ABSTRACT
This study investigates the resistive switching characteristics and underlying mechanism in 2D layered hexagonal boron nitride (h-BN) dielectric films using conductive atomic force microscopy. A combination of bipolar and threshold resistive switching is observed consistently on multi-layer h-BN/Cu stacks in the low power regime with current compliance (I comp ) of less than 100 nA. Standard random telegraph noise signatures were observed in the low resistance state (LRS), similar to the trends in oxygen vacancy-based RRAM devices. While h-BN appears to be a good candidate in terms of switching performance and endurance, it performs poorly in terms of retention lifetime due to the self-recovery of LRS state (similar to recovery of soft breakdown in oxide-based dielectrics) that is consistently observed at all locations without requiring any change in the voltage polarity for I comp ~1-100 nA.
ABSTRACT
In this study, we sought to learn whether adverse events such as chronic restraint stress (CRS), or 'nurture' in the form of environmental enrichment (EE), could modify depression-like behavior and blood biomarker transcript levels in a genetic rat model of depression. The Wistar Kyoto More Immobile (WMI) is a genetic model of depression that aided in the identification of blood transcriptomic markers, which successfully distinguished adolescent and adult subjects with major depressive disorders from their matched no-disorder controls. Here, we followed the effects of CRS and EE in adult male WMIs and their genetically similar control strain, the Wistar Kyoto Less Immobile (WLI), that does not show depression-like behavior, by measuring the levels of these transcripts in the blood and hippocampus. In WLIs, increased depression-like behavior and transcriptomic changes were present in response to CRS, but in WMIs no behavioral or additive transcriptomic changes occurred. Environmental enrichment decreased both the inherent depression-like behavior in the WMIs and the behavioral difference between WMIs and WLIs, but did not reverse basal transcript level differences between the strains. The inverse behavioral change induced by CRS and EE in the WLIs did not result in parallel inverse expression changes of the transcriptomic markers, suggesting that these behavioral responses to the environment work via separate molecular pathways. In contrast, 'trait' transcriptomic markers with expression differences inherent and unchanging between the strains regardless of the environment suggest that in our model, environmental and genetic etiologies of depression work through independent molecular mechanisms.
Subject(s)
Behavior, Animal , Depression/genetics , Environment , Hippocampus/metabolism , Restraint, Physical , Stress, Psychological/genetics , Transcriptome/genetics , Animals , Depression/metabolism , Depression/psychology , Disease Models, Animal , Gene Expression Profiling , Gene-Environment Interaction , Male , Rats , Rats, Inbred WKY , Real-Time Polymerase Chain Reaction , Restraint, Physical/psychology , Reverse Transcriptase Polymerase Chain Reaction , Stress, Psychological/metabolism , Stress, Psychological/psychologyABSTRACT
The freshwater snail, Biomphalaria glabrata is the obligate intermediate host for the transmission of the parasitic trematode, Schistosoma mansoni the causative agent of the chronic debilitating neglected tropical disease, schistosomiasis. We showed previously that in juvenile snails, early and significant induction of stress manifested by the expression of stress proteins, Hsp 70, Hsp 90 and reverse transcriptase (RT) of the non- LTR retrotransposon, nimbus, is a characteristic feature of juvenile susceptible NMRI but not resistant BS-90 snails. These latter, however, could be rendered susceptible after mild heat shock at 32°C, revealing that resistance in the BS-90 resistant snail to schistosomes is a temperature dependent trait. Here we tested the hypothesis that maintenance of BS-90 resistant snails at the permissive temperature for several generations affects the resistance phenotype displayed at the non-permissive temperature of 25°C. The progeny of BS-90 snails bred and maintained through several generations (F1 to F4) at 32°C were susceptible to the schistosome infection when returned to room temperature, shedding cercariae at four weeks post-infection. Moreover, the study of expression levels of the heat shock protein (Hsp) 70 protein by ELISA and western blot analysis, showed that this protein is also differentially expressed between susceptible and resistant snails, with susceptible snails expressing more protein than their resistant counterparts after early exposure to wild-type but not to radiation-attenuated miracidia. These data suggested that in the face of global warming, the ability to sustain a reduction in schistosomiasis by using refractory snails as a strategy to block transmission of the disease might prove challenging since non-lethal elevation in temperature, affects snail susceptibility to S. mansoni.
ABSTRACT
Pyoderma gangrenosum (PG) is a neutrophilic dermatosis of unknown aetiology. We report a 27-year-old male patient with diabetes, who presented with a nonhealing ulcer on the left leg, pruritic hyperpigmented papules distributed over the trunk and limbs, and chronic diarrhoea. He had eosinophilia, low haemoglobin and serum IgE levels, and raised erythrocyte sedimentation rate. Histopathology of the leg ulcer was consistent with the diagnosis of PG, while the histology of the hyperpigmented papule revealed tissue eosinophilia. Subsequent evaluation was conclusive of the diagnosis of PG, idiopathic hypereosinophilic syndrome (IHES) and selective IgE deficiency. Dexamethasone pulse therapy achieved resolution of the ulcer and reduction in the eosinophilia. Further evaluation for the persistent diarrhoea led to a diagnosis of lymphocytic colitis (LC), which responded to budesonide. To our knowledge, the association of PG with IHES, selective IgE deficiency or LC has not been previously reported.
Subject(s)
Colitis, Lymphocytic/complications , Diabetes Mellitus, Type 1/complications , Hypereosinophilic Syndrome/complications , Immunoglobulin E/deficiency , Pyoderma Gangrenosum/etiology , Adult , Humans , Leg Ulcer/etiology , MaleABSTRACT
Despite negative topline phase 3 clinical trial results for bapineuzumab and solanezumab in mild to moderate AD, findings from these trials and recent advances suggest renewed optimism for anti-amyloid therapies. Aß immunotherapy has now demonstrated its ability to engage CNS Aß and modify downstream CNS biomarkers in bapineuzumab treated patients, and to show likely cognitive benefits in mild patients treated with solanezumab. The current availability of potent BACE inhibitors provides additional opportunities to test the value of reducing Aß in the clinic. Trial enhancements, such as selecting and enriching for early stage AD, treating participants longer and using more sensitive composite endpoints may further improve our chances of demonstrating clinical efficacy and securing beneficial treatments for patients.
Subject(s)
Alzheimer Disease/diagnosis , Alzheimer Disease/drug therapy , Alzheimer Disease/prevention & control , Amyloid/drug effects , Amyloid/metabolism , Antibodies, Monoclonal, Humanized/therapeutic use , Biomarkers/analysis , Clinical Trials as Topic , Humans , Immunotherapy/methodsSubject(s)
Dyspnea/diagnostic imaging , Dyspnea/therapy , Lung Neoplasms/complications , Lung Neoplasms/radiotherapy , Pulmonary Disease, Chronic Obstructive/complications , Pulmonary Disease, Chronic Obstructive/radiotherapy , Radiotherapy/methods , Aged , Female , Humans , Lung/pathology , Lung/physiology , Oxygen/metabolism , Phenotype , Radionuclide Imaging , Respiratory Function Tests , Treatment OutcomeABSTRACT
We present an electrochemical study of carbon aerogel (CA) in aqueous sodium fluoride solutions, focusing on the comparison of two quantities that are related to the potential of zero charge (pzc): the capacitance minimum and the 'electrocapillary maximum' of the surface forces. Capacitance minima are well resolved in our samples. Their potential emerges reproducibly as around 90 mV (vs. Ag/AgCl in KCl), similar to the value, 70 mV, of bulk glassy carbon which we use for comparison, and similar to previous reported pzc values for carbon materials. Significantly, no electrocapillary maximum is found in this potential range. This demonstrates that the pzc does not necessarily coincide with the potential of the maximum of surface stress. We also determined the area-specific capacitances, c(a) = 2.8 microF cm(-2), which agrees well with reports for the basal-plane of graphite single crystals. Our experiments yield large reversible strain amplitudes, up to 0.45%.
ABSTRACT
The synthesis, molecular structures, and magnetic and optical properties of [Mn(32)Se(14)(SePh)(36)(PnPr(3))(4)] and [Na(benzene-15-crown-5)(C(4)H(8)O)(2)](2)[Mn(8)Se(SePh)(16)] have been investigated which are the first examples of manganese chalcogenide cluster complexes, despite known manganese oxo compounds, which comprise more than four manganese atoms.
Subject(s)
Manganese/chemistry , Organometallic Compounds/chemistry , Organometallic Compounds/chemical synthesis , Organoselenium Compounds/chemistry , Sodium/chemistry , Models, Molecular , Spectrophotometry, Ultraviolet/methods , TemperatureABSTRACT
As gene annotation databases continue to evolve and improve, it has become feasible to incorporate the functional and pathway information about genes, available in these databases into the analysis of gene expression data, for a better understanding of the underlying mechanisms. A few methods have been proposed in the literature to formally convert individual gene results into gene function results. In this paper, we will compare the various methods, propose and examine some new ones, and offer a structured approach to incorporating gene function or pathway information into the analysis of expression data. We study the performance of the various methods and also compare them on real data, using a case study from the toxicogenomics area. Our results show that the approaches based on gene function scores yield a different, and functionally more interpretable, array of genes than methods that rely solely on individual gene scores. They also suggest that functional class scoring methods appear to perform better and more consistently than overrepresentation analysis and distributional score methods.
Subject(s)
Databases, Genetic , Gene Expression , Oligonucleotide Array Sequence Analysis/methods , Research Design , ToxicogeneticsABSTRACT
By combining induced mutation, using NTG and UV irradiation, and protoplasting of a wild type strain of Aspergillus oryzae ATCC 22788, a hyper-producing strain was obtained that accumulated 41 g kojic acid l(-1) in shake-flasks, which was 100-fold higher than that in the wild type strains. Similar production of kojic acid was obtained in 5 l stirred-tank fermentations.
Subject(s)
Aspergillus oryzae/genetics , Aspergillus oryzae/metabolism , Biotechnology/methods , Mutation , Protoplasts/metabolism , Pyrones/metabolism , Bioreactors , Carbon/metabolism , Chromatography, High Pressure Liquid , Fermentation , Mutagenesis , Nitrogen/metabolism , Time Factors , Ultraviolet RaysABSTRACT
Parasite encapsulation and destruction in Biomphalaria glabrata has been shown to involve the cellular component of the snail's internal defence system, the haemocytes. To identify genes involved in the immunobiology of these cells, we used the method of differential display reverse transcriptase polymerase chain reaction (DDRT-PCR) to investigate differential gene regulation in haemocytes isolated from Schistosoma mansoni exposed and unexposed snails. RNA isolated from circulating haemocytes from resistant snails (BS-90 stock), previously exposed to S. mansoni, was analysed using 12 different arbitrary primers in conjunction with an anchored Oligo d(T(11)CG) primer. Transcription profiles between haemocytes of parasite exposed and unexposed snails were compared and a total of 87 differentially regulated bands were identified and isolated. Of these, 65 bands were cloned and used as probes in Southern blots to show the presence of corresponding sequences in the snail genome. RT-PCR was performed to verify the regulation of these transcripts. DNA sequence analysis showed that the majority of the cloned sequences were novel, although a few showed a high degree of sequence similarity to other sequences in the DNA and protein databases. One of these included a differentially expressed transcript that showed a significant degree of sequence identity to E. coli transposase Tn5, an enzyme whose activity is normally associated with generating mobility and instability in the genome.
Subject(s)
Gene Expression Regulation , Hemocytes/metabolism , Schistosoma mansoni , Snails/genetics , Snails/parasitology , Amino Acid Sequence , Animals , Blotting, Southern/veterinary , Electrophoresis, Polyacrylamide Gel/veterinary , Humans , Molecular Sequence Data , Reverse Transcriptase Polymerase Chain Reaction/veterinary , Sequence AlignmentABSTRACT
BACKGROUND AND PURPOSE: Our purpose was to evaluate the cost-effectiveness of clinical versus radiographic screening for an orbital foreign body before MR imaging. METHODS: Costs of screening were determined on the basis of published reports, disability rating guides, and a practice survey. Base case estimates were derived from published guidelines. A single-state change model was constructed using social cost as the unit of analysis. Sensitivity analysis was performed for each variable. The benefit of screening was avoidance of immediate, permanent, nonameliorable, unilateral blindness. RESULTS: Using base case estimates and a discount rate of zero, we calculated the cost of the current guideline as $328,580 per quality-adjusted life-year saved. Sensitivity analysis identified screening cost as a critical variable. Discount rates and effectiveness of foreign body removal also were found to be important factors. Probability of injury and prevalence of foreign body may impact the analysis. CONCLUSION: Clinical screening before radiography increases the cost-effectiveness of foreign body screening by an order of magnitude, assuming base case ocular foreign body removal rates. Asking the patient "Did a doctor get it all out?" serves this purpose. Occupational history by itself is not sufficient to mandate radiographic orbital screening. Current practice guidelines for foreign body screening should be altered.
Subject(s)
Foreign Bodies/diagnosis , Magnetic Resonance Imaging , Mass Screening/economics , Metals , Orbit , Adult , Aged , Blindness/economics , Blindness/prevention & control , Contraindications , Cost-Benefit Analysis , Female , Foreign Bodies/economics , Humans , Magnetic Resonance Imaging/economics , Male , Middle Aged , Models, Economic , Orbit/pathology , Quality-Adjusted Life YearsABSTRACT
The gene encoding the Wuchereria bancrofti orthologue of the Brugia malayi-derived diagnostic antigen SXP1 was identified from a W. bancrofti L3 cDNA library and characterized. The Wb-sxp-1 cDNA encoded a basic protein with a calculated molecular mass of 20.8 kDa. Wb-SXP-1 was 85% identical to the SXP1 protein described from B. malayi (Bm-SXP-1). The Wb-SXP-1 sequence also showed significant identity with proteins described from B. pahangi, Onchocerca volvulus, Acanthochilonema vitea, Ascaris suum, Loa loa, Litomosoides sigmodontis and Caenorhabditis elegans. The presence of a number of invariant and conserved residues in all of these nematode-derived molecules suggests that Wb-SXP-1 is a member of a new protein family. A recombinant form of Wb-SXP-1 was produced and it was determined that the anti-Wb-SXP-1 antibody response in patients with W. bancrofti infections was restricted to the IgG4 subclass. An anti-Wb-SXP-1 IgG4 ELISA was developed and this assay was found to be 100% sensitive for patients with patent W. bancrofti infection. Sera from individuals experiencing chronic pathology, endemic normals or patients with non-filarial nematode infections had no detectable IgG4 against Wb-SXP-1. While patients with patent Onchocerca volvulus infections were uniformly negative in the Wb-SXP-1 assay, 40% of sera from patent Loa loa infections were positive. When Bm-SXP-1 was used as the antigen under identical conditions, the assay was 88% specific for patent W. bancrofti infections and the antigen was recognized by antibodies from both O. volvulus and L. loa infections. The results strongly suggested that, for certain diagnostic filarial antigens, the use of same-species molecules can enhance the specificity of diagnostic tests.
Subject(s)
Antigens, Helminth/isolation & purification , Brugia malayi/immunology , Filariasis/diagnosis , Filariasis/immunology , Helminth Proteins/isolation & purification , Wuchereria bancrofti/immunology , Amino Acid Sequence , Animals , Antibodies, Helminth/blood , Antigens, Helminth/genetics , Brugia malayi/genetics , Helminth Proteins/genetics , Helminth Proteins/immunology , Humans , Immunoglobulin G/biosynthesis , Immunoglobulin G/blood , Immunoglobulin G/classification , Molecular Sequence Data , Recombinant Proteins/biosynthesis , Sequence Homology, Amino Acid , Wuchereria bancrofti/geneticsABSTRACT
A screen of an expression library from the fourth larval stage (L4) of the parasitic nematode Brugia malayi resulted in the identification of a 727 bp full-length cDNA with 29-40% identity to members of the small heat shock family of proteins (Bm-hsp-s1). The open reading frame encoded a protein of approximately 18 kDA (Bm-HSP-s1). An alignment of the Bm-HSP-s1 sequence with the sequences of small HSPs from vertebrate and invertebrate species demonstrated that a majority of the identity was concentrated in the central alpha-crystallin domain. Bm-HSP-s1 was constitutively produced by L4 and adult parasites and at low levels by third-stage larvae (L3), but not by first-stage larvae (microfilariae). In adult parasites, Bm-HSP-s1 was localized to the body wall muscle cells and to the cells of the hypodermis/lateral cord. Bm-HSP-s1 production was induced in adult and L3 incubated at 42 degrees C and in L3s during the developmental transition from vector-stage to vertebrate-stage parasites at 37 degrees C. Neither increased nor decreased temperatures induced Bm-HSP-s1 production in microfilariae. Nitric oxide induced low-level, transient Bm-HSP-s1 synthesis in adults, but not in microfilariae. Bm-HSP-s1 did not function as a molecular chaperone to prevent heat-induced aggregation of a test substrate. The developmentally regulated expression and inducable nature of Bm-HSP-s1 suggests that it may have a stage-restricted role in maintaining parasite homeostasis.
Subject(s)
Brugia malayi/genetics , Gene Expression Regulation, Developmental , Heat-Shock Proteins/genetics , Helminth Proteins , Amino Acid Sequence , Animals , Blotting, Western , Brugia malayi/growth & development , Brugia malayi/metabolism , DNA, Complementary/genetics , Female , Heat-Shock Proteins/biosynthesis , Heat-Shock Proteins/chemistry , Heat-Shock Proteins/metabolism , Heat-Shock Response , Immunohistochemistry , Mice , Mice, Inbred BALB C , Molecular Chaperones , Molecular Sequence Data , Oxidative Stress , Reverse Transcriptase Polymerase Chain Reaction , Sequence Analysis, DNAABSTRACT
Filarial nematode parasites establish long-term chronic infections in the context of an antiparasite immunity that is strongly biased toward a Th2 response. The mechanisms that lead to this Th2 bias toward filarial antigens are not clear, but one possibility is that the parasites produce molecules that have the capacity to proactively modify their immunological environment. Here we report that filarial parasites of humans secrete a homologue of the human proinflammatory cytokine macrophage migration inhibitory factor (MIF) that has the capability of modifying the activity of human monocytes/macrophages. A cDNA clone isolated from a Brugia malayi infective-stage larva expression library encoded a 12.5-kDa protein product (Bm-MIF) with 42% identity to human and murine MIF. MIF homologues were also found to be expressed in the related filarial species Wuchereria bancrofti and Onchocerca volvulus. Bm-mif was transcribed by adult and larval parasites, and the protein product was found in somatic extracts and in the parasite's excretory-secretory products. Immunohistocytochemistry revealed that Bm-MIF was localized to cells of the hypodermis/lateral chord, the uterine wall, and larvae developing in utero. Unexpectedly, the activities of recombinant Bm-MIF and human MIF on human monocytes/macrophages were found to be similar. When placed with monocytes/macrophages in a cell migration assay, Bm-MIF inhibited random migration. When placed away from cells, Bm-MIF induced an increase in monocyte/macrophage migration that was specifically inhibited by neutralizing anti-Bm-MIF antibodies. Bm-MIF is the first demonstration that helminth parasites produce cytokine homologues that have the potential to modify host immune responses to promote parasite survival.
Subject(s)
Filarioidea/metabolism , Macrophage Migration-Inhibitory Factors/metabolism , Amino Acid Sequence , Animals , Brugia malayi/genetics , Cell Movement , Female , Filarioidea/genetics , Gerbillinae , Humans , Macrophage Migration-Inhibitory Factors/genetics , Macrophage Migration-Inhibitory Factors/pharmacology , Macrophages/drug effects , Male , Molecular Sequence Data , Monocytes/drug effects , Onchocerca volvulus/genetics , Sequence Homology, Amino Acid , Wuchereria bancrofti/geneticsABSTRACT
STUDY DESIGN: The clinical and radiographic effect of a lumbar or lumbosacral fusion was studied in 42 patients who had undergone a posterolateral fusion with an average follow-up of 22.6 years. OBJECTIVE: To examine the long-term effects of posterolateral lumbar or lumbosacral fusion on the cephalad two motion segments (transition zone). SUMMARY OF BACKGROUND DATA: It is commonly held that accelerated degeneration occurs in the motion segments adjacent to a fusion. Most studies are of short-term, anecdotal, uncontrolled reports that pay particular attention only to the first motion segment immediately cephalad to the fusion. METHODS: Forty-two patients who had previously undergone a posterolateral lumbar or lumbosacral fusion underwent radiographic and clinical evaluation. Rate of fusion, range of motion, osteophytes, degenerative spondylolisthesis, retrolisthesis, facet arthrosis, disc ossification, dynamic instability, and disc space height were all studied and statistically compared with an age- and gender-matched control group. The patient's self-reported clinical outcome was also recorded. RESULTS: Degenerative changes occurred at the second level above the fused levels with a frequency equal to those occurring in the first level. There was no statistical difference between the study group and the cohort group in the presence of radiographic changes within the transition zone. In those patients undergoing fusion for degenerative processes, 75% reported a good to excellent outcome, whereas 84% of those undergoing fusion for spondylolysis or spondylolisthesis reported a good to excellent outcome. CONCLUSION: Radiographic changes occur within the transition zone cephalad to a lumbar or lumbosacral fusion. However, these changes are also seen in control subjects who have had no surgery.
Subject(s)
Lumbar Vertebrae/surgery , Postoperative Complications/surgery , Sacrum/surgery , Spinal Fusion , Adult , Animals , Arthritis/pathology , Calcinosis , Cricetinae , Female , Follow-Up Studies , Humans , Intervertebral Disc/pathology , Joint Instability/pathology , Joints/pathology , Joints/physiopathology , Lumbar Vertebrae/diagnostic imaging , Lumbar Vertebrae/pathology , Male , Middle Aged , Postoperative Complications/diagnostic imaging , Postoperative Complications/pathology , Radiography , Range of Motion, Articular , Sacrum/diagnostic imaging , Sacrum/pathology , Spinal Fusion/adverse effects , Spinal Osteophytosis/pathology , Spondylolisthesis/pathology , Treatment OutcomeABSTRACT
Parasite-derived antioxidant proteins have been implicated in playing an important role in protection against the oxygen radicals that are generated during aerobic metabolism and in defense against host immune cell attack. Here we report that filarial nematodes include the thioredoxin peroxidase/thiol-specific antioxidant (TPx/TSA) family of antioxidant proteins as part of their complex defense against radical-mediated damage. At the protein level, the TPx/TSA from Brugia malayi (Bm-TPx-1) was approximately 50% identical and approximately 60% similar to TPx/TSAs from mammals, amphibians and yeast. Bm-TPx-1 was also approximately 60% identical to putative TPx proteins from a related filarial nematode, Onchocerca volvulus, and from the free-living nematode Caenorhabditis elegans. That B. malayi may express multiple forms of molecules with TPx/TSA activity was indicated by the identification of a B. malayi gene encoding a second, distinct member of the TPx/TSA family (Bm-tpx-2). Bm-tpx-1 was found to be transcribed in all stages of the parasite present in the mammalian host and the 25 kDa translation product was present in all of the developmental stages studied. The results of immunohistochemical, immunofluorescent and immunoprecipitation studies showed Bm-TPx-1 to be localized in the cells of the hypodermis/lateral chord in adult parasites and not to be present at the surface or in excretory/secretory products. The distribution in the parasite suggests that Bm-TPx-1 may play its major role in countering radicals produced within cells. A recombinant form of Bm-TPx-1 was biologically active and capable of protecting DNA from oxygen radical-mediated damage. Thioredoxin peroxidases may prove to be a critical component in the parasite's defense against injury caused by oxygen radicals derived from endogenous and exogenous sources.
Subject(s)
Brugia malayi/enzymology , Neoplasm Proteins , Peroxidases , Proteins/metabolism , Amino Acid Sequence , Animals , Brugia malayi/genetics , Brugia malayi/growth & development , Female , Gene Expression Regulation, Developmental , Genes, Helminth , Immunohistochemistry , Molecular Sequence Data , Oxidation-Reduction , Peroxiredoxins , Protein Biosynthesis , Proteins/chemistry , Proteins/genetics , Recombinant Fusion Proteins/biosynthesis , Recombinant Fusion Proteins/genetics , Sequence Alignment , Sequence Analysis, DNA , Sequence Homology, Amino Acid , Transcription, GeneticSubject(s)
Amino Acid Isomerases/antagonists & inhibitors , Carrier Proteins/antagonists & inhibitors , Cyclosporine/pharmacology , Filarioidea/enzymology , Amino Acid Isomerases/genetics , Amino Acid Isomerases/metabolism , Amino Acid Sequence , Animals , Brugia/enzymology , Brugia/genetics , Carrier Proteins/genetics , Carrier Proteins/metabolism , Dirofilaria immitis/enzymology , Dirofilaria immitis/genetics , Filarioidea/genetics , Humans , Molecular Sequence Data , Onchocerca volvulus/enzymology , Onchocerca volvulus/genetics , Peptidylprolyl Isomerase , Plasmodium falciparum/enzymology , Plasmodium falciparum/genetics , Protozoan Proteins/genetics , Schistosoma/enzymology , Schistosoma/genetics , Sequence Alignment , Toxoplasma/enzymology , Toxoplasma/geneticsABSTRACT
We have used a tag sequencing approach to survey genes expressed in the third stage infective larvae of the human filarial nematode parasite Brugia malayi. RNA was isolated from late vector-stage L3 larvae after days 9 or 10 of infection in mosquitos, and converted to cDNA by reverse transcriptase. Double-stranded cDNA was produced by either conventional methods (non-SL cDNA library) or by PCR using the nematode spliced leader (SLI) and oligo(dT) primers (SL cDNA library). Two clone libraries (one from SL and one from non-SL cDNAs) were constructed in lambda ZapII. A set of these full-length clones was selected and 596 inserts were sequenced from the 5' end. We have identified 364 B. malayi genes (the majority of which are new) that encode housekeeping proteins, structural proteins, proteins of immediate immunological or drug-discovery interest as well as a large class of novel sequences which may prove to have significant involvement in host invasion. Extensive, genome-wide approaches to the analysis of larval gene expression are now possible for B. malayi. We present several examples of this approach.