Larisa Bender
University of Würzburg
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Publication
Featured researches published by Larisa Bender.
Zentralblatt Fur Bakteriologie-international Journal of Medical Microbiology Virology Parasitology and Infectious Diseases | 1992
Helmut Tschäpe; Larisa Bender; Manfred Ott; Walter Wittig; Jörg Hacker
Escherichia coli O139:K82:H1 strains originating from outbreaks and single cases of oedema disease in pigs were characterized by their genomic restriction fragment length polymorphism (RFLP), their virulence pattern, and by the occurrence as well as the genomic distribution of the determinants for hemolysin (hly) and verotoxins (shiga-like toxins; sltI, sltII). Whereas the RFLPs revealed considerable variation among the E. coli O139:K82:H1 isolates depending the origin and epidemic source of the strains, the virulence gene slt II was found to be present in nearly all strains in a particular chromosomal region. Similar to RFLPs, the plasmid profiles are useful for epidemiological analysis.
Microbial Pathogenesis | 1991
Manfred Ott; Larisa Bender; Elizabeth Chirinos; Werner Ehret; Jörg Hacker
The protein PpIA (19 kD) cloned from a genomic library of Legionella pneumophila, Philadelphia 1, represents a peptido-glycan associated outer membrane protein in recombinant E. coli K-12 and L. pneumophila. It exhibits distinct sequence homology to lipoproteins of Haemophilus influenzae and E. coli. A ppIA specific DNA probe generated by PCR was used in Southern hybridizations of chromosomal DNA of Legionella strains and other Gram-negative pathogens. Under conditions of high stringency, hybridization could only be observed in L. pneumophila isolates, but all other Legionella strains tested displayed hybridization under lower stringency. No signals appeared after hybridization of chromosomal DNA from a variety of other bacteria. Using anti-PpIA monospecific polyclonal antibodies in Western blots, it was demonstrated that PpIA related proteins of nearly the same size are found in all L. pneumophila isolates and in a variety of, but not all, the Legionella species analysed here.
Fems Microbiology Letters | 1992
Manfred Ott; Larisa Bender; P. Christian Lück; Peter Meyer; Jörg Hacker
A hospital warm water system was monitored for the presence and distribution of legionellae. Subtyping of ten selected Legionella pneumophila isolates, originating from four different sites in the system by using serogroup specific antisera in an indirect immunofluorescence test, revealed that nine of the ten isolates belong to serogroup 6, while the remaining one was serogroup 10. Two monoclonal antibodies (mAbs) specific for a subgroup of serogroup 6 strains were further used for characterization. None of the strains reacted with these mAbs. Genome analysis by elaborating NotI profiles using the pulsed field gel electrophoresis (PFGE) technique revealed that nearly all serogroup 6 isolates derived from different sites, including a new building connected by a ring pipe, were identical according to restriction fragment patterns. The patterns were distinguishable from those of the two L. pneumophila serogroup 6 reference strains, and from that of the L. pneumophila serogroup 10 isolate. These data argue for a relatively homogeneous L. pneumophila serogroup 6 population in the entire water system.
Microbial Pathogenesis | 1990
Jörg Hacker; Larisa Bender; Manfred Ott; Jochen Wingender; Björn Lund; Reinhard Marre; Werner Goebel
Infection and Immunity | 1991
Manfred Ott; Larisa Bender; G Blum; M Schmittroth; Mark Achtman; Helmut Tschäpe; Jörg Hacker
Fems Microbiology Letters | 1990
Larisa Bender; Manfred Ott; Reinhard Marre; Jörg Hacker
Journal of Basic Microbiology | 1992
Bunty Jain; Larisa Bender; P. Christian Lück; Manfred Ott
Archive | 1992
Helmut Tschäpe; Larisa Bender; Manfred Ott; Walter Wittig; Jörg Hacker; Robert Koch-Institut
Archive | 1991
Larisa Bender; Manfred Ott; Jürgen H. Helbig; Jörg Hacker
Archive | 1991
Manfred Ott; Larisa Bender; Reinhard Marre; Jörg Hacker