Objective

Anisakis pegreffii is a parasitic nematode belonging to the A. simplex (s.l.) species complex [1, 2]. It has a heteroxenous life cycle involving mainly cetaceans as definitive hosts, crustaceans as first intermediate hosts, fish, and squids as intermediate/paratenic ones. Its geographical distribution includes the Mediterranean Sea, the Iberian Atlantic coast waters, and the Austral region waters, between 30°S and 60°S. In humans, the accidental ingestion of third-stage larvae (L3) through the consumption of infected raw, undercooked, or improperly processed fish, causes a zoonosis, known as anisakiasis. Among the currently recognized nine biological species of the genus, so far only A. pegreffii and A. simplex (s.s.) cause anisakiasis [1, 3, 4].

The investigation of genes and proteins of A. pegreffii is crucial for understanding the parasite biological functions and its adaptation to abiotic and biotic conditions. It also represents a fundamental aspect to add knowledge about the molecular mechanisms involved in the evolutionary host-parasite interaction. Additionally, the molecules involved in the interaction between A. pegreffii and humans have not yet been elucidated. Finally, the absence of a suitable reference genome of this parasite species could make it difficult to achieve those goals. Although several RNA-seq analyses of L3 A. pegreffii at different experimental conditions and from different larvae tissues were carried out [5,6,7,8,9], a complete “ready to use” transcriptome is missing.

Objective of this research was to provide a robust high-confidence protein-coding transcriptome of the L3 stage of A. pegreffii acquired from the assembly of data newly generated in the present study with those previously stored. The findings were to provide a more accurate de novo reference transcriptome of A. pegreffii that will allow to shed light on genes implicated in the "cross-talk" between the parasite and its natural and accidental hosts.

Data description

The input dataset for de novo assembly of A. pegreffii L3 was composed by six RNA-seq datasets (Table 1, Data file 1, 2): one obtained in the present study (PRJNA752284) (Table 1, Data file 2) and five retrieved from SRA of NCBI (PRJNA589243, PRJNA602791, PRJNA374530, PRJNA316941, PRJNA312925). In order to obtain the RNA-seq dataset in this study, A. pegreffii L3, collected from the viscera of fish from the Mediterranean Sea, were maintained in vitro culture for 24 h. RNA and DNA were extracted from nine L3 using TRIzol reagent, as previously described [10, 11]. The extracted RNA from each three L3 was pooled, and the quantity check was performed by using Agilent 2100 Bioanalyzer. The cDNA library was prepared using the TruSeq Stranded mRNA kit (Illumina). Ligated products of 200 bp were excised from agarose gels and PCR amplified. Products were single end sequenced on an Illumina TruSeq platform. Genetic/molecular identification of L3 A. pegreffii was performed by sequences analysis of mitochondrial (mtDNA cox2), and nuclear (EF1 α − 1 nDNA, nas 10 nDNA) gene loci, as previously described [12].

Bioinformatic analysis was performed using a High-Performance-Computing platform [13]. For each bioproject, the quality control of reads was performed running FastQC v.0.11.2, before and after trimming step (Trimmomatic v.0.39 [14]). The quality assessment metrics for all trimmed data were aggregated with MultiQC v.1.9 [15]. Data file 3 (Table 1) shows both the mean read counts per quality scores and the mean quality scores in each base position higher than 35, for all the samples in the six analyzed bioprojects. A total of 393,512,048 cleaned reads (97% of whole raw reads) were obtained after the removal of the low-quality reads.

In order to construct a robust de novo transcriptome, three assembly tools with a multi-kmer approach were adopted: Trinity v.2.11.0 [16] (Table 1, Data file 4), rnaSPAdes v.3.14.1 [17] (Table 1, Data file 5) and Oases v.0.2.09 [18] (Table 1, Data file 6). Results for each assembler were merged with Transabyss v.2.0.1 [19] (Table 1, Data file 7). The merged assembly of A. pegreffii showed an average length of 939 bp and an N50 of 2859 bp. The assembly was validated with two algorithms: Busco v.4.1.4 [20] and Transrate v.1.0.3 [21]. A CD-HIT-est run v.4.8.1 was applied to the merged assembly to remove any redundant transcripts. A total of 394,635 unique genes were provided (Table 1, Data file 8) and a quality check was re-applied. A total of 260,872 ORFs were predicted by using Transdecoder v.5.5.0 [22] (Table 1, Data file 9).

The functional annotation of contigs was performed by using DIAMOND v.2.0.11 [23], calling both blastp and blastx functions against three databases (Nr, SwissProt and TremBL). The obtained results for blastx consisted in 86,982 (88.93%), 56,997 (58.47%) and 87,134 (89.39%) sequences against Nr (Table 1, Data file 10), SwissProt (Table 1, Data file 11) and TremBl (Table 1, Data file 12), respectively. Mapped transcripts listed in the Data file 10, yielded 38,972 matches (hits) with A. simplex. Blastp results also are available for Nr (Table 1, Data file 13), SwissProt (Table 1, Data file 14) and TremBl (Table 1, Data file 15). Output from InterProScan used to annotate protein signatures is available in Data file 16 (Table 1). In detail, 18,976 contigs were annotated: 5099 GO-annotated and 2800 KEGG-annotated.

Table 1 Overview of data files/data sets
Full size table

Limitations

The A. pegreffii transcriptome here obtained was assembled with those RNA-seq data sets from the third larval stage of the parasite species. The single transcriptome available from the fourth stage larva of A. pegreffii [8] was not included in this analysis because the main aim of this analysis was to provide a robust and "ready to use'' transcriptome of the infective stage (third larval stage) of the parasite also provoking the zoonotic disease (anisakiasis) to humans.