Variability of the mitochondrial CO1 gene in native and invasive populations of Harmonia axyridis Pall. comparative analysis.

Our study is focused on original and publicly accessible data on the intraspecific variability of the barcoding DNA fragment in ladybirds Harmonia axyridis Pall analysis. The complete dataset consists of 39 haplotypes, 16 of which we identified for the first time. The intra-population and geographical variability of the barcoding fragment was studied for seven populations of the western and eastern groups of the native range and in six invasive populations, in which 25 of the 39 haplotypes are found. Population structure inferred on base of molecular variability and haplotype frequencies showed a high level of differences between the eastern and western groups of native populations and confirm the hypothesis of the origin of all invasive populations from native populations of the eastern group. A comparative analysis of molecular variation indices testifies to various evolutionary scenarios of the formation of the western and eastern groups of native populations and confirms the hypothesis of the microevolutionary history of the species, previously suggested in morphological character based studies of the geographical variability of H. axyridis. A significant decrease in the molecular diversity of invasive populations confirms the hypothesis of a random nature of the primary invasion of this species in North America.

Spiroplasma infection in Harmonia axyridis - Diversity and multiple infection.

The heritable endosymbiotic bacterium Spiroplasma is found in the harlequin ladybird Harmonia axyridis. The proportion of beetles infected with Spiroplasma in different native H. axyridis populations varies from 2% to 49%. We investigated the polymorphism of Spiroplasma strains in samples from individual beetles from Kyoto, Vladivostok, Troitsa Bay, Novosibirsk, and Gorno-Altaisk. To identify Spiroplasma strains, we analyzed nucleotide polymorphisms of the 16S rRNA gene and the ribosomal internal transcribed spacer (ITS1). The majority of infected beetles were infected with two or more Spiroplasma strains. We measured Spiroplasma density in beetles with different infection status using quantitative PCR. The abundance of Spiroplasma in samples with a single infection is an order of magnitude lower than in samples with multiple infections. Density dependent biological effects of Spiroplasma are discussed.