Abstract

Juvenile hormone (JH) regulates development and reproductive maturation in insects. The corpora allata (CA) from female adult mosquitoes synthesize fluctuating levels of JH, which have been linked to the ovarian development and are influenced by nutritional signals. The rate of JH biosynthesis is controlled by the rate of flux of isoprenoids in the pathway, which is the outcome of a complex interplay of changes in precursor pools and enzyme levels. A comprehensive study of the changes in enzymatic activities and precursor pool sizes have been previously reported for the mosquito Aedes aegypti JH biosynthesis pathway. In the present studies, we used two different quantitative approaches to describe and predict how changes in the individual metabolic reactions in the pathway affect JH synthesis. First, we constructed generalized additive models (GAMs) that described the association between changes in specific metabolite concentrations with changes in enzymatic activities and substrate concentrations. Changes in substrate concentrations explained 50% or more of the model deviances in 7 of the 13 metabolic steps analyzed. Addition of information on enzymatic activities almost always improved the fitness of GAMs built solely based on substrate concentrations. GAMs were validated using experimental data that were not included when the model was built. In addition, a system of ordinary differential equations (ODE) was developed to describe the instantaneous changes in metabolites as a function of the levels of enzymatic catalytic activities. The results demonstrated the ability of the models to predict changes in the flux of metabolites in the JH pathway, and can be used in the future to design and validate experimental manipulations of JH synthesis.

Highlights

  • Mosquito-transmitted parasitic diseases are among the major causes of mortality in the world

  • The amounts of products generated by the seven enzymatic reactions included in the MVAP were modeled as a function of: 1) substrate, 2) enzymatic activity and, 3) the combination of substrate and enzymatic activity (Table 1)

  • The molecular bases for regulation of Juvenile hormone (JH) synthesis, as well as the roles of brain factors or other endocrine regulators changed during these four phases

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Summary

Introduction

Mosquito-transmitted parasitic diseases are among the major causes of mortality in the world. The wide-spread resistance of mosquitoes to insecticides underscores the need for new control approaches based on a better understanding of mosquito biology. The biosynthetic pathway of JH III in mosquitoes involves 13 discrete enzymatic reactions which are divided into early (mevalonic acid pathway—MVAP) and late (JH-branch) steps. The early steps of JH III biosynthesis follow the mevalonate pathway to form farnesyl pyrophosphate (FPP) [3]. The late steps involve the hydrolysis of FPP to farnesol (FOL), followed by oxidation to farnesal (FAL) [4] and farnesoic acid (FA) [5]. FA is converted to JH III by the activity of a methyl transferase [6, 7], and a P450 epoxidase [8, 9]

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