MbrlCatalogueTitleDetail

Do you wish to reserve the book?
Development of Novel Recombinant Antigens of Nucleoprotein and Matrix Proteins of IPorcine orthorubulavirus:/I Antigenicity and Structural Prediction
Development of Novel Recombinant Antigens of Nucleoprotein and Matrix Proteins of IPorcine orthorubulavirus:/I Antigenicity and Structural Prediction
Hey, we have placed the reservation for you!
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Development of Novel Recombinant Antigens of Nucleoprotein and Matrix Proteins of IPorcine orthorubulavirus:/I Antigenicity and Structural Prediction
Oops! Something went wrong.
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Title added to your shelf!
Title added to your shelf!
View what I already have on My Shelf.
Oops! Something went wrong.
Oops! Something went wrong.
While trying to add the title to your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Development of Novel Recombinant Antigens of Nucleoprotein and Matrix Proteins of IPorcine orthorubulavirus:/I Antigenicity and Structural Prediction
Development of Novel Recombinant Antigens of Nucleoprotein and Matrix Proteins of IPorcine orthorubulavirus:/I Antigenicity and Structural Prediction

Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
How would you like to get it?
We have requested the book for you! Sorry the robot delivery is not available at the moment
We have requested the book for you!
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Development of Novel Recombinant Antigens of Nucleoprotein and Matrix Proteins of IPorcine orthorubulavirus:/I Antigenicity and Structural Prediction
Development of Novel Recombinant Antigens of Nucleoprotein and Matrix Proteins of IPorcine orthorubulavirus:/I Antigenicity and Structural Prediction
Journal Article

Development of Novel Recombinant Antigens of Nucleoprotein and Matrix Proteins of IPorcine orthorubulavirus:/I Antigenicity and Structural Prediction

2022
Request Book From Autostore and Choose the Collection Method
Overview
Blue eye disease (BED) is a swine viral infection that affects the pork industry of Mexico. Porcine orthorubulavirus (PRV) is the etiological agent, and the hemagglutinin-neuraminidase protein (HN) is characterized as the best antigen for serological tests, although other structural proteins, including the nucleoprotein (NP) and the matrix (M) protein, have been investigated during the infection of members of the Paramyxoviridae family, generating promising results. Herein, for the first time, we successfully produced and characterized both the NP and M proteins of PRV by using a recombinant strategy in the E. coli heterologous system. The ORF of the NP and M genes were cloned in-frame with the pET-SUMO expression vector. Recombinant proteins proved to be a sensitive target to detect seroconversion at 7 days until 28 days in vaccinated mice (BALB/c) by indirect ELISAs. Immunoreactivity was also tested using porcine serum samples, in which antibodies were recognized from early stages to a persistence of PRV infection, which is indicative that these proteins contain properties similar to native antigens. The predicted tertiary structure showed that both proteins have a conserved structure that resembles those found in others Paramyxovirus. Our results pave the way for developing biotechnological tools based on these proteins for the control and prevention of BED.