Evidence map›Paper›PMID 24023678›Full record

ArticlePloS one2013

Characterization of microRNAs in mud crab Scylla paramamosain under Vibrio parahaemolyticus infection.

Shengkang Li, Shuo Zhu, Chuanbiao Li, Zhao Zhang, Lizhen Zhou, Shijia Wang, Shuqi Wang, Yueling Zhang, Xiaobo Wen

Abstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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.

2 · The registry

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Leucine regulates the mTOR pathway to improve growth and enhance immune responses inAnimal nutrition (Zhongguo xu mu shou yi xue hui) · 2026
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors.

Shengkang LiGuangdong Provincial Key Laboratory of Marine Biology, Marine Biology Institute, Shantou University, Shantou, China.
Shuo Zhu
Chuanbiao Li
Zhao Zhang
Lizhen Zhou
Shijia Wang
Shuqi Wang
Yueling Zhang
Xiaobo Wen

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInfection of bacterial Vibrio parahaemolyticus is common in mud crab farms. However, the mechanisms of the crab's response to pathogenic V. parahaemolyticus infection are not fully understood. MicroRNAs (miRNAs) are a class of small noncoding RNAs that function as regulators of gene expression and play essential roles in various biological processes. To understand the underlying mechanisms of the molecular immune response of the crab to the pathogens, high-throughput Illumina/Solexa deep sequencing technology was used to investigate the expression profiles of miRNAs in S. paramamosain under V. parahaemolyticus infection. METHODOLOGY/PRINCIPAL

findingsTwo mixed RNA pools of 7 tissues (intestine, heart, liver, gill, brain, muscle and blood) were obtained from V. parahaemolyticus infected crabs and the control groups, respectively. By aligning the sequencing data with known miRNAs, we characterized 421 miRNA families, and 133 conserved miRNA families in mud crab S. paramamosain were either identical or very similar to existing miRNAs in miRBase. Stem-loop qRT-PCRs were used to scan the expression levels of four randomly chosen differentially expressed miRNAs and tissue distribution. Eight novel potential miRNAs were confirmed by qRT-PCR analysis and the precursors of these novel miRNAs were verified by PCR amplification, cloning and sequencing in S. paramamosain. 161 miRNAs (106 of which up-regulated and 55 down-regulated) were significantly differentially expressed during the challenge and the potential targets of these differentially expressed miRNAs were predicted. Furthermore, we demonstrated evolutionary conservation of mud crab miRNAs in the animal evolution process. CONCLUSIONS/SIGNIFICANCE: In this study, a large number of miRNAs were identified in S. paramamosain when challenged with V. parahaemolyticus, some of which were differentially expressed. The results show that miRNAs might play some important roles in regulating gene expression in mud crab under V. parahaemolyticus infection, providing a basis for further investigation of miRNA-modulating networks in innate immunity of mud crab.

Indexed as

AnimalsBase SequenceBrachyuraConserved SequenceEvolution, MolecularGene Expression ProfilingGene Expression RegulationHigh-Throughput Nucleotide SequencingInverted Repeat SequencesMicroRNAsMolecular Sequence AnnotationMolecular Sequence DataNucleic Acid ConformationPhylogenyReproducibility of ResultsReverse Transcriptase Polymerase Chain ReactionMicroRNAs

Identifiers

PMID24023678
PMCPMC3758354

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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.