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Drewes, S.

Publications and source records attributed to Drewes, S..

2 recordsLinked to original sources

Maternal antibody-mediated elimination of a Puumala hantavirus outbreak in a bank vole colony

Bank voles (Myodes glareolus syn. Clethrionomys glareolus) are frequently used as an animal model in ecological and biomedical studies, and are important reservoir of viral and bacterial zoonotic pathogens, e.g. of Puumala hantavirus (PUUV). Here we describe an accidental PUUV outbreak in a large bank vole laboratory colony by incursion of infected wild-trapped bank voles, and a successful eradication of the virus. The eradication plan was based on results of previous studies, which showed that maternal antibodies (MatAb) protect the young from infection for up to 40 days after the weaning, four weeks longer than the estimated duration of maintaining infectivity of PUUV in the environment. After ensuring that most animals are infected, 620 pairs were mated on the same day. Only females that showed PUUV-specific antibodies and gave offspring within 26 days after the mating were retained. All individuals of the parental generation were euthanized before the last weaning. The weaned offspring was moved to individually ventilated cages (IVC) and repeatedly tested for the presence of PUUV-specific antibodies and RNA. A few infected and suspicious animals were euthanised. Then the animals were mated (in IVC) and after producing grand-offspring euthanised and tested for PUUV RNA in lungs. No PUUV RNA was detected, and no animals showed PUUV-specific antibodies in next generations. The successful clearance confirmed the protective efficiency of PUUV-specific MatAb. The procedure for clearance of PUUV in the bank vole colony may represent a blueprint for similar approaches in precious colonies of other rodents infected by similar pathogens. Author SummaryIn 2006 we started a unique long-term experiment on the bank vole, a common European rodent. Our goal was to study how animals can adapt to different challenges - a process called adaptive radiation. We established 16 vole lines: four control lines and others selected for specific behavioural and physiological traits. Over the years, this colony became an important model for studying evolution, physiology, and behaviour. Unfortunately, the colony became infected with Puumala hantavirus. The virus is mild for voles but can cause serious zoonotic illness in humans, without specific medical treatment available. At first, it seemed that the entire colony would have to be destroyed - a loss of thousands of animals and many years of research. However, we used a natural advantage: young voles born to infected mothers are temporarily protected by maternal antibodies. By carefully planning breeding, isolation, and testing, we created conditions where the virus lost its strength before the young lost their protection. This simple yet challenging approach worked - we saved the colony. Because many animals respond to viruses in a similar way, our method can help rescue other valuable research populations without complex procedures like embryo transfer or cross-fostering.

zoology↗

On the ecology of Acinetobacter baumannii - jet stream rider and opportunist by nature

The natural reservoirs of the nosocomial pathogen Acinetobacter baumannii are not well defined. We previously identified white storks as a model system to study the ecology of A. baumannii. Having screened more than 1,300 white stork nestlings over a period of six years across different regions of Poland and Germany (overall isolation rate of [~]29.5%), including food chain analyses and environmental samplings, we come up with a detailed picture of the dynamics and diversity of A. baumannii in their natural habitats. Adult storks, rather than being stably colonized with strains of A. baumannii which are successively transferred to their offspring, instead initially encounter these bacteria while foraging. Among their common food sources, consisting of earthworms, small mammals, and insects, we identified earthworms as a potential source of A. baumannii, but more so the associated soil as well as plant roots. Through this, hotspot soil and compost habitats were identified which enable population dynamics to be studied over the course of the year. We demonstrate that sterilized plant material is rapidly colonized by airborne A. baumannii suggesting they patrol to search for novel habitats, being opportunist by nature. The prevalence of A. baumannii exhibited a strong seasonality and peaked during summer. The strains we collected in Poland and Germany represent more than 50% of the worldwide known diversity in terms of the intrinsic OXA-51-like {beta}-lactamase. A set of [~]400 genomes was determined and compared to a diverse set of publicly available genomes. Our pan-genome estimate of the species ([~]51,000 unique genes) more than doubles the amount proposed by previous studies. Core-genome based phylogenetic analyses illustrated numerous links between wildlife isolates and hospital strains, including ancient as well as recent intercontinental transfer. Our data further suggest massive radiation within the species early after its emergence, matching with human activity during the Neolithic. Deforestation in particular seemed to set the stage for this bloom as we found that forests do not provide conducive conditions for the proliferation of A. baumannii. In contrast, wet and nutrient-rich soil alongside rivers sampled during the summer can yield an isolation rate of [~]30%. Linking published work on the interaction between A. baumannii and fungi and on aspergillosis as a major cause of mortality in white stork nestlings to our findings, we hypothesized that fungi and A. baumannii share a long history of coevolution. Interaction studies revealed the capability of A. baumannii to adhere to fungal spores and to suppress spore germination. Taken together, the intrinsic resistance endowment and potential to acquire antibiotic resistance can be explained by coevolution with antibiotic-producing fungi and other microorganisms within soil, and resistance to desiccation stress and radiation can be interpreted in the light of intercontinental hitchhiking through fungal spores. Originality - SignificanceThe ecology of the nosocomial pathogen Acinetobacter baumannii remains poorly understood outside the hospital. Here, we present the most comprehensive study on its environmental biology to date, after having collected more than 1,450 independent isolates of which around 400 were whole genome-sequenced. This study more than doubles the size of the pan-genome of the species, illustrating both the diversity of our collection and the bias of previous work, but also the bottleneck for the establishment of lineages within the hospital environment. We reached isolation rates of about 30% both in white stork (Ciconia ciconia) nestlings and in soil samples when considering for sampling all preferences of A. baumannii we uncovered. Thus, it is now possible to study the ecology and evolution of A. baumannii in nature at an unprecedented temporal and spatial resolution. We describe the worldwide spread of A. baumannii lineages in nature as an ancient phenomenon that even surpasses that of human-associated bacteria in magnitude. This is likely due to airborne spread, putatively facilitated by association with fungal spores. We propose that A. baumannii is an opportunist by nature, using airborne patrolling to rapidly enter new suitable habitats consisting of organic matter in early stages of decomposition. Our collective data suggest that A. baumannii, early after its speciation, went through massive radiation during the Neolithic, likely due to deforestation, settlement and farming producing numerous favorable habitats. Their natural lifestyle, which requires rapid adaptability to various habitats as well as tolerance to desiccation, radiation and antibiotic stress, perfectly predispose these opportunistic pathogens to establish within the hospital setting. Comparison of genomes from environmental and clinical isolates will now enable studies of the adaptive evolution of environmental bacteria towards multidrug-resistant opportunistic pathogens.

microbiology↗