http://orcid.org/0000-0002-9601-6140
Figures
Abstract
Relative gene expression analyses by qRT-PCR (quantitative reverse transcription PCR) require an internal control to normalize the expression data of genes of interest and eliminate the unwanted variation introduced by sample preparation. A perfect reference gene should have a constant expression level under all the experimental conditions. However, the same few housekeeping genes selected from the literature or successfully used in previous unrelated experiments are often routinely used in new conditions without proper validation of their stability across treatments. The advent of RNA-Seq and the availability of public datasets for numerous organisms are opening the way to finding better reference genes for expression studies. Globodera rostochiensis is a plant-parasitic nematode that is particularly yield-limiting for potato. The aim of our study was to identify a reliable set of reference genes to study G. rostochiensis gene expression. Gene expression levels from an RNA-Seq database were used to identify putative reference genes and were validated with qRT-PCR analysis. Three genes, GR, PMP-3, and aaRS, were found to be very stable within the experimental conditions of this study and are proposed as reference genes for future work.
Citation: Sabeh M, Duceppe M-O, St-Arnaud M, Mimee B (2018) Transcriptome-wide selection of a reliable set of reference genes for gene expression studies in potato cyst nematodes (Globodera spp.). PLoS ONE 13(3): e0193840. https://doi.org/10.1371/journal.pone.0193840
Editor: Istvan Rajcan, University of Guelph, CANADA
Received: November 17, 2017; Accepted: February 19, 2018; Published: March 2, 2018
Copyright: © 2018 Sabeh et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and available from the NCBI bioproject database at https://www.ncbi.nlm.nih.gov/bioproject/274143 (accession number PRJNA274143).
Funding: This work was supported by Agriculture and Agri-Food Canada (AAFC) and the United States Department of Agriculture (USDA) through a Coordinated Agricultural Project (CAP) titled “Risk Assessment and Eradication of Globodera spp. in U.S. Production of Potato”, supported by award #2015-69004-23634 from the National Institute for Food and Agriculture (https://www.globodera.org/).
Competing interests: The authors have declared that no competing interests exist.
Introduction
Quantitative reverse transcription PCR (qRT-PCR) is the most commonly used technique to measure the expression level of a particular gene and is considered to be the most accurate and reliable method so far [1,2]. However, sample preparation, from RNA extraction to complementary DNA (cDNA) synthesis, can introduce biases in the quantification. To overcome these sources of variation, reference genes are often used as internal controls to normalize the expression data [3]. However, it is now recognized that conventional housekeeping genes used as references (e.g., glyceraldehyde-3-phosphate dehydrogenase and β-actin) are not systematically appropriate, owing to their variability in some conditions [4–6]. It is therefore important to select and validate good reference genes based on their expression stability within all the experimental conditions, in order to ensure valid results [1].
Until now, microarrays were frequently used to test large numbers of genes simultaneously for the selection of good reference genes. Although this is not a bad approach, the technique requires previous knowledge of the nucleotide sequences of each candidate gene. With the advent of next-generation sequencing and, especially, RNA sequencing (RNA-Seq), this problem is now overcome, and quantifying a large number of gene transcripts without previous knowledge of their gene sequences can be done routinely. The RNA-Seq method yields millions of reads that can be assembled to generate a transcript database, which contains the sequences and expression levels of all expressed genes at a given time. Because RNA-Seq is quantitative, it can be used to study RNA expression [7,8]. Therefore, analyzing RNA-Seq data from different treatments should allow the identification of reliable reference genes for further qRT-PCR analyses, a strategy that has rarely been used to date, and to our knowledge, never applied to Globodera spp.
The potato cyst nematodes (PCNs), Globodera rostochiensis Wollenweber and G. pallida Stone, are plant-parasitic nematodes that affect exclusively Solanaceae plants, including potato (Solanum tuberosum L.), tomato (S. lycopersicum L.), and eggplant (S. melongena L.) [9]. Present in over 75 countries around the world [10] and recognized as quarantine organisms, PCNs limit plant growth and are among the most economically damaging nematodes [11]. They are responsible for estimated yield losses of 9% of the world’s production of potatoes, currently the fifth most important crop in the world, with an annual production of more than 368 million metric tons (FAOSTAT, 2015 [12]).
The nematodes enter the roots of the host plant, where they transform one of the plant cells to create a complex feeding site to pump plant nutrients. This will limits plant growth and eventually causes heavy yield loss. After maturation and fecundation, PCN females will dry to form a cyst containing up to 500 eggs. Inside their protective shell, these eggs can survive more than 20 years in the soil without a suitable host [13,14]. Because of the strength and durability of the cysts, PCN populations are difficult to control with currently available control strategies [15]. Hatching, host penetration, and establishment of the feeding cell are key stages of the life cycle that we need to focus on in order to find new PCN control methods. Studying gene expression during these stages could highlight essential genes against which control strategies could be developed. Therefore, we need a good technique to estimate gene expression levels during these key stages, as well as a reliable set of reference genes with constant expression across the experiment.
Many studies have been published reporting reference genes to analyze the expression of the plant gene transcripts, such as in potato roots infected with G. pallida [16] and in giant cells and syncytia induced by Meloidogyne incognita and Heterodera schachtii [17], but to our knowledge, no studies have yet focused on finding reference genes for PCN species. The aims of our study were to identify a set of potential reference genes for G. rostochiensis based on expression data obtained by RNA-Seq and to test reference genes previously reported in Caenorhabditis elegans for their expression in G. rostochiensis. In addition, the gene expression stability of the selected candidates was also evaluated in G. pallida.
Materials and methods
RNA-Seq dataset
This study took advantage of a recently published transcriptome dataset from a G. rostochiensis hatching experiment conducted by our team [18]. These data (NCBI bioproject accession number PRJNA274143) include sampling at different life stages, including dry cyst, hydrated cyst, hydrated cyst soaked in PRD for 1 h, 8 h, 24 h, 48 h, and 7 d, and fully hatched infective larvae (J2). Library preparation and sequencing were performed at McGill University and Génome Québec Innovation Centre (Montreal, Quebec, Canada) using the TruSeq RNA sample prep kit v2 (Illumina) and a HiSeq 2000 sequencer (Illumina, San Diego, California, United States). All eight samples were multiplexed and sequenced in one lane for 100 bp paired-end reads. Two replicates were processed and assembled into a de novo transcriptome using the Trinity assembler (for details, see Duceppe et al. [18]).
Selection of candidate reference genes
A set of 15 genes previously used as references in the model nematode C. elegans [3,19,20] were selected to be evaluated in G. rostochiensis. These genes were pmp-3, Y45F10D.4, tba-1, cdc-42, csq-1, eif-3, ama-1, mdh-1, gpd-2, act-1, act-2, F35G12.2, rbd-1, rgs-6, and unc-16. The nucleotide sequences of these genes were retrieved from GenBank [21] and searched in the G. rostochiensis RNA-Seq transcriptome using BLAST to identify orthologues. Only the genes expressed in all the experimental conditions were kept for further analyses. The RNA-Seq dataset was also screened to identify transcripts with constant expression values in all the experimental conditions. This measurement of stability was based on standard deviations and expression variation through treatments, using log-transformed quantiles from normalized data. Only the four most stable genes were kept for further analysis.
Expression stability analysis of candidate reference genes
RNA extraction and cDNA synthesis.
The nematode populations used in this study were from a greenhouse rearing of G. rostochiensis pathotype Ro1, initially isolated from St-Amable, Quebec, Canada (obtained from Guy Bélair, AAFC), and G. pallida pathotype Pa2/3 from Noirmoutier, Vendée, France (obtained from Éric Grenier, INRA). The experimental conditions used were the same as in Duceppe et al. [18]: dry cyst, hydrated cyst, hydrated cyst soaked in potato root diffusate (PRD) for 1 h, 8 h, 24 h, 48 h, and 7 d, and fully hatched infective larvae (J2). Each G. rostochiensis sample contained approximately 1000 cysts, while the G. pallida samples contained only approximately 100 cysts because of low availability. Each sample was homogenized in 650 μL of RLT Plus buffer (Qiagen, Hilden, Germany) with one 6-mm zirconium grinding bead and 200 μL of 1-mm zirconium beads using the PowerLyzer 24 Homogenizer (Mo Bio, Carlsbad, California, United States) before RNA extraction. Total RNA was extracted using the RNeasy Mini Kit (Qiagen) according to the manufacturer’s instructions. All samples were treated with DNase (DNase I, New England Biolabs, Ipswich, Massachusetts, United States). A 2100 Bioanalyzer system (Agilent Technologies, Santa Clara, California, United States) was used to assess RNA concentration and purity. First-strand cDNA was synthesized with the SuperScript II reverse transcriptase (Invitrogen, Carlsbad, California, United States) according to the manufacturer’s instructions, from 0.5 μg of total RNA and using oligo (dT)18. Three replicates were made for each treatment.
Primer design and qRT-PCR.
Primers were designed using PrimerQuest tool (Integrated DNA Technologies, Inc., Coralville, Iowa, United States) based on the sequences retrieved from the G. rostochiensis RNA-Seq dataset. Target fragments lengths were designed between 84 and 130 bp. Primer information for the candidate reference genes is listed in Table 1. Reactions were prepared using QuantiTect SYBR Green PCR kit (Qiagen) and amplified on a Mx3000P qPCR System (Agilent Technologies) in a final volume of 20 μL according to the manufacturer’s instructions. Melting curve analyses were done following the amplification cycles in order to examine the specificity of the reactions. Amplification efficiencies were calculated with dry cysts using the Real-time PCR Miner algorithm (ver. 4.0) [22].
Data analysis.
RefFinder [23], a wrapper tool that integrates the statistical algorithm of BestKeeper [24], NormFinder [25], and geNorm [26], and the ΔCt method [27], was used to compare and rank the tested candidate reference genes. Based on the rankings from each program, it assigns an appropriate weight to an individual gene and calculates the geometric mean of their weights for the overall comprehensive ranking. Gene expressions from both the RNA-Seq database (read numbers) and qRT-PCR data (Cq values) across all treatments were compared. The variability of each gene across all treatments and replicates was also directly observed by plotting the distribution of the raw Cq values from the qRT-PCR experiment.
Validation of reference genes
Relative expression analyses of three genes with published expression data (NEP-1, cht-2, and eng) were performed using the 2−ΔΔCt method [28] in order to validate the selected reference genes. The genes GR, PMP-3, and aaRS were used as a reference set to normalize the expression of the targeted genes. Dry cysts were treatment used as the calibrator to calculate the fold changes for the other treatments. Gene expression was also normalized using the Act-1 gene for comparison.
Results
Selection of candidate reference genes
Among the 15 putative reference genes previously reported in C. elegans and selected for this study, 11 were found to have orthologues in G. rostochiensis (PMP-3, Y45F10D.4, tba-1, cdc-42, CSQ-1, EIF-3, AMA-1, MDH-1, gpd-2, Act-1, and Act-2). However, four of them (tba-1, cdc-42, gpd-2, and act-2) were eliminated because they had no expression values for at least one experimental condition in the RNA-Seq experiment (data not shown). Four contigs from the analysis of the RNA-Seq database (aaRS, GR, mce1, and ArgRS) were also selected as candidate reference genes because their expression levels were stable across all experimental conditions. Specific primers were designed for these genes (Table 1).
Expression stability analysis of candidate reference genes in G. rostochiensis
According to the distributions of raw Cq values, the genes with the lowest ranges were GR, AMA-1, MDH-1, and aaRS. The genes EIF-3 and Act-1 were the worst candidates, with Cq values spanning several units (Fig 1). However, a comparison of the distribution of the raw Cq values is not sufficient to evaluate the expression stability of candidate reference genes. Overall gene expression stability for both methods was assessed with RefFinder (Fig 2). GR, PMP-3, and aaRS expression were found to be the most stable, while EIF-3, Act-1, and CSQ-1 showed the highest variability across treatments. Details of this ranking based on individual algorithms are given in Table 2. All four methods gave a roughly similar ranking except BestKeeper with the qRT-PCR data. The genes GR, PMP-3, and aaRS were rated among the four most stable genes across both methods.
The median of three replicates of the eight conditions is represented by the line inside the box, 50% of the values are inside the box, the upper and lower edges represent the 75th and 25th percentiles, respectively, and the circles represent outliers.
Expression variations were calculated on two RNA-Seq replicates and three qRT-PCR replicates for the eight developmental stages of G. rostochiensis.
Comparison of rankings of 11 candidate reference genes from (A) RNA-Seq data and (B) qRT-PCR data, given by RefFinder in G. rostochiensis.
Evaluation of reference genes in G. pallida
Candidate genes were also investigated in G. pallida, a closely related species. Both PCN species share the same host plants and have very similar morphological characteristics. The qRT-PCR analysis was performed using the same experimental design and primers that were designed for G. rostochiensis. The results for G. pallida were similar to those obtained for G. rostochiensis. Details of this ranking based on individual algorithms are given in Table 3. Based on the qRT-PCR analysis, AMA-1, GR, and PMP-3 were the most stable potential reference genes for expression analysis in G. pallida. The results are similar to those obtained for G. rostochiensis as we find nearly the same genes in the first, second and last tier of the ranking.
Validation of reference genes
Validation of these recommended reference genes was performed using three genes (NEP-1, cht-2, and eng) with known patterns of expression. A qRT-PCR analysis was performed across the life stages of G. rostochiensis for each of these genes using the selected reference genes (aaRS, PMP-3, and GR) to normalize the data. The gene NEP-1 was found to be overexpressed nearly 10 times after 8 h of exposure to PRD, cht-2 was overexpressed 6 to 7 times after 24 to 48 h of exposure to PRD, and eng was overexpressed nearly 4 times after 48 h of exposure to PRD (Fig 3). In comparison, when normalization was performed using the Act-1 gene, no significant difference was found in gene expression.
Expression of (A) NEP-1, (B) cht-2, and (C) eng assessed by qRT-PCR in dry cysts (DC), water hydrated eggs (W), hydrated eggs exposed to potato root diffusate (PRD) for 1 h, 8 h, 24 h, 48 h, and 7 d, and in J2 larvae. All expression levels were normalized using the geometric mean of aaRS, PMP-3, and GR, our selected reference genes (in black) and Act-1 (in grey). Dry cyst was used as the calibrator for relative expression calculation. Error bars represent the standard error of the mean, and significant differences among treatments are indicated by different letters (Tukey’s test).
Discussion
Even though the PCNs, G. rostochiensis and G. pallida, are major threats to agriculture worldwide, many aspects of the infection process remain largely unknown, and several plant-nematode genomics analyses are currently underway. However, a set of reliable reference genes for the normalization of gene expression in qRT-PCR studies is still lacking. A perfect reference genes should have a constant expression and be unaffected by the experimental treatments. Because this is rarely met in practice, the use of at least three reference genes is generally recommended in order to obtain reliable expression data [5,29]. Previous studies often used common housekeeping gene as reference genes. However, it is now recognized that some of them are not suitable owing to their variability [4–6]. In this study, we evaluated seven reference genes frequently used for C. elegans in addition to four other candidates selected from RNA-Seq expression data across a range of G. rostochiensis development stages and times of exposure to root exudates. This study demonstrates the feasibility of using RNA-seq expression data for the selection of RT-qPCR reference gene, as well as, to our knowledge, the first validation of reference gene published for PCNs. This work was carried out in parallel with an in-depth characterization of gene expression during hatching in G. rostochiensis which led to the identification of the NEP-1 gene in Duceppe et al. [18]. The lack of good reference genes adapted to cyst nematodes was hampering this kind of expression studies and although we already used these genes in the above-mentioned work [18], they need to be formally validated using recognized methods and on more genes.
Using RefFinder, the genes GR (glutathione reductase), PMP-3 (putative ABC transporter), and aaRS (aminoacyl tRNA synthetase) were found to be the most stable among all the candidates. Therefore, they are the best available to be used as reference genes for normalization in qRT-PCR gene expression experiments for G. rostochiensis within the same experimental condition. Two of the three recommended reference genes (GR and aaRS) were identified based on RNA-Seq expression data analysis. This shows that RNA-Seq is an efficient approach to identify more stable and reliable reference genes and that public repositories like the NCBI Short Read Archive should be more exploited. The third gene, PMP-3, had already been selected as a reliable reference gene for C. elegans in previous studies [3,19]. Our results showed that this gene was also appropriate in G. rostochiensis, and may be a good candidate overall since its expression was found to be very stable in experimental conditions that differed noticeably from those generally found in most C. elegans studies. RNA-Seq data mining was found to be a very useful strategy to identify new reference genes from a much larger pool of candidates than qRT-PCR.
The PMP-3 gene encodes a peroxisomal membrane protein putative ABC transporter [30], the GR gene encodes a glutathione reductase that is involved in oxidative stresses regulation [31], and the aaRS gene encodes an aminoacyl tRNA synthetase that is part of RNA translation [32]. Since none of these recommended reference genes belong to the same metabolic pathway, their combination decreases the probability that an experimental factor would affect the expression of all three reference genes, and therefore support their common use as a reference gene set.
The rankings given by the four calculation methods (ΔCt, BestKeeper, NormFinder, and geNorm) are slightly different because they use different algorithms and calculation approaches (Table 2). RefFinder proposes a comprehensive ranking that considers calculations from the four methods and was used here to select the reference genes. Some candidate reference genes that had been ranked at the top of the RNA-Seq analysis were not as stable when tested using qRT-PCR. This difference could be due to the sample preparation, in addition to the multiple bioinformatics steps required before the expression analysis could take place. Some genes that are routinely used as reference genes for other nematode species in the literature (e.g., EIF-3 and Act-1 [1,2,33]) were less stable than those that were found as the best potential reference genes in the present study. This suggests that different morphological and physiological stages of G. rostochiensis may influence the expression of these usual reference genes. This influence would not be surprising, considering the huge reshuffling of gene expression across the different developmental stages, spanning from dormant cyst to infective juvenile larvae [18,34,35].
Very similar results were found with the sister species, G. pallida, for the ranking of reference gene candidates according to their stability. This similarity was expected, given the close phylogenetic relationship between G. rostochiensis and G. pallida. Using the same primers (for two out of three reference genes) for these two species would also increase the practicality of this set of reference genes.
To test the set of reference genes, we used it to normalize the expression of the NEP-1, cht-2, and eng genes in multiple life stages of G. rostochiensis known to have different levels of expression. The results were consistent with those previously reported. Duceppe et al. [18] showed that NEP-1 was significantly overexpressed 6.7 times after 8h of exposure to PRD; cht-2 transcripts were 4.9 and 5.3 times more abundant 24 and 48h after exposure to PRD respectively and eng showed a 4.4 fold change after 48h in PRD. These data are very similar to our RT-qPCR results after normalization with the proposed set of reference genes (Fig 3). In comparison, data normalization using the Act-1 gene, revealed no significant difference in gene expression according to a Tukey’s test (Fig 3). This result is probably explained by the high variation in the Act-1 Cq values across the treatments (Fig 1) confirming that this gene is not stable enough to be used as reference. This was also confirmed in other organisms, for example expression levels of actin were found to be highly affected by biotic or abiotic stresses in potato [36]. These observations further support the efficiency and purpose of our selected set of reference genes. The NEP-1 gene, which is involved in the degradation of peptides and in post-transcriptional modification, was also found to be overexpressed prior to hatching in C. elegans [37]. The cht-2 gene, codes for a hydrolytic enzyme that degrades chitin. In plant-parasitic nematodes, chitin has been found only in the eggshell and was found to be overexpressed during hatching [38]. The eng gene codes for beta-endoglucanase, a polysaccharide-degrading enzyme. That gene was also found to be expressed prior to hatching in Globodera tabacum, a closely related species [39]. In the present study, the normalized expression of these three genes was consistent with expectations from the previously reported studies. This confirms the efficiency of the selected reference genes.
Conclusion
In this work, we showed that the expression of the genes GR, PMP-3, and aaRS was stable in all tested stages of the PCNs nematodes life cycle and duration of exposition of hydrated cysts in potato root exudates. We, therefore, recommend their use as reference genes in qRT-PCR analysis of PCNs nematodes. It is important however to remind that some life stages–J3 and J4 –were not tested in this work. Researchers willing to use these reference genes for sexual differentiation study, for example, should validate their stability in their experimental conditions. This study also demonstrated the benefit of using RNA-Seq expression data for the identification of novel candidate reference genes for qRT-PCR analyses as well as the concordance of the RNA-seq and RT-qPCR expression data.
Acknowledgments
The authors thank Guy Bélair and Éric Grenier for providing us with isolates of potato cyst nematodes.
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