Stefanie A. Barth

Dr. Stefanie A. Barth

Friedrich-Loeffler-Institut, Jena, Thuringia, Germany
orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 April 2006 in Digestive Diseases and Sciences
Verified
Journal Article
Closed access
PDF file
BSB. Schroeder
B. Schroeder
SDS. Duncker
S. Duncker
SBStefanie A. Barth
Stefanie A. Barth
RBR. Bauerfeind
R. Bauerfeind
AGA. D. Gruber
A. D. Gruber
GBG. Breves
G. Breves

10 January 2018 in Transboundary and Emerging Diseases
Verified
Journal Article
Closed access
PDF file
SBStefanie A. Barth
Stefanie A. Barth
Sandra  BlomeSandra Blome
Sandra Blome
DCD. Cornelis
D. Cornelis
JPJ. Pietschmann
J. Pietschmann
MLM. Laval
M. Laval
FJFerran Jori
Ferran Jori

1 September 2016 in Applied and Environmental Microbiology
Verified
Journal Article
Closed access
PDF file
SBStefanie A. Barth
Stefanie A. Barth
CMChristian Menge
Christian Menge
IEInga Eichhorn
Inga Eichhorn
TSTorsten Semmler
Torsten Semmler
LWLothar H. Wieler
Lothar H. Wieler
LGLutz Geue
Lutz Geue
Shiga toxin-producing Escherichia coli (STEC) strains can colonize cattle for several months and may, thus, serve as gene reservoirs for the genesis of highly virulent zoonotic enterohemorrhagic E. coli (EHEC). Attempts to reduce the human risk for acquiring EHEC infections should include strategies to control such STEC strains persisting in cattle. We therefore aimed to identify genetic patterns associated with the STEC colonization type in the bovine host. We included 88 persistent colonizing STEC (STEC per ) (shedding for ≥4 months) and 74 sporadically colonizing STEC (STEC spo ) (shedding for ≤2 months) isolates from cattle and 16 bovine STEC isolates with unknown colonization types. Genoserotypes and multilocus sequence types (MLSTs) were determined, and the isolates were probed with a DNA microarray for virulence-associated genes (VAGs). All STEC per isolates belonged to only four genoserotypes (O26:H11, O156:H25, O165:H25, O182:H25), which formed three genetic clusters (ST21/396/1705, ST300/688, ST119). In contrast, STEC spo isolates were scattered among 28 genoserotypes and 30 MLSTs, with O157:H7 (ST11) and O6:H49 (ST1079) being the most prevalent. The microarray analysis identified 139 unique gene patterns that clustered with the genoserotypes and MLSTs of the strains. While the STEC per isolates possessed heterogeneous phylogenetic backgrounds, the accessory genome clustered these isolates together, separating them from the STEC spo isolates. Given the vast genetic heterogeneity of bovine STEC strains, defining the genetic patterns distinguishing STEC per from STEC spo isolates will facilitate the targeted design of new intervention strategies to counteract these zoonotic pathogens at the farm level. IMPORTANCE Ruminants, especially cattle, are sources of food-borne infections by Shiga toxin-producing Escherichia coli (STEC) in humans. Some STEC strains persist in cattle for longer periods of time, while others are detected only sporadically. Persisting strains can serve as gene reservoirs that supply E. coli with virulence factors, thereby generating new outbreak strains. Attempts to reduce the human risk for acquiring STEC infections should therefore include strategies to control such persisting STEC strains. By analyzing representative genes of their core and accessory genomes, we show that bovine STEC with a persistent colonization type emerged independently from sporadically colonizing isolates and evolved in parallel evolutionary branches. However, persistent colonizing strains share similar sets of accessory genes. Defining the genetic patterns that distinguish persistent from sporadically colonizing STEC isolates will facilitate the targeted design of new intervention strategies to counteract these zoonotic pathogens at the farm level.

1 November 2009 in Journal of Applied Microbiology
Verified
Journal Article
Closed access
PDF file
SBStefanie A. Barth
Stefanie A. Barth
SDS. Duncker
S. Duncker
JHJ. Hempe
J. Hempe
GBG. Breves
G. Breves
GBG. Baljer
G. Baljer
RBR. Bauerfeind
R. Bauerfeind

22 June 2015 in PLOS ONE
Verified
Journal Article
Open access
PDF file
MBMichael Black
Michael Black
PMPaula M. Moolhuijzen
Paula M. Moolhuijzen
RBRoberto Barrero
Roberto Barrero
TLTom La
Tom La
NPNyree Phillips
Nyree Phillips
MBMatthew Bellgard
Matthew Bellgard
The intestinal spirochete Brachyspira hyodysenteriae is an important pathogen in swine, causing mucohemorrhagic colitis in a disease known as swine dysentery. Based on the detection of significant linkage disequilibrium in multilocus sequence data, the species is considered to be clonal. An analysis of the genome sequence of Western Australian B. hyodysenteriae strain WA1 has been published, and in the current study 19 further strains from countries around the world were sequenced with Illumina technology. The genomes were assembled and aligned to over 97.5% of the reference WA1 genome at a percentage sequence identity better than 80%. Strain regions not aligned to the reference ranged between 0.2 and 2.5%. Clustering of the strain genes found on average 2,354 (88%) core genes, 255 (8.6%) ancillary genes and 77 (2.9%) unique genes per strain. Depending on the strain the proportion of genes with 100% sequence identity to WA1 ranged from 85% to 20%. The result is a global comparative genomic analysis of B. hyodysenteriae genomes revealing potential differential phenotypic markers for numerous strains. Despite the differences found, the genomes were less varied than those of the related pathogenic species Brachyspira pilosicoli, and the analysis supports the clonal nature of the species. From this study, a public genome resource has been created that will serve as a repository for further genetic and phenotypic studies of these important porcine bacteria. This is the first intra-species B. hyodysenteriae comparative genomic analysis.

1 January 2020 in Veterinary Microbiology
Verified
Journal Article
Closed access
MGMayada Gwida
Mayada Gwida
Amal AwadAmal Awad
Amal Awad
Maged El-AshkerMaged El-Ashker
Maged El-Ashker
HHHelmut Hotzel
Helmut Hotzel
SMStefan Monecke
Stefan Monecke
SBSascha Daniel Braun
Sascha Daniel Braun