Pseudocohnilembus persalinus genome database - the first genome database of facultative scuticociliatosis pathogens
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Pseudocohnilembus persalinus, a unicellular ciliated protozoan, is one of commonest facultative pathogens. We sequenced the macronuclear genome of P. persalinus in 2015, which provided new insights into its pathogenicity.
Here, we present the P. persalinus genome database (PPGD) (http://ciliates.ihb.ac.cn/database/home/#pp), the first genome database for the scuticociliatosis pathogens. PPGD integrates P. persalinus macronuclear genomic and transcriptomic data, including genome sequence, transcript, gene expression data, and gene annotation, as well as relevant information on its biology, morphology and taxonomy. The database also provides functions for visualizing, analyzing, and downloading the data.
PPGD is a useful resource for studying scuticociliates or scuticociliatosis. We will continue to update the PPGD by integrating more data and aim to integrate the PPGD with other ciliate databases to build a comprehensive ciliate genome database.
KeywordsPseudocohnilembus persalinus Genome database Useful resource Scuticociliate
Basic Local Alignment Search Tool
Generic Genome Browser
National Center for Biotechnology Information
Pseudocohnilembus persalinus genome database
Reads per kilobase per million mapped reads
The Pseudocohnilembus persalinus scuticociliate is a free-living marine ciliate first reported by Evans and Thompson in 1964 . Since then, its morphological, ecological, and phylogenetic have been well studied [2, 3, 4]. Since Kim and colleagues (2004) isolated P. persalinus from a diseased olive flounder in Korea, the organism has been recognized as a common facultative pathogen. P. persalinus infection causes scuticociliatosis, one of the most important fish diseases that has led to serious economic losses in marine aquaculture worldwide [5, 6]. P. persalinus is a facultative parasite and can be easily grown in the laboratory by feeding with bacteria. It is therefore a suitable model for studying the life cycle, genetics, and genomics of ciliates. Therefore, P. persalinus is an ideal model for investigating scuticociliatosis and the molecular mechanisms of its pathogenicity.
Like other ciliates, it has two types of functionally diverse nuclei within the same cytoplasm: a micronucleus (MIC) and a macronucleus (MAC). The MIC is transcriptionally silent and undergoes meiosis and transmits the genetic information to the progeny by sexual reproduction. In contrast, the MAC is highly polyploid and transcriptionally active, and controls the non-reproductive features of cell function. In 2015, we reported the P. persalinus MAC genome sequence . This was the first report of its type for a scuticociliate and a marine ciliate. Before that, the genomes of Tetrahymena thermophila, Paramecium tetraurelia and Ichthyophthirius multifiliis have first been sequenced and their comparative genomics analyses have comprehensively provided a better understanding of the unique features between the free-living (T. thermophila and P. tetraurelia) and typical parasitic (I. multifiliis) ciliates. As has been done for these ciliates, we have constructed the P. persalinus genome database (PPGD), which integrates genomic data, transcriptomic data, and gene annotation, thereby providing a useful resource for studying scuticociliates or scuticociliatosis.
PPGD mainly contains three types of datasets containing: (i) genomic sequence; (ii) gene expression data; and (iii) genome annotation. The PPGD also includes a brief summary of the biological, morphological, and taxonomical characteristics of P. persalinus.
The P. persalinus genome was sequenced with the Illumina platform and then assembled with SOAPdenovo . The 55.5 Mb genome was assembled from 288 scaffolds; the scaffold N50 is approximately 368 kb . A total of 13,186 genes were predicted by an ab initio prediction pipeline. Three types of annotation were included for these genes. The first type was functional prediction based on the BLAST hits when searched against the NCBI non-redundant protein database. The function of 4,265 genes (32%) could be assigned in this way; all other genes were annotated as “hypothetical protein”. The second type was protein domain or structure annotation based on InterProScan prediction . InterProScan integrates the results from multiple protein domain databases (Pfam, PRINTS, PANTHER, Gene3D and InterProScan) and some protein domain structures (coiled-coil, signal peptide, and transmembrane helix). A total of 11,948 genes could be annotated and 5,869 genes could be assigned GO (gene ontology) numbers based on InterProScan predictions. The third type was based on gene information on homologs in other ciliates. Ortholog groups in six ciliates (Ichthyophthirius multifiliis, Oxytricha trifallax, Paramecium tetraurelia, P. persalinus, Stylonychia lemnae, and Tetrahymena thermophila) were obtained using OrthoMCL , finally, 5,962 P. persalinus genes could be assigned, and thus provided in PPGD. We also used RNA-Seq data to obtain gene expression data for P. persalinus fed with bacteria to determine changes in gene transcription level under growth condition. The RNA-seq data was mapped to the P. persalinus MAC assembly using TopHat2 , then raw read counts were calculated for each gene using Subread  program, and the gene expression values were obtained by normalized the raw read counts to RPKM (reads per kilobase per million mapped reads) values. For all the 13,186 predicted genes, 92% (12,145) of genes have more or less reads mapped in the growth condition. Among them, 56% (6765) of genes showed an expression value larger than 10.
Utility and discussion
PPGD can be accessed via an easy-to-use web interface. The top row of navigation tabs (including “HOME,” “SEARCH,” “GENOME BROWSER,” “BLAST,” “MORPHOLOGY,” and “DATA DOWNLOAD”) directs the user to retrieve the information. The “HOME” page displays some background information on P. persalinus, introduces the database, and contains news and references related to the PPGD.
The PPGD also offers a search function for homologous sequence in BLAST, which is embedded into the database to provide a graphical interface (Fig. 2b). This allows users to search for gene information on homologs by directly inserting a query sequence into the text box. The CDS, protein sequence, and whole draft genome sequence of P. persalinus are organized as datasets for BLAST searching. Furthermore, “Expect value” and “Number alignments” options are included as advanced settings to filter low-comparability sequence. Finally, users can select an output format for downloading the homologous sequence.
The “MORPHOLOGY” page of PPGD displays detailed morphological information and the taxonomic status of P. persalinus, based on previous studies [5, 14, 15, 16, 17, 18]. Users can also download P. persalinus genomic sequence, protein sequence, and CDS in FASTA format and gene annotation information in CSV format via the “DATA DOWNLOAD” page.
We will continue to update PPGD by integrating more data, such as functional genomics data. As more and more ciliate genomes are sequenced, we will try to integrate these into PPGD to build a comprehensive genome database for ciliates.
PPGD is the first genome database for a scuticociliate. It integrates basic genomic information of P. persalinus and provides a useful resource for studying scuticociliates and scuticociliatosis.
We thank Ying Zhu (Nextomics Biosciences Co., Ltd.) for his help and suggestion on constructing the database.
This project was supported by grants from National Natural Science Foundation of China (No. 31525021) to WM, National Natural Science Foundation of China (No. 31672281) to JX, Knowledge Innovation Program of the Chinese Academy of Sciences to JX, Youth Innovation Promotion Association of the Chinese Academy of Sciences to JX.
Availability of data and materials
The database is freely available at http://ciliates.ihb.ac.cn/database/home/#pp.
JX, WM and WY conceived the work. KC, WW, JX, WY, and WM constructed the database. WW and KC wrote the manuscript. All authors have approved the final version of the manuscript.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
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