Next-generation technologies for studying host-pathogen interactions: a focus on dual transcriptomics, CRISPR/Cas9 screening and organs-on-chips

被引:10
作者
Baddal, Buket [1 ]
机构
[1] Near East Univ, Fac Med, Dept Med Microbiol & Clin Microbiol, Near East Blvd, CY-99010 Nicosia, Cyprus
关键词
infectious disease; host-pathogen interaction; dual RNA-seq; genome editing; CRISPR screening; organ-on-chips; RNA-SEQ; INSIGHTS; DISCOVERY; RECEPTOR; REVEALS;
D O I
10.1093/femspd/ftz060
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pathogens constantly interact with their hosts and the environment, and therefore have evolved unique virulence mechanisms to target and breach host defense barriers and manipulate host immune response to establish an infection. Advances in technologies that allow genome mining, gene editing such as CRISPR/Cas9, genomic, epigenomic and transcriptomic studies such as dual RNA-seq, coupled with bioinformatics, have accelerated the field of host-pathogen interactions within a broad range of infection models. Underpinning of the molecular changes that accompany invasion of eukaryotic cells with pathogenic microorganisms at the intersection of host, pathogen and their local environment has provided a better understanding of infectious disease mechanisms and antimicrobial strategies. The recent evolution of physiologically relevant three-dimensional (3-D) tissue/organ models and microfluidic organ-on-chip devices also provided a window to a more predictive framework of infectious disease processes. These approaches combined hold the potential to highly impact discovery of novel drug targets and vaccine candidates of the future. Here, we review three of the available and emerging technologies-dual RNA-seq, CRISPR/Cas9 screening and organs-on-chips, applicable to the high throughput study and deciphering of interaction networks between pathogens and their hosts that are critical for the development of novel therapeutics.
引用
收藏
页数:8
相关论文
共 92 条
[1]   Time-resolved dual RNA-seq reveals extensive rewiring of lung epithelial and pneumococcal transcriptomes during early infection [J].
Aprianto, Rieza ;
Slager, Jelle ;
Holsappel, Siger ;
Veening, Jan-Willem .
GENOME BIOLOGY, 2016, 17
[2]   Twin arginine translocation, ammonia incorporation, and polyamine biosynthesis are crucial for Proteus mirabilis fitness during bloodstream infection [J].
Armbruster, Chelsie E. ;
Forsyth, Valerie S. ;
Johnson, Alexandra O. ;
Smith, Sara N. ;
White, Ashley N. ;
Brauer, Aimee L. ;
Learman, Brian S. ;
Zhao, Lili ;
Wu, Weisheng ;
Anderson, Mark T. ;
Bachman, Michael A. ;
Mobley, Harry L. T. .
PLOS PATHOGENS, 2019, 15 (04)
[3]  
Baddal B, 2016, MBIO, V7, DOI [10.1128/mbio.00373-16, 10.1128/mBio.00373-16]
[4]   Subdiffusive motion of bacteriophage in mucosal surfaces increases the frequency of bacterial encounters [J].
Barr, Jeremy J. ;
Auro, Rita ;
Sam-Soon, Nicholas ;
Kassegne, Sam ;
Peters, Gregory ;
Bonilla, Natasha ;
Hatay, Mark ;
Mourtada, Sarah ;
Bailey, Barbara ;
Youle, Merry ;
Felts, Ben ;
Baljon, Arlette ;
Nulton, Jim ;
Salamon, Peter ;
Rohwer, Forest .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015, 112 (44) :13675-13680
[5]   Modeling Host-Pathogen Interactions in the Context of the Microenvironment: Three-Dimensional Cell Culture Comes of Age [J].
Barrila, Jennifer ;
Crabbe, Aurelie ;
Yang, Jiseon ;
Franco, Karla ;
Nydam, Seth D. ;
Forsyth, Rebecca J. ;
Davis, Richard R. ;
Gangaraju, Sandhya ;
Ott, C. Mark ;
Coyne, Carolyn B. ;
Bissell, Mina J. ;
Nickerson, Cheryl A. .
INFECTION AND IMMUNITY, 2018, 86 (11)
[6]   Proteomics and integrative omic approaches for understanding host-pathogen interactions and infectious diseases [J].
Beltran, Pierre M. Jean ;
Federspiel, Joel D. ;
Sheng, Xinlei ;
Cristea, Ileana M. .
MOLECULAR SYSTEMS BIOLOGY, 2017, 13 (03)
[7]  
Benam KH, 2016, NAT METHODS, V13, P151, DOI [10.1038/NMETH.3697, 10.1038/nmeth.3697]
[8]  
Biron DG, GENETICS EVOLUTION I
[9]   Genomic-scale analysis of bacterial gene and protein expression in the host [J].
Boyce, JD ;
Cullen, PA ;
Adler, B .
EMERGING INFECTIOUS DISEASES, 2004, 10 (08) :1357-1362
[10]   Unique features in the intracellular transport of typhoid toxin revealed by a genome-wide screen [J].
Chang, Shu-Jung ;
Jin, Sheng Chih ;
Jiao, Xuyao ;
Galan, Jorge E. .
PLOS PATHOGENS, 2019, 15 (04)