Synthesis, depletion and cell-type expression of a protein from the male accessory glands of the dengue vector mosquito Aedes aegypti

作者: Catalina Alfonso-Parra , Frank W. Avila , Prasit Deewatthanawong , Laura K. Sirot , Mariana F. Wolfner

DOI: 10.1016/J.JINSPHYS.2014.07.004

关键词:

摘要: Aedes aegypti males transfer sperm and seminal fluid proteins (Sfps), primarily produced by male accessory glands (AGs), to females during mating. When collectively injected or transplanted into females, AG tissues and/or homogenates have profound effects on female physiology behavior. To identify targets design new strategies for vector control, it is important understand the biology of AGs. Thus, we examined characteristics secretion development in A. aegypti, using AG-specific protein, AAEL010824, as a marker. We showed that AAEL010824 first detectable 12h post-eclosion, increases amount over 3 days adult life. then AAEL0010824 decreases after mating, with each successive mating depleting further; 5 matings no time recovery, its levels are very low. depleted replenished 48 h post-mating. In addition examining level also characterized expression gene. did this making transgenic mosquito line carries an Enhanced Green Fluorescence Protein (EGFP) fused promoter defined here. expressed anterior cells glands, RNA respond further characterizing expression, our results EGFP fusion provide driving expression. By providing information reproductive tissue production one proteins, lay foundation future work aimed at identifying novel population control.

参考文章(38)
Geoffrey D Findlay, Xianhua Yi, Michael J MacCoss, Willie J Swanson, Proteomics Reveals Novel Drosophila Seminal Fluid Proteins Transferred at Mating PLOS Biology. ,vol. 6, pp. 1417- 1426 ,(2008) , 10.1371/JOURNAL.PBIO.0060178
Chiara Naccarati, Neil Audsley, Jeffrey N Keen, Jung-Ha Kim, Gareth J Howell, Young-Joon Kim, R Elwyn Isaac, None, The host-seeking inhibitory peptide, Aea-HP-1, is made in the male accessory gland and transferred to the female during copulation Peptides. ,vol. 34, pp. 150- 157 ,(2012) , 10.1016/J.PEPTIDES.2011.10.027
S. Ramalingam, G.B. Craig, Fine structure of the male accessory glands in Aedes triseriatus Journal of Insect Physiology. ,vol. 24, pp. 251- 259 ,(1978) , 10.1016/0022-1910(78)90043-4
Vimla Adlakha, M.K.K. Pillai, Involvement of male accessory gland substance in the fertility of mosquitoes. Journal of Insect Physiology. ,vol. 21, pp. 1453- 1455 ,(1975) , 10.1016/0022-1910(75)90207-3
A. Leiblich, L. Marsden, C. Gandy, L. Corrigan, R. Jenkins, F. Hamdy, C. Wilson, Bone morphogenetic protein- and mating-dependent secretory cell growth and migration in the Drosophila accessory gland Proceedings of the National Academy of Sciences of the United States of America. ,vol. 109, pp. 19292- 19297 ,(2012) , 10.1073/PNAS.1214517109
Amy C Morrison, Emily Zielinski-Gutierrez, Thomas W Scott, Ronald Rosenberg, Defining challenges and proposing solutions for control of the virus vector Aedes aegypti. PLOS Medicine. ,vol. 5, ,(2008) , 10.1371/JOURNAL.PMED.0050068
Woodbridge A. Foster, Arden O. Lea, Renewable fecundity of male Aedes aegypti following replenishment of seminal vesicles and accessory glands Journal of Insect Physiology. ,vol. 21, pp. 1085- 1090 ,(1975) , 10.1016/0022-1910(75)90120-1
Duane J Gubler, The Global Emergence/Resurgence of Arboviral Diseases As Public Health Problems Archives of Medical Research. ,vol. 33, pp. 330- 342 ,(2002) , 10.1016/S0188-4409(02)00378-8
K. R. Ram, M. F. Wolfner, A network of interactions among seminal proteins underlies the long-term postmating response in Drosophila. Proceedings of the National Academy of Sciences of the United States of America. ,vol. 106, pp. 15384- 15389 ,(2009) , 10.1073/PNAS.0902923106
J. M. Kalb, A. J. DiBenedetto, M. F. Wolfner, Probing the function of Drosophila melanogaster accessory glands by directed cell ablation Proceedings of the National Academy of Sciences of the United States of America. ,vol. 90, pp. 8093- 8097 ,(1993) , 10.1073/PNAS.90.17.8093