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1.
Parasitol Res ; 116(5): 1479-1486, 2017 May.
Artigo em Inglês | MEDLINE | ID: mdl-28324166

RESUMO

The traditional taxonomy of the genus Chloromyxum Mingazzini, 1890 has been intensively challenged to be paraphyletic by recent ribosomal DNA (rDNA)-based phylogenetic analysis. Undersampling to get rich sequence data to infer more scientific phylogenetic relationships makes scientists conservatively assign all non-marine elasmobranch-infecting species as Chloromyxum sensu lato. Although complex ridge pattern on the spore surface observed by scanning electron microscopy was thought to be critical for the identification of Chloromyxum species, insufficient data also prevent this ultrastructural data to be a valid taxonomic feature for this genus. It is especial for Chloromyxum species to be reported in China. Molecular and ultrastructural characteristics are yet available for all 22 Chloromyxum species recorded in China. During the investigation of the diversity of coelozoic fish myxosporeans, Chloromyxum ellipticum Li & Nie, 1973 was found to highly infect the gall bladder of Ctenopharyngodon idellus Valenciennes, 1844 in Poyang Lake watershed of Jiangxi province, Eastern China. Here, we redescribed it by the currently recommended holistic approach of combining morphological, ultrastructural, and molecular characteristics. Mature spores were found floating free in the gall bladder, but no plasmodium observed. Spores are typical freshwater teleost-infecting Chloromyxum species, spherical or subspherical in lateral view, measuring 7.7 ± 0.08 µm (6.9-9.1) in length, 6.3 ± 0.09 µm (5.6-7.6) in width, and 5.8 ± 0.20 µm (5.2-6.3) in thickness. Four pyriform polar capsules, located at the anterior end of the spores, were equal in size, 3.3 ± 0.06 µm (2.2-4.1) long and 2.1 ± 0.03 µm (1.7-2.5) wide. Polar filaments coiled with four to five turns. Two equal spore valves are symmetrical, with 10-16 surface extrasutural ridges per valve, aligned along the longitudinal axis. The obtained partial 18S rDNA of C. ellipticum did not match any sequences available in GenBank. Phylogenetic analysis showed that C. ellipticum clustered firstly with Chloromyxum legeri with robust nodal support and grouped then with urinary system of freshwater teleost-infecting Chloromyxum clade, rather than other gall bladder of freshwater teleost-infecting clade.


Assuntos
Carpas/parasitologia , Doenças dos Peixes/parasitologia , Vesícula Biliar/parasitologia , Myxozoa/classificação , Myxozoa/isolamento & purificação , Doenças Parasitárias em Animais/parasitologia , Esporos de Protozoários/ultraestrutura , Animais , China , DNA Ribossômico/genética , Lagos , Microscopia Eletrônica de Varredura , Myxozoa/genética , Filogenia , Esporos de Protozoários/isolamento & purificação , Bexiga Urinária/parasitologia
2.
Blood Cells Mol Dis ; 52(4): 181-5, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24351655

RESUMO

In this study, we investigated the molecular basis of two unrelated Chinese patients with hemostatic disorders. The proband of the first family had severe hemophilia A (HA) coexisting with type 1 von Willebrand disease (VWD) and the proband of the second family had type 2N VWD. Both probands had similar phenotypes, which included joint and mucosal bleeding, very low factor VIII (FVIII) activity (FVIII:C), and moderate reductions in VWF antigen (VWF:Ag) and VWF ristocetin cofactor activity (VWF:Rco), as well as a normal multimeric pattern. One FVIII mutation and three VWF mutations were identified: FVIII p.R446* and VWF heterozygous p.E216K mutations were detected in proband 1 and compound heterozygosity of VWF mutations (p.R816W and c.1911delC) in proband 2. Transient expression studies in HEK293T cells proved that R816W mutation abolished the binding of FVIII to VWF and slightly impaired protein synthesis and secretion; 1911delC mutation mainly impaired VWF protein synthesis and secretion. These results provided insight into the possible pathogenic mechanism of type 2N VWD in Chinese patients carrying these mutations.


Assuntos
Hemofilia A/complicações , Hemofilia A/diagnóstico , Hemorragia/etiologia , Mucosa/patologia , Doença de von Willebrand Tipo 1/complicações , Doença de von Willebrand Tipo 1/diagnóstico , Doença de von Willebrand Tipo 2/complicações , Doença de von Willebrand Tipo 2/diagnóstico , Adulto , Testes de Coagulação Sanguínea , Pré-Escolar , Diagnóstico Diferencial , Fator VIII/genética , Fator VIII/metabolismo , Feminino , Genótipo , Hemartrose/etiologia , Hemofilia A/tratamento farmacológico , Hemofilia A/genética , Humanos , Masculino , Mutação , Fenótipo , Ligação Proteica , Doença de von Willebrand Tipo 1/tratamento farmacológico , Doença de von Willebrand Tipo 1/genética , Doença de von Willebrand Tipo 2/tratamento farmacológico , Doença de von Willebrand Tipo 2/genética , Fator de von Willebrand/genética , Fator de von Willebrand/metabolismo
4.
Appl Opt ; 33(24): 5783-95, 1994 Aug 20.
Artigo em Inglês | MEDLINE | ID: mdl-20935981

RESUMO

The analyticity of the complex extinction efficiency is examined numerically in the size-parameter domain for homogeneous prolate and oblate spheroids and finite cylinders. The T-matrix code, which is the most efficient program available to date, is employed to calculate the individual particle-extinction efficiencies. Because of its computational limitations in the size-parameter range, a slightly modified Hilbert-transform algorithm is required to establish the analyticity numerically. The findings concerning analyticity that we reported for spheres (Astrophys. J. 399, 164-175, 1992) apply equally to these nonspherical particles.

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