Please wait a minute...
Journal of Integrative Agriculture  2016, Vol. 15 Issue (8): 1808-1815    DOI: 10.1016/S2095-3119(15)61301-6
Plant Protection Advanced Online Publication | Current Issue | Archive | Adv Search |
Characterization of a native whitefly vitellogenin gene cDNA and its expression pattern compared with two invasive whitefly cryptic species
GUO Jian-yang1, 2, DU Yu-ping1, WAN Fang-hao2, YE Gong-yin1
1 Key Laboratory of Agricultural Entomology, Ministry of Agriculture/Institute of Insect Sciences, Zhejiang University, Hangzhou 310058, P.R.China
2 State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, P.R.China
Download:  PDF in ScienceDirect  
Export:  BibTeX | EndNote (RIS)      
Abstract     The whitefly Bemisia tabaci is a species complex, of which two invasive species, called MEAM1 and MED whiteflies, have invaded many parts of the world in the past 30 years and replaced native whitefly populations in many regions of invasions including many areas in China. One of the possible reasons for the invasion is that MEAM1 and MED whiteflies are more fecund than the native species. However, factors that affect reproduction and the molecular mechanism of vitellogenesis among various B. tabaci cryptic species are not clearly known. In this study, cDNAs of vitellogenin (Vg) genes were sequenced from native B. tabaci Asia II 1 and invasive B. tabaci MED in China. The deduced amino acid sequences were 2 182 residues in Asia II 1 and 2 217 residues in MED. Compared to the Vg gene cDNA sequence of Asia II 1 species, the Vg gene in MED could be cleaved at least into four subunits, with deduced molecular weight of 50, 90, 150 and 190 kDa, respectively. However, only two different subunits were cleaved between residues 459 and 460 in the Asia II 1. In addition, more than two serine-rich stretches located in both the N-terminal and the C-terminal region in invasive species. More GHN domains were revealed only in the N-terminal region of B. tabaci MED. Vg gene expression pattern was characterized using quantitative real-time (qRT)-PCR to compare the dynamic of vitellogenin gene mRNA level. Vg gene transcription reached the peak level at 13 d after eclosion in B. tabaci Asia II 1, 3 d later than that in MED and another invasive species of the B. tabaci complex MEAM1. We assumed that the present difference of Vg gene expression pattern is due to the different regulation pattern of vitellogenesis among species of the B. tabaci complex. These results provide useful information to reveal the mechanisms of reproduction in whitefly species complex.
Keywords:  vitellogenin gene        Bemisia tabaci        MED        Asia II 1        MEAM1        vitellogenesis        displacement  
Received: 12 November 2015   Accepted:
Fund: 

This work was supported by grants from the National Basic Research Program of China (2014CB138404), the China National Science Fund for Innovative Research Groups of Biological Control (31321063), the National Basic Research Program of China (973 Program, 2009CB119203) and the National Natural Science Foundation for Young Scientists in China (31101674).

Corresponding Authors:  YE Gong-yin, Tel: +86-571-88982696, Fax: +86-571-8795124, E-mail: chu@zju.edu.cn   
About author:  GUO Jian-yang, Tel: +86-10-82109572, E-mail: guojianyang@caas.cn;

Cite this article: 

GUO Jian-yang, DU Yu-ping, WAN Fang-hao, YE Gong-yin. 2016. Characterization of a native whitefly vitellogenin gene cDNA and its expression pattern compared with two invasive whitefly cryptic species. Journal of Integrative Agriculture, 15(8): 1808-1815.

Boykin L M. 2014. Bemisia tabaci nomenclature: Lessons learned. Pest Management Science, 70, 1454–1459.

Boykin L M, De Barro P J. 2014. A practical guide to identifying members of the Bemisia tabaci species complex: and other morphologically identical species. Frontiers in Ecology Evolution, 2, 45.

Chu D, Wan F H, Zhang Y J, Brown J K. 2010. Change in the biotype composition of Bemisia tabaci in Shandong Province of China from 2005 to 2008. Environmental Entomology, 39, 1028–1036.

De Barro P J, Liu S S, Boykin L M, Dinsdale A B. 2011. Bemisia tabaci: a statement of species status. Annual Review of Entomology, 56, 1–19.

Dong S Z, Ye G Y, Guo J Y, Hu C. 2009. Roles of ecdysteroid and juvenile hormone in vitellogenesis in an endoparasitic wasp, Pteromalus puparum (Hymenoptera: Pteromalidae). General and Comparative Endocrinology, 160, 102–108.

Dong S Z, Ye G Y, Zhu J Y, Chen Z X, Hu C, Liu S S. 2007. Vitellin of Pteromalus puparum (Hymenoptera: Pteromalidae), a pupal endoparasitoid of Pieris rapae (Lepidoptera: Pieridae): Biochemical characterization, temporal patterns of production and degradation. Journal of Insect Physiology, 53, 468–477.

Ghanim M, Kontsedalov S. 2007. Gene expression in pyriproxyfen-resistant Bemisia tabaci Q biotype. Pest Management Science, 63, 776–783.

Guo J Y, Cheng L, Ye G Y, Fang Q. 2014. Feeding on a begomovirus-infected plant enhances fecundity via increased expression of an insulin-like peptide in the whitefly, MEAM1. Archives of Insect Biochemistry and Physiology, 85, 164–179.

Guo J Y, Dong S Z, Yang X L, Cheng L, Wan F H, Liu S S, Zhou X P, Ye G Y. 2012. Enhanced vitellogenesis in a whitefly via feeding on a begomovirus-infected plant. PLOS ONE, 7, e43567.

Guo J Y, Ye G Y, Dong S Z, Liu S S. 2010. An invasive whitefly feeding on a virus-infected plant increased its egg production and realized fecundity. PLoS ONE, 5, e11713.

Horowitz A R, Kontsedalov S, Khasdan V, Ishaaya I. 2005. Biotypes B and Q of Bemisia tabaci and their relevance to neonicotinoid and pyriproxyfen resistance. Archives of Insect Biochemistry and Physiology, 58, 216–225.

Hu J, De Barro P J, Zhao H, Wang J, Nardi F, Liu S S. 2011. An extensive field survey combined with a phylogenetic analysis reveals rapid and widespread invasion of two alien whiteflies in China. PLoS ONE, 6, e16061.

Jiu M, Zhou X P, Tong L, Xu J, Yang X, Wan F H, Liu S S. 2007. Vector-virus mutualism accelerates population increase of an invasive whitefly. PLoS ONE, 2, e182.

Leshkowitz D, Gazit S, Reuveni E, Ghanim M, Czosnek H, McKenzie C, Shatters Jr R L, Brown J K. 2006. Whitefly (Bemisia tabaci) genome project: Analysis of sequenced clones from egg, instar, and adult (viruliferous and non-viruliferous) cDNA libraries. BMC Genomics, 7, 79.

Liu S S, Colvin J J, De Barro P J. 2012. Species concepts as applied to the whitefly Bemisia tabaci systematics: How many species are there? Journal of Integrative Agriculture, 11, 176–186.

Liu S S, De Barro P J, Xu J, Luan J B, Zang L S, Ruan Y M, Wan F H. 2007. Asymmetric mating interactions drive widespread invasion and displacement in a whitefly. Science, 318, 1769–1772.

Liu Y Q, Liu S S. 2012. Species status of Bemisia tabaci complex and their distributions in China. Journal of Biosafety, 21, 247–255. (in Chinese)

Livak K J, Schmittgen T D. 2001. Analysis of relative gene expression data using real-time quantitative PCR and the 2(T)(-Delta Delta C) method. Methods, 25, 402–408.

Luan J B, Xu J, Lin K K, Zalucki M P, Liu S S. 2012. Species exclusion between an invasive and an indigenous whitefly on host plants with differential levels of suitability. Journal of Integrative Agriculture, 11, 215–224.

Ndunguru J, Sseruwagi P, Tairo F, Stomeo F, Maina S, Djinkeng A, Kehoe M, Boykin L M. 2015. Analyses of twelve new whole genome sequences of Cassava brown streak virus and Ugandan cassava brown streak virus from east Africa: Diversity, supercomputing and evidence for further speciation. PLoS ONE, 10, e0139321.

Raikhel A S, Dhadialla T S. 1992. Accumulation of yolk proteins in insect oocytes. Annual Review of Entomology, 37, 217–251.

Raikhel A S. 2005. Vitellogenesis of disease vectors, from physiology to genes. In: Marquardt W C, ed., Biology of Disease Vectors. Elsevier Academic Press, USA. pp. 329–346.

Richard D S, Rybczynski R, Wilson T G, Wang Y, Wayne M L, Zhou Y, Patridge L, Harshman L G. 2005. Insulin signaling is necessary for vitellogenesis in Drosophila melanogaster independent of the roles of juvenile hormone and ecdysteroids: Female sterility of the chico1 insulin signaling mutation is autonomous to the ovary. Journal of Insect Physiology, 51, 455–464.

Riehle M A, Brown M R. 2002a. Insulin receptor expression during development and a reproductive cycle in the ovary of the mosquito Aedes aegypti. Cell and Tissue Research, 308, 409–420.

Riehle M A, Garczynski S F, Crim J W, Hill C A, Brown M R. 2002b. Neuropeptides and peptide hormones in Anopheles gambiae. Science, 298, 172–175.

Sappington T W, Raikhel A S. 1998. Molecular characteristics of insect vitellogenins and vitellogenin receptors. Insect Biochemistry and Molecular Biology, 28, 277–300.

Sun D B, Li J, Liu Y Q, Crowder D W, Liu S S. 2014. Effects of reproductive interference on the competitive displacement between two invasive whiteflies. Bulletin of Entomological Research, 104, 334–346.

Sun D B, Liu Y Q, Qin L, Xu J, Li F F, Liu S S. 2013. Competitive displacement between two invasive whiteflies: insecticide application and host plant effects. Bulletin of Entomological Research, 103, 344–353.

Tamura K, Stecher G, Peterson D, Filipski A, Kumar S. 2013. MEGA6: Molecular evolutionary genetics analysis version 6.0. Molecular Biology and Evolution, 30, 2725–2729.

Tufail M, Nagaba Y, Elgendy A M, Takeda M. 2014. Regulation of vitellogenin genes in insects. Entomological Science, 17, 269–282.

Tufail M, Takeda M. 2008. Molecular characteristics of insect vitellogenins. Journal of Insect Physiology, 54, 1447–1458.

Tufail M, Takeda M. 2009. Insect vitellogenin/lipophorin receptors: molecular structures, role in oogenesis, and regulatory mechanisms. Journal of Insect Physiology, 55, 87–103.

Wang X W, Luan J B, Li J M, Bao Y Y, Zhang C X, Liu S S. 2010. De novo characterization and comparison of the whitefly transcriptomes reveals genes associated with development and insecticide resistance. BMC Genomics, 11, 400.

Xie W, Wu Q J, Wang S L, Jiao X G, Guo L T, Zhou X G, Zhang Y J. 2014. Transcriptome analysis of host-associated differentiation in Bemisia tabaci (Hemiptera: Aleyrodidae). Frontiers in Physiology, 5, 487.

Xu J, De Barro P J, Liu S S. 2010. Reproductive incompatibility among genetic groups of Bemisia tabaci supports the proposition that the whitefly is a cryptic species complex. Bulltin of Entomological Reseatch, 100, 1–8.

Yamamoto R, Bai H, Dolezal A G, Amdam G, Tatar M. 2013. Juvenile hormone regulation of Drosophila aging. BMC Biology, 11, 85.

Zang L S, Chen W Q, Liu S S. 2006. Comparison of performance on different host plants between the B biotype and a non-B biotype of Bemisia tabaci from Zhejiang, China. Entomologia Experimentalis et Applicata, 121, 221–227.

Zang L S, Liu S S, Liu Y Q, Chen W Q. 2005. A comparative study on the morphological and biological characteristics of the B biotype and a non-B biotype (China-ZHJ-1) of Bemisia tabaci (Homoptera: Aleyrodidae) from Zhejiang, China. Acta Entomologica Sinica, 48, 742–748. (in Chinese)

Zhong R, Ding T B, Niu J Z, Xia W K, Liao C Y, Dou W, Wang J J. 2015. Molecular characterization of vitellogenin and its receptor genes from citrus red mite, Panonychus citri (McGregor). International Journal of Molecular Sciences, 16, 4759–4773.
No related articles found!
No Suggested Reading articles found!