SummaryThe natural habitats and potential reservoirs of the nosocomial pathogen Acinetobacter baumannii are poorly defined. Here, we put forth and tested the hypothesis of avian reservoirs of A. baumannii. We screened tracheal and rectal swab samples from livestock (chicken, geese) and wild birds (white stork nestlings) and isolated A. baumannii from 3% of sampled chicken (n 5 220), 8% of geese (n 5 40) and 25% of white stork nestlings (n 5 661). Virulence of selected avian A. baumannii isolates was comparable to that of clinical isolates in the Galleria mellonella infection model. Whole genome sequencing revealed the close relationship of an antibiotic-susceptible chicken isolate from Germany with a multidrug-resistant human clinical isolate from China and additional linkages between livestock isolates and human clinical isolates related to international clonal lineages. Moreover, we identified stork isolates related to human clinical isolates from the United States. Multilocus sequence typing disclosed further kinship between avian and human isolates. Avian isolates do not form a distinct clade within the phylogeny of A. baumannii, instead they diverge into different lineages. Further, we provide evidence that A. baumannii is constantly present in the habitats occupied by storks. Collectively, our study suggests A. baumannii could be a zoonotic organism that may disseminate into livestock.
Animal home‐ranges are expressions of the biology and ecology of a species, and their size is often considered to be a proxy for habitat quality. Understanding the factors affecting variation in home‐range size may aid prediction of the impact of local or global environmental change on studied populations. To this end, we established an international collaborative programme to gather GPS telemetry data on the Lesser Spotted Eagle Clanga pomarina across a large part of its range. The breeding season home‐ranges of 58 individuals from Estonia, Lithuania, Poland, Hungary and Romania were estimated using autocorrelated kernel density estimation. Differences in home‐range size were analysed using linear mixed‐effects models incorporating global (latitude, longitude, climate) and local (habitat heterogeneity, land cover, topography, human disturbance) variables. Home‐range was significantly affected by habitat heterogeneity, vegetation cover and human disturbance, and also by climate, increasing with greater temperature seasonality. A quadratic relationship between home‐range and Shannon diversity index, found in males, suggests that Eagles use less space in the least and most diverse habitats. Home‐ranges were also smaller close to human settlements, but range size was positively correlated with human population density. The first result reflects the positive influence of agricultural management on prey availability, whereas the second reflects negative impacts of disturbance and loss of foraging space. Home‐ranges of male Eagles were relatively consistent in size and were more linked to environmental conditions compared with those of females. Female home‐ranges were significantly more variable in size and showed less distinctive patterns of relationship with the tested predictors. Sex‐dependent variation in home‐range may result from the different roles of males and females in breeding activities and territoriality limitations of males. The latter factor both limited and increased the home‐range size in different individuals.
Whether Ca and other micronutrients are equally distributed in an avian eggshell over its longitudinal section and what portion of these local resources are utilized by developing embryos are unanswered questions in avian reproductive physiology. Here, we measured the thickness and concentrations of Ca and 16 other chemical elements (Al, As, Cd, Co, Cr, Cu, Fe, Hg, K, Mg, Mn, Na, Ni, Pb, Se, and Sr) in 4 shell regions (sharp pole, equator, shoulder, blunt pole) of White Stork (Ciconia ciconia) eggs representing different stages of embryonic development, from unresorbed eggshells to almost fully resorbed ones (with near-to-hatch embryos). We found that unresorbed eggshells displayed several significant differences in the concentrations of 15 elements (Al, As, Ca, Cd, Co, Cr, Fe, K, Hg, Mg, Mn, Na, Ni, Se, and Sr) between various regions of the same shell. Only 2 metals (As and Ca) showed a cross-sectional decrease in concentrations from the sharp pole to the blunt one. In particular, we observed that unresorbed eggshells at the blunt pole were less calcified (with 2.4% less Ca) compared to the sharp pole. In contrast, the concentrations of 6 other metals (Co, Fe, Mg, Mn, Na, and Se) peaked in the relatively less calcified region of the blunt pole, where concentrations (such as Se) were up to 10 times as high as in other regions of unresorbed eggshells. Our findings highlight that eggshells over their longitudinal sections are not chemically homogeneous. Surprisingly, however, and contrary to our expectations, we found that unresorbed eggshells were thinner (2.1–5.9% less depending on the region) and at the same time more strongly calcified than resorbed eggshells. This suggests that some modification has occurred in the shell structure and raises the question of thin-shelled eggs in populations of wild birds.
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