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Status |
Public on Dec 07, 2019 |
Title |
Mycobacterium avium ssp. paratuberculosis Infection Induces an Immune Tolerance Phenotype in Primary Bovine Macrophages from Johne’s Disease Cows (Agriculture and Agri-Food Canada_N.Bissonnette_J000079) |
Organism |
Bos taurus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Mycobacterium avium ssp. paratuberculosis (MAP) is the causative agent of Johne’s disease (JD), which is also known as paratuberculosis, in ruminants. The mechanisms of JD pathogenesis are still unclear, but it is known that MAP subverts the host immune system for years by using macrophages as its primary reservoir. The effect of MAP infection on macrophages is often studied in healthy or experimentally infected cows, but reports on primary macrophages from naturally infected cows are lacking. In our study, the transcriptome of primary monocyte-derived macrophages challenged with live MAP was analyzed using next-generation sequencing (RNA‑seq). The gene expression signatures of macrophages from cows diagnosed as negative or positive for JD [JD(–) or JD(+), respectively] revealed differential host–pathogen interplay, highlighting long-term mechanisms established during mycobacterial disease. In JD(–) cows, a considerable number of genes (1,436) were differentially expressed at 8 h post-infection (hpi). Interestingly, while expected inflammatory immune response pathways were among the significant pathways, others related to Hepatic fibrosis/hepatic stellate cell activation, lipid homeostasis, such as the LXR/RXR [liver X receptor/retinoid X receptor] activation, and autoimmune diseases such as atherosclerosis and rheumatoid arthritis were consistently among the top significant pathways. Unexpectedly, the macrophages from JD(+) cows did not present a clear response pattern to ex vivo MAP infection, neither during the early period nor at 24 hpi. Analyzing of the transcriptomic profile of the uninfected macrophages, revealed 868 genes that were differentially expressed in JD(+) versus JD(–) cows. The down-regulated genes particularly modified the general cell metabolism by down-regulating amino acid synthesis, cholesterol biosynthesis, and other energy production pathways while introducing a pro-fibrotic pattern associated with foam cells. These modifications show the apparent importance of the metabolic pathways hijacked by MAP to subvert the immune cells. Our findings support the hypothesis that MAP could induce a tolerant-like state in circulating peripheral blood monocytes when they are differentiating into macrophages, which could further promote the persistence. Similar to other mycobacteria and pathogen-associated molecular patterns, MAP could influence macrophage behavior in the long term. This report contributes to a better understanding of MAP control of immune cells and its mechanisms of survival.
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Overall design |
A total of 12 dairy cows were selected for RNA-seq analysis. Cows were assigned to one of the two groups (six biological replicates) according their Johne's disease (JD) status : JD negative [JD(–)] (n = 6) or JD positive [JD(+)] (n = 6) cows. Cows from the JD(+) group were identified A to F, and cows in the JD(–) group were assigned from G to L. For each cow, monocyte-derived macrophages were cultured and exposed ex vivo to MAP infection for 1h, 4h, 8h, or 24h or conserved as non-infected controls harvested at 4 or 24h). The 72 libraries (2 controls + 4 infection time points per cow for 12 cows = 72 libraries) were sequenced.
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Contributor(s) |
Ariel O, Bissonnette N |
Citation(s) |
31969876, 33969037 |
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Submission date |
Apr 29, 2017 |
Last update date |
Jul 25, 2021 |
Contact name |
Nathalie Bissonnette |
E-mail(s) |
nathalie.bissonnette@agr.gc.ca
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Phone |
1(819)780-7253
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Organization name |
Agriculture and Agri-food Canada
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Department |
Sherbrooke research center
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Street address |
2000 rue College
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City |
Sherbrooke |
State/province |
Quebec |
ZIP/Postal code |
J1M 0C8 |
Country |
Canada |
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Platforms (1) |
GPL15749 |
Illumina HiSeq 2000 (Bos taurus) |
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Samples (72)
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Relations |
BioProject |
PRJNA384849 |
SRA |
SRP105462 |
Supplementary file |
Size |
Download |
File type/resource |
GSE98363_RAW.tar |
31.8 Mb |
(http)(custom) |
TAR (of TSV) |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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