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Transcriptional profiling of Brucella ovis strains cultivated in the presence of high (5%) and low (0.04%) CO2

ABSTRACT: Transcriptional profiling of Brucella ovis strains cultivated in the presence of high (5%) and low (0.04%) CO2

PROVIDER: PRJNA540968 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR9007020.fastq.gz	Fastqsanger.gz
	SRR9007021.fastq.gz	Fastqsanger.gz
	SRR9007022.fastq.gz	Fastqsanger.gz
	SRR9007013.fastq.gz	Fastqsanger.gz
	SRR9007014.fastq.gz	Fastqsanger.gz

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Project description:Brucella dynamically engage macrophages while trafficking to an intracellular replicative niche as macrophages, the first line of innate host defense, attempt to eliminate organisms. Brucella melitensis, B. neotomae, and B. ovis are highly homologous, yet exhibit a range of host pathogenicity and specificity. RAW 264.7 macrophages infected with B. melitensis, and B. ovis exhibit divergent patterns of bacterial persistence and clearance; conversely, B. melitensis and B. neotomae exhibit similar patterns of infection. Evaluating early macrophage interaction with Brucella spp. allows discovery of host entry and intracellular translocation mechanisms, rather than bacterial replication. Microarray analysis of macrophage transcript levels following a 4 hr Brucella spp. infection revealed 130 probe sets altered compared to uninfected macrophages; specifically, 72 probe sets were increased and 58 probe sets were decreased with any Brucella spp. Interestingly, much of the inflammatory response was not regulated by the number of Brucella gaining intracellular entry, as macrophage transcript levels were often equivalent among B. melitensis, B. ovis, and B. neotomae infections. An additional 33 probe sets were identified with altered macrophage transcript levels among Brucella spp. infections that may correlate with species specific host defenses and intracellular survival. Gene ontological categorization unveiled genes altered among species are involved in cell growth and maintenance, response to external stimuli, transcription regulation, transporter activity, endopeptidase inhibitor activity and G-protein mediated signaling. Host transcript profiles provide a foundation to understand variations in Brucella spp. infections, while structure of the macrophage response and intracellular niche of Brucella spp. will be revealed through piecewise consideration of host signaling pathways. Keywords: Macrophage, intracellular pathogen, Brucella melitensis, Brucella neotomae, Brucella ovis, inflammatory immune response, species specificity

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Transcriptional profiling of Brucella ovis strains cultivated in the presence of high (5%) and low (0.04%) CO2

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