2018
DOI: 10.1016/j.fsi.2017.11.045
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De novo transcriptome assembly and analysis of differential gene expression following lipopolysaccharide challenge in Pelteobagrus fulvidraco

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Cited by 17 publications
(4 citation statements)
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“…Thus, transcriptome technology addresses key gene expression patterns of non-model organisms in specific environments and enables detection of unknown genes and discovery of new transcripts. In recent years, transcriptome technology has been widely used in transcriptome assembly and annotation of many non-model fish, such as Megalobrama amblycephala [ 18 ], Pelteobagrus fulvidraco [ 19 ] and Atlantic salmon [ 20 ].…”
Section: Introductionmentioning
confidence: 99%
“…Thus, transcriptome technology addresses key gene expression patterns of non-model organisms in specific environments and enables detection of unknown genes and discovery of new transcripts. In recent years, transcriptome technology has been widely used in transcriptome assembly and annotation of many non-model fish, such as Megalobrama amblycephala [ 18 ], Pelteobagrus fulvidraco [ 19 ] and Atlantic salmon [ 20 ].…”
Section: Introductionmentioning
confidence: 99%
“…Lipopolysaccharide (LPS) is considered to be a potential immunostimulant and it is the main component of the Gram-negative bacterial cell wall. The yellow catfish stimulated with LPS showed a significant upregulation in the nonspecific immune responses, such as CXCL2-like chemokine, goose-type lysozyme, and cathepsin K [ 148 ]. Plant-based immunostimulants are considered to be an effective prophylactic measure to prevent diseases by enhancing the nonspecific immune system of fish [ 149 ].…”
Section: Rna-seq Analysis Of Healthy Fishmentioning
confidence: 99%
“…Although infectious disease outbreaks associated with pathogenic microorganisms have caused high mortality rates and led to catastrophic economic losses in farmed P. fulvidraco, little is known about the immune system of this species. We previously screened a cDNA library of P. fulvidraco upon immune challenge [37][38][39][40] and identified an ITLN homolog that showed high similarity with other fish ITLNs. The full-length cDNA was obtained via rapid amplification of cDNA ends (RACE)-PCR for the investigation of expression patterns in different tissues and of the immune responses.…”
Section: Introductionmentioning
confidence: 99%