A Rickettsia-specific phylogenetic tree elucidated that one M. pygmaeus Rickettsia endosymbiont belonged to the ‘Limoniae’ group, selleck whereas the other is a member of the ‘Bellii’ group (Fig. 1). The M. pygmaeus Rickettsia endosymbiont

belonging to the ‘Bellii’ group was phylogenetically closely related to the symbionts of natural prey species of the mirid predator, including the two-spotted spider mite T. urticae, the pea aphid A. pisum and the tobacco whitefly B. tabaci. This finding may indicate a possible horizontal transfer between predator and prey. The horizontal transfer of an endosymbiont has, however, currently only been established in an arthropod parasitoid-host system. Chiel et al. [67] investigated the interspecies horizontal transfer of Rickettsia from B. tabaci (belonging to the ‘Bellii’ group) to its aphelinid parasitoids Eretmocerus emericus and E. emiratus.

BAY 80-6946 molecular weight This Rickettsia infection reached the reproductive tissues of its host, but was not transmitted to its progeny. Sharing the same habitat and using the same plant tissues may also constitute a transmission route for bacterial endosymbionts. Macrolophus spp. are facultatively phytophagous predators with piercing-sucking mouthparts and may inoculate plant tissues with micro-organisms. Other species, feeding on the same host plant may then take up these micro-organisms. Furthermore, the PCR-DGGE profile showed the presence of R. limoniae and R. bellii in the gut, suggesting that an infection of the faeces is likely. However, more research is needed to confirm these hypothetical horizontal transmission routes. Conclusions In this study, the microbial community of the mirid predators M. pygmaeus and M. caliginosus was explored by 16S rRNA gene cloning and

PCR-DGGE. Both species were infected with Wolbachia and a Rickettsia species related to R. limoniae. Furthermore, M. pygmaeus was infected with a Rickettsia species belonging to the ‘Bellii’ group. The latter is phylogenetically related PRKACG to Rickettsia species in their arthropod prey, including B. tabaci and T. urticae, which may be indicative of a potential horizontal transmission in a predator-prey system. All endosymbionts were vertically transmitted to their progeny, as demonstrated by a FISH analysis and a diagnostic PCR on the ovaries. A bio-assay with M. pygmaeus indicated that infection with the endosymbionts did not have fitness costs for the predator. Further research is warranted to elucidate the role of Rickettsia in its Macrolophus host. Authors’ contributions TM performed the experiments and wrote the manuscript. TM, TVL and PDC designed the experiments. TVDW and NB helped with the PCR-DGGE experiments. JAS and MN collected Macrolophus bugs in Spain and Italy, respectively. WDV helped with the FISH experiments. TVL, TVDW, GG and PDC revised the manuscript. All authors read and approved the final manuscript.