Abstract

BackgroundConcerted efforts to identify the pathogenesis and mechanism(s) involved in pansteatitis, (a generalized inflammation of the adipose tissue), that was attributed to the recent crocodile die off in the Olifants River and Loskop Dam in Kruger National Park, Mpumalanga, South Africa have been in the forefront of research in recent time. As part of the efforts, molecular characterization of healthy and pansteatitis adipose tissue was carried out by RNA sequencing (RNA-Seq) using Next Generation Sequencing (NGS) and de novo assembly of the adipose transcriptome, followed by differential gene expression analysis.MethodologyHealthy adipose tissue consisting of fifty samples was collected from the subcutaneous, visceral, intermuscular adipose tissues and the abdominal fat body of ten 4 years old juvenile crocodiles from a local crocodile farm in Pretoria, South Africa. Ten pansteatitis samples were collected from visceral and intermuscular adipose tissues of five crocodiles that were dying of pansteatitis.ResultsForty-two thousand, two hundred and one (42,201) transcripts were assembled, out of which 37, 835 had previously been characterized. The de novo assembled transcriptome had an N50 (average sequence) of 436 bp, percentage GC content of 43.92, which compared well with previously assembled transcripts in the saltwater crocodile. Seventy genes were differentially expressed and upregulated in pansteatitis. These included genes coding for extracellular matrix (ECM) signaling ligands, inflammatory cytokines and tumour necrosis factor alpha (TNFα) receptors, fatty acid synthase and fatty acid binding proteins, peroxisome proliferator-activated receptor gamma (PPARγ), nuclear factor and apoptosis signaling ligands, and mitogen activated protein kinase enzymes among others. Majority (88.6%) of the upregulated genes were found to be involved in hypoxia inducible pathways for activation of NFkβ and inflammation, apoptosis, Toll-like receptor pathway and PPARγ. Bicaudal homologous 2 Drosophila gene (BICD2) associated with spinal and lower extremity muscle atrophy was also upregulated in pansteatitis while Sphingosine -1-phosphate phosphatase 2 (SGPP2) involved in Sphingosine -1- phosphate metabolism was downregulated. Futhermore, Doublesex–mab-related transcription factor 1 (DMRT1) responsible for sex gonad development and germ cell differentiation was also downregulated.ConclusionThus, from the present study, based on differentially expressed genes in pansteatitis, affected Nile crocodiles might have died partly due to their inability to utilize stored triglycerides as a result of inflammation induced insulin resistance, leading to starvation in the midst of plenty. Affected animals may have also suffered muscular atrophy of the lower extremities and poor fertility.

Highlights

  • The use of RNA sequencing (RNA-Seq) and de novo transcript assembly is an attempt to characterize all expressed mRNA transcripts, especially in organism with no reference genome that is already sequenced [1]

  • From the present study, based on differentially expressed genes in pansteatitis, affected Nile crocodiles might have died partly due to their inability to utilize stored triglycerides as a result of inflammation induced insulin resistance, leading to starvation in the midst of plenty

  • Pansteatitis samples of the visceral and intermuscular adipose tissues were collected from five adult Nile crocodiles, which were dying of pansteatitis in the wild at the Loskop Dam, Olifant River in Mpumalanga, South Africa

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Summary

Introduction

The use of RNA-Seq and de novo transcript assembly is an attempt to characterize all expressed mRNA transcripts, especially in organism with no reference genome that is already sequenced [1]. Using the domestic chicken (Gallus gallus) as a reference, the evolutionary development and relationship between Tuatara, snake, bearded dragon and the Nile crocodile have been reported [3]. These authors have made efforts to update the study and produce better annotation as well as include more reptilian species in an attempt to produce a unique repository of Saurapoda genomics and transcriptomics using personally developed algorithm–LANE runner 2.0 (www.reptilian-transcriptomes.org) [4]. As part of the efforts, molecular characterization of healthy and pansteatitis adipose tissue was carried out by RNA sequencing (RNA-Seq) using Generation Sequencing (NGS) and de novo assembly of the adipose transcriptome, followed by differential gene expression analysis

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