Corrigendum: De novo Assembly and Characterization of the Testis Transcriptome and Development of EST-SSR Markers in the Cockroach Periplaneta americana

The cockroach Periplaneta americana is a notorious pest and threat to health worldwide, with a high reproductive ability. However, a limited amount of data is available on the developmental stage-specific transcriptomes of P. americana. To identify genes involved in developmental processes and to develop additional SSR markers in P. americana, we carried out de novo assembly of the P. americana transcriptome using Illumina sequencing. After removing low-quality sequences, we obtained 64,954,709 contigs, which were further assembled into 125,390 unigenes with an average length of 711 bp. Based on similarity searches against known proteins, we identified 48,300 unigenes based on a cut-off E-value of 10−5. The assembled sequences were annotated according to gene descriptions, gene ontology and clusters of orthologous groups. A total of 14,195 potential SSRs were identified, and 41 of 63 randomly chosen primer pairs successfully amplified the predicted SSR markers, seven of which were polymorphic in size in P. americana. Furthermore, the Spag6 gene was confirmed to be testes specific, and the fru and RPSA genes were related to the development of the testis. This is the special report of a P. americana transcriptome obtained using Illumina sequencing technology, and a large number of molecular markers were developed.

genomes previously confirmed that relatively short reads can be effectively assembled and used for gene discovery and comparison of gene expression profiles 10,11 . For non-model organisms with limited genomic information, transcriptome sequencing is a cost-effective tool because it focuses mostly on the sequencing of functional and protein-coding RNAs 12 . Despite the feasibility of this methodology, Illumina next-generation sequencing has not yet been applied to P. americana.
Transcriptome sequencing is an effective method for obtaining EST sequences, which are essential for developing molecular markers and identifying novel genes. We focus on two types of markers, simple sequence repeats (SSRs) and single-nucleotide polymorphisms (SNPs). SSRs have been widely used in studies for gene identification and fingerprint mapping because they exhibit high levels of polymorphism and are associated with simple protocols and high reproducibility. Currently, only a few SSR primers have been developed in P. americana because the standard methods for developing SSR markers are time-consuming and expensive. Deep transcriptome sequencing provides a good resource for the development of SSRs because of its high throughput. Another type of marker, SNPs, are the most abundant type of marker and can be easily detected via high-throughput sequencing, which will be helpful in future linkage and associated studies.
Using transcriptome data, we closely examined several candidate genes involved in mating in males. For example, the Sperm-associated Antigen 6 (Spag6) gene was confirmed to be testes specific, and the fruitless (fru) and RPSA genes were related to the development of the testis. Spag6 is essential for flagellar motility and maintenance of the structure of the axoneme of mature sperm in mice 13 . Spag6 may play similar roles in testicular function in P. americana. Another gene, fru, appears to be the master regulator affecting male courtship behaviours. These courtship behaviours are either abnormal or absent in male flies lacking the fru gene, and the male-specific variants of fru are necessary and sufficient to elicit male courtship behavior 14 . This function is also very likely to be conserved in Blattella germanica 15 .
In this study, we generated over six billion bases of high-quality DNA sequences through Illumina sequencing and confirmed the suitability of using short-read sequencing for the de novo assembly and annotation of genes expressed in a eukaryote without reference genome information.

Results
Illumina sequencing and read assembly. cDNA samples were prepared from the testes of adult males of P. americana and sequenced using Illumina sequencing. After cleaning and quality checks, we obtained 6.3 Gb of reads. To facilitate sequence assembly, these raw reads were randomly clipped into 25-mers for sequence assembly using Trinity software 16 . These short 25-mers were subsequently assembled, resulting in 64,954,709 contigs, which were further assembled into 125,390 unigenes with an average length of 711 bp, ranging from 351 bp to 21,092 bp, including 24,887 unigenes larger than 1,000 bp (Table 1). To double check the quality of the sequencing data, we randomly selected 10 unigenes and designed 10 primer pairs for RT-PCR amplification. Amplification resulted in the expected product size in 8 of the 10 unigenes, and the sequences of all eight PCR products were confirmed using Sanger sequencing (data not shown).
Annotation of predicted proteins. For annotation, the unique gene sequences were first subjected to BLAST searches against the non-redundant NCBI nucleotide database (nr) employing Blastx with a cut-off E-value of 10 −5 . Using this approach, 48,300 unigenes (38.5% of all distinct sequences) returned a BLAST hit above the cut-off. These annotated unigenes formed a potential pool for gene identification in P. americana. Because of the relatively short length of the query sequences and the lack of genome information for cockroaches, most of the 77,090 assembled transcripts (61.5%) could not be matched to known genes. The proportion of sequences showing hits in nr databases was higher among the longer assembled sequences. Specifically, 76.3% of assembled sequences longer than 2,000 bp returned significant BLAST hits, whereas the proportion decreased to 60.5% for sequences ranging from 1,000 to 2,000 bp, to 38.9% for those between 500 and 1,000 bp and to 25.6% for sequences of less than 500 bp (Fig. 1). Regarding the species distribution, 11.4% of the distinct sequences showed top matches with sequences from the red flour beetle (Tribolium castaneum), followed by the body louse (Pediculus humanus corporis) (10.7%), the pea aphid (Acyrthosiphon pisum) (4.9%), and the jewel wasp (Nasonia vitripennis) (4.4%) (Fig. 2). Given the scarcity of prior information from P. americana, only 697 unigene sequences (0.56%) were matched with the highest degree of homology to genes from P. americana, and the majority of these hits were matched to lectin-related proteins (data not shown).
Gene ontology (GO) classification. Based on the nr annotation, GO assignments were employed to classify the functions of the P. americana transcripts. Among the 48,300 nr hits, a total of 25,661 sequences could be categorized into 61 functional groups (Fig. 3). Within the three main categories (biological process, cellular component and molecular function) of the GO classification, the 'Cellular process', 'Cell part' and 'Binding' terms were most prevalent, respectively. We also noted that a high percentage of genes were classified under the 'Metabolic process', 'Cell' and 'Catalytic activity' terms, while only a few genes were classified under the terms 'Cell killing', 'Virion part' and 'Morphogen activity' (Fig. 3).

SNP detection.
A total of 1,379 high-quality SNPs were identified among all of the unigenes ( Table 2).
In the quality filtering steps, the filtered SNPs were required to have at least 150 bp of flanking sequence on both sides of the SNP for further analysis. The predicted SNPs included 581 transitions (298 C/T and 283 A/G transitions) and 798 transversions (224 A/T, 160 A/C, 166 T/G and 248 C/G transversions).

Development and characterization of SSR markers.
To evaluate the quality of the assembly and develop new molecular markers, 125,390 unigenes assembled in this study were used to mine potential SSRs. The potential SSRs were defined as ranging from mononucleotide motifs with a minimum of ten repeats to hexanucleotide motifs with a minimum of three repeats. A total of 14,195 potential SSRs were identified, which could be divided into two types of mononucleotide SSRs, four types of dinucleotide SSRs, ten types of trinucleotide SSRs, twenty-nine types of tetranucleotide SSRs, thirty-four types of pentanucleotide SSRs and six types of hexanucleotide SSRs. The largest fraction of identified SSRs consisted of mononucleotides, which accounted for 59.8% (8,488) of the SSRs. The second most common type of SSR was trinucleotides, accounting for 26.9% (3,817) of the SSRs, followed by dinucleotides (1,190,8.4%), tetranucleotides (633, 4.5%), pentanucleotides (61, 0.4%) and hexanucleotides (6, 0.04%). Among the identified SSRs, A (T) (57.1%) accounted for 95.5% of the mononucleotide repeats, and AC (GT) (3.3%)  accounted for 39.1% of the dinucleotide repeats, while AAT (ATT) (8.1%), ATC (GAT) (5.5%) and AAG (CTT) (3.9%) together accounted for 65.5% of the trinucleotide repeats (Table 3).
To verify the identified SSR markers, we attempted to amplify the predicted SSRs via PCR. BatchPrime3 was used to design appropriate primers based on the flanking sequences. A total of 1,292 primer pairs for 1,186 out of 3,756 SSRs were successfully designed, while the remaining SSRs were not suitable for primer design. 63 primer pairs were randomly selected to amplify the genomic DNA of P. americana. Among the 63 primer pairs, 41 resulted in successful PCR amplification, whereas the remaining 12 primer pairs failed to generate PCR products at various annealing temperatures. Among the 41 successfully generated PCR products, 32 showed specific amplification, with 26 of these products presented the correct size, while five were longer than expected, and one primer pair amplified a significantly shorter product than expected.
Two P. americana clusters, including 10 individuals from Nanjing (Jiangsu province) and 10 from Taizhou (Zhejiang province), were randomly selected for amplification and polymorphism analysis. PCR  Genes related to the development of the testis. In the gene ontology (GO) classification, we focused on the 'Reproduction' term in the biological process category. A total of 386 unigenes were assigned to the 'Reproduction' term, which are likely to participate in reproductive processes. A further Blastx research was performed for these 386 unigenes, and scores above 80 for Blastx and a query cover above 30% were considered significant 1 . Among the remaining 261 unigenes (Table S1), the Sperm-associated Antigen 6 (Spag6) and fruitless (fru) genes were confirmed to be testes specific in previous studies. qRT-PCR was carried out to verify whether these two genes were also testes specific in P. americana. The primers used to amplify these two genes are listed in Table 5.
The RT-PCR results showed that the Spag6 gene was expressed only in the testis of male P. americana, and not in the ovary of females. The qRT-PCR results revealed that fru transcripts were approximately 1.6-fold more abundant in male P. americana than that in females (Fig. 5). Real-time PCR showed that RPSA was expressed in almost all of the tissues of P. americana (Fig. 6), presenting the highest expression level in the thorax, followed by the testis, head and leg, whereas it exhibited a low expression level in the ovary and intestine.

Discussion
To determine the gene expression profile in the testes of adult male P. americana, cDNA samples were prepared from the testes of adult males and sequenced through Illumina sequencing. After cleaning and quality checks, we obtained 6.3 Gb of reads. The genome size of P. americana was 3,338 Mb 18 , and approximately 6.3 Gb of transcriptome sequence data likely represented 1.9-fold coverage of the genome of P. americana. The de novo assembly of lower eukaryotic transcriptomes is straightforward, with more than 30-fold coverage being required for the full length of most yeast transcripts, whereas the de novo assembly of higher eukaryotic transcriptomes is much more challenging because of the larger sizes of the datasets and the difficulties involved in identifying alternatively spliced variants 5,19,20 . In spite of the limitation in terms of coverage, a large set of P. americana transcripts can provide valuable information for further gene identification and the identification of molecular markers. To facilitate sequence assembly, these raw reads were further assembled into 25,390 unigenes with an average length of 711 bp. The KEGG Pathway database is a collection of manually drawn pathway maps representing current knowledge regarding molecular interaction and reaction networks. Pathway-based analysis is helpful to better understand biological functions and gene interactions. Among the 312 KEGG pathways to which the obtained unigenes were assigned in this work, 'metabolic pathways' represented the largest category (3,929, 18%), followed by 'biosynthesis of secondary metabolites' (864, 4%), 'PURINE METABOLISM' (676, 3.1%) and 'pathways in cancer' (569, 2.6%). These results imply that active metabolic processes were underway in the testes 21 . The KEGG functional classification provided a valuable resource for investigating specific processes, functions and pathways in the testes of P. americana.
Genetic markers are important for studying population structure, diversity and the genetic basis of adaptive traits 22,23 . Markers based on transcriptome sequences are useful for the detection of variation and functional genetic analysis 24 . To verify the identified SSR markers, we attempted to amplify the predicted SSRs via PCR. A total of 1,292 primer pairs for 1,186 out of 3,756 SSRs were successfully designed using BatchPrime3, while the remaining SSRs were not suitable for primer design. For these SSRs, no appropriate primer pairs could be found for the following reasons: (1) the SSRs were located  too close to the end of the flanking region, or (2) the base composition of the flanking sequence was unsuitable. In our results, the observed Ho value varied from 0.3333 to 0.8333 (0.5 ± 0.1925), while the expected He varied from 0.3182 to 0.803 (0.5476 ± 0.1881). PIC values ranged from 0.2723 to 0.6874 (0.4389 ± 0.1718) ( Table 4). These results suggested that the primers designed to amplify SSR loci could serve as tools for polymorphism evaluation in P. americana. Furthermore, the predicted SSR loci could serve as a useful resource for SSR marker development.
In the Gene Ontology (GO) classification, we focused on the 'Reproduction' term in the biological process category. Spag6 was confirmed to be a testes-specific gene, and the fru and RPSA genes were related to the development of the testis. The results of RT-PCR showed that the Spag6 gene was expressed only in the testis of male P. americana, and not in the ovary of females. Spag6 is essential for sperm motility in mice, and a lack of Spag6 leads to inviability or infertility 13 . We speculate that Spag6 may play a similar role in controlling the testicular development of P. americana. Additionally, the qRT-PCR results showed that fru transcripts were approximately 1.6-fold more abundant in male P. americana than that in females, suggesting that the fru gene might play an important role in testicular development. In Drosophila melanogaster, more than 30 genes have been shown to affect behavioural steps in male courtship, and fru appears to be the master regulator. Male flies lacking the fru gene are sterile, with male-specific courtship behaviours being either abnormal or absent 14 , and the male-specific variants of fru are necessary and sufficient to elicit male courtship behaviour. A previous study on the German cockroach (B. germanica) showed that fru plays a similar role in controlling male sexual behaviour in this species. Therefore, this role has been conserved during insect evolution, at least from the phylogenetically basal order Blattaria to the most distal Diptera 15 . This function is also very likely to be conserved in P. americana.
RPSA has numerous known functions. It is a multifunctional protein that is present in several cellular compartments. In our GO classification, RPSA was assigned to the "Cell part" and "Macromolecular complex" terms. This receptor is an extracellular matrix glycoprotein that mediates cell attachment, movement, differentiation and growth 25 . It has also been associated with the regulation of cytoskeletal dynamics 26 and is expressed in a wide variety of tissues, including showing expression in tumour cells 27,28 . In a previous study by our group 29 , the transcription level of RPSA in the testis of P. americana was found to be 2.83-fold higher than in the ovary, in accord with a previous study in which the non-normalized gene expression level of RPSA in the testis was 6.3-fold higher than in the ovary 30 . Therefore, we speculate that RPSA may play a greater functional role in the testes than in the ovaries. In a previous study, this protein was shown to be upregulated by testicular heat shock 31 , and we predict that it might be involved in regulating the process of capacitation necessary for fertilization. The real-time PCR results showed that RPSA was expressed almost in all tissues of P. americana. Interestingly, it exhibited the highest expression level in the thorax, followed by the testis, head and leg, whereas a low expression level was observed in the ovary and intestine. Hence, it is suggested that RPSA plays a more important role in the thorax than in other tissues. However, we are still a long way from understanding how a specific ribosomal protein gene might contribute to the development of the thorax as well as gonadal development. Although the function of RPSA in reproduction has not yet been reported, RPSA would be a candidate gene for further research on fertilization. Additional studies on the molecular mechanisms of this gene involved in controlling the development of the thorax and testis should be carried out to obtain a better understanding of the development of a number of the organs of P. americana.
The assembled, annotated transcriptome sequences and gene expression profiles can serve as an invaluable resource for future identification of P. americana genes involved in reproduction.

Conclusion
In this study, we sequenced and analysed P. americana transcriptomes. A large-scale transcriptome dataset with 125,390 unigenes was produced, with 48,300 of these unigenes showing a BLAST hit below a cut-off E-value of 10 −5 . A total of 14,195 potential SSRs were identified, and 1,292 primer pairs were successfully designed. The SSR markers developed in this work constitute a valuable resource for studying genetic diversity, linkage mapping, and germplasm characterization analysis in cockroaches. The results confirmed that transcriptome analysis based on Illumina paired-end sequencing is a cost-effective and reliable approach in non-model organisms. In addition, the Spag6 gene was confirmed to be testes specific in P. americana using RT-PCR, and the fru and RPSA genes were related to the development of the testis in P. americana via real-time PCR. The present study provides new clues towards elucidating the molecular mechanisms underlying gonad development in P. americana. The obtained transcriptome information will also serve as an important public dataset for further research on gene expression, genomics, and functional genomics in P. americana.

Methods
Insect rearing and sample preparation. The specimens of P. americana were obtained in our laboratory. The colony was maintained at 25 °C, 60-70% r.h., with a 12 h:12 h daily light:dark cycle. Cockroaches that had moulted to the adult stage twenty to thirty days earlier were selected. We collected the testes from 10 males. All dissections and tissue samplings were carried out in carbon dioxide-anaesthetized specimens 32 .
Scientific RepoRts | 5:11144 | DOi: 10.1038/srep11144 RNA isolation and library preparation for transcriptome analysis. Total RNA was extracted from the head, thorax, legs, intestines, testes and ovaries of P. americana using the RNeasy® Plant Mini Kit (Qiagen, Hilden, Germany), following the manufacturer's protocols 32 . Considerable care was taken to ensure that all of the total RNA samples used in this study were of high quality (showing an A260/ A280 > 1.8 in nuclease-free water), with minimal degradation 33 . Briefly, mRNA was purified from 5 μ g of total RNA using oligo (dT) magnetic beads. Following purification, the mRNA was fragmented into small pieces using divalent cations under elevated temperature, and the cleaved RNA fragments were employed for first-strand cDNA synthesis using reverse transcriptase and random primers. This was followed by second-strand cDNA synthesis using DNA polymerase I and RNaseH. These cDNA fragments then underwent an end repair process and were ligated with adapters. These products were finally amplified via PCR to generate a cDNA library for sequencing.
Analysis of the Illumina sequencing results. The cDNA library was sequenced on the Illumina HiSeq2000 sequencing platform. The raw reads were cleaned by removing adaptor sequences, empty reads and short sequences with a length of less than 25 nt. The obtained reads were randomly clipped into overlapping K-mers (default K = 25) for assembly using Trinity software 16 . Distinct sequences were subjected to BLAST searches and annotation against the NCBI nr database using an E-value cut-off of 10 −5 . The obtained functional annotations according to Gene Ontology terms (GO; http://www.geneontology. org) were analysed using Blast2GO software. COG annotation was performed using Blastx 2.2.24 + software against the STRING 9.0 database. KEGG pathway annotation was performed using Blastx/Blastp 2.2.24 + software against the Kyoto Encyclopedia of Genes and Genomes database. Potential SNPs were detected using Samtools (http://samtools.sourceforge.net/) and VarScan (http://varscan.sourceforge.net/).

Quantitative RT-PCR expression analysis.
The quantitative RT-PCR was performed using the Rotor-Gene Q real-time PCR system. The SYBR Premix Ex Taqkit (Takara) was employed according to the manufacturer's protocol. In each amplification reaction, gene-specific primers were used; each primer set exhibited a unique optimal Tm in the real-time PCR assays. The β-actin rRNA gene was used as the internal reference, and the expression level of each gene was normalized against the β-actin rRNA gene. Melting curves were checked to ensure that the primers were amplifying the desired amplicons, and the obtained values reflected increases in the amplicons, rather than primer dimers or other unrelated sequences. The calculated efficiency values for the above genes and the β-actin rRNA gene amplicons were all within the range of 95 to 100%; therefore, no correction for efficiency was applied in further calculations. Relative expression values were calculated from three biological replicates using a modified 2 −∆∆CT method 34 . All of the data collected from the real-time PCR analyses are presented as averages ± SE. SNP detection. SNPs were inferred from sequence variations in mixed individual pools of P.

Development and detection of SSR markers.
Msatcommander was employed to identify repetitive elements in the assembled transcriptome of P. americana 35 . We focused on EST-SSRs with motifs ranging from two to six nucleotides and a minimum of 3 contiguous repeat units. Primer sequences were designed using BatchPrimer3 based on the flanking sequences, and the following criteria were required: 1) EST-SSRs with a minimum of seven repeats for dinucleotide motifs, five for trinucleotides, four for tetranucleotides and three for penta-and hexanucleotides; 2) a primer length between 18-22 bp, with an optimum of 20 bp; 3) a GC content between 40-60%, with an optimum of 50%; 4) a Tm of 55-65 °C (with a difference of no greater than 4 °C between the Tm values of the forward and reverse primers); and 5) an amplicon length of 100-300 bp with no secondary structure; for other parameters, the default settings were used.
Genomic DNA was isolated from the legs of different P. americana individuals using the Wizard TM Genomic DNA purification kit (Promega, USA) following the manufacturer's protocol. A total of 63 primer pairs were designed to check the correctness of the randomly selected SSR loci. The PCR products were analysed via electrophoresis on 8.0% non-denaturing polyacrylamide gels with silver staining 36 .
The appearance of each band was recorded as present (coded as 1) or absent (coded as 0). The scored data from polymorphic loci were used to calculate the polymorphism information content (PIC) according to the formula PIC = 1-∑p i 2 (where p i is the frequency of the i th allele at each locus) 37 . We used Popgene version 1.31 38 to calculate the observed heterozygosity (Ho) and expected heterozygosity (He) [39][40][41][42][43][44][45] .