Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 7 de 7
Filtrar
Mais filtros

Base de dados
Tipo de documento
Intervalo de ano de publicação
1.
Fish Shellfish Immunol ; 44(1): 224-31, 2015 May.
Artigo em Inglês | MEDLINE | ID: mdl-25542377

RESUMO

Mud crab reovirus (MCRV) is the causative agent of a severe disease in cultured mud crab (Scylla paramamosain), which has caused huge economic losses in China. MCRV is a double-stranded RNA virus with 12 genomic segments. In this paper, SDS-PAGE, mass spectrometry and Western blot analyses revealed that the VP12 protein encoded by S12 gene is a structural protein of MCRV. Immune electron microscopy assay indicated that MCRV VP12 is a component of MCRV outer shell capsid. Yeast two hybrid cDNA library of mud crab was constructed and mud crab voltage-dependent anion-selective channel (mcVDAC) was obtained by MCRV VP12 screening. The full length of mcVDAC was 1180 bp with an open reading frame (ORF) of 849 bp encoding a 282 amino acid protein. The mcVDAC had a constitutive expression pattern in different tissues of mud crab. The interaction between MCRV VP12 and mcVDAC was determined by co-immunoprecipitation assay. The results of this study have provided an insight on the mechanisms of MCRV infection and the interactions between the virus and mud crab.


Assuntos
Proteínas de Artrópodes/metabolismo , Braquiúros , Reoviridae , Proteínas Estruturais Virais/metabolismo , Canais de Ânion Dependentes de Voltagem/metabolismo , Sequência de Aminoácidos , Animais , Proteínas de Artrópodes/genética , Sequência de Bases , Braquiúros/metabolismo , Braquiúros/virologia , Escherichia coli/genética , Brânquias/metabolismo , Células HeLa , Hepatopâncreas/metabolismo , Humanos , Microscopia Eletrônica , Dados de Sequência Molecular , Reoviridae/fisiologia , Reoviridae/ultraestrutura , Proteínas Estruturais Virais/genética , Canais de Ânion Dependentes de Voltagem/genética
2.
J Int Med Res ; 52(9): 3000605241274570, 2024 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-39225009

RESUMO

Wernicke encephalopathy (WE) is an acute life-threatening neurological condition caused by thiamine (vitamin B1) deficiency. Patients with WE often present with a triad of symptoms consisting of ophthalmoplegia, gait ataxia, and mental confusion. If WE is not treated in a timely manner, it can lead to serious complications such as confusion, coma, or death. Although alcohol abuse is the most commonly reported cause of WE, nonalcoholic causes-although rare-do exist. Herein, we present the case of a nonalcoholic woman with medullary infarctions who presented with intractable vomiting. Her clinical state subsequently progressed to include ophthalmoplegia and gait ataxia. A diagnosis of WE was suspected based on her clinical presentation; this was confirmed by brain magnetic resonance imaging (MRI) and the finding of decreased serum thiamine levels. Brain magnetic resonance imaging demonstrated the complete resolution of abnormal hyperintensities during a follow-up visit, 6 months after treatment.


Assuntos
Imageamento por Ressonância Magnética , Bulbo , Encefalopatia de Wernicke , Humanos , Encefalopatia de Wernicke/diagnóstico , Encefalopatia de Wernicke/etiologia , Encefalopatia de Wernicke/diagnóstico por imagem , Encefalopatia de Wernicke/complicações , Feminino , Bulbo/patologia , Bulbo/diagnóstico por imagem , Bulbo/irrigação sanguínea , Tiamina/uso terapêutico , Tiamina/sangue , Pessoa de Meia-Idade , Infartos do Tronco Encefálico/diagnóstico por imagem , Infartos do Tronco Encefálico/complicações
3.
World J Clin Cases ; 11(20): 4961-4965, 2023 Jul 16.
Artigo em Inglês | MEDLINE | ID: mdl-37583998

RESUMO

BACKGROUND: Anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis is a rare autoimmune disorder. The symptoms of anti-NMDAR encephalitis include behavioral problems, speech problems, psychosis, seizures, and memory deficits, among others. However, laryngospasm is rare. We present the case of a patient with anti-NMDAR antibodies and severe laryngospasms. CASE SUMMARY: The patient was a 15-year-old female with normal psychomotor development. She was initially admitted to our neurological intensive care unit with seizures. She received anti-epilepsy treatment, and the seizures disappeared. However, 2 wk later, she developed behavioral problems and speech impairment. Then, she developed severe laryngospasms, which were treated with intubation and a tracheotomy. Antibodies against the NMDAR were detected in the patient's cerebrospinal fluid. Therefore, she was diagnosed with anti-NMDAR encephalitis. In addition, she received intravenously administered immunoglobulins, and methylprednisolone was administered. The patient's symptoms gradually improved, and she was discharged from our hospital. Approximately 9 mo later, the patient could speak sentences, walk independently, and carry out activities of daily living independently. Through our case report, we highlighted laryngospasm as an uncommon presentation in patients with anti-NMDAR encephalitis. CONCLUSION: Laryngospasm may be an uncommon clinical manifestation of anti-NMDAR encephalitis.

4.
Guang Pu Xue Yu Guang Pu Fen Xi ; 31(5): 1309-13, 2011 May.
Artigo em Zh | MEDLINE | ID: mdl-21800589

RESUMO

Due to the high data dimensionality of a hyperspectral image, dimensionality reduction algorithm has attracted much attention in hyperspectral image analysis. Band selection algorithm, which selects appropriate bands from the original set of spectral bands, can preserve original information from the data and is useful for image classification and recognition. In the present paper, a novel band selection algorithm based on orthogonal projection divergence (OPD) is proposed, it aims to discriminate the interesting objects from background and noise information, maximize the spectral similarity between different spectral vectors by projecting the original data to feature space. Two HYDICE Washington DC Mall images and an HYMAP Purdue campus image data were experimented, and support vector machine (SVM) classifier was used for classification. The selected band number varies from 5 to 40 in order to study the impacts of different band selection algorithms on different features. For the computation complex, the sequential floating forward search (SFFS) was used to get the appropriate bands. The experiments have proved that our proposed OPD algorithm can outperform other traditional band selection methods such as SAM, ED, SID, and LCMV-BCC for hyperspectral image analysis. It is proven that OPD band selection is effective and robust in hyperspectral remote sensing dimensionality reduction

5.
J Int Med Res ; 48(10): 300060520964349, 2020 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-33070690

RESUMO

Short-lasting unilateral neuralgiform headache with conjunctival injection and tearing (SUNCT) is a rare primary headache syndrome. However, some cases of secondary SUNCT are attributed to underlying diseases such as demyelination. We herein report a case of SUNCT with progression to neuromyelitis optica spectrum disorder (NMOSD). A 43-year-old woman developed headaches; 6 weeks later, she developed bilateral visual loss and numbness on the left side of her body. She was ultimately diagnosed with NMOSD.


Assuntos
Neuralgia , Neuromielite Óptica , Síndrome SUNCT , Adulto , Feminino , Cefaleia/etiologia , Humanos , Neuromielite Óptica/complicações , Neuromielite Óptica/diagnóstico por imagem
6.
J Int Med Res ; 46(8): 3411-3416, 2018 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-29806512

RESUMO

Autoantibodies targeting aquaporin 4 (AQP4) water channels are a sensitive and specific biomarker for neuromyelitis optica spectrum disorder (NMOSD). Presence of AQP4 antibodies distinguishes NMOSD from multiple sclerosis. We present our experience with an anti-AQP4 antibody-positive patient diagnosed with NMOSD who complained of intractable nausea and vomiting, not restricted to optic neuritis or acute myelitis during the first attack. Her symptoms partially resolved after appropriate therapy with intravenous methylprednisolone and oral prednisolone. Through this case, we hope to draw attention to an unusual neurological presentation of NMOSD which should be included in the differential diagnosis of intractable nausea and vomiting.


Assuntos
Aquaporina 4/imunologia , Autoanticorpos/imunologia , Náusea/etiologia , Neuromielite Óptica/diagnóstico , Vômito/etiologia , Administração Intravenosa , Administração Oral , Adulto , Autoanticorpos/sangue , Feminino , Glucocorticoides/administração & dosagem , Humanos , Metilprednisolona/administração & dosagem , Mielite Transversa/diagnóstico , Mielite Transversa/tratamento farmacológico , Náusea/tratamento farmacológico , Náusea/imunologia , Neuromielite Óptica/diagnóstico por imagem , Neuromielite Óptica/tratamento farmacológico , Neuromielite Óptica/imunologia , Prednisolona/administração & dosagem , Vômito/tratamento farmacológico , Vômito/imunologia
7.
Virology ; 422(2): 185-94, 2012 Jan 20.
Artigo em Inglês | MEDLINE | ID: mdl-22088215

RESUMO

Mud crab reovirus (MCRV) is the causative agent of a serious disease with high mortality in cultured mud crab (Scylla serrata). This study sequenced and analyzed 12 genome segments of MCRV. The 12 genome segments had a total length of 24.464 kb, showing a total G+C content of 41.29% and predicted 15 ORFs. Sequence analysis showed that the majority of MCRV genes shared low homology with the counterpart genes of other reoviruses, e.g., the amino acid identity of RNA-dependent RNA polymerase (RdRp) was lower than 13.0% compared to the RdRp sequences of other reoviruses. Nucleotide and amino acid sequences of RdRp and capping enzyme suggested MCRV as a single group. Further genome-based phylogenetical analysis of conserved termini and reovirus polymerase motif indicates that this MCRV belongs to a new genus of the Reoviridae family, tentatively named as Crabreovirus.


Assuntos
Genoma Viral , Reoviridae/genética , Sequência de Aminoácidos , Animais , Braquiúros , Proteínas do Capsídeo/genética , Proteínas do Capsídeo/metabolismo , Clonagem Molecular , Regulação Viral da Expressão Gênica/fisiologia , Dados de Sequência Molecular , Conformação de Ácido Nucleico , Filogenia , RNA Viral/química , RNA Viral/genética
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA