Genome Degradation in Brucella ovis Corresponds with Narrowing of Its Host Range and Tissue Tropism

Brucella ovis is a veterinary pathogen associated with epididymitis in sheep. Despite its genetic similarity to the zoonotic pathogens B. abortus, B. melitensis and B. suis, B. ovis does not cause zoonotic disease. Genomic analysis of the type strain ATCC25840 revealed a high percentage of pseudogenes and increased numbers of transposable elements compared to the zoonotic Brucella species, suggesting that genome degradation has occurred concomitant with narrowing of the host range of B. ovis. The absence of genomic island 2, encoding functions required for lipopolysaccharide biosynthesis, as well as inactivation of genes encoding urease, nutrient uptake and utilization, and outer membrane proteins may be factors contributing to the avirulence of B. ovis for humans. A 26.5 kb region of B. ovis ATCC25840 Chromosome II was absent from all the sequenced human pathogenic Brucella genomes, but was present in all of 17 B. ovis isolates tested and in three B. ceti isolates, suggesting that this DNA region may be of use for differentiating B. ovis from other Brucella spp. This is the first genomic analysis of a non-zoonotic Brucella species. The results suggest that inactivation of genes involved in nutrient acquisition and utilization, cell envelope structure and urease may have played a role in narrowing of the tissue tropism and host range of B. ovis

Forest-fire regimes affect thermoregulatory opportunities for terrestrial ectotherms

Fire-induced changes in canopy openness may affect sunlight penetration to the forest floor, and thus the operative temperatures available to terrestrial ectotherms. We examined thermal regimes for two types of ectotherms: diurnally active species that utilize sun-exposed patches to regulate their body temperatures, and nocturnally active species that depend upon solar radiation striking the rocks under which they shelter. We measured canopy openness, shrub height, radiation transmission and operative environmental temperatures in the open and inside reptile retreat-sites, at 24 study sites in eucalypt forests in two regions (Gosford and Yengo) in south-eastern Australia. All sites were last burnt in 2000-2001, but had experienced different fire frequencies (1-4 fires over the previous 37years). In Gosford, higher fire frequencies reduced canopy openness and radiation transmission at ground and shrub level, and thus reduced environmental temperatures and the thermal quality of reptile habitats. Our modelling based on thermal preferenda of an endangered snake species (the broad-headed snake Hoplocephalus bungaroides) suggests that increased fire frequency at Gosford halved the amount of time an animal could spend within its preferred (set-point) range, regardless of whether it thermoregulated beneath rocks or basked out in the open. At Yengo, however, fire frequency did not affect the thermal quality of reptile habitats. Thus, the effects of fire frequency on forest structure and the thermal environment at ground level differed between adjacent areas, and relatively small changes in canopy openness translated into major effects on thermoregulatory opportunities for reptiles. Although fire is a useful management tool for creating open habitats, we need to understand more about the effects of fire frequency on vegetation structure and thermal environment before we can use fire to manage habitats for reptiles. © 2012 Ecological Society of Australia

Evidence for a Role of the Polysaccharide Capsule Transport Proteins in Pertussis Pathogenesis

Polysaccharide (PS) capsules are important virulence determinants for many bacterial pathogens. Bordetella pertussis, the agent of whooping cough, produces a surface associated microcapsule but its role in pertussis pathogenesis remained unknown. Here we showed that the B. pertussis capsule locus is expressed in vivo in murine lungs and that absence of the membrane-associated protein KpsT, involved in the transport of the PS polymers across the envelope, but not the surface-exposed PS capsule itself, affects drastically B. pertussis colonization efficacy in mice. Microarray analysis revealed that absence of KpsT in B. pertussis resulted in global down-regulation of gene expression including key virulence genes regulated by BvgA/S, the master two-component system. Using a BvgS phase-locked mutant, we demonstrated a functional link between KpsT and BvgA/S-mediated signal transduction. Whereas pull-down assays do not support physical interaction between BvgS sensor and any of the capsule locus encoded proteins, absence of KpsT impaired BvgS oligomerization, necessary for BvgS function. Furthermore, complementation studies indicated that instead of KpsT alone, the entire PS capsule transport machinery spanning the cell envelope likely plays a role in BvgS-mediated signal transduction. Our work thus provides the first experimental evidence of a role for a virulence-repressed gene in pertussis pathogenesis