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1.
PLoS One ; 15(4): e0231827, 2020.
Article in English | MEDLINE | ID: mdl-32325482

ABSTRACT

The diagnosis of infective endocarditis (IE) remains a challenge. One of the rare bacterial species recently associated with biofilms and negative cultures in infective endocarditis is Aerococcus urinae. Whether the low number of reported cases might be due to lack of awareness and misidentification, mainly as streptococci, is currently being discussed. To verify the relevance and biofilm potential of Aerococcus in endocarditis, we used fluorescence in situ hybridization to visualize the microorganisms within the heart valve tissue. We designed and optimized a specific FISH probe (AURI) for in situ visualization and identification of A. urinae in sections of heart valves from two IE patients whose 16S rRNA gene sequencing had deteced A. urinae. Both patients had a history of urinary tract infections. FISH visualized impressive in vivo grown biofilms in IE, thus confirming the potential of A. urinae as a biofilm pathogen. In both cases, FISH/PCR was the only method to unequivocally identify A. urinae as the only causative pathogen for IE. The specific FISH assay for A. urinae is now available for further application in research and diagnostics. A. urinae should be considered in endocarditis patients with a history of urinary tract infections. These findings support the biofilm potential of A. urinae as a virulence factor and are meant to raise the awareness of this pathogen.


Subject(s)
Aerococcus/isolation & purification , Biofilms , Endocarditis, Bacterial/diagnosis , Endocarditis, Bacterial/microbiology , Heart Valves/microbiology , Aerococcus/physiology , Aged , Aged, 80 and over , Female , Humans , In Situ Hybridization, Fluorescence/methods , Male , Urinary Tract Infections/microbiology , Urinary Tract Infections/pathology
2.
Eur J Appl Physiol ; 88(6): 497-505, 2003 Feb.
Article in English | MEDLINE | ID: mdl-12560947

ABSTRACT

It was hypothesized that subjects with metabolic syndrome (hypertension, obesity, hyperlipidemia, diabetes mellitus): (1) develop measurable peripheral edema at moderate altitude and (2) might show differences on erythropoiesis, iron status and vascular endothelial growth factor (VEGF) in comparison to healthy subjects during and after a long-term stay (3-week exposure) at moderate altitude (congruent with 1700 m). Twenty-two male subjects with metabolic syndrome were selected. Baseline investigations (t1) were performed in Innsbruck (500 m). All participants were transferred by bus to 1700 m (Alps) and remained there for 3 weeks with examinations on day 1 (after the first night at altitude, t2), day 4 (t3), day 9 (t4) and day 19 (t5). After returning to Innsbruck, post-altitude examinations were conducted after 7-10 days (t6) and 6-7 weeks (t7), respectively. Body mass was decreased from t1 to t7 (P<0.01). Total body water was decreased at t2 (P<0.01), returned to control level (t3, t4), and was found elevated at t7 (P<0.01). Lean body mass did not change, but body fat decreased during the study (P<0.01). Tissue thickness at the forehead decreased during and after altitude exposure (P<0.01), whereas tissue thickness at the tibia did not alter. Erythropoietin (EPO) was elevated as early as t2 and remained increased until t5. Reticulocyte count was increased at t3 and remained above pre-altitude values. VEGF levels were unchanged. After a 3-week exposure to moderate altitude, patients with metabolic syndrome had reduced their body mass, mainly because of a reduction in body fat. The moderate altitude was found to stimulate erythropoiesis in these patients but this was not sufficient to increase serum VEGF concentration.


Subject(s)
Altitude , Body Fluids , Endothelial Growth Factors/metabolism , Erythropoiesis , Intercellular Signaling Peptides and Proteins/metabolism , Lymphokines/metabolism , Metabolic Diseases/physiopathology , Neovascularization, Pathologic/physiopathology , Adaptation, Physiological , Adult , Atmospheric Pressure , Austria , Body Composition , Body Water , Endothelial Growth Factors/blood , Humans , Intercellular Signaling Peptides and Proteins/blood , Iron/metabolism , Lymphokines/blood , Male , Metabolic Diseases/blood , Middle Aged , Skinfold Thickness , Vascular Endothelial Growth Factor A , Vascular Endothelial Growth Factors , Water-Electrolyte Balance
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