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Published on: September 27, 2018
Roles of mdh and MAP1981c in Mycobacterium avium subsp. paratuberculosis intracellular survival within bovine
Jun Ho Lee1, Eun-Seo Lee1, Xi-Rui Xiang1
1Department of Infectious Disease, College of Veterinary Medicine, Seoul National University, Seoul, 08826, Republic of Korea; BK21 FOUR Future Veterinary Medicine Leading Education and Research Center, College of Veterinary Medicine, Seoul National University, Seoul, Republic of Korea.
Abstract:
Mycobacterium avium subsp. paratuberculosis (MAP) is the causative agent of Johne's disease, a chronic enteritis in ruminants, and is capable of persisting within macrophages despite the activation of host immune defenses. Although this intracellular persistence is a key determinant of MAP pathogenicity, the bacterial factors and host responses that regulate this process remain poorly understood. In this study, we established the first CRISPR interference (CRISPRi) platform applied to bovine monocyte-derived macrophages (MDM) to evaluate the functions of MAP genes involved in intracellular survival and to perform an integrative analysis of host transcriptomic responses. MAP mutants were targeted to two genes (mdh and MAP1981c). The optimal concentration of anhydrotetracycline (ATc) was determined to be 2 μg/ml by measuring the survival of the cells and the downregulation of gene expression levels in the cells up to 72 h. The gene expression profiles and intracellular MAP levels were investigated using RNA-seq and colony-forming units, respectively. The survival rates of the MAP mutants significantly decreased with the time course of infection in MAP-mdhKD and MAP1981cKD (KD, knockdown). RNA-seq-based gene expression profiling suggested that target gene silencing in MAP mutants led to altered expression of host genes involved in lipid metabolism, T-cell activation reduction, and antimicrobial response in bovine MDM, contributing to reduced intracellular survival of MAP. Our study demonstrates that the downregulation of mdh and MAP1981c in MAP significantly alters the host transcriptomic landscape in bovine MDM, revealing their critical roles in subverting host immune defenses for intracellular persistence.
Insights
We developed a CRISPR interference (CRISPRi) platform to study Mycobacterium avium subsp. paratuberculosis (MAP) gene function in bovine macrophages. Silencing MAP genes mdh and MAP1981c reduced bacterial survival and altered host immune responses, revealing their role in persistent infections.
Area of Science:
- Veterinary Microbiology
- Immunology
- Genetics
Background:
- Mycobacterium avium subsp. paratuberculosis (MAP) causes Johne's disease in ruminants.
- MAP's ability to persist inside host macrophages is crucial for its pathogenicity.
- Bacterial factors and host responses governing MAP intracellular survival are not well understood.
Purpose of the Study:
- To establish a CRISPR interference (CRISPRi) platform in bovine monocyte-derived macrophages (MDM) for MAP gene functional analysis.
- To investigate the role of MAP genes mdh and MAP1981c in intracellular survival.
- To analyze host transcriptomic responses to MAP gene manipulation.
Main Methods:
- Development of a CRISPRi system in bovine MDM targeting MAP genes.
- Optimization of anhydrotetracycline (ATc) concentration for gene knockdown.
- RNA sequencing (RNA-seq) to profile host gene expression.
- Colony-forming unit (CFU) assays to quantify intracellular MAP survival.
Main Results:
- CRISPRi-mediated knockdown of MAP genes mdh and MAP1981c significantly reduced MAP survival in bovine MDM.
- Gene silencing altered host gene expression related to lipid metabolism, T-cell activation, and antimicrobial responses.
- The study identified optimal ATc concentration (2 μg/ml) for effective gene knockdown.
Conclusions:
- The mdh and MAP1981c genes are critical for MAP's intracellular persistence in bovine MDM.
- Downregulation of these MAP genes impacts host immune pathways, including lipid metabolism and immune cell activation.
- This study provides a novel tool for dissecting MAP pathogenesis and host-pathogen interactions.
