of resistance to the Cry1Ab Bacillus thuringiensis toxin in Ostrinia nubilalis (Lepidoptera: crambidae) [J].
Alves, AP ;
Spencer, TA ;
Tabashnik, BE ;
Siegfried, BD .
JOURNAL OF ECONOMIC ENTOMOLOGY, 2006, 99 (02) :494-501
[2]   Diversity of aminopeptidases, derived from four lepidopteran gene duplications, and polycalins expressed in the midgut of Helicoverpa armigera:: Identification of proteins binding the δ-endotoxin, Cry1Ac of Bacillus thuringiensis [J].
Angelucci, Constanza ;
Barrett-Wilt, Gregory A. ;
Hunt, Donald F. ;
Akhurst, Raymond J. ;
East, Peter D. ;
Gordon, Karl H. J. ;
Campbell, Peter M. .
INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2008, 38 (07) :685-696
[3]   Improved prediction of signal peptides: SignalP 3.0 [J].
Bendtsen, JD ;
Nielsen, H ;
von Heijne, G ;
Brunak, S .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 340 (04) :783-795
[4]   Long-term selection for resistance to bacillus thuringiensis Cry1Ac endotoxin in a Minnesota population of European corn borer (Lepidoptera: Crambidae) [J].
Bolin, PC ;
Hutchison, WD ;
Andow, DA .
JOURNAL OF ECONOMIC ENTOMOLOGY, 1999, 92 (05) :1021-1030
[5]   Partial purification and characterization of midgut leucyl aminopeptidase of Morimus funereus (Coleoptera: Cerambycidae) larvae [J].
Bozic, N ;
Vujcic, Z ;
Nenadovic, V ;
Ivanovic, J .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 2003, 134 (02) :231-241
[6]   Oligomerization triggers binding of a Bacillus thuringiensis Cry1Ab pore-forming toxin to aminopeptidase N receptor leading to insertion into membrane microdomains [J].
Bravo, A ;
Gómez, I ;
Conde, J ;
Muñoz-Garay, C ;
Sánchez, J ;
Miranda, R ;
Zhuang, M ;
Gill, SS ;
Soberón, M .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2004, 1667 (01) :38-46
[7]   Characterization of Bacillus thuringiensis Cry toxin binding novel GPI anchored aminopeptidase from fat body of the moth Spodoptera litura [J].
Budatha, Madhusudhan ;
Meur, Gargi ;
Kirti, P. B. ;
Gupta, Aparna Dutta .
BIOTECHNOLOGY LETTERS, 2007, 29 (11) :1651-1657
[8]   A novel aminopeptidase in the fat body of the moth Achaea janata as a receptor for Bacillus thuringiensis Cry toxins and its comparison with midgut aminopeptidase [J].
Budatha, Madhusudhan ;
Meur, Gargi ;
Dutta-Gupta, Aparna .
BIOCHEMICAL JOURNAL, 2007, 405 (287-297) :287-297
[9]   Chronic exposure of the European corn borer (Lepidoptera: Crambidae) to CrylAb Bacillus thuringiensis toxin [J].
Chaufaux, J ;
Seguin, M ;
Swanson, JJ ;
Bourguet, D ;
Siegfried, BD .
JOURNAL OF ECONOMIC ENTOMOLOGY, 2001, 94 (06) :1564-1570
[10]   Mining an Ostrinia nubilalis midgut expressed sequence tag (EST) library for candidate genes and single nucleotide polymorphisms (SNPs) [J].
Coates, B. S. ;
Sumerford, D. V. ;
Hellmich, R. L. ;
Lewis, L. C. .
INSECT MOLECULAR BIOLOGY, 2008, 17 (06) :607-620