@article{HlinakMuehleWerneretal.2006, author = {Hlinak, Andreas and M{\"u}hle, Ralf-Udo and Werner, Ortrud and Globig, Anja and Starick, Elke and Schirrmeier, Horst and Hoffmann, Bernd and Engelhardt, Andreas and H{\"u}bner, Dagmar and Conraths, Franz J. and Wallschl{\"a}ger, Hans-Dieter and Kruckenberg, Helmut and M{\"u}ller, Thomas}, title = {A virological survey in migrating waders and other waterfowl in one of the most important resting sites of Germany}, issn = {0931-1793}, year = {2006}, abstract = {Wild birds are considered a potential reservoir or a carrier of viral diseases and may therefore play a role in the epidemiology of economically important or zoonotic diseases. In 2001 and 2002, a survey with special emphasis oil virus isolation in migrating waders and some other birds were conducted. In one of the most important inland resting sites for migratory waterfowl, tracheal and cloacal swabs were collected from 465 waders representing 19 different species, and 165 other birds that were not captured on purpose. A total of 42 avian viruses were isolated, 34 of these were identified as paramyxoviruses (PMVs). The majority of isolates came from waders and wild ducks, and were characterized as PMV-1. In contrast, PMV-4 was found in wild ducks only, PMV-6 was mainly detected in wader species. Four avian influenza viruses (ATVs), belonging to H4 and H3 haemagglutinin subtype, were isolated from wild duck species. Furthermore, four reo-like viruses were isolated from one particular wader species for the first time. The majority of virus positive birds were < 1 year old and did not show any clinical symptoms. There was no evidence for the presence of West Nile virus in these birds. These results confirm that the restricted resting sites in Western Europe must be considered as important locations for the intra- and interspecies transmission of avian viruses}, language = {en} } @article{BauerStammVirnichetal.2006, author = {Bauer, Joachim and Stamm, Axel and Virnich, Katharina and Wissing, Karen and M{\"u}ller, Udo and Wirsching, Michael and Schaarschmidt, Uwe}, title = {Correlation between burnout syndrome and psychological and psychosomatic symptoms among teachers}, issn = {0340-0131}, doi = {10.1007/s00420-005-0050-y}, year = {2006}, abstract = {Objectives: Psychosomatic disorders and symptoms that correlate with the so-called burnout syndrome turned out to be the main cause of increasing rates of premature retirement of school teachers. The aim of this study was to evaluate the relation between occupational burden and psychological strain of teachers who are still in work. Methods: A sample of 408 teachers at ten grammar schools (am: High school; German: Gymnasium) in south-western Germany was evaluated. To determine the styles of coping with occupational burden we used the measure of coping capacity questionnaire (MECCA). To analyse the psychopathological and psychosomatic symptom load we applied SCL 90 R questionnaire. Results: According to the MECCA questionnaire, 32.5\% of the sample suffered from burnout (type B), 17.7\% suffered severe strain (type A), 35.9\% showed an unambitious (type S) and 13.8\% showed a healthy-ambitious coping style (type G). Burnout was significantly higher among women, divorced teachers and teachers working part-time. As part of the MECCA, teachers were asked to rate what they regarded as the strongest factor resulting in occupational burden. Teachers indicated that, besides high numbers of pupils in one class, they regarded destructive and aggressive behaviour of pupils as the primary stress factor. According to the SCL 90 R, 20\% of the sample showed a severe degree (defined as > 70 points in the SCL90R GSI) of psychological and psychosomatic symptoms. MECCA type B (burnout) correlated significantly with high psychological and psychosomatic symptom load according to the SCL90R. Conclusions: In school teachers, burnout syndrome, a construct that derived from occupational psychology and occupational medicine, is significantly correlated with psychological and psychosomatic symptoms. Teachers rate destructive and aggressive behaviour of pupils as the primary stress factor.}, language = {en} } @article{HlinakMuellerKrameretal.1998, author = {Hlinak, Andreas and M{\"u}ller, Thomas and Kramer, Matthias and M{\"u}hle, Ralf-Udo and Liebherr, Helga and Ziedler, Klaus}, title = {Serological survey of viral pathogens in bean and white-fronted geese from Germany}, issn = {0090-3558}, year = {1998}, language = {en} } @article{KruckenbergMuellerFreulingetal.2011, author = {Kruckenberg, Helmut and M{\"u}ller, Thomas and Freuling, Conrad and M{\"u}hle, Ralf-Udo and Globig, Anja and Schirrmeier, Horst and Buss, Melanie and Harder, Timm and Kramer, Matthias and Teske, Kathrin and Polderdijk, Kees and Wallschl{\"a}ger, Hans-Dieter and Hlinak, Andreas}, title = {Serological and virological survey and resighting of marked wild geese in Germany}, series = {European journal of wildlife research}, volume = {57}, journal = {European journal of wildlife research}, number = {5}, publisher = {Springer}, address = {New York}, issn = {1612-4642}, doi = {10.1007/s10344-011-0514-1}, pages = {1025 -- 1032}, year = {2011}, abstract = {In order to investigate the potential role of arctic geese in the epidemiology, the spatial and temporal spread of selected avian diseases, in autumn 2002, a virological and serological survey designed as capture-mark-resighting study was conducted in one of the most important coastal resting sites for migratory waterfowl in Germany. Orophatyngeal, cloacal swabs and blood samples were collected from a total of 147 birds comprising of three different arctic geese species including White-fronted Goose (Anser albifrons), Tundra Bean Goose (Anser fabalis rossicus), Pink-footed Goose (Anser brachyrhynchus) as well as from 29 non-migratory Canada Geese (Branta canadensis). Altogether, six adeno-like viruses (ALV; 95\% CI, 1.74-9.92\%) and two avian paramyxoviruses (APMV-4; 95\% Cl, 0.19-5.53\%) were isolated mainly from juvenile White-fronted Geese. In addition, four Canada Geese were infected with lentogenic APMV-1 (95\% CI, 3.89-31.66\%) at the date of sampling. No avian influenza viruses, reo-like viruses could be isolated despite serological evidence. Likewise, no evidence of current or previous infection by West Nile virus was found. Of the 147 birds tagged in the following years, 137 birds were resighted between 2002 and 2008 accumulating to 1925 sightings. About 90\% of all sightings were reported from the main wintering and resting sites in Germany and The Netherlands. Eight of the resighted geese were virus positive (ALV and APMV-4) at the time point of sampling in 2002.}, language = {en} } @article{SchatzFreulingAueretal.2014, author = {Schatz, Juliane and Freuling, Conrad Martin and Auer, Ernst and Goharriz, Hooman and Harbusch, Christine and Johnson, Nicholas and Kaipf, Ingrid and Mettenleiter, Thomas Christoph and Muehldorder, Kristin and Muehle, Ralf-Udo and Ohlendorf, Bernd and Pott-D{\"o}rfer, B{\"a}rbel and Prueger, Julia and Ali, Hanan Sheikh and Stiefel, Dagmar and Teubner, Jens and Ulrich, Rainer G{\"u}nter and Wibbelt, Gudrun and M{\"u}ller, Thomas}, title = {Enhanced passive bat rabies surveillance in indigenous bat species from Germany - A retrospective study}, series = {PLoS neglected tropical diseases}, volume = {8}, journal = {PLoS neglected tropical diseases}, number = {5}, publisher = {PLoS}, address = {San Fransisco}, issn = {1935-2735}, doi = {10.1371/journal.pntd.0002835}, pages = {9}, year = {2014}, abstract = {In Germany, rabies in bats is a notifiable zoonotic disease, which is caused by European bat lyssaviruses type 1 and 2 (EBLV-1 and 2), and the recently discovered new lyssavirus species Bokeloh bat lyssavirus (BBLV). As the understanding of bat rabies in insectivorous bat species is limited, in addition to routine bat rabies diagnosis, an enhanced passive surveillance study, i.e. the retrospective investigation of dead bats that had not been tested for rabies, was initiated in 1998 to study the distribution, abundance and epidemiology of lyssavirus infections in bats from Germany. A total number of 5478 individuals representing 21 bat species within two families were included in this study. The Noctule bat (Nyctalus noctula) and the Common pipistrelle (Pipistrellus pipistrellus) represented the most specimens submitted. Of all investigated bats, 1.17\% tested positive for lyssaviruses using the fluorescent antibody test (FAT). The vast majority of positive cases was identified as EBLV-1, predominately associated with the Serotine bat (Eptesicus serotinus). However, rabies cases in other species, i.e. Nathusius' pipistrelle bat (Pipistrellus nathusii), P. pipistrellus and Brown long-eared bat (Plecotus auritus) were also characterized as EBLV-1. In contrast, EBLV-2 was isolated from three Daubenton's bats (Myotis daubentonii). These three cases contribute significantly to the understanding of EBLV-2 infections in Germany as only one case had been reported prior to this study. This enhanced passive surveillance indicated that besides known reservoir species, further bat species are affected by lyssavirus infections. Given the increasing diversity of lyssaviruses and bats as reservoir host species worldwide, lyssavirus positive specimens, i.e. both bat and virus need to be confirmed by molecular techniques.}, language = {en} } @article{HlinakMuellerKrameretal.1999, author = {Hlinak, Andreas and M{\"u}ller, Thomas and Kramer, Matthias and M{\"u}hle, Ralf-Udo and Liebherr, Helga and Ziedler, Klaus}, title = {A descriptive analysis of the potenrial association between migration patterns of bean and white-fronted geese and the occurence of newcastle disease outbreaks in domestic birds}, issn = {0005-2086}, year = {1999}, abstract = {Sightings and migration patterns of 65 bean and 65 white-fronted geese are reported. These geese were tagged and serologically screened. 19 of the 53 birds sighted had serologic evidence of Newcastle Disease. The migration patterns of the wild geese provided further evidence that the main resting and wintering sites of migratory waterfowl are likely to be important for the inter- and intraspecies transmission of avian diseases.}, language = {en} } @misc{SchatzOhlendorfBusseetal.2013, author = {Schatz, Juliane and Ohlendorf, Bernd and Busse, Peter and Pelz, Gerrit and Dolch, Dietrich and Teubner, Jens and Encarnacao, Jorge A. and M{\"u}hle, Ralf-Udo and Fischer, M. and Hoffmann, Bernd and Kwasnitschka, Linda and Balkema-Buschmann, Anne and Mettenleiter, Thomas Christoph and M{\"u}ller, T. and Freuling, Conrad M.}, title = {Twenty years of active bat rabies surveillance in Germany}, series = {Postprints der Universit{\"a}t Potsdam Humanwissenschaftliche Reihe}, journal = {Postprints der Universit{\"a}t Potsdam Humanwissenschaftliche Reihe}, number = {533}, issn = {1866-8364}, doi = {10.25932/publishup-41514}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-415140}, pages = {12}, year = {2013}, abstract = {In Germany, active bat rabies surveillance was conducted between 1993 and 2012. A total of 4546 oropharyngeal swab samples from 18 bat species were screened for the presence of EBLV-1- , EBLV-2- and BBLV-specific RNA. Overall, 0 center dot 15\% of oropharyngeal swab samples tested EBLV-1 positive, with the majority originating from Eptesicus serotinus. Interestingly, out of seven RT-PCR-positive oropharyngeal swabs subjected to virus isolation, viable virus was isolated from a single serotine bat (E. serotinus). Additionally, about 1226 blood samples were tested serologically, and varying virus neutralizing antibody titres were found in at least eight different bat species. The detection of viral RNA and seroconversion in repeatedly sampled serotine bats indicates long-term circulation of the virus in a particular bat colony. The limitations of random-based active bat rabies surveillance over passive bat rabies surveillance and its possible application of targeted approaches for future research activities on bat lyssavirus dynamics and maintenance are discussed.}, language = {en} } @article{BroekerGohlkeMuelleretal.2013, author = {Br{\"o}ker, Nina Kristin and Gohlke, Ulrich and M{\"u}ller, J{\"u}rgen J. and Uetrecht, Charlotte and Heinemann, Udo and Seckler, Robert and Barbirz, Stefanie}, title = {Single amino acid exchange in bacteriophage HK620 tailspike protein results in thousand-fold increase of its oligosaccharide affinity}, series = {Glycobiology}, volume = {23}, journal = {Glycobiology}, number = {1}, publisher = {Oxford Univ. Press}, address = {Cary}, issn = {0959-6658}, doi = {10.1093/glycob/cws126}, pages = {59 -- 68}, year = {2013}, abstract = {Bacteriophage HK620 recognizes and cleaves the O-antigen polysaccharide of Escherichia coli serogroup O18A1 with its tailspike protein (TSP). HK620TSP binds hexasaccharide fragments with low affinity, but single amino acid exchanges generated a set of high-affinity mutants with submicromolar dissociation constants. Isothermal titration calorimetry showed that only small amounts of heat were released upon complex formation via a large number of direct and solvent-mediated hydrogen bonds between carbohydrate and protein. At room temperature, association was both enthalpy- and entropy-driven emphasizing major solvent rearrangements upon complex formation. Crystal structure analysis showed identical protein and sugar conformers in the TSP complexes regardless of their hexasaccharide affinity. Only in one case, a TSP mutant bound a different hexasaccharide conformer. The extended sugar binding site could be dissected in two regions: first, a hydrophobic pocket at the reducing end with minor affinity contributions. Access to this site could be blocked by a single aspartate to asparagine exchange without major loss in hexasaccharide affinity. Second, a region where the specific exchange of glutamate for glutamine created a site for an additional water molecule. Side-chain rearrangements upon sugar binding led to desolvation and additional hydrogen bonding which define this region of the binding site as the high-affinity scaffold.}, language = {en} } @article{SeulMuellerAndresetal.2014, author = {Seul, Anait and M{\"u}ller, J{\"u}rgen J. and Andres, Dorothee and Stettner, Eva and Heinemann, Udo and Seckler, Robert}, title = {Bacteriophage P22 tailspike: structure of the complete protein and function of the interdomain linker}, series = {Acta crystallographica : Section D, Biological crystallography}, volume = {70}, journal = {Acta crystallographica : Section D, Biological crystallography}, publisher = {Wiley-Blackwell}, address = {Hoboken}, issn = {1399-0047}, doi = {10.1107/S1399004714002685}, pages = {1336 -- 1345}, year = {2014}, abstract = {Attachment of phages to host cells, followed by phage DNA ejection, represents the first stage of viral infection of bacteria. Salmonella phage P22 has been extensively studied, serving as an experimental model for bacterial infection by phages. P22 engages bacteria by binding to the sugar moiety of lipopolysaccharides using the viral tailspike protein for attachment. While the structures of the N-terminal particle-binding domain and the major receptor-binding domain of the tailspike have been analyzed individually, the three-dimensional organization of the intact protein, including the highly conserved linker region between the two domains, remained unknown. A single amino-acid exchange in the linker sequence made it possible to crystallize the full-length protein. Two crystal structures of the linker region are presented: one attached to the N-terminal domain and the other present within the complete tailspike protein. Both retain their biological function, but the mutated full-length tailspike displays a retarded folding pathway. Fitting of the full-length tailspike into a published cryo-electron microscopy map of the P22 virion requires an elastic distortion of the crystal structure. The conservation of the linker suggests a role in signal transmission from the distal tip of the molecule to the phage head, eventually leading to DNA ejection.}, language = {en} } @article{BarbirzMuellerUetrechtetal.2008, author = {Barbirz, Stefanie and M{\"u}ller, J{\"u}rgen J. and Uetrecht, Charlotte and Clark, Alvin J. and Heinemann, Udo and Seckler, Robert}, title = {Crystal structure of Escherichia coli phage HK620 tailspike : podoviral tailspike endoglycosidase modules are evolutionarily related}, issn = {0950-382X}, year = {2008}, abstract = {Bacteriophage HK620 infects Escherichia coli H and is closely related to Shigella phage Sf6 and Salmonella phage P22. All three Podoviridae recognize and cleave their respective host cell receptor polysaccharide by homotrimeric tailspike proteins. The three proteins exhibit high sequence identity in the 110 residues of their N-terminal particle- binding domains, but no apparent sequence similarity in their major, receptor-binding parts. We have biochemically characterized the receptor-binding part of HK620 tailspike and determined its crystal structure to 1.38 {\AA} resolution. Its major domain is a right-handed parallel ;-helix, as in Sf6 and P22 tailspikes. HK620 tailspike has endo-N- acetylglucosaminidase activity and produces hexasaccharides of an O18A1-type O-antigen. As indicated by the structure of a hexasaccharide complex determined at 1.6 {\AA} resolution, the endoglycosidase-active sites are located intramolecularly, as in P22, and not between subunits, as in Sf6 tailspike. In contrast, the extreme C-terminal domain of HK620 tailspike forms a ;-sandwich, as in Sf6 and unlike P22 tailspike. Despite the different folds, structure-based sequence alignments of the C-termini reveal motifs conserved between the three proteins. We propose that the tailspike genes of P22, Sf6 and HK620 have a common precursor and are not mosaics of unrelated gene fragments.}, language = {en} } @article{MuellerBarbirzHeinleetal.2008, author = {M{\"u}ller, J{\"u}rgen J. and Barbirz, Stefanie and Heinle, Karolin and Freiberg, Alexander and Seckler, Robert and Heinemann, Udo}, title = {An intersubunit active site between supercoiled parallel beta helices in the trimeric tailspike endorhamnosidase of Shigella flexneri phage Sf6}, doi = {10.1016/j.str.2008.01.019}, year = {2008}, abstract = {Sf6 belongs to the Podoviridae family of temperate bacteriophages that infect gram-negative bacteria by insertion of their double-stranded DNA. They attach to their hosts specifically via their tailspike proteins. The 1.25 {\AA} crystal structure of Shigella phage Sf6 tailspike protein (Sf6 TSP) reveals a conserved architecture with a central, right-handed ; helix. In the trimer of Sf6 TSP, the parallel ; helices form a left-handed, coiled;; coil with a pitch of 340 {\AA}. The C-terminal domain consists of a ; sandwich reminiscent of viral capsid proteins. Further crystallographic and biochemical analyses show a Shigella cell wall O-antigen fragment to bind to an endorhamnosidase active site located between two ;-helix subunits each anchoring one catalytic carboxylate. The functionally and structurally related bacteriophage, P22 TSP, lacks sequence identity with Sf6 TSP and has its active sites on single subunits. Sf6 TSP may serve as an example for the evolution of different host specificities on a similar general architecture.}, language = {en} }