Wolbachia infection and incompatibility dynamics in experimental selection lines

• Published in: Journal of evolutionary biology Vol. 12; no. 2; pp. 272 - 282
• Main Authors: Perrot‐Minnot, Werren
• Format: Journal Article
• Language: English
• Published: Oxford UK Blackwell Publishing Ltd 01-03-1999
• Subjects: bacterial load; cytoplasmic incompatibility; introgression; Nasonia vitripennis; parasitic wasp; Pteromalidae; Wolbachia
• ISSN: 1010-061X; 1420-9101
• DOI: 10.1046/j.1420-9101.1999.00025.x

High and low levels of Wolbachia‐induced cytoplasmic incompatibility (CI) were selected for in the parasitic wasp Nasonia vitripennis, in the single‐infected strain Ti277. After nine generations of selection, males from lines selected for high incompatibility level (HI lines) were significantly more incompatible with uninfected females (AsymC) than the maternal strain. The reverse response, a full compatibility with AsymC, was observed in eight out of 12 lines selected for low incompatibility (LO lines), correlated with loss of Wolbachia infection. Bacterial density estimates in the eggs of some HI lines increased significantly. The procedure for line maintenance resulted in introgression of AsymC nuclear genome into the Ti277 background. Significant changes of CI level and bacterial density due to the introgression were also observed in the control lines, possibly reflecting an effect of host genotype on bacterial density and CI. After selection had been relaxed for six generations, bacterial density in the five high‐infected HI lines declined back to a level comparable to the other lines. The data are consistent with the ‘bacterial dosage’ model, but with an upper threshold of bacterial infection above which there is no correlation between infection level and CI level. We further investigate the maternal transmission of bacterial density by a mother–daughter regression on bacterial density. The pattern observed is consistent with a density dependent regulation of bacterial numbers around an ‘equilibrium’ density, independent of any effects of CI. The equilibrium value is likely to be determined by both bacterial strain and host genotype.