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1.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-277288

RESUMO

Porcine circovirus type 2 (PCV2) is closely related to the postweaning multisystemic wasting syndrome (PMWS). In this study, the pig serum and tissue samples collected from different regions of Hangzhou District in Zhejiang Province of China between 2003 and 2005 were analyzed by enzyme-linked immunosorbent assay (ELISA) for PCV2 antibody and by polymerase chain reaction (PCR) for ORF2 gene. The results show that out of 1250 randomly collected serum samples, 500 sera (40%) were seropositive for PCV2. PCR results demonstrate that Hangzhou PCV2 with more than 50% Chinese PCV2 strains and French PCV2 formed Cluster A. Only one PCV2 from Hangzhou belonged to Cluster B with some other Chinese PCV2 and Netherlands's isolates. Cluster C consisted of PCV2 isolates from China, US, Canada, UK and Germany. The results indicate that the PCV2 infection was widespread in Hangzhou.


Assuntos
Animais , Humanos , Antígenos , Química , China , Infecções por Circoviridae , Genética , Ensaio de Imunoadsorção Enzimática , Métodos , Fases de Leitura Aberta , Filogenia , Reação em Cadeia da Polimerase , Métodos , Análise de Sequência de DNA , Suínos , Doenças dos Suínos , Genética
2.
Biotechnol Adv ; 25(1): 1-12, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-16997527

RESUMO

The absence of an outer membrane in Bacillus subtilis can simplify the protein secretion pathways and allow the organism to secrete high levels of extracellular proteins. Of the three known secretory routes, Sec-SRP pathway can direct the majority of secretory proteins into the growth medium. Alternatively, a small number of exoproteins with specific functions are secreted via Tat pathway or ABC transporters in B. subtilis. The discriminating function of precursor proteins among these pathways is largely attributed to the distinct structure of their cleavable signal peptides. Individual secretion machinery components with their special functions are involved in the total flow of proteins from the cytoplasm to the medium. Notably, multiple regulators with signal transduction functions can affect expression of secretion machinery as well as their post-transcriptional actions for protein secretion, resulting in the complicated networks in B. subtilis. Ultimately, according to the available knowledge of secretion machinery, several approaches aimed at optimizing protein secretion are discussed.


Assuntos
Bacillus subtilis/metabolismo , Proteínas de Bactérias/metabolismo , Transportadores de Cassetes de Ligação de ATP/metabolismo , Proteínas de Bactérias/química , Humanos , Redes e Vias Metabólicas , Transporte Proteico , Partícula de Reconhecimento de Sinal
3.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-309021

RESUMO

We developed an assay for the detection and quantitation of porcine circovirus type 2 (PCV2) with the SYBR Green I-based real-time PCR. The real-time PCR provides a broad dynamic range, detecting from 10(3) to 10(11) copies of DNA per reaction. No cross-reactions were found in specimens containing PCV1. Because of the high sensitivity and specificity of the assay with a relatively rapid and simple procedure, real-time PCR can be used as a routine assay for the clinical diagnosis of PCV2 infection. In this study we applied real-time PCR assay to 80 clinical samples, collected from 40 pigs with postweaning multisystemic wasting syndrome (PMWS) and 40 healthy pigs in comparison with conventional PCR assay. In 56 of 80 samples, PCV2 DNA was detected by conventional PCR assay. All samples positive for PCV2 DNA in conventional PCR assay were also positive in real-time assay, and 12 of 24 samples that tested negative for PCV2 DNA in the conventional assay were tested positive in real-time PCR assay. Real-time PCR assay increased the number of samples in which PCV2 was detected by 15%. It is, therefore, considered to be a useful tool for the detection of PCV2.


Assuntos
Animais , Circovirus , Genética , Primers do DNA , DNA Viral , Compostos Orgânicos , Reação em Cadeia da Polimerase , Métodos , Reprodutibilidade dos Testes , Sensibilidade e Especificidade , Suínos , Carga Viral
4.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-309052

RESUMO

Specific immunoglobulin (IgY) from egg yolk against Aeromonas hydrophila was produced by immunization of White Leghorn hens with formalin-killed whole cells of A. hydrophila. ELISA test using A. hydrophila as the coating antigen revealed that the specific antibody titer started to increase in the egg yolk at the 13th day post-immunization (P/N=2.18), reached the peak at the 56th day (P/N=13.82), and remained at high level until day 133 (P/N=7.03). The antibody was purified by saturated ammonium sulphate with a recovery rate of 63.5%. The specific IgY inhibited the growth of A. hydrophila at a concentration of 1.0 mg/ml during the 18 h incubation. Pre-treatment of polyploid gibel carps Carassius auratus Gibelio with specific IgY had a protection rate of 60% (6/10) against challenge with A. hydrophila, while none of the fishes in the control groups receiving sterile phosphate buffered saline (PBS) or non-specific IgY survived the challenge. Treatment of fishes with the specific IgY 4 h after the challenge also had lower mortality (70%, 7/10), a 30% reduction against the control PBS or non-specific IgY groups (10/10). These results indicate that specific IgY antibodies could be obtained easily from hens immunized with an inactivated A. hydrophila and could provide a novel alternative approach to control of diseases in fishes caused by this organism.


Assuntos
Animais , Aeromonas hydrophila , Alergia e Imunologia , Especificidade de Anticorpos , Reações Antígeno-Anticorpo , Galinhas , Alergia e Imunologia , Relação Dose-Resposta a Droga , Gema de Ovo , Química , Carpa Dourada , Alergia e Imunologia , Microbiologia , Infecções por Bactérias Gram-Negativas , Alergia e Imunologia , Imunoglobulinas , Farmacologia , Usos Terapêuticos , Testes de Sensibilidade Microbiana , Taxa de Sobrevida , Fatores de Tempo
5.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-251873

RESUMO

Infectious bursal disease virus (IBDV) was inactivated by two different chemicals--formaldehyde and binary ethylenimine (BEI). Formaldehyde was used at 0.1% and 0.2%, while BEI was used at concentrations of 0.001 and 0.002 mol/L. These four vaccines were tested for their efficiency in generating humoral immune response in different groups of broiler chicks. Both BEI-inactivated vaccines gave relatively higher antibody titers and were almost twice as efficient as formaldehyde-inactivated ones.


Assuntos
Animais , Anticorpos Antivirais , Sangue , Aziridinas , Farmacologia , Galinhas , Formaldeído , Farmacologia , Vírus da Doença Infecciosa da Bursa , Alergia e Imunologia , Vacinação , Vacinas de Produtos Inativados , Alergia e Imunologia , Vacinas Virais , Alergia e Imunologia
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