As more than 10% of insect species depend on obligate bacterial mutualists for their viability and reproduction [29], the research on symbiosis between bacteria and animals appears to be a new and promising field, particularly in social insects. Methods Camponotus fellah: sampling sites and culture Camponotus ants develop by complete metamorphosis, like all hymenopterans, going through stages of the egg, larva, pupa, and adult worker or reproductive. Pupae exist in conspicuous silk cocoons. Newly fecundated females start a new colony,

caring for their first brood of larvae until they develop into workers, which then begin to forage for food. Founding queens of C. fellah were collected in Tel-Aviv in March 2006 and 2007. Colonies were kept in plastic see more containers (20 × 20 × 10 cm) with plaster nests in www.selleckchem.com/products/lcl161.html a climate chamber (constant temperature of 28°C, 12 h light per day),

and were fed twice a week with AUY-922 Tenebrio molitor larvae and commercial honey solution (BeeHappy®, France). In 2006 and 2007 we used 10 control colonies (fed with Tenebrio and honey) and 10 treated colonies (fed with Tenebrio and honey in the first week, and Tenebrio larvae and honey solution containing 1% of the antibiotic Rifampin the second week and after). In previous studies on other Camponotus species [30] Rifampin was shown to reduce the number of bacteria without increasing mortality and did not cause damage to the ant midgut tissues. The treatment was maintained during three months. Because the occurrence of Phosphoglycerate kinase Wolbachia is widespread in ants [31] and these symbiotic bacteria can have negative effects on immunity-related traits of insects [32], their incidence was checked in the C. fellah colonies studied, using two pairs of primers based on Wolbachia ftsZ sequences [31], so as to amplify A and B-group Wolbachia specific product [31]. No incidence of Wolbachia was detected. Symbiont identification Symbiont identification was based on sequencing of the 16S rRNA gene and Fluorescent in situ hybridization. The 16S rRNA gene was amplified using the previously described primers SL (TTGGGATCCAGAGTTTGATCATGGCTCAGAT)

and SR (CACGAATTCTACCTTGTTACGACTTCACCCC) [33]. The PCR reactions were performed in a total volume of 25 μl containing 2.5 mM dNTPs, 7.5 mM MgCl2, 5 pmol each oligonucleotide and 2.5 U/μl Taq DNA polymerase (GoldStar®). Amplification was performed in an Eppendorf thermocycler according to the following conditions: 30 s denaturation at 94°C, 30 s primers annealing at 55 °C and 1.5 min primer extension at 72°C, running 35 cycles. The amplified DNA fragment of approximately 1,550 bp was purified using a QIAquick PCR purification Kit (Qiagen) and directly sequenced using the ABI PRISM™ dye terminator cycle. The sequencing reactions were performed using the SL and SR primers and using the two internal primers sequences CampL (5′-GAATTACTGGGCGTAAAGAGT-3′) and CampR (5′-GGAACGTATTCACCG TGAC-3′).