Core genome phylogenetic analysis of the avian associated Borrelia turdi indicates a close relationship to Borrelia garinii.

Borrelia burgdorferi sensu lato comprises a species complex of tick-transmitted bacteria that includes the agents of human Lyme borreliosis. Borrelia turdi is a genospecies of this complex that exists in cryptic transmission cycles mainly between ornithophilic tick vectors and their avian hosts. The species has been originally discovered in avian transmission cycles in Asia but has increasingly been found in Europe. Next generation sequencing was used to sequence the genome of B. turdi isolates obtained from ticks feeding on birds in Portugal to better understand the evolution and phylogenetic relationship of this avian and ornithophilic tick-associated genospecies. Here we use draft genomes of these B. turdi isolates for comparative analysis and to determine the taxonomic position within the B. burgdorferi s.l. species complex. The main chromosomes showed a maximum similarity of 93% to other Borrelia species whilst most plasmids had lower similarities. All three isolates had nine or 10 plasmids and, interestingly, one plasmid with a novel partitioning protein; this plasmid was termed lp30. Phylogenetic analysis of multilocus sequence typing housekeeping genes and 113 single copy orthologous genes revealed that the isolates clustered according to their classification as B. turdi. In phylogenies generated from these 113 genes the isolates cluster together with other Eurasian genospecies and form a sister clade to the avian associated B. garinii and the rodent associated B. bavariensis. These findings show that Borrelia species maintained in cryptic ecological cycles need to be included to fully understand the complex ecology and evolutionary history of this bacterial species complex.

Experimental infection by microparasites affects the oxidative balance in their avian reservoir host the blackbird Turdus merula.

By draining resources, microparasites can negatively affect the host fitness, which in turn can result in reduced transmission when virulence leads to reductions in host population size. Therefore, for a microparasite to persist in nature, the level of harm it can do to its host is expected to be limited. We tested this hypothesis for tick-borne Borrelia burgdorferi sensu lato (s.l.) infections in the blackbird Turdus merula, one of the most important avian reservoir hosts in Europe. Experimental and observational data were combined to examine the physiological effects caused by B. burgdorferi s.l. infection in blackbirds. Pathogen-free blackbirds were exposed to B. burgdorferi s.l.-infected Ixodes ricinus and I. frontalis nymphs, and compared with a control group (exposed to naïve laboratory-derived I. ricinus nymphs). Their physiological status was evaluated before and after infection with B. burgdorferi s.l., through a set of immunological (erythrocyte sedimentation rate, haptoglobin, white blood cell count and heterophil/lymphocyte ratio), oxidative stress (glutathione peroxidase activity, protein carbonyls and nitric oxide) and general body condition variables (body condition, glucose and haematocrit). Infected males showed higher levels of oxidative damage to proteins (increased levels of protein carbonyls), decreased glutathione peroxidase activity and increased body mass. Infected females had higher levels of glutathione peroxidase activity after infection by B. burgdorferi s.l. than the control group. No significant effects of B. burgdorferi s.l. infection were detected on erythrocyte sedimentation rate, haptoglobin, heterophil/lymphocyte ratio, nitric oxide, glucose and haematocrit. The first experimental study on the effects of B. burgdorferi s.l. on its avian reservoir hosts shows that these bacteria may inflict non-negligible physiological costs. We speculate that during energetically demanding periods, these physiological costs may reduce host fitness and affect pathogen transmission.

High Resilience of Seed Dispersal Webs Highlighted by the Experimental Removal of the Dominant Disperser.

The pressing need to conserve and restore habitats in the face of ongoing species loss [1, 2] requires a better understanding of what happens to communities when species are lost or reinstated [3, 4]. Theoretical models show that communities are relatively insensitive to species loss [5, 6]; however, they disagree with field manipulations showing a cascade of extinctions [7, 8] and have seldom been tested under field conditions (e.g., [9]). We experimentally removed the most abundant seed-dispersing ant species from seed dispersal networks in a Mediterranean landscape, replicating the experiment in three types of habitat, and then compared these communities to un-manipulated control communities. Removal did not result in large-scale changes in network structure. It revealed extensive structural plasticity of the remaining community, which rearranged itself through rewiring, while maintaining its functionality. The remaining ant species widened their diet breadth in a way that maintained seed dispersal, despite the identity of many interactions changing. The species interaction strength decreased; thus, the importance of each ant species for seed dispersal became more homogeneous, thereby reducing the dependence of seed species on one dominant ant species. Compared to the experimental results, a simulation model that included rewiring considerably overestimated the effect of species loss on network robustness. If community-level species loss models are to be of practical use in ecology or conservation, they need to include behavioral and population responses, and they need to be routinely tested under field conditions; doing this would be to the advantage of both empiricists and theoreticians.