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. 2009 Jun;5(6):e1000467.
doi: 10.1371/journal.ppat.1000467. Epub 2009 Jun 5.

Mosquitoes put the brake on arbovirus evolution: experimental evolution reveals slower mutation accumulation in mosquito than vertebrate cells

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Mosquitoes put the brake on arbovirus evolution: experimental evolution reveals slower mutation accumulation in mosquito than vertebrate cells

Nikos Vasilakis et al. PLoS Pathog. 2009 Jun.

Abstract

Like other arthropod-borne viruses (arboviruses), mosquito-borne dengue virus (DENV) is maintained in an alternating cycle of replication in arthropod and vertebrate hosts. The trade-off hypothesis suggests that this alternation constrains DENV evolution because a fitness increase in one host usually diminishes fitness in the other. Moreover, the hypothesis predicts that releasing DENV from host alternation should facilitate adaptation. To test this prediction, DENV was serially passaged in either a single human cell line (Huh-7), a single mosquito cell line (C6/36), or in alternating passages between Huh-7 and C6/36 cells. After 10 passages, consensus mutations were identified and fitness was assayed by evaluating replication kinetics in both cell types as well as in a novel cell type (Vero) that was not utilized in any of the passage series. Viruses allowed to specialize in single host cell types exhibited fitness gains in the cell type in which they were passaged, but fitness losses in the bypassed cell type, and most alternating passages, exhibited fitness gains in both cell types. Interestingly, fitness gains were observed in the alternately passaged, cloned viruses, an observation that may be attributed to the acquisition of both host cell-specific and amphi-cell-specific adaptations or to recovery from the fitness losses due to the genetic bottleneck of biological cloning. Amino acid changes common to both passage series suggested convergent evolution to replication in cell culture via positive selection. However, intriguingly, mutations accumulated more rapidly in viruses passed in Huh-7 cells than in those passed in C6/36 cells or in alternation. These results support the hypothesis that releasing DENV from host alternation facilitates adaptation, but there is limited support for the hypothesis that such alternation necessitates a fitness trade-off. Moreover, these findings suggest that patterns of genetic evolution may differ between viruses replicating in mammalian and mosquito cells.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Experimental design for DENV in vitro adaptation studies.
Sylvatic strain P8-1407 or endemic strain IQT-1950 were serially passaged in vertebrate Huh-7 cells (left) or invertebrate C6/36 cells (Ae. albopictus cell line) (right) to artificially bypass one host, or alternately passaged (center) to simulate natural transmission. The fitness of DENV derived from these passage series compared to parent viruses was determined by direct replication comparison.
Figure 2
Figure 2. Replication of Huh-7 – passaged uncloned DENV-2.
(a) Huh-7 – passaged sylvatic P8-1407 DENV-2 on Huh-7 cells. (b) Huh-7 – passaged endemic IQT-1950 DENV-2 on Huh-7 cells. (c) Huh-7 – passaged sylvatic P8-1407 DENV-2 on the bypassed cell line C6/36. (d) Huh-7 – passaged endemic IQT-1950 DENV-2 on the bypassed cell line C6/36. (e) Huh-7 – passaged sylvatic P8-1407 DENV-2 on a control cell line (Vero). (f) Huh-7 – passaged endemic IQT-1950 DENV-2 on a control cell line (Vero). Timepoint T = 0 represents residual virus after washing.
Figure 3
Figure 3. Replication of Huh-7 – passaged cloned DENV-2.
(a) Huh-7 – passaged sylvatic P8-1407 DENV-2 on Huh-7 cells. (b) Huh-7 – passaged endemic IQT-1950 DENV-2 on Huh-7 cells. (c) Huh-7 – passaged sylvatic P8-1407 DENV-2 on the bypassed cell line C6/36. (d) Huh-7 – passaged endemic IQT-1950 DENV-2 on the bypassed cell line C6/36. (e) Huh-7 – passaged sylvatic P8-1407 DENV-2 on a control cell line (Vero). (f) Huh-7 – passaged endemic IQT-1950 DENV-2 on a control cell line (Vero). Timepoint T = 0 represents residual virus after washing.
Figure 4
Figure 4. Replication of C6/36 – passaged uncloned DENV-2.
(a) C6/36 – passaged sylvatic P8-1407 DENV-2 on C6/36 cells. (b) C6/36 – passaged endemic IQT-1950 DENV-2 on C6/36 cells. (c) C6/36 – passaged sylvatic P8-1407 DENV-2 on the bypassed cell line Huh-7. (d) C6/36 – passaged endemic IQT-1950 DENV-2 on the bypassed cell line Huh-7. (e) C6/36 – passaged sylvatic P8-1407 DENV-2 on a control cell line (Vero). (f) C6/36 – passaged endemic IQT-1950 DENV-2 on a control cell line (Vero). Timepoint T = 0 represents residual virus after washing.
Figure 5
Figure 5. Replication of C6/36 – passaged cloned DENV-2.
(a) C6/36 – passaged sylvatic P8-1407 DENV-2 on C6/36 cells. (b) C6/36 – passaged endemic IQT-1950 DENV-2 on C6/36 cells. (c) C6/36 – passaged sylvatic P8-1407 DENV-2 on the bypassed cell line Huh-7. (d) C6/36 – passaged endemic IQT-1950 DENV-2 on the bypassed cell line Huh-7. (e) C6/36 – passaged sylvatic P8-1407 DENV-2 on a control cell line (Vero). (f) C6/36 – passaged endemic IQT-1950 DENV-2 on a control cell line (Vero). Timepoint T = 0 represents residual virus after washing.

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