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1.
BMC Genomics ; 10: 267, 2009 Jun 15.
Article in English | MEDLINE | ID: mdl-19527522

ABSTRACT

BACKGROUND: Filarial nematode parasites cause serious diseases such as elephantiasis and river blindness in humans, and heartworm infections in dogs. Third stage filarial larvae (L3) are a critical stage in the life cycle of filarial parasites, because this is the stage that is transmitted by arthropod vectors to initiate infections in mammals. Improved understanding of molecular mechanisms associated with this transition may provide important leads for development of new therapies and vaccines to prevent filarial infections. This study explores changes in gene expression associated with the transition of Brugia malayi third stage larvae (BmL3) from mosquitoes into mammalian hosts and how these changes are affected by radiation. Radiation effects are especially interesting because irradiated L3 induce partial immunity to filarial infections. The underlying molecular mechanisms responsible for the efficacy of such vaccines are unkown. RESULTS: Expression profiles were obtained using a new filarial microarray with 18, 104 64-mer elements. 771 genes were identified as differentially expressed in two-way comparative analyses of the three L3 types. 353 genes were up-regulated in mosquito L3 (L3i) relative to cultured L3 (L3c). These genes are important for establishment of filarial infections in mammalian hosts. Other genes were up-regulated in L3c relative to L3i (234) or irradiated L3 (L3ir) (22). These culture-induced transcripts include key molecules required for growth and development. 165 genes were up-regulated in L3ir relative to L3c; these genes encode highly immunogenic proteins and proteins involved in radiation repair. L3ir and L3i have similar transcription profiles for genes that encode highly immunogenic proteins, antioxidants and cuticle components. CONCLUSION: Changes in gene expression that normally occur during culture under conditions that support L3 development and molting are prevented or delayed by radiation. This may explain the enhanced immunogenicity of L3ir. Gene Ontology and KEGG analyses revealed altered pathways between L3 types. Energy and "immune pathways" are up-regulated and may be needed for L3i invasion and survival, while growth and development are priorities for L3c. This study has improved our understanding of molecules involved in parasite invasion and immune evasion, potential targets of protective immunity, and molecules required for parasite growth and development.


Subject(s)
Brugia malayi/genetics , Gene Expression Profiling , Genes, Helminth , Aedes/parasitology , Ancylostoma/genetics , Animals , Brugia malayi/immunology , Brugia malayi/pathogenicity , Brugia malayi/radiation effects , Caenorhabditis elegans/genetics , Cesium Radioisotopes , Gene Expression Regulation, Developmental/radiation effects , Larva/genetics , Larva/immunology , Larva/pathogenicity , Larva/radiation effects , Oligonucleotide Array Sequence Analysis , RNA, Helminth/genetics , Up-Regulation
2.
Mol Biochem Parasitol ; 149(2): 201-7, 2006 Oct.
Article in English | MEDLINE | ID: mdl-16824625

ABSTRACT

Third-stage infective larvae (L3i) of Brugia malayi are developmentally arrested in mosquitoes but must quickly adapt to a new environment when they enter mammalian hosts to initiate infections. These changes can be studied by in vitro culture of L3 (L3c) under conditions that permit molting of L3-L4. Irradiated L3 (L3ir) have stunted growth and limited lifespan in mammalian hosts, and they induce high levels of immunity to challenge infections in animal models. This study explored differences in gene expression in L3i, L3c and L3ir by expressed sequence tag EST generation and qRT-PCR. 2506 ESTs generated from cDNA libraries constructed from L3i, L3c and L3ir were grouped into 1309 gene clusters. Despite extensive prior sampling from B. malayi (>22,000 ESTs in dbEST), 73% of the L3 clusters described here are novel. Sixty-three percentage of the clusters have homology to proteins from other species including 187 specific to nematodes and 141 that have to date only been described in non-nematode species. The transcript levels of 62 candidates for up- or down-regulation in L3i, L3c and L3ir based on EST frequencies were evaluated by qRT-PCR. Twenty-eight were confirmed to have > or = 3-fold differences in expression. Genes coding for proteins believed to be involved in establishment of infection, host adaptation and targets of protective immunity were confirmed to have higher expression in L3i than in L3c. Some of the genes that were down-regulated in L3c were highly expressed in L3ir. This study provides an improved description of the adaptations that accompany the transition from L3i to L3c and the special ability of L3ir to induce protective immunity.


Subject(s)
Brugia malayi/genetics , Genes, Helminth , Aedes/parasitology , Animals , Brugia malayi/growth & development , Brugia malayi/immunology , Brugia malayi/radiation effects , Expressed Sequence Tags , Gene Expression/radiation effects , Gene Expression Profiling , Gene Library , Larva/genetics , Larva/growth & development , Larva/radiation effects , Multigene Family , Reverse Transcriptase Polymerase Chain Reaction
3.
Parasitol Res ; 97(3): 219-27, 2005 Oct.
Article in English | MEDLINE | ID: mdl-15997407

ABSTRACT

Prior studies have shown that irradiated filarial larvae are developmentally stunted but capable of inducing partial immunity to filariasis in animals. The mechanisms for these effects are poorly understood. Recent studies suggest that intracellular Wolbachia bacteria are necessary for the normal development, reproduction and survival of filarial nematodes. The purpose of this study was to examine the effects of irradiation on Wolbachia in Brugia malayi infective larvae (L3) and on L3 development. The L3 were exposed to 0, 25, 35, 45, 55, 65 or 75 krad of gamma irradiation from a (137) Cesium source and cultured in vitro at 37 degrees C in NCTC/IMDM medium with 10% FCS for 12 days. Irradiation prevented molting of L3 to the L4 stage in a dose-dependent manner. Electron microscopy studies showed that irradiation damaged Wolbachia (25 krad) or cleared them from worm tissues (45 krad). In addition, majority of the irradiated L3s failed to develop the L4 cuticle. Real-time PCR studies showed that irradiation reduced Wolbachia DNA in worm tissues. Parallel in vivo studies confirmed decreased development of irradiated L3 in jirds, with associated effects on Wolbachia. Jirds injected s.c with normal L3 developed antibodies to Wolbachia surface protein (wsp) shortly after the onset of microfilarial patency. In contrast, jirds injected with irradiated L3 did not develop microfilaremia or antibodies to wsp. Additional studies are needed to test the hypothesis that irradiation retards growth and development of filarial L3 by killing Wolbachia.


Subject(s)
Brugia malayi/radiation effects , Filariasis/radiotherapy , Gamma Rays/adverse effects , Gamma Rays/therapeutic use , Host-Parasite Interactions/radiation effects , Wolbachia/radiation effects , Animals , Antibodies, Bacterial/immunology , Bacterial Outer Membrane Proteins/immunology , Brugia malayi/microbiology , DNA, Bacterial/radiation effects , Dose-Response Relationship, Radiation , Filariasis/immunology , Filariasis/prevention & control , Gerbillinae , Host-Parasite Interactions/immunology , Larva/microbiology , Larva/radiation effects , Parasitemia/diagnosis , Parasitemia/immunology , Reverse Transcriptase Polymerase Chain Reaction , Vaccination , Wolbachia/genetics , Wolbachia/isolation & purification , Wolbachia/ultrastructure
4.
Exp Parasitol ; 109(2): 87-93, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15687015

ABSTRACT

Prior studies have shown that intracellular Wolbachia endobacteria are necessary for the normal development, reproduction, and survival of filarial nematodes. The purpose of this study was to examine effects of gamma radiation on Wolbachia and reproduction in Brugia malayi adult worms. Worms were exposed to 0, 10, 25, 45, 75, and 105 krad of gamma radiation from a 137cesium source and cultured in vitro for 10 days. Irradiation reduced production of microfilariae in a dose-dependent manner. Embryograms of irradiated female worms showed dose-related abnormalities with arrested development at the early embryo stage. Irradiation reduced the viability of adult worms in a dose-dependent manner, but no lethal effect was observed. Electron microscopy studies showed that irradiation cleared Wolbachia from worm tissues. Real-time polymerase chain reaction studies demonstrated greatly reduced Wolbachia DNA in irradiated worms. These effects are essentially the same as those observed in adult worms treated with doxycycline. These studies suggest that effects of irradiation on reproduction in Brugia malayi may be caused by effects of irradiation on Wolbachia.


Subject(s)
Brugia malayi/radiation effects , Gamma Rays , Wolbachia/radiation effects , Aedes , Animals , Brugia malayi/embryology , Brugia malayi/microbiology , Brugia malayi/physiology , DNA, Bacterial/radiation effects , DNA, Helminth/radiation effects , Dose-Response Relationship, Radiation , Embryonic Development/radiation effects , Female , Gerbillinae , Male , Microfilariae/radiation effects , Microscopy, Electron , Movement/radiation effects , Reproduction/radiation effects , Symbiosis , Wolbachia/physiology , Wolbachia/ultrastructure
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