Transcriptional comparison between the PhoPR system of Mycobacterium tuberculosis and Mycobacterium bovis on an M. bovis AF2122/97 genetic background

Tuberculosis (TB) is an infectious disease that affects humans and animals. The pathogens that cause TB belong to the Mycobacterium tuberculosis Complex (MTBC), with Mycobacterium tuberculosis and Mycobacterium bovis as the main representatives of human- and animal-adapted strains, respectively. One key genetic regulator of the MTBC members is the PhoPR system, which controls many processes including the stress response, lipid metabolism and pathogenesis, among others. Previous studies identified a key G71I substitution in the M. bovis PhoR ortholog relative to M. tuberculosis PhoR and suggested that PhoPR might be non-functional in animal-adapted strains, but recent work has highlighted the functionality of PhoPR in M. bovis despite the G71I substitution. Here we compare the transcriptional effects of the PhoPR system of M. tuberculosis H37Rv and M. bovis AF2122/97 on an M. bovis AF2122/97 ΔphoPR knockout background. Our results show common patterns of gene expression between the two orthologs, but also clear differences in the expression of rubredoxin genes and lipid biosynthetic loci. This work adds on to the evidence that the PhoPR system is indeed functional in M. bovis, and suggests that PhoPR controls differential transcriptional programs that are important in adapting to human or animal different hosts.

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Published
2025-07-25
DOI
https://doi.org/10.1099/acmi.0.001087.v1
Primary Topic
Mycobacterium research and diagnosis
Type
article
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0.00

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article

Transcriptional comparison between the PhoPR system of Mycobacterium tuberculosis and Mycobacterium bovis on an M. bovis AF2122/97 genetic background

Apoorva Bhatt, Gabriel González, Ruoyao Ma, Chie Nakajima et al.
Mycobacterium research and diagnosis
article

Transcriptional comparison between the PhoPR system of Mycobacterium tuberculosis and Mycobacterium bovis on an M. bovis AF2122/97 genetic background

Apoorva Bhatt, Gabriel González, Ruoyao Ma, Chie Nakajima, Jose Maria Urtasun-Elizari, Viktor Perets, Hayleah Pickford, David E. MacHugh, Damien Farrell, Stephen V. Gordon, Yasuhiko Suzuki, Jesus Urtasun-Elizari
article en

Abstract

Tuberculosis (TB) is an infectious disease that affects humans and animals. The pathogens that cause TB belong to the Mycobacterium tuberculosis Complex (MTBC), with Mycobacterium tuberculosis and Mycobacterium bovis as the main representatives of human- and animal-adapted strains, respectively. One key genetic regulator of the MTBC members is the PhoPR system, which controls many processes including the stress response, lipid metabolism and pathogenesis, among others. Previous studies identified a key G71I substitution in the M. bovis PhoR ortholog relative to M. tuberculosis PhoR and suggested that PhoPR might be non-functional in animal-adapted strains, but recent work has highlighted the functionality of PhoPR in M. bovis despite the G71I substitution. Here we compare the transcriptional effects of the PhoPR system of M. tuberculosis H37Rv and M. bovis AF2122/97 on an M. bovis AF2122/97 ΔphoPR knockout background. Our results show common patterns of gene expression between the two orthologs, but also clear differences in the expression of rubredoxin genes and lipid biosynthetic loci. This work adds on to the evidence that the PhoPR system is indeed functional in M. bovis, and suggests that PhoPR controls differential transcriptional programs that are important in adapting to human or animal different hosts.

University College Dublin (IE), Hokkaido University (JP), MRC London Institute of Medical Sciences (GB), Imperial College London (GB), University of Birmingham (GB), Vrije Universiteit Amsterdam (NL)
Science Foundation Ireland, Biotechnology and Biological Sciences Research Council
Openalex Percentile: Top 73%
Mycobacterium research and diagnosis
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