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1.
Parasitol Res ; 115(8): 2981-94, 2016 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-27083187

RESUMO

Serine protease inhibitors, known as serpins, are pleiotropic regulators of endogenous and exogenous proteases, and molecule transporters. They have been documented in animals, plants, fungi, bacteria, and viruses; here, we characterize a serpin from the trematode platyhelminth Schistosoma mansoni. At least eight serpins have been found in the genome of S. mansoni, but only two have characterized molecular properties and functions. Here, the function of S. mansoni serpin isoform 3 (SmSPI) was analyzed, using both computational and molecular biological approaches. Phylogenetic analysis showed that SmSPI was closely related to Schistosoma haematobium serpin and Schistosoma japonicum serpin B10. Structure determined in silico confirmed that SmSPI belonged to the serpin superfamily, containing nine α-helices, three ß-sheets, and a reactive central loop. SmSPI was highly expressed in schistosomules, predominantly in the head gland, and in adult male and female with intensive accumulation on the spines, which suggests that it may have a role in facilitating intradermal and intravenous survival. Recombinant SmSPI was overexpressed in Escherichia coli; the recombinant protein was of the same size (46 kDa) as the native protein. Immunological analysis suggested that mice infected with S. mansoni responded to rSmSPI at 8 weeks postinfection (wpi) but not earlier. The inhibitory activity of rSmSPI was specific to chymotrypsin but not trypsin, neutrophil elastase, and porcine pancreatic elastase. Elucidating the biological and physiological functions of SmSPI as well as other serpins will lead to further understanding of host-parasite interaction machinery that may provide novel strategies to prevent and control schistosomiasis in the future.


Assuntos
Schistosoma mansoni/fisiologia , Inibidores de Serina Proteinase/fisiologia , Serpinas/fisiologia , Animais , Feminino , Interações Hospedeiro-Parasita/efeitos dos fármacos , Masculino , Camundongos , Filogenia , Isoformas de Proteínas/genética , Isoformas de Proteínas/imunologia , Proteínas Recombinantes/genética , Proteínas Recombinantes/imunologia , Schistosoma mansoni/química , Schistosoma mansoni/imunologia , Esquistossomose mansoni/parasitologia , Inibidores de Serina Proteinase/genética , Inibidores de Serina Proteinase/imunologia , Inibidores de Serina Proteinase/isolamento & purificação , Serpinas/genética , Serpinas/imunologia , Serpinas/isolamento & purificação , Suínos
2.
Am J Trop Med Hyg ; 92(2): 336-9, 2015 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-25487731

RESUMO

Neotricula aperta (Gastropoda: Pomatiopsidae), the snail intermediate host of Schistosoma mekongi, is found in Cambodia, Laos, and Thailand. We update information on the distribution of this species in the Mekong River and its tributary, the Mun River, in Thailand. DNA sequences of a portion of the mitochondrial cytochrome c oxidase subunit 1 were obtained from N. aperta collected from different locations and used to confirm species and strain identities. Specimens of the ß-strain were found in the Mun River, whereas specimens of the γ-strain were found in the Mekong River. The γ-strain (with molecular confirmation of identity) is newly reported from Nong Khai Province, where it occurred in a habitat novel for this species: under paving slabs instead of under natural bed rocks, where agal aufwuchs is extensively located on the islet in the middle of the Mekong River. The new location is approximate 400 km upstream from the nearest previously known site for this species.


Assuntos
Caramujos , Animais , Sequência de Bases , DNA/genética , DNA Mitocondrial/genética , Ecossistema , Complexo IV da Cadeia de Transporte de Elétrons/genética , Dados de Sequência Molecular , Filogenia , Rios , Caramujos/genética , Tailândia/epidemiologia
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