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A Mycobacterial Systems Resource for the Research Community

Authors :
Daniel A. Russell
J. A. Judd
Alexander Dills
Joseph T. Wade
Jemila C. Kester
M. Mir
Erica Lasek-Nesselquist
E. Dove
Sarah M. Fortune
Rebekah M. Dedrick
Pascal Lapierre
Christopher G Meier
Keith M. Derbyshire
Ian D. Wolf
A. Joseph
Ryan R Clark
M. Stone
Graham F. Hatfull
Jill G. Canestrari
Junhao Zhu
Todd A. Gray
Samantha E. Wirth
Ashutosh Upadhyay
E. R. Rubin
Michael J. Palumbo
Carol Smith
Source :
mBio, mBio, Vol 12, Iss 2 (2021)
Publication Year :
2021
Publisher :
American Society for Microbiology, 2021.

Abstract

Diseases caused by mycobacterial species result in millions of deaths per year globally, and present a substantial health and economic burden, especially in immunocompromised patients. Difficulties inherent in working with mycobacterial pathogens have hampered the development and application of high-throughput genetics that can inform genome annotations and subsequent functional assays.<br />Functional characterization of bacterial proteins lags far behind the identification of new protein families. This is especially true for bacterial species that are more difficult to grow and genetically manipulate than model systems such as Escherichia coli and Bacillus subtilis. To facilitate functional characterization of mycobacterial proteins, we have established a Mycobacterial Systems Resource (MSR) using the model organism Mycobacterium smegmatis. This resource focuses specifically on 1,153 highly conserved core genes that are common to many mycobacterial species, including Mycobacterium tuberculosis, in order to provide the most relevant information and resources for the mycobacterial research community. The MSR includes both biological and bioinformatic resources. The biological resource includes (i) an expression plasmid library of 1,116 genes fused to a fluorescent protein for determining protein localization; (ii) a library of 569 precise deletions of nonessential genes; and (iii) a set of 843 CRISPR-interference (CRISPRi) plasmids specifically targeted to silence expression of essential core genes and genes for which a precise deletion was not obtained. The bioinformatic resource includes information about individual genes and a detailed assessment of protein localization. We anticipate that integration of these initial functional analyses and the availability of the biological resource will facilitate studies of these core proteins in many Mycobacterium species, including the less experimentally tractable pathogens M. abscessus, M. avium, M. kansasii, M. leprae, M. marinum, M. tuberculosis, and M. ulcerans.

Details

Language :
English
ISSN :
21507511
Volume :
12
Issue :
2
Database :
OpenAIRE
Journal :
mBio
Accession number :
edsair.doi.dedup.....26779fa33222648452693fc48bf4c821