Published July 1, 2024 | Version v1
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Drosophila serrata mutation accumulation lines: Phenotypic data on survival following infection with Drosophila C virus and reproduction

  • 1. University of Queensland

Description

The impact of selection on host immune function genes has been widely documented. However, it remains essentially unknown how mutation influences the quantitative immune traits that selection acts on. Applying a classical mutation accumulation (MA) experimental design in Drosophila serrata, we found the mutational variation in susceptibility (median time of death, LT50) to Drosophila C virus (DCV) was of similar magnitude to that reported for intrinsic survival traits. Mean LT50 did not change as mutations accumulated, suggesting no directional bias in mutational effects. Maintenance of genetic variance in immune function is hypothesised to be influenced by pleiotropic effects on immunity and other traits that contribute to fitness. To investigate this, we assayed female reproductive output for a subset of MA lines with relatively long or short survival times under DCV infection. Longer survival time tended to be associated with lower reproductive output, suggesting that mutations affecting susceptibility to DCV had pleiotropic effects on investment in reproductive fitness. Further studies are needed to uncover the general patterns of mutational effect on immune responses and other fitness traits, and to determine how selection might typically act on new mutations via their direct and pleiotropic effects.

Notes

Funding provided by: Australian Research Council
ROR ID: https://ror.org/05mmh0f86
Award Number:

Methods

This project first determined that D. serrata is a susceptible host of the Drosophila C virus. Second, survival time following DCV infection was measured for a panel of 65 inbred lines that differed from one another by fixation of spontaneous mutations over 30 generations , and that data used to determine how mutations affected DCV susceptibility. Finally, for a subset of lines with extreme differences in survival time, we also measured female offspring production to determine whether mutations affecting immune function also affected productivity.

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