Ticks transmit pathogens and harbour non-pathogenic, vertically transmitted intracellular bacteria termed endosymbionts. Almost all ticks studied to date contain 1 or more of Coxiella, Francisella, Rickettsia or Candidatus Midichloria mitochondrii endosymbionts, indicative of their importance to tick physiology. Genomic and experimental data suggest that endosymbionts promote tick development and reproductive success. Here, we review the limited information currently available on the potential roles endosymbionts play in enhancing tick metabolism and fitness. Future studies that expand on these findings are needed to better understand endosymbionts’ contributions to tick biology. This knowledge could potentially be applied to design novel strategies that target endosymbiont function to control the spread of ticks and pathogens they vector.

Thanks to modern molecular biology methods, our understanding of the impact of (endo)symbiotic bacteria on parasitic protists and helminths is growing fast. In this issue, 9 papers have been brought together that describe various facets of the relationships between these microorganisms, reveal their range and high frequency, as well as their capacity to create novel biological complexity. Comparative analyses of these host–endosymbiont interactions indicate that there may be no discrete types of relationships but rather a continuum ranging from a dispensable endosymbiont minimally integrated within the host cell to organelles, such as mitochondria and plastids that evolved into an indispensable, deeply integrated components of the cell. We hope that this series of studies on parasites and (endo)symbiotic bacteria will increase awareness about these relationships and their representation in microbial ecology models.

Mutualistic bacterial endosymbionts provide many benefits to their insect hosts, but their role in mating has not been studied in the past. In this study, we examined copulatory success and mating latency as two parameters of mating success to assess the influence of Candidatus Erwinia dacicola on mating between a laboratory population of olive flies (Bactrocera oleae Rossi) of Israel origin and a wild population of olive flies from Israel. Previous studies have shown that in many species of tephritid flies, laboratory-reared males have lower fitness and achieve fewer matings than wild males. Our research has shown that this Israeli population of olive flies reared in the laboratory on an artificial diet lacked an endosymbiont, Ca. E. dacicola, found in wild-caught insects from Israel. We hypothesized that decreased fitness and mating ability in laboratory-reared flies could be due to the absence of this endosymbiont. Mating assays between both sexes of these two Israeli populations revealed matings to occur primarily between laboratory-reared females and wild males. Laboratory-reared males achieved only 22% of the total matings. Candidatus Erwinia dacicola was found in significantly fewer insects from the laboratory population than in the wild population; within populations, male and female olive flies were equally likely to have the endosymbiont. However, differences in readiness to mate between the two populations, and not the presence of the endosymbiont, explained mating latency.

To determine whether host body size is the currency used by the aphidiine parasitoid, Lysiphlebus ambiguus Haliday (Hymenoptera: Braconidae), in assessing host quality, the aphid, Aphis fabae Scopoli (Homoptera: Aphididae), was reared at either high or low temperature to yield hosts of the same instar with different body sizes. Cohorts of A. fabae raised at 15°C and 30°C and exposed to individual female L. ambiguus in no-choice tests were successfully parasitized in all host stages from 1st instar nymphs to adults. However, younger and smaller aphids were more susceptible to parasitism than older and larger nymphs or adults, as measured by the number of mummies produced. For aphid cohorts reared at 15°C, the proportion of female progeny, progeny adult size, and development time all increased linearly with aphid size at the time of attack. In contrast, for aphid cohorts raised at 30°C, the proportion of female progeny and progeny adult size declined with aphid size, while development time remained unaffected. Through manipulation of host rearing temperature, we have shown that at cooler temperatures the koinobiont parasitoid, L. ambiguus, responds to host size in the same way as an idiobiont parasitoid, but that this response is compromised at higher temperatures. Our results suggest that differential mortality during development is likely to influence the observed secondary sex ratio in relation to aphid size for aphid cohorts raised at higher temperatures due to disruption of the activity of the host's primary endosymbiont and that such reduced nutritional quality of aphids cannot be compensated by increased development time.

Blastocrithidia culicis is an insect trypanosomatid that presents bacterial endosymbionts. The cell-associated and secreted proteinases of the endosymbiont-bearing and aposymbiotic strains were compared through the incorporation of proteinaceous substrates into sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). Few qualitative changes could be detected in the proteolytic zymograms in the 2 strains studied when gelatin, casein, haemoglobin or bovine serum albumin (BSA) were tested. However, the level of proteolytic activities was significantly higher in the aposymbiotic strain. Some of the B. culicis proteins reacted in Western blots with antibodies raised against gp63, a zinc-metalloproteinase, and cruzipain, a cysteinyl-proteinase, which are virulence factors of the human pathogenic trypanosomatids, Leishmania spp. and Trypanosoma cruzi, respectively. The anti-cross-reacting determinant (CRD) antibody recognized 2 polypeptides (50 and 58 kDa) in the spent culture media and in the supernatant from glycosylphosphatidylinositol-phospholipase C (GPI-PLC)-treated cells, suggesting that these proteins are GPI-anchored to the plasma membrane. In addition, the anti-gp63 reacted with the 50 kDa protein. The identification of protein homologues in trypanosomatids with distinct life-cycles may help to determine the importance of proteinases in trypanosomatids.