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. 2008 Sep 10:6:38.
doi: 10.1186/1741-7007-6-38.

Viral cystatin evolution and three-dimensional structure modelling: a case of directional selection acting on a viral protein involved in a host-parasitoid interaction

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Viral cystatin evolution and three-dimensional structure modelling: a case of directional selection acting on a viral protein involved in a host-parasitoid interaction

Céline Serbielle et al. BMC Biol. .

Abstract

Background: In pathogens, certain genes encoding proteins that directly interact with host defences coevolve with their host and are subject to positive selection. In the lepidopteran host-wasp parasitoid system, one of the most original strategies developed by the wasps to defeat host defences is the injection of a symbiotic polydnavirus at the same time as the wasp eggs. The virus is essential for wasp parasitism success since viral gene expression alters the immune system and development of the host. As a wasp mutualist symbiont, the virus is expected to exhibit a reduction in genome complexity and evolve under wasp phyletic constraints. However, as a lepidopteran host pathogenic symbiont, the virus is likely undergoing strong selective pressures for the acquisition of new functions by gene acquisition or duplication. To understand the constraints imposed by this particular system on virus evolution, we studied a polydnavirus gene family encoding cyteine protease inhibitors of the cystatin superfamily.

Results: We show that cystatins are the first bracovirus genes proven to be subject to strong positive selection within a host-parasitoid system. A generated three-dimensional model of Cotesia congregata bracovirus cystatin 1 provides a powerful framework to position positively selected residues and reveal that they are concentrated in the vicinity of actives sites which interact with cysteine proteases directly. In addition, phylogenetic analyses reveal two different cystatin forms which evolved under different selective constraints and are characterized by independent adaptive duplication events.

Conclusion: Positive selection acts to maintain cystatin gene duplications and induces directional divergence presumably to ensure the presence of efficient and adapted cystatin forms. Directional selection has acted on key cystatin active sites, suggesting that cystatins coevolve with their host target. We can strongly suggest that cystatins constitute major virulence factors, as was already proposed in previous functional studies.

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Figures

Figure 1
Figure 1
Cystatin gene tree obtained by maximum likelihood. Node supports are shown by bootstraps and by posterior probabilities from Bayesian inferences above and below each branch, respectively. Bootstrap scores or posterior probabilities lower than 50% are not represented. Sequences were obtained from bracoviruses of Cotesia congregata (CcBV), Cotesia flavipes (CfBV), Cotesia chilonis (CchBV), Cotesia melanoscela (CmBV), Cotesia vestalis (CvBV), Cotesia rubecula (CrBV), Cotesia sesamiae (CsBV), Cotesia karyai (CkBV)and Cotesia glomerata (CgBV). Cystatin sequences from CcBV genome are noted CcBVcyst1, CcBVcyst2 and CcBVcyst3.
Figure 2
Figure 2
Molecular model of CcBV cystatin 1 obtained from the average structure. (A) The superimposed molecular dynamics (MD) average structure of CcBV cystatin 1 orange (1–5 ns), cyan (5–7 ns) and purple (8–10 ns) of 10 ns MD simulation trajectory. (B) Positively selected residues (probability 95%) are represented as a red colour capped stick model on the secondary structure (green) of the final model of CcBV cystatin 1 average structure (1–10 ns). Glycine in N-terminal and Valine and Alanine in the L1 are important for C1 protease binding. CcBV mature cystatin 1 amino acid numbering is used.
Figure 3
Figure 3
Graphic representation of variable selective pressures (ω) along the protein sequence. The * indicates a posterior probability greater than 95% of having ω > 1 and ** indicates a posterior probability greater than 99% of having ω > 1. Conserved amino acids implicated in the interaction with target proteases are indicated by arrows and are numbered according to the mature protein.
Figure 4
Figure 4
Cystatin sequence tree under local substitution model. (A) Tree scaled on expected number of nonsynonymous substitutions per site. (B) Tree scaled on expected number of synonymous substitutions per site.
Figure 5
Figure 5
Branches under positive selection estimated according to the genetic algorithm-branch analysis. Percentages for branch classes in the legend reflect the proportion of total tree length (measured in expected substitutions per site per time unit) and evolving under the corresponding value of dN/dS. The * indicates a posterior probability greater than 95% of having ω > 1.

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