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International audience; As phytohormones lie at the very core of molecular mechanisms controlling the plant physiology and development, they have long been hypothesized to be involved in insect-induced plant manipulations. Cytokinins (CKs) are phytohormones now widely recognized to be utilized by leaf-mining and gall-inducing insects in the control of the physiology of their host plant. In some leaf-mining moth species, larvae can supply the hormones themselves, bacterial symbionts contributing to the production of CKs. Our objective was to investigate whether closely related leaf-miner species sharing the same ecological niche but differing in their Wolbachia infection status develop similar strategies to manipulate their host plant. An extensive identification and quantification of CKs has been used to elucidate physiological patterns relevant for the plant-insect interactions. Our results show that modulation of plant CK levels is impaired in the Wolbachia-free leaf-mining moth Phyllonoryc-ter mespilella (H€ ubner) (Lepidoptera: Gracillariidae) contrasting with results previously observed in the closely related moth species Phyllonorycter blancardella (Fabricius) that produce and deliver CKs to the plant through an intricate interaction with Wolbachia. Our study suggests that mechanisms underlying colonization of the host plant and adaptation to fluctuating environmental conditions are different between the two leaf-miner species and that P. mespilella larvae most likely do not produce CKs. This species rather only buffers the degradation of CKs naturally occurring during the senescence of leaves leading to few active CKs being maintained at a sufficiently high level to induce and maintain a 'green island' phenotype (photosynthetically active green patches in otherwise senescing leaves). This study further provides converging experimental evidence pointing toward the influence of bacterial symbionts in the ability of leaf-mining moths to control the physiology of their host plant with consequences for their ecology and evolutionary diversification.

Summary Termite gut flagellates are colonized by host-specific lineages of ectosymbiotic and endosymbiotic bacte- ria. Previous studies have shown that flagellates of the genus Trichonympha may harbour more than one type of symbiont. Using a comprehensive approach that combined cloning of SSU rRNA genes with fluo- rescence in situ hybridization and electron micros- copy, we investigated the phylogeny and subcellular locations of the symbionts in a variety of Trichonym- pha species from different termites. The flagellates in Trichonympha Cluster I were the only species asso- ciated with 'Endomicrobia', which were located in the posterior part of the cell, confirming previous results. Trichonympha species of Cluster II from the termite genus Incisitermes (family Kalotermitidae) lacked 'Endomicrobia' and were associated with endo- symbiotic Actinobacteria, which is highly unusual. The endosymbionts, for which we suggest the name 'Candidatus Ancillula trichonymphae', represent a novel, deep-branching lineage in the Micrococcineae that consists exclusively of clones from termite guts. They preferentially colonized the anterior part of the flagellate host and were highly abundant in all species of Trichonympha Cluster II except Tricho- nympha globulosa. Here, they were outnumbered by a Desulfovibrio species associated with the cytoplas- mic lamellae at the anterior cell pole. Such symbionts are present in both Trichonympha clusters, but not in all species. Unlike the intracellular location reported for the Desulfovibrio symbionts of Trichonympha agilis (Cluster I), the Desulfovibrio symbionts of T. globulosa (Cluster II) were situated in deep invagi- nations of the plasma membrane that were clearly connected to the exterior of the host cell.

Summary Endomicrobia represent a candidate class in the Elusimicrobia phylum (formerly Termite Group 1) and were originally described as obligate intracellular symbionts of gut flagellates in lower termites. However, 16S rRNA gene sequences of Endomicrobia have been detected also in the gut of insects that do not possess such flagellates, e.g. higher termites and cockroaches. When we eliminated the large gut flagellates of Reticulitermes santonensis by feeding a starch diet, we discovered novel lineages of Endomicrobia that were hitherto undetected in normally faunated specimens. The new phylotypes are clearly separated from the endosymbionts of gut flagellates and fall into the radiation of those from flagellate-free insects. Comprehensive phylogenetic analysis documented that Endomicrobia comprise an apical cluster of endosymbionts that is not necessarily monophyletic and several apparently basal lineages that include bacteria present in the gut of defaunated lower termites, the naturally flagellate-free guts of higher termites and scarab beetle larvae, and in the cow rumen. We propose that these lineages represent hitherto undetected free-living Endomicrobia that share a common ancestor with the intracellular symbionts.