P and S symbionts can AZD6244 solubility dmso coexist in the same host.

When an S-symbiont is also present, the irreversible genomic degenerative process could lead to the loss of some P-endosymbiont metabolic capabilities needed by the host. In this situation, two outcomes are possible: the host insect can recruit those functions from the S-symbiont, which then becomes a co-primary endosymbiont, establishing metabolic complementation https://www.selleckchem.com/products/a-769662.html with the former P-endosymbiont to fulfill the host needs or [5–8]; alternatively, the S-symbiont may replace its neighbor [9]. Mealybugs (Hemiptera: Sternorrhyncha: Pseudoccidae) form one of the largest families of scale insects, including many agricultural pest species that cause direct crops RepSox damage or vector plant diseases while feeding on sap [10]. All mealybug species analyzed so far possess P-endosymbionts. Two subfamilies have been identified, Phenacoccinae and Pseudococcinae [11], the latter having been studied in greater depth, all of which live in symbiosis with the β-proteobacterium “Candidatus Tremblaya princeps” (T. princeps from now on, for the sake of simplicity). Universal

presence, along with the cocladogenesis of endosymbionts and host insects, led to T. princeps being considered the mealybug P-endosymbiont [12]. However, recently, other P-endosymbionts from the β-proteobacteria and Bacteroidetes groups have been identified in the subfamily Phenacoccinae [13]. Most genera of the subfamily Pseudococcinae also harbor additional γ-proteobacteria endosymbionts that, due to their discontinuous presence and polyphyletic origin, have been considered as S-symbionts [14]. An unprecedented structural selleck inhibitor organization of the endosymbionts of the citrus mealybug Planococcus citri was revealed by von Dohlen and coworkers [15]: each T. princeps cell harbors several S-endosymbiont cells, being the first known case of prokaryote-prokaryote endocelullar symbiosis. The

S-endosymbiont has recently been named “Candidatus Moranella endobia” (M. endobia from now on) [16]. The dynamics of both endosymbiont populations throughout the insect life-cycle and their differential behavior depending on host sex [17] suggest that both play an important role in their hosts’ nutritional and reproductive physiology, putting into question the secondary role of M. endobia. The sequencing of two fragments of the genome of T. princeps from the pineapple mealybug, Dysmicoccus brevipes[18], showed a set of unexpected genomic features compared with that found in most P-endosymbiont reduced genomes. This species presents a rather high genomic G + C content – a rare condition among P-endosymbionts with the only known exception being “Candidatus Hodgkinia cicadicola” (P-endosymbiont of the cicada Diceroprocta semicincta[7]) –, a partial genomic duplication including the ribosomal operon and neighbor genes, and low gene density.