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1.
BMC Genomics ; 19(1): 592, 2018 Aug 07.
Article in English | MEDLINE | ID: mdl-30086708

ABSTRACT

BACKGROUND: Anisakis simplex sensu stricto and Anisakis pegreffii are sibling species of nematodes parasitic on marine mammals. Zoonotic human infection with third stage infective larvae causes anisakiasis, a debilitating and potentially fatal disease. These 2 species show evidence of hybridisation in geographical areas where they are sympatric. How the species and their hybrids differ is still poorly understood. RESULTS: Third stage larvae of Anisakis simplex s.s., Anisakis pegreffii and hybrids were sampled from Merluccius merluccius (Teleosti) hosts captured in waters of the FAO 27 geographical area. Specimens of each species and hybrids were distinguished with a diagnostic genetic marker (ITS). RNA was extracted from pools of 10 individuals of each taxon. Transcriptomes were generated using Illumina RNA-Seq, and assembled de novo. A joint assembly (here called merged transcriptome) of all 3 samples was also generated. The inferred transcript sets were functionally annotated and compared globally and also on subsets of secreted proteins and putative allergen families. While intermediary metabolism appeared to be typical for nematodes in the 3 evaluated taxa, their transcriptomes present strong levels of differential expression and enrichment, mainly of transcripts related to metabolic pathways and gene ontologies associated to energy metabolism and other pathways, with significant presence of excreted/secreted proteins, most of them allergens. The allergome of the 2 species and their hybrids has also been thoroughly studied; at least 74 different allergen families were identified in the transcriptomes. CONCLUSIONS: A. simplex s.s., A. pegreffi and their hybrids differ in gene expression patterns in the L3 stage. Strong parent-of-origin effects were observed: A. pegreffi alleles dominate in the expression patterns of hybrids albeit the latter, and A. pegreffii also display significant differences indicating that hybrids are intermediate biological entities among their parental species, and thus of outstanding interest in the study of speciation in nematodes. Analyses of differential expression based on genes coding for secreted proteins suggests that co-infections presents different repertoires of released protein to the host environment. Both species and their hybrids, share more allergen genes than previously thought and are likely to induce overlapping disease responses.


Subject(s)
Anisakis/genetics , Gadiformes/parasitology , Gene Expression Profiling/methods , Helminth Proteins/genetics , Allergens/genetics , Animals , Anisakis/isolation & purification , Anisakis/pathogenicity , Breeding , Energy Metabolism , Fish Diseases/parasitology , Gene Expression Regulation , Larva/genetics , Larva/pathogenicity , Molecular Sequence Annotation , Sequence Analysis, RNA/methods , Virulence Factors/genetics
2.
Neuropathol Appl Neurobiol ; 33(4): 420-30, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17442060

ABSTRACT

Ciliary neurotrophic factor (CNTF) may be implicated in the pathogenetic mechanisms of hepatic encephalopathy. We tested this hypothesis by treating confluent primary cultures of rat astroglial cells with ammonium chloride for various periods and analysing the effect of ammonia on the signalling pathway that regulates CNTF mRNA and protein expression. Ammonia treatment induced a dose- and time-dependent reduction in CNTF mRNA and protein expression. Surface-enhanced laser desorption/ionization-time-of-flight mass spectrometry analysis of CNTF in the culture medium demonstrated that ammonia also induced a significant decrease in CNTF release. In addition, ammonia affected Sp1 and c-fos, transcription factors that regulate CNTF mRNA and protein expression, which showed partial dephosphorylation and significantly lower mRNA and protein levels. Total content of p38MAPK (for which Sp1 and c-fos are substrates) was unaffected by ammonia, although the diphosphorylated (active) form was significantly reduced after ammonia exposure.


Subject(s)
Ammonia/pharmacology , Astrocytes/metabolism , Ciliary Neurotrophic Factor/biosynthesis , Genes, fos/drug effects , RNA, Messenger/biosynthesis , Signal Transduction/drug effects , Sp1 Transcription Factor/biosynthesis , p38 Mitogen-Activated Protein Kinases/biosynthesis , Animals , Astrocytes/drug effects , Blotting, Western , Cells, Cultured , Electrophoresis, Gel, Two-Dimensional , Phosphorylation , Rats , Rats, Wistar , Reverse Transcriptase Polymerase Chain Reaction , Sp1 Transcription Factor/drug effects , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization , p38 Mitogen-Activated Protein Kinases/drug effects
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