ABSTRACT: MinION sequencing of Francisella guangzhouensis FSC996 (08HL01032, 5, CCUG 60119, NCTC 13503) isolated from air conditioning systems in Guangzhou city, China.
Project description:To understand differences of gene expression profiles between Francisella strains RNA profiles of Francisella strains were generated by deep sequencing, in triplicate, using NovaSeq6000. qRT–PCR validation was performed using SYBR Green assays. Our study represents the first detailed differential transcriptomic analysis of Francisella strains , with biologic replicates, generated by RNA-seq technology.
Project description:This study aimed to investigate the differences in the immunity of Manis javanica and Manis pentadactyla through proteomics and microbiotas conjoint analysis.The nasal mucus of 10 pangolins (weight 5.71 kg ± 0.96 kg) was collected from the Wildlife Rescue Center of Shenzhen (Shenzhen City) and Guangdong Province (Guangzhou City). The pangolins from two different Wildlife Rescue Center were all in a healthy condition, although their feeding diets were not completely consistent.
Project description:Comparison of expression profiles of strains of Francisella to identify virulence factors We used custom microarrays to detail the global gene expression of four strains of Francisella (Schu4, LVS, OR960246, U112) and identified distinct classes of differentially expressed genes during this process.
Project description:Differential expression in human peripheral blood monocytes between F. novicida-infected and uninfected, and between Francisella tularensis tularensis isolate Schu S4 and uninfected. The goal was to examine genomewide transcriptional reponses to these two strains, and identify differentially-regulated genes that may help explain the virulence of Schu S4. Keywords: Immune Response, Human Monocytes, Bacteria, Francisella
Project description:The genus Francisella includes several species that cause zoonotic diseases and that have evolved to develop different strategies for survival within the host cells. Despite the critical importance of the diseases caused by members of the genus Francisella, the DNA repair mechanisms of this pathogen remain understudied. In this work, the transcriptional response of Francisella hispaniensis to the DNA-damaging agent ciprofloxacin was studied using RNA sequencing. Among the differentially expressed genes, we identified a S24 family peptidase-encoding gene. Electrophoretic mobility shift assays demonstrated that the product of this gene specifically binds to the palindromic sequence GTG-N11-CAC present in its promoter region, resulting in autoregulation. In silico analyses revealed that this S24 peptidase, here termed FddR, is most likely a co-opted phage repressor that implements a DNA-damage response across the Francisella genus. Our results provide insights into the SOS repair system of Francisella spp. and suggest that the identified S24 family peptidase is a direct regulator of the DNA damage response in F. hispaniensis.
Project description:Francisella tularensis may enter the body thorugh the lungs and cause fatal infection. In this study the inflammatory response to the virulent strain of Francisella (Schu4) was mapped over a 96h time-course using a custom microarray.