F Allerberger

Österreichische Agentur für Gesundheit und Ernährungssicherheit, Wien, Vienna, Austria

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Publications (293)975.83 Total impact

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    ABSTRACT: The detection of West Nile virus (WNV) nucleic acid in a blood donation from Vienna, Aus-tria, as well as in Culex pipiens pupae and egg rafts, sampled close to the donor's residence , is reported. Complete genomic sequences of the human-and mosquito-derived viruses were established, genetically compared and phylogenetically analyzed. The viruses were not identical, but closely related to each other and to recent Czech and Italian isolates, indicating co-circulation of related WNV strains within a confined geographic area. The detection of WNV in a blood donation originating from an area with low WNV prevalence in humans (only three serologically diagnosed cases between 2008 and 2014) is surprising and emphasizes the importance of WNV nucleic acid testing of blood donations even in such areas, along with active mosquito surveillance programs.
    PLoS ONE 05/2015; 10(5). DOI:10.1371/journal.pone.0126381 · 3.53 Impact Factor
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    ABSTRACT: The European, multi-centre, quarterly point prevalence study of community-acquired diarrhea (EUCODI) analyzed stool specimens received at ten participating clinical microbiology laboratories (Austria, Finland, France, Germany, Greece, Ireland, Italy, Portugal, Romania and United Kingdom) in 2014. On four specified days, each local laboratory submitted samples from ≤20 consecutive patients to the Austrian Study Centre for further testing using FilmArray® GI Panel (BioFire Diagnostics, Salt Lake City, Utah). Of the 709 specimens from as many patients received, 325 (45.8%) tested negative, 268 (37.8%) specimens yielded only one organism, and 116 (16.4%) specimens yielded multiple organisms. Positivity rates ranged from 41% (30/73 samples) in France to 74% (59/80 samples) in Romania. With the exception of Entamoeba histolytica and Vibrio cholerae, all of the 22 targeted pathogens were detected at least once. Enteropathogenic E. coli (EPEC), Campylobacter spp., toxigenic Clostridium difficile, enteroaggregative E. coli (EAEC), norovirus and enterotoxigenic E. coli (ETEC) were the six most commonly detected pathogens. When tested by local protocols, 7/128 positive samples (5.5%) yielded multiple organisms. Overall, the FilmArray® GI Panel detected at least one organism in 54.2% (384/709) of the specimens, as compared to 18.1% (128/709) when tested by conventional techniques locally. This underlines the considerable potential of multiplex PCR to improve routine stool diagnostics in community acquired diarrhea. Classical culture methods directed at isolation of specific pathogens are increasingly becoming second line tools, deployed when rapid molecular tests are positive. This optimizes yield from stool examinations and dramatically improves timeliness of diagnosis. Copyright © 2015. Published by Elsevier Ltd.
    Clinical Microbiology and Infection 04/2015; DOI:10.1016/j.cmi.2015.04.007 · 5.20 Impact Factor
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    ABSTRACT: Methicillin-resistant Staphylococcus aureus is one of the most significant pathogens associated with health care. For efficient surveillance, control and outbreak investigation, S. aureus typing is essential. A high resolution melting curve analysis was developed and evaluated for rapid identification of the most frequent spa types found in an Austrian hospital consortium covering 2,435 beds. Among 557 methicillin-resistant Staphylococcus aureus isolates 38 different spa types were identified by sequence analysis of the hypervariable region X of the protein A gene (spa). Identification of spa types through their characteristic high resolution melting curve profiles was considerably improved by double spiking with genomic DNA from spa type t030 and spa type t003 and allowed unambiguous and fast identification of the ten most frequent spa types t001 (58%), t003 (12%), t190 (9%), t041 (5%), t022 (2%), t032 (2%), t008 (2%), t002 (1%), t5712 (1%) and t2203 (1%), representing 93% of all isolates within this hospital consortium. The performance of the assay was evaluated by testing samples with unknown spa types from the daily routine and by testing three different high resolution melting curve analysis real-time PCR instruments. The ten most frequent spa types were identified from all samples and on all instruments with 100% specificity and 100% sensitivity. Compared to classical spa typing by sequence analysis, this gene scanning assay is faster, cheaper and can be performed in a single closed tube assay format. Therefore it is an optimal screening tool to detect the most frequent endemic spa types and to exclude non-endemic spa types within a hospital.
    PLoS ONE 03/2015; 10(3). DOI:10.1371/journal.pone.0116713 · 3.53 Impact Factor
  • F Allerberger
    Clinical Microbiology and Infection 01/2015; DOI:10.1016/j.cmi.2015.01.010 · 5.20 Impact Factor
  • Franz Allerberger, Steliana Huhulescu
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    ABSTRACT: Listeriosis during pregnancy usually presents as an unremarkable febrile illness in the mother but can be fatal for the fetus and newborn. Reliable laboratory testing for early diagnosis is lacking. Serological antibody tests and bacteriological stool tests are not helpful since Listeria-specific antibodies and stool cultures yielding the organism can be found in healthy pregnant women. Because early diagnosis is difficult, diagnosis is usually made by culturing the pathogen from blood, cerebrospinal fluid, placenta or meconium. The mortality rate for fetal and newborn listeriosis remains approximately 20%. Two to three cases of pregnancy-associated listeriosis are reported annually in Austria among approximately 79,000 births, 20-30 cases are reported annually in Germany among approximately 680,000 births and 50-100 cases are reported annually in the USA among approximately 4 million births. Although Listeria infections in pregnancy are rare, they should be considered as a cause of fever of unknown origin during pregnancy.
    Expert Review of Anti-infective Therapy 01/2015; 13(3):1-9. DOI:10.1586/14787210.2015.1003809 · 2.28 Impact Factor
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    ABSTRACT: Contamination of surfaces by spores of Clostridium difficile is a major factor influencing the spread of healthcare-associated C. difficile infection. The aim of this study was to test the effect of an automated room disinfection system that provides an aerosol of 7.5 % hydrogen peroxide (H2O2) disinfectant, on spores of two different strains of C. difficile, and to evaluate the impact of biological soiling on the efficacy of H2O2 disinfection. The strains used were a C. difficile PCR ribotype 027 and a C. difficile ATCC 9689. Spore suspensions of each strain were applied to ceramic tiles and exposed to aerosolized H2O2 at different locations in a test room. Biological soiling was simulated by bovine serum albumin and sheep erythrocytes. At set time points spores were recovered, plated onto Columbia 5 % sheep blood agar, and surviving bacteria were counted as colony-forming units (cfu). No viable spores of either strain were recovered after a 3 h exposure to gaseous H2O2. Spores located inside a drawer showed recovery of approximately 1E5 cfu/ml for C. difficile ribotype 027 after 1 h. In the presence of organic matter, a more than fivefold log reduction compared with not exposed controls could be observed for spores of either strain tested. Appropriate decontamination of surfaces exposed to spores of C. difficile is challenging for conventional cleaning methods. Aerosolized H2O2 delivered by automated room disinfection systems could possibly improve surface decontamination and thereby reduce transmission of healthcare-associated C. difficile infection. Also in the presence of organic matter H2O2 disinfection appears to be an effective adjunct for decontamination of environmental surfaces.
    Wiener klinische Wochenschrift 12/2014; DOI:10.1007/s00508-014-0682-6 · 0.79 Impact Factor
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    ABSTRACT: The intestinal microbiota has a pivotal role in the maintenance of health of the human organism, especially in the defense against pathogenic microorganisms. Alterations in the microbiota, also termed dysbiosis, seem to be involved in the pathogenesis of a variety of intestinal and extraintestinal diseases. Fecal microbiota transplantation (FMT), also known as stool transplantation, is a therapeutic procedure aiming at restoring an altered intestinal microbiota by administration of stool microorganisms from a healthy donor into the intestinal tract of a patient. FMT is most commonly used for recurrent forms of Clostridium difficile infections (CDI). There are currently many cohort studies in a large number of patients and a randomized controlled trial showing a dramatic effect of FMT for this indication. Therefore FMT is recommended by international medical societies for the treatment of recurrent CDI with high scientific evidence. Other potential indications are the treatment of fulminant CDI or the treatment of inflammatory bowel diseases. In the practical utilization of FMT there are currently several open questions regarding the screening of stool donors, the processing of stool and the mode of FMT application. Different modes of FMT application have been described, the application into the colon has to be preferred due to less reported side effects than the application into the upper gastrointestinal tract. So far only very few side effects due to FMT have been reported, nevertheless the use and risks of FMT are currently intensely debated in the medical community. This consensus report of the Austrian society of gastroenterology and hepatology (ÖGGH) in cooperation with the Austrian society of infectious diseases and tropical medicine provides instructions for physicians who want to use FMT which are based on the current medical literature. © Georg Thieme Verlag KG Stuttgart · New York.
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    ABSTRACT: The intestinal microbiome is essential for maintaining human health and defending against intestinal pathogens. Alterations of the intestinal microbiota, also termed dysbiosis, play a pivotal role in the pathogenesis of various human diseases. Fecal microbiota transplantation (FMT) aims on correcting these alterations by delivering fecal microorganisms from a healthy person to the intestines of a patient. Up to now, recurrent Clostridium difficile (CDI) infection is the only indication supported by solid scientific evidence, but many ongoing studies are investigating FMT in other dysbiosis-related diseases such as inflammatory bowel disease. As there are no systematic methodological investigations, several questions about techniques, donor screening and safety issues remain. This shortage of evidence, especially on long-term safety concerns, is leading to worldwide controversy on the use of FMT. Regulations by health care authorities vary among different countries. This review reflects the Austrian situation and its FMT guidelines concerning indications, techniques and donor screening, recently developed by local scientific societies.This article is protected by copyright. All rights reserved.
    Clinical Microbiology and Infection 10/2014; DOI:10.1111/1469-0691.12801 · 5.20 Impact Factor
  • Jürgen J Wenzel, Franz Allerberger
    The Lancet Infectious Diseases 10/2014; 14(10). DOI:10.1016/S1473-3099(14)70897-7 · 19.45 Impact Factor
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    ABSTRACT: We tested 19 sera from Austrian patients with acute hepatitis A. A serum from a 48-year-old female patient yielded HAV-nucleic acid that showed 99.7 % homology to the HAV-sequence obtained from samples taken during the current outbreak in several European countries, which is associated with consumption of frozen berries. So far, Austria was considered not to be affected by this hepatitis A outbreak.
    Food and Environmental Virology 09/2014; 6(4). DOI:10.1007/s12560-014-9165-1 · 1.98 Impact Factor
  • Frauenheilkunde up2date 08/2014; 8(04):263. DOI:10.1055/s-004-27552
  • Eurosurveillance: bulletin europeen sur les maladies transmissibles = European communicable disease bulletin 07/2014; 19(26). DOI:10.2807/1560-7917.ES2014.19.26.20845 · 4.66 Impact Factor
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    ABSTRACT: Introduction: Little is known about prevailing ribotypes of Clostridium difficile infection in Romania where CDI is not a mandatory notifiable disease. Methodology: We studied 64 non-duplicate C. difficile isolates from patients hospitalised at the National Institute of Infectious Diseases, Bucharest, Romania between March 2011 and March 2012. Results: Sixty-three of the 64 C. difficile isolates produced toxins A and B whereas 44 (69%) isolates produced a binary toxin. Ribotype 027 accounted for 43 (68%) of the 63 toxigenic strains. The remaining 20 isolates belonged to ribotypes 018 (n = 9), 012 (n = 3), and, with one isolate each, 014, 031, 081, 416, 433, 500, 507 and PR03035 (new ribotype). Information on hospital mortality was available for 62 of the 64 patients; among these 62 cases, 4 (6.4%) ended fatal. Recurrence was documented for 11 (18.3%) of the 60 patients for whom this information was available. Multilocus variable-number tandem repeat analysis of the 43 isolates of ribotype 027 yielded a unique cluster for the Romanian isolates when compared to Austrian or Italian isolates. Conclusion: Our findings sustain the hypothesis of a recent emerged outbreak of C. difficile PCR ribotype 027 infections in the area of Bucharest.
    The Journal of Infection in Developing Countries 06/2014; 8(6):694-8. DOI:10.3855/jidc.4435 · 1.27 Impact Factor
  • B Springer, F Allerberger, C Kornschober
    Eurosurveillance: bulletin europeen sur les maladies transmissibles = European communicable disease bulletin 06/2014; 19(22). DOI:10.2807/1560-7917.ES2014.19.22.20818 · 4.66 Impact Factor
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    ABSTRACT: BackgroundIn Europe animal and human infections due to Dirofilaria repens are increasing.FindingsIn a nationwide screening for filarioid parasites in Austria, 7,632 mosquitoes were collected from June till October 2012 and divided into 437 pools according to same trapping date and sight and mosquito species. For the molecular detection, a real-time PCR approach was followed by conventional PCR. D. repens was detected in the villages Moerbisch and Rust, Burgenland in one Anopheles maculipennis group and one Anopheles algeriensis species pool, respectively.ConclusionsThe geographical distribution of the two positive pools points to the invasion of D. repens from Eastern neighboring countries. The finding of D. repens in mosquito vectors suggests the occurrence of the causative agent for cutaneous dirofilariosis in Austria.
    Parasites & Vectors 05/2014; 7(1):226. DOI:10.1186/1756-3305-7-226 · 3.25 Impact Factor
  • B Seidel, F Allerberger, P Hufnagl, A Indra
    Parasites & Vectors 04/2014; 7(Suppl 1):O6. DOI:10.1186/1756-3305-7-S1-O6 · 3.25 Impact Factor
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    ABSTRACT: A cluster of 7 human cases of listeriosis occurred in Austria and in Germany between April 2011 and July 2013. The L. monocytogenes SV 1/2b isolates shared PFGE and fAFLP patterns indistinguishable from those from 5 food producers. The 7 human isolates, a control strain with a different PFGE/fAFLP profile, and 10 food isolates were subjected to whole genome sequencing (WGS) in a blinded fashion. A gene-by-gene comparison (MLST+) was performed and the resulting whole genome allelic profiles were compared using SeqSphere software version 1.0 (Ridom GmbH, Muenster, Germany). Analyzing 2298 genes, the 4 human outbreak isolates from 2012 and 2013 had different alleles at ≤6 genes, i.e. differed by ≤6 genes from each other; the dendrogram placed these isolates in between 5 Austrian unaged soft cheese isolates from producer A (≤19 genes difference to human cluster) and 2 Austrian ready-to-eat-meat isolates from producer B (≤8 genes to human cluster). Both food products appeared on grocery bills prospectively collected by these outbreak cases after hospital discharge. Epidemiological results on food consumption and MLST+ clearly separated the 3 cases in 2011 from the 4 2012/2013- outbreak cases (>48 differing genes). We showed that WGS is capable of discriminating L. monocytogenes SV 1/2b clones not distinguishable by PFGE and fAFLP. The listeriosis outbreak described, clearly underlines the potential of sequence-based typing methods in offering new perspectives of enhanced resolution and comparability of typing systems for public health applications.This article is protected by copyright. All rights reserved.
    Clinical Microbiology and Infection 04/2014; 17(5). DOI:10.1111/1469-0691.12638 · 5.20 Impact Factor
  • Parasites & Vectors 04/2014; 7(Suppl 1):P14. DOI:10.1186/1756-3305-7-S1-P14 · 3.25 Impact Factor
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    ABSTRACT: The prevalence of Coxiella burnetii, Francisella tularensis, Brucella abortus, and Brucella melitensis infections in Austria and the exposure risk of military personnel were assessed in an exploratory nationwide cross-sectional seroprevalence survey in 526 healthy adult individuals, 222 of which were soldiers and 304 were civilians. Screening for IgA/IgG antibodies to C. burnetii (Phase I) and IgG/IgM antibodies to C. burnetii (Phase II), and to F. tularensis was done with commercial enzyme-linked immunosorbent assays. To detect antibodies against B. abortus and B. melitensis, an in-house complement fixation test was used. Overall, 11 individuals (2.0%) showed antibodies to C. burnetii, 3 individuals (0.5%) were seropositive for F. tularensis, and one (0.3%) individual was borderline positive. All individuals positive or borderline for F. tularensis tested negative for antibodies against C. burnetii. All individuals tested negative for antibodies against B. melitensis/B. abortus. There were no significant differences between the seroprevalence of C. burnetii and F. tularensis among military personnel and civilians. Our data demonstrate serological evidence of a low rate of exposure to C. burnetii and F. tularensis among the Austrian adult population and military personnel.
    Ticks and Tick-borne Diseases 04/2014; DOI:10.1016/j.ttbdis.2013.12.007 · 2.88 Impact Factor
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    ABSTRACT: A large listeriosis outbreak occurred in Austria, Germany and the Czech Republic in 2009 and 2010. The outbreak was traced back to a traditional Austrian curd cheese called "Quargel" which was contaminated with two distinct serovar 1/2a Listeria monocytogenes strains (QOC1 and QOC2). In this study we sequenced and analysed the genomes of both outbreak strains in order to investigate the extent of genetic diversity between the two strains belonging to MLST sequence types 398 (QOC2) and 403 (QOC1). Both genomes are highly similar, but also display distinct properties: The QOC1 genome is approximately 74 kbp larger than the QOC2 genome. In addition, the strains harbour 93 (QOC1) and 45 (QOC2) genes encoding strain-specific proteins. A 21 kbp region showing highest similarity to plasmid pLMIV encoding three putative internalins is integrated in the QOC1 genome. In contrast to QOC1, strain QOC2 harbours a vip homologue, which encodes a LPXTG surface protein involved in cell invasion. In accordance, in vitro virulence assays revealed distinct differences in invasion efficiency and intracellular proliferation within different cell types. The higher virulence potential of QOC1 in non-phagocytic cells may be explained by the presence of additional internalins in the pLMIV-like region, whereas the higher invasion capability of QOC2 into phagocytic cells may be due to the presence of a vip homologue. In addition, both strains show differences in stress-related gene content. Strain QOC1 encodes a so-called stress survival islet 1, whereas strain QOC2 harbours a homologue of the uncharacterized LMOf2365_0481 gene. Consistently, QOC1 shows higher resistance to acidic, alkaline and gastric stress. In conclusion, our results show that strain QOC1 and QOC2 are distinct and did not recently evolve from a common ancestor.
    PLoS ONE 02/2014; 9(2):e89964. DOI:10.1371/journal.pone.0089964 · 3.53 Impact Factor

Publication Stats

4k Citations
975.83 Total Impact Points


  • 2003–2015
    • Österreichische Agentur für Gesundheit und Ernährungssicherheit
      Wien, Vienna, Austria
  • 2011–2012
    • Paracelsus Medical University Salzburg
      • University Institute of Medical Microbiology, Hygiene and Infectious Diseases
      Salzburg, Salzburg, Austria
  • 2009
    • Institut Pasteur
      Lutetia Parisorum, Île-de-France, France
  • 1990–2009
    • University of Innsbruck
      • • Institute of Biochemistry
      • • Institute of Microbiology
      Innsbruck, Tyrol, Austria
  • 2005
    • University of Padova
      Padua, Veneto, Italy
  • 1999
    • Robert Koch Institut
      Berlín, Berlin, Germany
  • 1997
    • IST Austria
      Klosterneuberg, Lower Austria, Austria
  • 1991
    • Friedrich-Alexander Universität Erlangen-Nürnberg
      Erlangen, Bavaria, Germany
    • Mayo Clinic - Rochester
      Rochester, Minnesota, United States