- Open Access
Transcript and protein expression profile of PF11_0394, a Plasmodium falciparum protein expressed in salivary gland sporozoites
© Schlarman et al; licensee BioMed Central Ltd. 2012
- Received: 16 December 2011
- Accepted: 23 March 2012
- Published: 23 March 2012
Plasmodium falciparum malaria is a significant problem around the world today, thus there is still a need for new control methods to be developed. Because the sporozoite displays dual infectivity for both the mosquito salivary glands and vertebrate host tissue, it is a good target for vaccine development.
The P. falciparum gene, PF11_0394, was chosen as a candidate for study due to its potential role in the invasion of host tissues. This gene, which was selected using a data mining approach from PlasmoDB, is expressed both at the transcriptional and protein levels in sporozoites and likely encodes a putative surface protein. Using reverse transcription-polymerase chain reaction (RT-PCR) and green fluorescent protein (GFP)-trafficking studies, a transcript and protein expression profile of PF11_0394 was determined.
The PF11_0394 protein has orthologs in other Plasmodium species and Apicomplexans, but none outside of the group Apicomplexa. PF11_0394 transcript was found to be present during both the sporozoite and erythrocytic stages of the parasite life cycle, but no transcript was detected during axenic exoerythrocytic stages. Despite the presence of transcript throughout several life cycle stages, the PF11_0394 protein was only detected in salivary gland sporozoites.
PF11_0394 appears to be a protein uniquely detected in salivary gland sporozoites. Even though a specific function of PF11_0394 has not been determined in P. falciparum biology, it could be another candidate for a new vaccine.
- Plasmodium falciparum
- Gene expression
- Protein expression
Malaria is still a major problem around the world due to the development of insecticide-resistant mosquitoes, drug-resistant Plasmodium parasites, and economic/political instability in areas of the world where malaria is a significant problem . It is estimated that 225 million cases of malaria occur annually and, of those, 750,000 are fatal [2, 3]. Because of these issues, it is critical for improved and/or new malaria control methods to be developed. The Plasmodium falciparum gene, PF11_0394, was chosen as a candidate for study due to its potential role in the invasion of host tissues based on an in silico data mining protocol. PF11_0394 was selected based on data collected from PlasmoDB, the Plasmodium database, indicating that this gene likely encodes a putative surface protein, and is present in the sporozoite both at the mRNA transcript and protein levels [4–7]. These specific criteria were set for two reasons: first, not many sporozoite proteins are well characterized based on the difficulty of working with P. falciparum mosquito stages in a laboratory setting and, second, many Plasmodium proteins that have been shown to be critical for invasion and/or development of the parasite are surface or secreted proteins, including the sporozoite proteins, circumsporozoite (CS) protein and thrombospondin-related anonymous protein (TRAP) [8–10].
This study characterized in depth the P. falciparum gene, PF11_0394, at the transcript and protein levels to determine its expression profile during various life cycle stages. Using reverse transcriptase-polymerase chain reaction (RT-PCR) and green fluorescent protein (GFP)-trafficking studies, it was determined that PF11_0394 has transcript present during several life cycle stages, but its protein is only detected during the salivary gland sporozoite stage.
Parasite maintenance, parasite transmission, and cell cultures
Plasmodium falciparum strain NF54 was used for the following experiments and was maintained according to procedures described by Carter and colleagues . Briefly, P. falciparum cultures were maintained in human blood (O + male, BioChemed Services) at a 6% haematocrit in complete culture medium, RPMI 1640 (Gibco) supplemented with 25 mM HEPES (Gibco), 0.5% Albumax (Invitrogen), and 0.005% hypoxanthine (Sigma). The medium was changed every 48 hours and the parasites were kept in a gas mixture (3% O2, 3% CO2, and 94% N2) at 37°C . Cultures were diluted/split to prevent the parasitaemia from becoming too high by addition of fresh, washed 50% blood (blood washed three times with sterile RPMI and diluted 50:50 with RPMI), maintaining a 6% haematocrit level. The use of human blood was in compliance with federal guidelines and institutional policies. All experiments described in this paper were approved by the Institutional Biosafety Committee (IBC), the Institutional Review Board (IRB), and the University of Missouri Institutional Animal Care and Use Committee (IACUC).
In order to obtain infected mosquitoes to study the parasite stages within the vector host, four-five day old, female Anopheles stephensi were exposed to P. falciparum-infected blood (1:1 ratio of infected blood and human serum), using induced gametocyte cultures. Gametocyte cultures were produced by setting a standard culture (described above) at a parasitaemia of between 0.5-1.0% and maintaining them in complete culture media supplemented with 10% human serum (A + male, Interstate Blood Bank); however, instead of splitting the parasites with fresh red blood cells (RBCs), the culture was left undiluted such that a high parasitaemia developed and the parasites became stressed. This was done for 16 days and resulted in a mixture of male and female gametocyte stages (I-V), with a majority of them being mature stages. The mosquitoes were fed the infected blood for approximately 30 minutes, using a 37°C water-jacketed membrane feeding system. After the blood feed, only colony cages where at least 75% of females fed were utilized and the infected mosquitoes were maintained in an incubator (Low Temperature Illuminated Incubator 818, Precision) at 26-27°C with 82-88% humidity.
To obtain exoerythrocytic stages, axenic cultures (producing liver stage parasites without hepatocytes) were utilized and were produced by following an online protocol by Kappe and colleagues . In brief, approximately 5 × 104 salivary gland sporozoites were added to a well of a 48-well plate (Corning) and allowed to incubate in RPMI 1640 medium (Invitrogen) supplemented with 10% foetal bovine serum (Hyclone) and 500 units/ml and 500 μg/ml penicillin and streptomycin, respectively. These cultures were maintained in a 37°C incubator with 5% CO2 for 24 hours before collection for transcript expression studies .
Anopheles stephensi were used for all studies. Mosquitoes were reared using protocols available from the Malaria Research and Reference Reagent Resource Center (MR4). In brief, larvae and adults were maintained in an insectary with 78-85% humidity at approximately 26-27°C on a 12-hour light/dark cycle. Larvae were fed both a mixture of 0.33 g yeast (Fleischmann's) and 0.66 g micron (Sera) per 50 ml water and game fish chow (Purina). Adults were fed sucrose (0.3 M) ad libitum.
Selection of candidate gene, PF11_0394
An in silico data mining procedure was used to select PF11_0394 as a gene of interest. Briefly, PlasmoDB was utilized to search for P. falciparum proteins predicted to be expressed only by the sporozoite and containing a signal peptide, increasing its probability of being a surface protein [6, 13]. Next, additional sequence analysis programs available on the ExPASy Bioinformatics Resource Portal and SoftBerry, such as PSORT and ProtComp, were used to verify that the proteins encoded by the genes were predicted to either be located on the surface and/or secreted by the parasite [14, 15]. Those proteins that were verified by these two programs to meet the required criteria (and were not proteins that had been studied or were currently being studied) became the genes of interest, including PF11_0394.
PF11_0394 sequence analysis
Using PlasmoDB, the full genomic DNA (gDNA), complimentary DNA (cDNA), and protein sequence of PF11_0394 were obtained. A list of orthologs of PF11_0394 was compiled using both PlasmoDB and the National Center for Biotechnology Information's (NCBI) BLAST analysis program . The ortholog sequences were then aligned using Vector NTI (Explorer or Contig Express, Invitrogen). Additional sequence information for PF11_0394 was obtained by using software programs such as TargetP, SignalP, PSORT II, WoLF PSORT, and PROSITE, all found via the ExPASy Bioinformatics Resource Portal [14, 15, 17].
Isolation of Plasmodium falciparum-infected tissues for transcript expression studies
Anopheles stephensi were infected with P. falciparum as described previously. Ten days post-infection (PI), when oocyst sporozoites were mature using laboratory conditions, 50 mid-guts were dissected from the abdomens of An. stephensi that had fed on a P. falciparum-infected blood meal. The tissues were placed in 50 μl IX phosphate buffered saline (10X PBS, 0.2 M phosphate buffer and 1.5 M NaCl pH 7.0, diluted 1:10 with Millipore water) in microcentrifuge tubes, snap-frozen in liquid nitrogen, and stored at-80°CCutil needed for RNA isolation.
Salivary gland sporozoites
Fifty sets of An. stephensi salivary glands were dissected from mosquitoes that had fed on a P. falciparum-infected blood meal 14 days PI because sporozoites are found in the glands at this time under laboratory conditions. The tissues were put in 50 μl 1X PBS in microcentrifuge tubes, snap-frozen in liquid nitrogen, and stored at -80°C until needed for RNA isolation.
Axenic exoerythrocytic stages were generated as previously described. After 24 hours, Trizol (Invitrogen) was directly added to the cultures to begin the process of RNA isolation.
Mixed erythrocytic stages and gametocytes
Plasmodium falciparum cultures were maintained as previously described. Either mixed erythrocytic stage (ES) cultures (containing a mixture of rings, trophozoites, and schizonts) or 16-day-old mixed gametocyte cultures (containing a mixture of stage I-V gametocytes, but with more mature forms present) were collected by centrifugation at 2,650 × g for five minutes. The infected RBCs were lyzed with 0.05% saponin (Invitrogen) in complete culture medium for three minutes at room temperature (RT) and parasites collected by centrifugation for five minutes at 2,650 × g. Purified parasites were then washed once with RPMI 1640 medium and collected again by centrifugation as previously described. The parasite pellets were stored at -80°C until needed for RNA isolation.
RNA/DNA isolation and transcriptional analysis by reverse transcription-polymerase chain reaction (RT-PCR)
Total RNA was isolated from Plasmodium-infected tissues using a Trizol reagent-based protocol, following the manufacturer's instructions (Invitrogen). The samples were all DNase-treated (Promega), according to the manufacturer's instructions, to remove any contaminating gDNA. Approximately 2-3 μg of the DNase-treated RNA was used to synthesize cDNA using OligoDT primers from a SuperScript™ III First-Strand Synthesis System (Invitrogen), following the manufacturer's instructions.
Genomic DNA was isolated following the manufacturer's instructions using a DNeasy® Blood and Tissue Kit (Qiagen) and was used as a positive control for all RT-PCR experiments. PF11_0394 full-length gene specific primers (5'-atgaaaatttttaattacatatgtg-3' forward and 5'-ttatataatatttctattatcttcc-3' reverse) were used to amplify a 762 base pair (bp) gDNA fragment and a 561 bp cDNA fragment in a polymerase chain reaction (PCR) using 2.0 μl gDNA (~100 ng total)/cDNA (~1/10 the volume synthesized from above), 1.25 units GoTaq® DNA Polymerase (Promega), 1X GoTaq® Flexi Buffer, 1 mM MgCl2, 0.2 mM di-nucleotide tri-phosphate mix, and 0.5 μM primers. PCR conditions were as follows: an initial denaturing step of 95°C for three minutes, 35 repetitive cycles of denaturing at 95°C for 30 seconds, primer annealing at 56°C for 30 seconds and an extension at 62°C for three minutes, and then a final extension at 62°C for 10 minutes . Plasmodium falciparum heat shock protein-70 was used as a positive control during the axenic exoerythrocytic stage studies since PF11_0394 transcript was not detected and the primers used were 5'-aggtatagaaactgtgggtgg-3' forward and 5'-gattggttggcatacagcttc-3' reverse. After PCR amplification, all samples were separated on a 1% agarose gel and stained with ethidium bromide (EtBr) for UV detection. The experiments using oocyst sporozoites and axenic exoerythrocytic stages were done in biological duplicates. The experiments with salivary gland sporozoites, mixed ES, and mixed gametocytes were done in biological triplicates.
Creation of a PF11_0394/GFP-trafficking construct
To detect the presence of PF11_0394 protein throughout the life cycle of the parasite, a PF11_0394/GFP-trafficking construct was made by cloning base pairs 28-759 (excluding the stop codon) of the open reading frame of the gene into the pPM2GT vector (obtained from MR4) . The primers used to amplify the region were 5'-ccgctcgag cgtcctttaagaaatggtg-3' forward and 5'-ccgcctagg tataatatttctattatcttcc-3' reverse. The restriction enzymes XhoI and AvrII (New England Biolabs) are underlined and were used for cloning into the pPM2GT vector. These primers were used to amplify a 732 bp product via PCR using 2.0 μl DNA (~100 ng total), 1.0 μl FastStart High Fidelity Taq Polymerase (5 U/μl Roche), 1X FastStart Buffer, 1 mM MgCl2, 0.2 mM di-nucleotide tri-phosphate mix, and 0.5 μM primers. The PCR was conducted using conditions previously described, but with an annealing temperature of 54°C .
The product was double-digested with XhoI and AvrII, along with the pPM2GT vector, separated via gel electrophoresis, gel-purified according to the manufacturer's instructions using QIAquick® Gel Extraction Kit (Qiagen), and ligated with T4 DNA Ligase (Promega) following the manufacturer's instructions. Two microlitres of the ligation products were transformed into DH10B electrocompetant cells via electroporation and streaked on antibiotic resistant plates. Using colonies that grew on the plates, gDNA was isolated as previously described. The DNA was sequenced at the DNA Core Facility at the University of Missouri and aligned with the PF11_0394 sequence available from PlasmoDB using Vector NTI (Invitrogen) to confirm that the correct protein coding sequence was obtained.
Transfection of parasites with the trafficking construct
Transfections of P. falciparum were carried out according to Crabb and colleagues . Before performing the transfections, mixed ES parasite cultures were synchronized with 5% D-sorbitol (Sigma) for 10 minutes followed by two washes with RPMI 1640 (Gibco) at 1,600 × g for five minutes two days before transfection. In addition, plasmid DNA was isolated using a Plasmid Maxi Kit (Qiagen) and equilibrated in CytoMix (120 mM KCl, 0.15 mM CaCl2, 2 mM EGTA, 5 mM MgCl2, 10 mM K2HPO4 pH 7.6, and 25 mM HEPES pH 7.6). The synchronized P. falciparum ring stage NF54 parasites were electroporated (BTX 600, BTX Harvard Apparatus; 0.2 cm cuvette, 0.31 kV, 950 μF, maximum resistance) with 50 μg of the plasmid DNA in CytoMix . Transfected P. falciparum cultures were maintained as previously described.
Two days following electroporation, media containing WR99210 (2.5 nM, Sigma) was added to the cultures to begin the process of selecting transfected parasites utilizing the human dihydrofolate reductase gene drug cassette present in all constructs . To enrich for GFP-trafficking recombinants and eliminate episomal plasmids, parasites were subjected to at least three rounds of drug selection (three weeks on drug and three weeks off drug for each round).
To obtain a clonal population of parasites with no presence of wild-type parasites carrying episomes, a limiting dilution was performed on the transfected parasites. Parasites were seeded in 96-well plates (200 μl volume) at two concentrations, either 25% or 50% of wells would contain a single parasite, and maintained in a gassed modular incubator chamber (Billups-Rothenberg, Inc., 3% O2, 3% CO2, and 94% N2) at 37°C. Cultures were gassed every other day for 20 days. On days 7, 14, and 17, 0.4% fresh red blood cells were added. On day 20, 150 μl of the parasite culture were transferred to a 96-well plate to begin gDNA isolation for use in PCR and Southern blot analysis to determine if clonal populations of parasites had been successfully created. To isolate the gDNA, 50 μl of 6% saponin (Sigma) was added to the 150 μl of cultures in the 96-well plate and incubated for five minutes at RT. The plate was centrifuged for 15 minutes at 2,650 × g and supernatant removed. One hundred microlitres of 1X PBS was added to each well to wash the parasites and the plate was centrifuged as previously described. The 1X PBS was removed and 40 μl of down scale prep buffer (DSP, 1 M Tris-Cl pH 8.0, 1 M KCl, and 1 M MgCl2) working stock (985 μl DSP stock, 10 μl proteinase K, and 5 μl Tween 20) was added to each well and parasite pellets re-suspended in the DSP solution . The plate was incubated for 30 minutes at 50°C and then for 10 minutes at 95°C. The resulting gDNA was stored at 4°C until further use. The remaining 50 μl of parasites were used for expansion and cryopreservation of promising clonal parasite populations.
PCR and Southern blot verification of the GFP-trafficking construct
Integration of the transfected DNA at the correct location was verified for the PF11_0394/GFP clones by PCR and Southern blot analysis. To verify integration at the PF11_0394 locus by PCR, the primers 5'-atgaaaatttttaattacatatgtg-3' PF11_0394 gene specific forward primer and 5'-tccgtatgttgcatcacc-3' GFP reverse primer were used for the GFP-trafficking construct and 4.0 μl gDNA (isolated from the 96-well plates above), 1.25 units GoTaq® DNA Polymerase (Promega), 1X GoTaq® Flexi Buffer, 1 mM MgCl2, 0.2 mM di-nucleotide tri-phosphate mix, and 0.5 μM primers were used. PCR conditions were as follows: an initial denaturing step of 95°C for three minutes, 35 repetitive cycles of denaturing at 95°C for 30 seconds, primer annealing at 52°C for 30 seconds and an extension at 62°C for three minutes and 30 seconds, and then a final extension at 62°C for 10 minutes. The samples were all separated via gel electrophoresis (1% gel) and visualized via UV detection using EtBr.
Southern blotting was performed with gDNA isolated as previously described from ES parasites and DIG nonradioactive nucleic acid labelling technology (Roche) was used for visualization of the DNA. Genomic DNA (2-3 μg) that was digested with SapI and KpnI was hybridized with a 732 bp fragment of PF11_0394 created with the PCR DIG Probe Synthesis Kit following the manufacturer's instructions (Roche). Before hybridization, the DNA was separated on a 0.7% agarose gel and transferred to a positively charged nylon membrane (Osmonics) overnight via an upward transfer method. Following the manufacturer's instructions, the membrane was washed, hybridized with the above probes, and DNA products detected by autoradiography using the DIG Nucleic Acid Detection Kit (Roche).
The GFP-trafficking studies described below were done using two independent PF11_0394/GFP clones obtained via the limiting dilution process previously described. Each independent clone was used in a biological replicate, with a technical replicate conducted for each as well.
Mixed erythrocytic stages and gametocytes
Both P. falciparum mixed ES cultures and day 16 mixed gametocyte cultures were obtained by collecting 200 μl of infected blood from culture flaks. This protocol was followed for all experimental groups: PF11_0394/GFP, NF54 WT negative control parasites, and 3D7HT-GFP (obtained from MR4) positive control parasites . The collected, infected blood was centrifuged for five minutes at 2,650 × g and the supernatant removed. The infected red blood cells (iRBCs) were re-suspended in 200 μl 1X PBS containing DAPI nuclear stain (1:1,000 dilution, Invitrogen) and incubated in the dark for five minutes at RT. The iRBCs were centrifuged again for five minutes at 2,650 × g, washed once with 200 μl IX PBS, centrifuged a final time for five minutes at 2,650 × g, and a small drop of the blood was placed on a slide. Coverslips were placed on the slides and they were viewed with a 100X objective using an Olympus BX51 inverted fluorescent microscope coupled with a X-Cite® Series 120 fluorescent light source. The entire slide was scanned, with at least 100 iRBCs and 50 gametocytes observed for each group.
Zygotes and ookinetes
For all experimental groups listed above, six mid-guts were dissected from P. falciparum-infected An. stephensi 24-30 hours PI. The mid-guts were placed in 1X PBS containing DAPI nuclear stain (1:1,000 dilution) and incubated at RT for five minutes. The mid-guts were then placed three per slide into 15 μl of Matrigel™ (BD Biosciences) and coverslips placed on top. The infected mid-guts were then viewed as described above. Due to limited numbers, at least nine zygotes and five ookinetes were observed for each group per replicate.
For all experimental groups listed above, six mid-guts were dissected from P. falciparum-infected An. stephensi 10 days PI. The mid-guts were placed in 1X PBS containing DAPI nuclear stain (1:1,000 dilution) and incubated at RT for five minutes. Three mid-guts per slide were then placed into 15 μl of 1X PBS and coverslips placed on the slides. The infected mid-guts were viewed as previously described. At least 75% of the mid-guts had infections with three-18 oocysts per mid-gut for each group.
Haemolymph sporozoites were collected by perfusing the body cavity of 10 P. falciparum-infected An. stephensi 12 days PI with 1X PBS. Haemolymph for all experimental groups described above was collected in microcentrifuge tubes containing 40 μl 1X PBS with DAPI nuclear stain (1:1,000 dilution). The sporozoites were concentrated by centrifugation at 18,000 × g for five minutes, supernatant removed, and 10 μl of sporozoites spotted on slides containing 10 μl of Matrigel™ . Coverslips were placed on top of the slides and they were viewed as described above. Due to the difficulty of isolating haemolymph sporozoites from An. stephensi, only three to five haemolymph sporozoites were observed for each group per replicate.
Salivary gland sporozoites
For all three experimental groups, six pairs of salivary glands were dissected from P. falciparum-infected An. stephensi 13-20 days PI. The glands were placed in 1X PBS containing DAPI nuclear stain (1:1,000 dilution) and incubated at RT for five minutes. The glands were then placed into 15 μl of 1X PBS on a slide and coverslips placed on top. The infected salivary glands were viewed as previously described. For each experimental condition, at least 75% of the salivary glands were infected with hundreds of sporozoites observed per set of infected glands for each replicate.
PF11_0394 sequence analysis
PF11_0394 is a 762 base pair (bp) gene on chromosome eleven, containing one intron, resulting in a 561 bp cDNA product. The cDNA product encodes a 186 amino acid P. falciparum protein with an estimated molecular weight of 21,026 Daltons. Initial PlasmoDB data, based upon mass spectrometry results and sequence analysis, suggested that the PF11_0394 protein was expressed by salivary gland sporozoites, has a signal anchor, and four transmembrane domains (amino acids 28-50, 65-84, 97-119, and 149-171) [7, 24]. To confirm these data and obtain more information about PF11_0394, additional sequence analysis programs were utilized. SignalP revealed that PF11_0394 is predicted to have a non-cleavable signal anchor . Analysis using TargetP predicted that the protein enters the secretory pathway and, more specifically, is predicted to be a plasma membrane protein (located on the surface of the parasite) according to PSORTII and WoLF PSORT [26, 27]. Additional sequence analysis using PROSITE, PROTCOMP, Profam, and NCBI (BLASTp) sites predicted that the protein has no GPI-anchor, has multiple glycosylation and phosphorylation sites and has no functional identity with other known proteins [16, 28].
PF11_0394 transcript is present throughout a majority of the Plasmodium falciparum life cycle
Since generating exoerythrocytic stage parasites using primary human hepatocytes was not successful, a method to produce exoerythrocytic stages using axenic cultures (without the presence of liver cells) was utilized . Data obtained using the axenic exoerythrocytic stages suggest that the PF11_0394 transcript is not present during exoerythrocytic stages when compared to an exoerythrocytic stage control gene, P. falciparum heat shock protein-70 (PfHsp70), which did amplify a transcript (Figure 2E). The PfHsp70 gene was used as a positive control since its transcript is highly up-regulated in exoerythrocytic stage parasites, but barely detectable in sporozoites . This result indicated that exoerythrocytic stage parasites were indeed produced in the axenic cultures. Genomic DNA was used as a positive control and a no-reverse transcriptase reaction was used as a negative control as described above. Primers specific to the P. falciparum circumsporozoite protein gene (PfCS) were also used in the RT-PCR (data not shown). A transcript for PfCS was not amplified, even though the gene and protein have been shown to be expressed during the early exoerythrocytic stages . This result demonstrates that even though axenic liver stage parasites were generated, as indicated by the presence of PfHsp70 transcript, they were likely produced at low levels. Therefore, the PF11_0394 transcript could potentially be detected if greater parasite numbers were present.
In addition to data available on PlasmoDB, a literature search was conducted for PF11_0394 and its predicted orthologs in two rodent malaria models, P. berghei and P. yoelii, to assess previous transcript and protein detection data generated throughout the life cycle of the parasite. According to the literature and PlasmoDB, PF11_0394 transcript is present during the salivary gland sporozoite stage and erythrocytic stages (specifically free merozoites, rings, trophozoites, schizonts, and gametocytes) [5, 30–33]. Transcript results for exoerythrocytic stages vary between species, with a study in P. falciparum indicating no transcript expression and two studies, one using P. yoelii and one using P. berghei, confirming transcript expression [34–36]. Data obtained during these studies in P. falciparum for the salivary gland sporozoite stage, exoerythrocytic stages, mixed erythrocytic stages, and mixed gametocyte stages confirm results in the literature [5, 30–36]. The presence of PF11_0394 transcript in oocyst sporozoites has not been described elsewhere and represents new knowledge about the P. falciparum transcriptome.
The PF11_0394 protein is present in salivary gland sporozoites, as demonstrated by GFP-trafficking studies
Several attempts to produce PF11_0394 recombinant protein were employed, but were never successful. These included the use of several types of bacterial expression systems (Novagen), as well as a baculovirus expression system (Invitrogen). When using these systems, the PF11_0394 protein appeared to be expressed at low levels, but it could never be purified (even in the presence of protease inhibitors). Then, synthetic peptides were produced, using a commercial source (Genscript), and were used for IgY antibody production in chickens (Avian Immunology). Unfortunately, the peptides proved to be non-immunogenic, as the antibodies did not detect any proteins following Western blot analysis or produce any signals on immunofluorescent assays. PF11_0394 sequence analysis revealed that this protein has a signal anchor and four transmembrane domains, resulting in a largely hydrophobic protein embedded within the membrane of the parasite . Thus, this feature of the PF11_0394 protein may have caused the protein production techniques used to be unsuccessful. Therefore, a PF11_0394/GFP-trafficking construct was created and used for protein trafficking studies.
Due to the difficulty of generating liver stage parasites in vitro, protein detection studies were not able to be conducted for PF11_0394 during this particular life cycle stage. Nevertheless, based on data suggesting transcript is not present during the exoerythrocytic stages, it is predicted that the PF11_0394 protein is not present during the liver stages; however, there is always the possibility that the PF11_0394 protein is expressed during the liver stages, especially early exoerythrocytic stage development.
Attempts to generate a clonal population of mutant PF11_0394 parasites to assess a potential function of PF11_0394 were not successful
PF11_0394 gene disruption constructs were made for functional analysis by cloning base pairs 37-700 of PF11_0394 into both the pHD22y and pCAM-BSD vectors [15, 38, 39]. Unfortunately, once the constructs were transfected into P. falciparum, integration of the constructs was never observed via PCR analysis, even after four rounds of drug selection. The PF11_0394 protein is not expressed in mixed erythrocytic stage parasites (the stage of the life cycle when transfections are conducted), so the failure to obtain a mutant PF11_0394 parasite population was not likely due to it being essential during this life cycle stage. The lack of integration could be due to the genome of P. falciparum being highly AT-rich (~80%) with greater than 90% of it occurring in the intronic regions of the genome . Because PF11_0394 has one intron, it is a possibility that when the PF11_0394 disruption constructs were transfected into the P. falciparum genome, the highly AT-rich intron of PF11_0394 may have caused the constructs to homologously recombine with either other AT-rich areas of the P. falciparum genome or perhaps, with another gene that has an intron of similar sequence.
In summary, data obtained from these studies demonstrate that PF11_0394 is a P. falciparum protein that has orthologs in other Plasmodium species and also has orthologs with other Apicomplexans. PF11_0394 does not have orthologs with any protein outside of the Apicomplexan group and shares no functional identity with other known proteins. PF11_0394 is thus a novel protein to study in P. falciparum biology. Transcript detection studies determined that PF11_0394 transcript is present throughout a majority of the life cycle of the parasite, including mixed ES, mixed gametocyte stages, oocyst sporozoites, and salivary gland sporozoites, but is not detectable during axenic exoerythrocytic stages. Protein detection studies demonstrated that the PF11_0394 protein is present in salivary gland sporozoites and not in other stages examined.
Overall, these data obtained for PF11_0394 have determined that the PF11_0394 protein is present in salivary gland sporozoites and, therefore, may be required for parasite or sporozoite development/survival in the mosquito salivary glands and/or development within and/or invasion of human host tissues. A few Plasmodium sporozoite proteins have been found to be critical for development and/or invasion of host tissues. For example, both the CS protein and TRAP are sporozoite proteins that are essential for proper development and invasion of both mosquito salivary glands and human hepatocytes [9, 10, 41–45]. Thus, based on the protein detection profile of PF11_0394, it could be another candidate gene for a pre-erythrocytic stage vaccine since it does not share identity with any known human protein.
This study was supported by a NIH/NIAID grant, R01AI64306. The following reagents were obtained through the MR4 as part of the BEI Resources Repository, NIAID, NIH: Plasmodium falciparum PM2GT (MRA-805) deposited by D E Goldberg; P. falciparum 3D7HT-GFP parasites (MRA-1029); P. falciparum pCAM-BSD vector (MRA-848) deposited by D A Fidock; Homo sapiens pHD22Y vector (MRA-90) deposited by D A Fidock, T E Wellems. Lastly, the wild-type P. falciparum NF54 parasites were a gift from Dr Shirley Luckhart at the University of California-Davis.
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