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Genome-Wide Expression Profiling Reveals S100B as Biomarker for Invasive Aspergillosis

Overview of attention for article published in Frontiers in Microbiology, March 2016
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Title
Genome-Wide Expression Profiling Reveals S100B as Biomarker for Invasive Aspergillosis
Published in
Frontiers in Microbiology, March 2016
DOI 10.3389/fmicb.2016.00320
Pubmed ID
Authors

Andreas Dix, Kristin Czakai, Jan Springer, Mirjam Fliesser, Michael Bonin, Reinhard Guthke, Anna L. Schmitt, Hermann Einsele, Jörg Linde, Jürgen Löffler

Abstract

Invasive aspergillosis (IA) is a devastating opportunistic infection and its treatment constitutes a considerable burden for the health care system. Immunocompromised patients are at an increased risk for IA, which is mainly caused by the species Aspergillus fumigatus. An early and reliable diagnosis is required to initiate the appropriate antifungal therapy. However, diagnostic sensitivity and accuracy still needs to be improved, which can be achieved at least partly by the definition of new biomarkers. Besides the direct detection of the pathogen by the current diagnostic methods, the analysis of the host response is a promising strategy toward this aim. Following this approach, we sought to identify new biomarkers for IA. For this purpose, we analyzed gene expression profiles of hematological patients and compared profiles of patients suffering from IA with non-IA patients. Based on microarray data, we applied a comprehensive feature selection using a random forest classifier. We identified the transcript coding for the S100 calcium-binding protein B (S100B) as a potential new biomarker for the diagnosis of IA. Considering the expression of this gene, we were able to classify samples from patients with IA with 82.3% sensitivity and 74.6% specificity. Moreover, we validated the expression of S100B in a real-time reverse transcription polymerase chain reaction (RT-PCR) assay and we also found a down-regulation of S100B in A. fumigatus stimulated DCs. An influence on the IL1B and CXCL1 downstream levels was demonstrated by this S100B knockdown. In conclusion, this study covers an effective feature selection revealing a key regulator of the human immune response during IA. S100B may represent an additional diagnostic marker that in combination with the established techniques may improve the accuracy of IA diagnosis.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 23 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 23 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 8 35%
Student > Bachelor 3 13%
Student > Master 3 13%
Student > Ph. D. Student 2 9%
Student > Doctoral Student 1 4%
Other 4 17%
Unknown 2 9%
Readers by discipline Count As %
Agricultural and Biological Sciences 7 30%
Engineering 4 17%
Medicine and Dentistry 3 13%
Computer Science 3 13%
Biochemistry, Genetics and Molecular Biology 2 9%
Other 2 9%
Unknown 2 9%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 23 March 2016.
All research outputs
#20,315,221
of 22,856,968 outputs
Outputs from Frontiers in Microbiology
#22,466
of 24,866 outputs
Outputs of similar age
#253,688
of 299,504 outputs
Outputs of similar age from Frontiers in Microbiology
#482
of 558 outputs
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