scholarly journals Erratum: Corrigendum: Dual-species transcriptional profiling during systemic candidiasis reveals organ-specific host-pathogen interactions

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Betty Hebecker ◽  
Sebastian Vlaic ◽  
Theresia Conrad ◽  
Michael Bauer ◽  
Sascha Brunke ◽  
...  
2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Betty Hebecker ◽  
Sebastian Vlaic ◽  
Theresia Conrad ◽  
Michael Bauer ◽  
Sascha Brunke ◽  
...  

Abstract Candida albicans is a common cause of life-threatening fungal bloodstream infections. In the murine model of systemic candidiasis, the kidney is the primary target organ while the fungal load declines over time in liver and spleen. To better understand these organ-specific differences in host-pathogen interaction, we performed gene expression profiling of murine kidney, liver and spleen and determined the fungal transcriptome in liver and kidney. We observed a delayed transcriptional immune response accompanied by late induction of fungal stress response genes in the kidneys. In contrast, early upregulation of the proinflammatory response in the liver was associated with a fungal transcriptome resembling response to phagocytosis, suggesting that phagocytes contribute significantly to fungal control in the liver. Notably, C. albicans hypha-associated genes were upregulated in the absence of visible filamentation in the liver, indicating an uncoupling of gene expression and morphology and a morphology-independent effect by hypha-associated genes in this organ. Consistently, integration of host and pathogen transcriptional data in an inter-species gene regulatory network indicated connections of C. albicans cell wall remodelling and metabolism to the organ-specific immune responses.


Author(s):  
Gabriela Arévalo-Pinzón ◽  
Diego Garzón-Ospina ◽  
Fredy A. Pulido ◽  
Maritza Bermúdez ◽  
Johanna Forero-Rodríguez ◽  
...  

Virulence ◽  
2018 ◽  
Vol 9 (1) ◽  
pp. 1449-1467 ◽  
Author(s):  
Abeer M. Alkhaibari ◽  
Alex M. Lord ◽  
Thierry Maffeis ◽  
James C. Bull ◽  
Fabio L. Olivares ◽  
...  

2019 ◽  
Vol 3 (4) ◽  
pp. 371-378
Author(s):  
Joshua M. Peters ◽  
Sydney L. Solomon ◽  
Christopher Y. Itoh ◽  
Bryan D. Bryson

Abstract Interactions between pathogens and their hosts can induce complex changes in both host and pathogen states to privilege pathogen survival or host clearance of the pathogen. To determine the consequences of specific host–pathogen interactions, a variety of techniques in microbiology, cell biology, and immunology are available to researchers. Systems biology that enables unbiased measurements of transcriptomes, proteomes, and other biomolecules has become increasingly common in the study of host–pathogen interactions. These approaches can be used to generate novel hypotheses or to characterize the effects of particular perturbations across an entire biomolecular network. With proper experimental design and complementary data analysis tools, high-throughput omics techniques can provide novel insights into the mechanisms that underlie processes from phagocytosis to pathogen immune evasion. Here, we provide an overview of the suite of biochemical approaches for high-throughput analyses of host–pathogen interactions, analytical frameworks for understanding the resulting datasets, and a vision for the future of this exciting field.


BMC Genomics ◽  
2015 ◽  
Vol 16 (1) ◽  
Author(s):  
Laura A. L. Dillon ◽  
Rahul Suresh ◽  
Kwame Okrah ◽  
Hector Corrada Bravo ◽  
David M. Mosser ◽  
...  

Peptides ◽  
2010 ◽  
Vol 31 (12) ◽  
pp. 2165-2172 ◽  
Author(s):  
Jeison García ◽  
Hernando Curtidor ◽  
Magnolia Vanegas ◽  
Gabriela Arévalo-Pinzon ◽  
Manuel A. Patarroyo ◽  
...  

2009 ◽  
Vol 174 (3) ◽  
pp. 308
Author(s):  
Soubeyrand ◽  
Laine ◽  
Hanski ◽  
Penttinen

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