The two other groups included either two distinct COI groups

The two other groups included either two distinct COI groups learn more of B. tabaci ASL and AnSL or individuals from two different host check details species : B. tabaci (with Ms genetic group individuals from Madagascar, Tanzania and Reunion) and T. vaporariorum (Tables

3, 4). Comparative analysis of the genetic divergence of these groups at the three loci (Tables 3, 4) revealed that the group composed of ASL and AnSL individuals is the most polymorphic (π = 0.0068), while the Q2 group is highly homogeneous despite several sampling origins (Table 1). Overall, DNA polymorphism was rather low with an average value of group π means of 0.002. Phylogenetic relatedness of Arsenophonus strains from other insects species The Arsenophonus isolates observed in our B. tabaci samples proved to be phylogenetically very close to the Arsenophonus strains found in other insect species (Figure 3). One clade, composed of T. vaporariorum, B. afer, the B. tabaci groups Ms, Q2, and some individuals belonging to ASL, fell into the Aphis sp. and Triatoma sp. Arsenophonus clade described by Duron et al. [17]. The other clade was comprised mainly Arsenophonus infecting Hymenoptera (Nasonia vitripennis, Pachycrepoideus vindimmiae, Muscidifurax uniraptor) and the dipteran Protocalliphora azurea. Discussion In this paper we report on a survey

of the Arsenophonus bacterial symbiont in whitefly species, and in particular in B. tabaci. The data revealed considerable within-genus diversity at this fine host taxonomic level. Previous studies conducted in several arthropod species have found Selleck MX69 Arsenophonus to be one of the richest and most widespread symbiotic bacteria in arthropods [9, 15]. However, those studies were performed with 16S rRNA, which is present in multiple copies

in the genome of the bacterium [25] and has proven to be a marker that is highly sensitive to methodological artifacts, leading to an overestimation of the diversity [15]. The phylogenetic analyses performed on concatenated sequences of three Arsenophonus genes from whiteflies identified two well-resolved clades corresponding to the two clades obtained in the MLST study performed by Duron et al. on a larger insect species scale [17]. One clade was composed of Arsenophonus lineages from three B. tabaci genetic groups Decitabine nmr (Ms, ASL, Q2), T. vaporariorum and B. afer, and strains found in other Hemiptera. The other clade, initially clustering Arsenophonus strains found in Hymenoptera and Diptera, also contained whitefly symbionts of the AnSL, ASL and Q3 genetic groups of the B. tabaci species complex. This clade thus combines insect hosts from phylogenetically distant taxa. The lineages of Arsenophonus from this clade were most likely acquired by whiteflies more recently through lateral transfers from other insect species. The genetic groups of B.

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