Host gene expression profiling in pathogen–host interactions

2006 ◽  
Vol 18 (4) ◽  
pp. 422-429 ◽  
Author(s):  
Hamid Hossain ◽  
Svetlin Tchatalbachev ◽  
Trinad Chakraborty
2012 ◽  
Vol 66 (4) ◽  
pp. 282-285 ◽  
Author(s):  
Olga Bourmenskaya ◽  
Ekaterina Shubina ◽  
Dmitry Trofimov ◽  
Denis Rebrikov ◽  
Elina Sabdulaeva ◽  
...  

2007 ◽  
Vol 1 (2) ◽  
pp. e86 ◽  
Author(s):  
Joshua Fink ◽  
Feng Gu ◽  
Ling Ling ◽  
Thomas Tolfvenstam ◽  
Farzad Olfat ◽  
...  

2003 ◽  
Vol 49 (7) ◽  
pp. 1045-1049 ◽  
Author(s):  
Baochuan Lin ◽  
Maryanne T Vahey ◽  
Dzung Thach ◽  
David A Stenger ◽  
Joseph J Pancrazio

Abstract With the increased threat posed by biological weapons, detection techniques for biothreat pathogens are critically needed to monitor and assess the severity of the illness once exposure has occurred. Current approaches for detecting biological threats are either time-consuming or highly specific but provide little information regarding pathogenicity. Genotyping of pathogens by PCR provides a fast and definitive means for identifying pathogens, but reliance on pathogen genotypic endpoints has several limitations. Current progress in DNA microarrays technology provides an alternative way to address the issues faced by traditional detection systems through host gene expression profiles of peripheral blood cells. We discuss the advantages and critical issues facing the use of host gene expression profiling for biological threat detection.


2005 ◽  
Vol 3 (3) ◽  
pp. 119-129 ◽  
Author(s):  
Chad J. Creighton ◽  
Jennifer L. Bromberg-White ◽  
David E. Misek ◽  
David J. Monsma ◽  
Frank Brichory ◽  
...  

2018 ◽  
Vol 2 (2) ◽  
pp. 151-163 ◽  
Author(s):  
Wayne A. Warner ◽  
David H. Spencer ◽  
Maria Trissal ◽  
Brian S. White ◽  
Nichole Helton ◽  
...  

Key Points A subset of snoRNAs is expressed in a developmental- and lineage-specific manner during human hematopoiesis. Neither host gene expression nor alternative splicing accounted for the observed differential expression of snoRNAs in a subset of AML.


2021 ◽  
Vol 7 (6) ◽  
pp. eabe7386 ◽  
Author(s):  
Ke Zhang ◽  
Lisa Miorin ◽  
Tadashi Makio ◽  
Ishmael Dehghan ◽  
Shengyan Gao ◽  
...  

The ongoing unprecedented severe acute respiratory syndrome caused by the SARS-CoV-2 outbreak worldwide has highlighted the need for understanding viral-host interactions involved in mechanisms of virulence. Here, we show that the virulence factor Nsp1 protein of SARS-CoV-2 interacts with the host messenger RNA (mRNA) export receptor heterodimer NXF1-NXT1, which is responsible for nuclear export of cellular mRNAs. Nsp1 prevents proper binding of NXF1 to mRNA export adaptors and NXF1 docking at the nuclear pore complex. As a result, a significant number of cellular mRNAs are retained in the nucleus during infection. Increased levels of NXF1 rescues the Nsp1-mediated mRNA export block and inhibits SARS-CoV-2 infection. Thus, antagonizing the Nsp1 inhibitory function on mRNA export may represent a strategy to restoring proper antiviral host gene expression in infected cells.


Sign in / Sign up

Export Citation Format

Share Document