Evidence map›Paper›PMID 22955963›Full record

ArticleFish physiology and biochemistry2013

Identification and expression analysis of a CC chemokine from cobia (Rachycentron canadum).

Juan Feng, Youlu Su, Zhixun Guo, Liwen Xu, Xiuxiu Sun, Yunxin Wang

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Article in Fish physiology and biochemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Juan FengKey Laboratory of South China Sea Fishery Resources Exploitation and Utilization, Ministry of Agriculture, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510300, Guangdong, China. juanfeng@scsfri.ac.cn
Youlu Su
Zhixun Guo
Liwen Xu
Xiuxiu Sun
Yunxin Wang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemokines are small, secreted cytokine peptides known principally for their ability to induce migration and activation of leukocyte populations and regulate the immune response mechanisms. The cobia (Rachycentron canadum), a marine finfish species, has a great potential for net cage aquaculture in the South China Sea. We isolated and characterized a CC chemokine cDNA from cobia-designated RcCC2. Its cDNA is 783 bp in length and encodes a putative protein of 110 amino acids. Homology and phylogenetic analysis revealed that the RcCC2 gene, which contains four conserved cysteine residues, shares a high degree of similarity with other known CC chemokine sequences and is closest to the CCL19/21 clade. The mRNA of RcCC2 is expressed constitutively in all tested tissues, including gill, liver, muscle, spleen, kidney, head kidney, skin, brain, stomach, intestine and heart, but not blood, with the highest level of expression in gill and liver. The reverse transcription quantitative polymerase chain reaction was used to examine the expression of the RcCC2 gene in immune-related tissues, including head kidney, spleen and liver, following intraperitoneal injection of the viral mimic polyriboinosinic polyribocytidylic acid, formalin-killed Vibrio carchariae (bacterial vaccine) and phosphate-buffered saline as a control. RcCC2 gene expression was up-regulated differentially in head kidney, spleen and liver during 12 h after challenge. These results indicate that the RcCC2 gene is inducible and is involved in immune responses, suggesting RcCC2 has an important role in the early stage of viral and bacterial infections.

Indexed as

AnimalsBacterial VaccinesBase SequenceChemokines, CCCloning, MolecularCluster AnalysisDNA, ComplementaryDNA PrimersGene Expression ProfilingGene Expression RegulationMolecular Sequence DataPerciformesPhylogenyPolynucleotidesReverse Transcriptase Polymerase Chain ReactionSequence Analysis, DNABacterial VaccinesChemokines, CCDNA, ComplementaryDNA PrimersPolynucleotidespoly(rI).poly(dC)

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.