Generation and analysis of expressed sequence tags from the ciliate protozoan parasite Ichthyophthirius multifiliis

Generation of the Ich ESTs

The processed sequences were subjected to cluster analysis using Vector NTI to evaluate sequence redundancies. Of the 8,432 sequences, 4,702 sequences fell within 976 contigs while 3,730 sequences were singletons. On average, each contig contained 4.8 sequences. Taken together, the 976 contigs and the 3,730 singletons made up 4,706 unique sequences (Table 1).

This work demonstrated that pooling of samples from all three stages of Ich life cycle followed by normalization was an effective way to reduce common messages across all three life stages. As one would expect, many structural genes would be expressed highly abundantly in all stages of the life cycle. In addition to making savings economically, pooling of samples allowed very effective normalization of these common transcripts without going through three rounds of normalization. This is consistent with our previous experience for the generation of a large number of catfish and oyster ESTs [32–36]. It is obvious that the pooling of samples from three developmental stages made it impossible to provide information concerning expression profiling in relation to developmental stages. However, such information would not be highly meaningful in normalized cDNA libraries where the major focus was to develop EST resources, rather than expression profiling. The other limitation caused by construction of a pooled cDNA library is the loss of sequencing flexibility as to the number of clones to be sequenced from each developmental stage library if they had been separately constructed.

The putative identities of the sequenced ESTs were assessed using BLASTX searches against the non-redundant (NR) database in GenBank [39]. All the search results are summarized in supplemental Table 1. Of the 4,706 unique ESTs, 2,518 (53.5%) had significant (E-value < 10^-5) hits. The remaining 2,188 (46.5%) EST sequences were not similar to any known sequences. Additional searches using the Swiss-Prot database resulted in putative identities for six additional unknown ESTs (Supplemental Table 1).

Identification of putative secretory proteins

Secretory proteins have been shown to be an important component in many biological processes, including pathogenesis of parasites [40–42]. We therefore searched for transcripts with putative signal peptides (suggestive of peptides of secretory proteins) within the EST set using the program SignalP 3.0 [43]. We found 314 ESTs with signal peptides, representing 6.7% of the unique sequences. Of these, 180 (3.8%) were from ESTs with no significant (E-value < 10^-5) BLASTX hit to the NR database in GenBank (Supplemental Table 1).

Comparative analysis to related taxa

The parasite Ich is phylogenetically placed between the protozoan's Plasmodium falciparum and Tetrahymena thermophila. Previous studies using 18S rDNA, histone genes, and I-antigens [44–46] suggested that Ich was more related to T. thermophila than to P. falciparum. Furthermore, T. thermophila and Ich share the ciliate nuclear genetic code, while P. falciparum uses the standard genetic code for translation. As the entire genome sequence of P. falciparum is available and the macronuclear sequencing project of T. thermophila was just recently completed, we made comparative BLAST analyses against both genome sequences.

The tBLASTx or BLASTX searches of Ich ESTs against the T. thermophila and P. falciparum genomes are summarized in Supplemental Table 2, and are presented in Figure 1. As expected based on the phylogenetic relationships, more Ich ESTs were similar to the genome sequences of T. Thermophila than to that of P. falciparum. Of the 4,706 Ich ESTs, 1,759 sequences were similar (E-value < 10^-5) to the T. thermophila genome sequences; whereas 817 were similar to the P. falciparum genome sequences. In total, 695 ESTs were similar to both T. thermophila and P. falciparum genomes, and thus are common to all three protists.

Of the 1,759 significant hits against the T. thermophila genome, 1,673 had been identified with a putative identity using BLASTX searches against the NR database, while the tBLASTx searches against the T. thermophila genome allowed identification of putative identities for additional 86 unique ESTs. Similarly, BLASTX searches against the P. falciparum genome allowed identification of 9 additional ESTs. Taken together, the BLAST searches against these two genomes allowed putative identities of 95 additional unique ESTs, bringing the total number of ESTs with significant similarities to known genes to 2,613.

Such genome searches also revealed that of the 2,518 ESTs that had significant hits in BLASTX searches against the NR database, 845 had no significant hits to the Tetrahymena genome. Clearly, these ESTs were similar to sequences of organisms other than the ciliate Tetrahymena.

These results clearly suggest conservation of a large fraction of gene sequences among the three protozoa parasites, with a higher level of conservation between Ich and the T. thermophila genome than between the Ich genome and the P. falciparum genome; although a significant fraction of gene sequences are also shared between the genomes of T. thermophila and P. falciparum. The results of this comparative analysis are compatible with existing phylogenetic analyses using several molecular markers such as the 18S rDNA, histone genes, and the I-antigens. Obviously, use of a large set of sequences should provide a greater confidence concerning genome evolution. The comparative analysis suggested that the EST resource generated from this study should be useful for phylogenetic analysis and studies concerning genome evolution.

Gene ontology

The unique Ich sequences were compared to annotations through the Gene Ontology Consortium [47] using the automated software Blast2GO [48]. We were able to obtain GO terms for 1,008 unique sequences using this method. Of these, 304 were contigs and 704 were singletons. Sequence descriptions, gene ontology (GO) and enzyme commission (EC) numbers are summarized in Supplemental Table 3. There were 258 sequences with both GO terms and EC numbers.

Gene ontology graphs using percentages of 2^nd level GO terms are presented in Figure 2 under the categories of cellular components (Fig. 2A), molecular functions (Fig. 2B), and biological processes (Fig. 2C). Of the cellular component GO terms, 45% and 26% were related directly with cellular and organelle components, respectively. In the category of molecular functions, the vast majority were involved in catalytic activity (41%) and binding activities (39%). Under the category of biological processes, 45% were involved in physiological processes; 43% were involved in cellular processes, 6% in regulation of biological processes, 4% in response to stimuli, and 2% in development (Figure 2).

Samples

The source of mRNA for this analysis was derived and expanded from a single parasite cloned from the infected fish. The source of the original Ichthyophthirius multifiliis was isolated from an infected fish obtained from a local pet shop and the parasite was transmitted to channel catfish held in a 50-l glass aquarium at the USDA-ARS Aquatic Animal Health Research Laboratory, Auburn, AL. The transmission of I. multifiliis was achieved through co-habitation of the infected fish with two fingerlings of channel catfish (3 inches in size). When the two catfish were infected, the symptoms of Ich, white spots, started to emerge when trophonts were collected by scraping with a glass slide. Channel catfish infected with maturing trophonts were rinsed in dechlorinated water and the skin was gently scraped to dislodge the parasites. Trophonts were harvested by filtering through a 0.22 μ m filter to remove fish skin. The trophonts were placed into a Petri dish to allow them to develop into theronts that were used to infect 8 fish each for the collection of trophonts, toments, and theronts, respectively. Trophonts were directly collected from the skin surface of the 8 infected fish. To collect tomonts and theronts, trophonts isolated from fish were placed in Petri dishes and allowed to attach. After replacing the water in the Petri dishes with fresh dechlorinated water to remove contaminating mucus, the trophonts were incubated at 24°C for 8 h to harvest tomonts (32–128 cells/cyst) or 24 h to harvest theronts. Trophonts, tomonts and theronts were washed with PBS (pH 7.4), concentrated with a centrifuge (Beckman Coulter, Inc., Miami, FL) at 228 × g for 5 min and discarded supernatant. After washing 3 times with PBS, parasite samples from the three life stages were stored in liquid nitrogen and used for the isolation of RNA for the construction of normalized cDNA library.

RNA isolation

Total RNA was isolated from the samples using the TRIzol reagent method from Invitrogen (Carlsbad, CA, USA) according to manufacturer's instructions. Briefly, samples of tomont, theront, and trophont were resuspended after thawing on ice, and 100 μl each were combined in a sterile tube to provide a total of 300 μl of Ich samples with equal fractions from each of its three life stages. As the major objective of this study was to generate EST resources with maximal efficiency of gene discovery, a pooled sample followed with normalization would allow inclusion of all transcripts in the library while reducing cost for library construction and increasing gene discovery rate. Three milliliters of TRIzol reagent was added to the sample tube. Cells were lysed by repetitively pipetting up and down. RNA was isolated following the manufacturer's protocol. The RNA pellet was resuspended in 100 μl of RNase-free double distilled water and divided into 25 μl aliquots. RNA aliquots were checked for quality using agarose gel electrophoreses containing formaldehyde.

Normalized library construction

The Creator Smart cDNA Library Construction Kit from Clontech (Mountain View, CA) and components from the TRIMMER-DIRECT Kit from Evrogen (Moscow, Russia) were used for the construction of the normalized cDNA library. Total RNA concentration was checked on a spectrophotometer and 1 μg RNA was combined with 1 μl of SMART IV oligonucleotide (Clontech) and 1 μl CDS-3M adapter (Evrogen) for first-strand cDNA synthesis. The reaction was incubated at 72°C for 2 min followed by immediate cooling on ice for 2 min. Next, 2 μl of 5× first strand buffer, 1 μl of DTT (20 mM), 1 μl of dNTP mix (10 mM), and 1 μl of PowerScript reverse transcriptase were added to the tube and incubated at 42°C for 1 h in a thermal cycler (PTC-100, Bio-Rad, Hercules, CA) then placed on ice. The SMART cDNA cloning system allows the enrichment of full-length cDNA through the use of a 5'-linker with 3'-GGG tails. Reverse transcriptase has terminal transferase activity that preferentially adds three additional Cs at the end of first strand cDNA. As a result, the first strand cDNA is able to base pair with the 5'-linker with 3'-GGG tails. Once base paired, the reverse transcriptase would switch the template and extend into the linker sequences allowing PCR amplification of full-length cDNA using a single primer (the 5'-linker has the same sequences as the linker containing poly T used for the synthesis of the first strand cDNA). Truncated cDNAs are not able to base pair with the 5'-linker and, therefore, get lost in the PCR amplification of the full-length cDNA.

The first strand cDNA was initially amplified by long-distance PCR (LD-PCR) using hot-start amplification. For the reaction, the following were combined in a reaction tube: 1.5 μl of the first strand cDNA, 60 μl of sterile deionized water, 7.5 μl of 10× Advantage 2 PCR buffer, 1.5 μl of 50× dNTP mix, 3 μl of 5' PCR primer and 1.5 μl of 50× Advantage 2 polymerase mix. The tube was mixed and briefly centrifuged and added to a pre-heated (95°C) thermal cycler. Cycle settings were 95°C for 1 min followed by 19 cycles of 95°C for 7 s, 66°C for 20 s, and 72°C for 5.5 min. The product was analyzed on a 1.1% agarose gel to determine the sizes and amount of the cDNA products before proceeding to the next step. The LD-PCR reaction was purified and eluted in 30 μl of sterile Nanopure water using the QIAquick PCR Purification Kit (Qiagen, Valencia, CA).

For the normalization procedure, the TRIMMER-DIRECT Kit from Evrogen (Moscow, Russia) was used. This system is specially developed to normalize cDNA enriched with full length sequences [49, 50]. The cDNA from the LD-PCR was quantified [~100 ng/μl] and 1 μl was mixed with 1 μl of the 4× hybridization buffer and 2 μl of sterile water. The mix was overlaid with mineral oil and incubated for 3 min at 98°C followed by 4 h at 70°C. Then, 5 μl of 2× DSN buffer (preheated to 70°C) and 0.25 Kunitz units of DSN enzyme were added and incubated at 70°C for 20 min. The DSN enzyme specifically degrades double-stranded molecules. The reaction was inactivated by adding 10 μl of DSN stop solution, and sterile water added to a final volume of 40 μl.

Following normalization, two rounds of PCR were performed using 1 μl of the normalization reaction as template. A shorter primer M1 (first 23 bases of the SMART IV oligonucleotide) was used in the first round of PCR with 15 amplification cycles using the same thermal cycling parameters as above; and an even shorter primer M2 (first 20 bases of the SMART IV oligonucleotide) was used in the second round of PCR for 15 amplification cycles of 95°C for 7 s, 64°C for 20 s, and 72°C for 5.5 min. Products were checked on a 1.1% agarose gel. The PCR products were quantified and 3 μg were used for treatment with proteinase K. All the subsequent procedures including proteinase K treatment, restriction digestion with Sfi I, size fractionation, and ligation followed the manufacture's instructions (Clontech). The cDNA was ligated to the pDNR-LIB vector. Electroporation (MicroPulser, Bio-Rad, Hercules, CA) was performed using DH12S electrocompetent cells following supplier's instructions (Invitrogen). A total of approximately 700,000 primary recombinant clones were obtained, and the library was amplified, titered, and stored in glycerol stocks in a -80°C freezer.

Plasmid isolation and EST sequencing

Independent colonies were picked and grown for 20 h at 37°C in 1.2 ml LB broth containing 30 μg/ml chloramphenicol. Plasmid DNA was isolated using the Perfectprep Plasmid 96 Vacuum Direct Bind Kit from Eppendorf (Westbury, NY). Plasmids were stored at -20°C until usage. The cDNA inserts were directionally sequenced from the 5'-end of the cDNAs using universal M13(-21) primer and the BigDye terminator sequencing kit version 3.1 from Applied Biosystems (Foster City, CA) on a 3130XL DNA analyzer (Applied Biosystems).

Sequence analysis

Base calling was performed using the Phred program [30, 31] at quality cut-off set at Phred 20. Raw sequences were then imported into the Vector NTI Advance 10 software (Invitrogen) and were subjected to trimming of vector sequences and 5'adapter sequences using default settings. Afterwards, poly (A) tails were trimmed where necessary and sequences less than 100 bases were removed. Contigs were built in Vector NTI ContigExpress using default settings. All unique sequences were compared to the GenBank database using BLASTX in the non-redundant (NR), Swiss-Prot, and Plasmodium falciparum 3D7 genome database. For comparison to the Tetrahymena thermophila SB210 genome, tBLASTx was used. The cut-off for sequence similarity used was E-value < 10^-5 for all analyses. Ciliate nuclear translation code was used in the BLAST searches. Search results from genome comparisons were summarized using a Venn diagram.

Gene ontology (GO) annotations were assigned using the program Blast2GO [48]. BLASTX results were loaded into the program and the default settings were used to assign GO terms to all unique sequences. From these annotations, pie charts were made using 2^nd level GO terms based on biological process, molecular function, and cellular component.

Putative secretory proteins and signal peptides were identified using both neural networks and hidden Markov model methods in SignalP 3.0 [43]. All 4,706 unique ESTs were used as the tester sequences. Open reading frames were predicted using both OrfPredictor [51] and BLASTX, with ciliate nuclear genetic code for ESTs of known genes and just OrfPredictor with unknown ESTs. The resulting deduced protein sequences from the ORFs were uploaded into SignalP 3.0. Sequences were identified as putatively secretory, predicted with signal peptides if both D-score in the neural network model and prediction probability in the hidden Markov model were significant.

Total lengths of all ESTs, G+C% content and simple repetitive elements were estimated using the Repeatmasker program [52].

Accession numbers

All Ich EST sequences were submitted to the dbEST database of NCBI. Continuous accession numbers are from EG957858–EG966289.