40 results about "Bovine parainfluenza virus" patented technology

The present invention relates to recombinant bovine parainfluenza virus (bPIV) cDNA or RNA which may be used to express heterologous gene products in appropriate host cell systems and/or to rescue negative strand RNA recombinant viruses that express, package, and/or present the heterologous gene product. In particular, the heterologous gene products include gene product of another species of PIV or from another negative strand RNA virus, including but not limited to, influenza virus, respiratory syncytial virus, human metapneumovirus and avian pneumovirus. The chimeric viruses and expression products may advantageously be used in vaccine formulations including vaccines against a broad range of pathogens and antigens.

The present invention relates to recombinant bovine parainfluenza virus (bPIV) cDNA or RNA which may be used to express heterologous gene products in appropriate host cell systems and/or to rescue negative strand RNA recombinant viruses that express, package, and/or present the heterologous gene product. The chimeric viruses and expression products may advantageously be used in vaccine formulations including vaccines against a broad range of pathogens and antigens.

The invention discloses a reverse transcription-polymerase chain reaction (RT-PCR) detection method and a kit for quickly diagnosing bovine parainfluenza virus 3 (BPIV-3), and belongs to the field of biomedical detection. The invention adopts the technical scheme that the method comprises acquisition of a sample, extraction of virus RNA, design optimization of a specific primer, RT-PCR amplification, agarose gel electrophoresis and result judgment; the specific primer is designed for a specific fragment of BPIV-3 nucleoprotein (NP) genes, and the upstream and downstream sequences of the specific primer are respectively P1: 5'-GGATGTTTGGGAGTGATCTTGAGTA-3' and P2: 5'-TGTGTTGAAAAATGAAGCAAGACCT-3'; the quick RT-PCR diagnosing kit for detecting the BPIV-3 comprises a sample virus RNA extracting reagent, a reverse transcription reagent, a PCR reagent, a positive reference substance and a negative reference substance; and by verifying, the method is sensitive and specific and has applicationprospect.

Chimeric human-bovine parainfluenza viruses (PIVs) are infectious and attenuated in humans and other mammals and useful individually or in combination in vaccine formulations for eliciting an immune response to PIV or other pathogens. Also provided are isolated polynucleotide molecules and vectors incorporating a chimeric PIV genome or antigenome which includes a partial or complete human or bovine PIV “background” genome or antigenome combined or integrated with one or more heterologous gene(s) or genome segment(s) of a different PIV. Chimeric human-bovine PIV of the invention include a partial or complete “background” PIV genome or antigenome derived from or patterned after a human or bovine PIV virus combined with one or more heterologous gene(s) or genome segment(s) of a different pathogen, including different PIV virus to form the human-bovine chimeric PIV genome or antigenome.

The invention discloses a primer, a probe and a method for detecting knopvelsiekte virus by a RAA fluorescence method. The primer and the probe are suitable for the detection by the RAA fluorescence method, can accurately detect knopvelsiekte virus plasmids without cross reaction with mycoplasma, bovine infectious rhinotracheitis virus, bovine viral diarrhea virus, bovine parainfluenza virus, bovine respiratory syncytial virus, goat pox virus and sheep pox virus, and have a specificity of 100%. The method is fast and easy to achieve high throughput, and can reduce time and cost for detection.The method for rapid detection of DNA of the knopvelsiekte virus based on the RAA fluorescence method has high sensitivity reaching 10 copies / reaction.

The invention discloses a primer and a probe for detecting BPIV3 (Bovine parainfluenza virus type 3) aerosol through a RPA (Recombinase Ploymerase Amplification)-lateral flow assay, a kit and a detection method. The kit contains primer probe liquid formed by a RPA primer and a probe for detecting the BPIV3, wherein the forward primer sequence is shown as SEQ ID No.1; the reverse primer sequence isshown as SEQ ID No.2; the probe sequence is shown as SEQ ID No.3. The used primer probe group has a good RPA effect; the strip specificity is high; no cross reaction with other viruses exists; strongpositive reaction exists in a detection region; the detection sensitivity is enhanced. The RPA-lateral flow assay technology is used for building a BPIV3 fast detection method for the first time; through specificity and sensitivity evaluation, the method can be used for clinical field detection; a flexible and reliable novel method is provided for BPIV3 field detection.

The invention relates to an indirect competitive enzyme linked immunosorbent assay aptamer method used for detecting bovine parainfluenza virus 3 antibodies, and belongs to the field of bioengineering. The indirect competitive enzyme linked immunosorbent assay aptamer method comprises following steps: coating; plate washing; blocking; adding of a nucleic acid aptamer and bovine serum; plate washing; adding of second antibodies; color developing; reaction killing; reading; determining of a negative and positive critical value; Ic-ELAA method specific detection; and clinical bovine serum detection. The indirect competitive enzyme linked immunosorbent assay aptamer method is high in specificity; compared with commercially available ELISA kits, the positive detection rate of Ic-ELAA is higher, and is more suitable for clinical serological investigation of bovine parainfluenza virus.

Chimeric human-bovine parainfluenza viruses (PIVs) are infectious and attenuated in humans and other mammals and useful individually or in combination in vaccine formulations for eliciting an anti-PIV immune response. Also provided are isolated polynucleotide molecules and vectors incorporating a chimeric PIV genome or antigenome which includes a partial or complete human or bovine PIV “background” genome or antigenome combined or integrated with one or more heterologous gene(s) or genome segment(s) of a different PIV. Chimeric human-bovine PIV of the invention include a partial or complete “background” PIV genome or antigenome derived from or patterned after a human or bovine PIV virus combined with one or more heterologous gene(s) or genome segment(s) of a different PIV virus to form the human-bovine chimeric PIV genome or antigenome. In certain aspects of the invention, chimeric PIV incorporate a partial or complete human PIV background genome or antigenome combined with one or more heterologous gene(s) or genome segment(s) from a bovine PIV, whereby the resultant chimeric virus is attenuated by virtue of host-range restriction. In alternate embodiments, human-bovine chimeric PIV incorporate a partial or complete bovine PIV background genome or antigenome combined with one or more heterologous gene(s) or genome segment(s) from a human PIV gene that encode a human PIV immunogenic protein, protein domain or epitope, for example encoded by PIV HN and/or F glycoprotein gene(s) or genome segment(s). Human-bovine chimeric PIV of the invention are also useful as vectors for developing vaccines against other pathogens. A variety of additional mutations and nucleotide modifications are provided within the human-bovine chimeric PIV of the invention to yield desired phenotypic and structural effects.

The invention discloses a PCR (Polymerase Chain Reaction) method for simultaneously detecting four bovine infectious disease RNA (Ribose Nucleic Acid) viruses by a single tube. The PCR method is used for detecting a bovine parainfluenza virus, a foot and mouth disease virus, a bovine diarrhea virus and a bovine reovirus. The PCR method is rapid in operation without one step. In addition, the invention also relates to a reagent related in the PCR method, which is used in a detection kit of the method and preparation and application of the detection kit.

The invention discloses a dual RPA detection kit for bovine parainfluenza virus (BPIV) and bovine respiratory syncytial virus (BRSV). The dual RPA detection kit comprises aBPIV RPA detection primer group consisting of nucleotide sequences shown in SEQ. ID. NO.2 and SEQ. ID. NO.5, and a BRSV RPA detection primer group consisting of nucleotide sequences shown in SEQ. ID. NO.8 and SEQ. ID. NO.10. Thekit is based on a recombinase polymerase amplification method, cDNA formed by RNA reverse transcription is used as a template, an amplification reaction is carried out at an optimized reaction temperature and time, and a detection result is obtained by nucleic acid gel electrophoresis. The kit can be used for simultaneously detecting the bBPIV and the BRSV, is simple to operate, has higher sensitivity and specificity, and provides a rapid detection reagent for on-site screening of bovine pathogens.

The invention discloses a blocking ELISA kit for detecting a bovine parainfluenza virus type 3 antibody. The kit comprises a pre-coated elisa plate and an enzyme-labeled antibody, the pre-coated elisaplate is an elisa plate coated with purified goat parainfluenza virus type 3; the enzyme labeled antibody is a monoclonal antibody 2E6 labeled by horse radish peroxidase; the monoclonal antibody 2E6is secreted by a hybridoma cell strain 2E6; the hybridoma cell strain 2E6 is preserved in China Center for Type Culture collecting on February 1, 2016, the preservation address is Wuhan University, Wuhan, China, the preservation number is CCTCC NO: C201627, and the hybridoma cell strain 2E6 is classified and named as hybridoma cell strain 2E6. The kit disclosed by the invention is good in specificity, high in sensitivity, good in stability, capable of rapidly, simply, conveniently and efficiently detecting the bovine parainfluenza virus type 3 antibody, low in cost and suitable for high-throughput detection of samples.

The invention belongs to the technical field of biology and particularly relates to an immunofluorescence reagent for detecting bovine parainfluenza virus type 3 and a detection kit of the immunofluorescence reagent. The immunofluorescence reagent is an anti-bovine parainfluenza virus type 3 monoclonal antibody marked by fluorescent dye, and the monoclonal antibody is prepared by taking virus particles obtained by concentrating and purifying the bovine parainfluenza virus type 3 as an antigen and adopting a hybridoma cell monoclonal antibody technology. The fluorescent dye is fluorescein isothiocyanate (FITC). The subtype of the monoclonal antibody is IgG2. An immune reagent in an immunofluorescence kit for detecting the bovine parainfluenza virus type 3 is an immunofluorescence reagent for detecting the bovine parainfluenza virus type 3. The invention has the advantages of high sensitivity, strong specificity, good stability, high diagnosis speed and the like.

The invention particularly relates to application of sulfamethoxypyrazine in preparation of a product for preventing and/or treating bovine parainfluenza virus. Bovine parainfluenza virus type 3 is an important pathogen causing cattle respiratory syndrome in a livestock farm, and the transmission route comprises respiratory tract and reproductive organ transmission which may cause serious pneumonia and even infertility. The research result provides the application of sulfamethoxypyrazine in development of products for preventing and/or treating bovine parainfluenza virus, and verification shows that in a safe dosage range of normal cells, sulfamethoxypyrazine shows an inhibition effect on bovine parainfluenza virus type 3, blocks an adsorption effect of the virus on the normal cells, and can be used for preventing and/or treating the bovine parainfluenza virus type 3. Sulfamethoxypyrazine is expected to be applied to development of veterinary drugs or feed additives.

The invention discloses a RT-PCR (Reverse Transcription-Polymerase Chain Reaction) amplification primer for quickly detecting a bovine parainfluenza 3 virus, and application thereof, which belong to the field of animal bacteriology and molecular biology. The RT-PCR amplification primer is formed by an upstream primer with a nucleotide sequence as shown in an SEQ ID NO:1 and a downstream primer with a nucleotide sequence as shown in an SEQ ID NO:2; the primer is used for preparing a RT-PCR amplification kit for detecting the bovine parainfluenza 3 virus. An RT-PCR detection method provided by the kit has high specificity and sensibility, good repeatability, and high reliability, can specifically detect the bovine parainfluenza 3 virus and quickly and accurately obtain a detection result, islow in price, simple and convenient to operate, and suitable for a basic level at the same time, and can be used as a quick, accurate, simple and convenient detection tool for quick identification ina bovine parainfluenza 3 virus laboratory and large-scale epidemiological investigation.