A new study from University of California, Davis, and the U.S. Department of Agriculture describes how vaccines work against a deadly virus in chickens, and could offer a model for related human diseases such as chickenpox.
The study, published and highlighted in the November issue of the journal , describes how three common vaccines for Marek鈥檚 disease, a deadly herpesvirus disease in chickens, insert themselves into the chicken鈥檚 chromosomes.
Herpesviruses in animals and humans have developed a number of strategies to evade the immune system and persist for later infection.
鈥淥ne of the key questions surrounding herpesviruses in animals and humans is how do these viruses go latent and where do they 鈥榟ide out鈥 in cells of the body during a latent period, with the opportunity to re-emerge later,鈥 said Mary Delany, a professor of animal science and a noted poultry geneticist.
鈥淔or example, the virus that causes chickenpox in children can seem to go away only to reappear years later as a painful case of shingles in the adult,鈥 Delany said.
In earlier work, Delany and colleagues showed that the Marek鈥檚 disease herpesvirus integrates into the chicken鈥檚 DNA, and the timing of that is associated with the timing of viral latency. This apparent strategy for evading the immune system allows the virus to persist in the cells of the host, with the potential for later re-emergence causing infectious cycles.
Marek鈥檚 disease is largely controlled by vaccination with related strains of the virus, which prime the immune system to defend against the disease virus but do not cause disease themselves.
鈥淚n this recent study, we were quite surprised to find that Marek鈥檚 vaccines also integrate into the host鈥檚 chromosome just as the disease-causing virus does,鈥 Delany said.
She noted that the chicken-based study has tremendous biomedical and economic implications, given that the chicken is one of the major sources of meat, as well as eggs, for much of the world. The United Nations鈥 Food and Agriculture Organization estimates that 59 billion chickens were used for food production in 2010.
About Marek鈥檚 disease
Marek鈥檚 disease, first described in 1907, is a highly contagious herpesvirus disease, which in chickens causes recurrent infections and tumors within and among the organ systems.
Like other herpesviruses, the Marek鈥檚 disease virus can transition from an active infection stage to a temporary latent stage. This enables the virus to evade the chicken鈥檚 defensive immune system and re-emerge later.
Vaccines key to controlling Marek鈥檚
Marek鈥檚 disease can be managed by selectively breeding for chickens with increased genetic resistance to the virus; however vaccination is the predominant and most efficient method used to control, although not eradicate, the disease in commercial and even backyard chicken flocks.
The vaccines are prepared from related, weakened strains of the Marek鈥檚 disease virus. Although they don鈥檛 prevent infection, they do interfere with tumor formation and so prevent death in infected chickens.
However, even after 40 years of vaccinating chickens against Marek鈥檚 disease, the exact mechanisms by which vaccines create immunity against the disease have not been clearly understood.
In response to the vaccination, Marek鈥檚 disease has evolved to ever more virulent forms. Better understanding of vaccine mechanisms should lead to development of improved vaccines.
Vaccines may lie low to provide lasting protection
In this study, the researchers monitored chicks that had each been vaccinated with one of three commonly used vaccines, as well as a control group of chicks that had not been vaccinated.
They found that all three of the vaccine strains that were tested quickly integrated into the chicken genome, which is characteristic of virulent viruses. The chromosomal integration happened as early as one day after the chicks were vaccinated
鈥淚t was completely unexpected that the vaccines would behave similarly to the disease-causing virus with regard to their interactions with the chicken genome,鈥 Delany said. 鈥淎nd it was especially interesting that all three of these vaccines share the capacity to integrate into the genome, even though each shares different features with the Marek鈥檚 disease virus.鈥
She added that it is now important to determine whether the vaccines can re-emerge from their sites in the host genome to allow for long-lasting protection.
Her research group is now studying whether the vaccines may provide protection by out-competing the virus for location in the host鈥檚 genome, perhaps preventing latency and the creation of the specific cell population that can be transformed into deadly cancerous conditions.
鈥淲e need to find out whether genomic integration of the vaccine offers protection because it competes with integration of the disease-causing virus or if the vaccine鈥檚 integration into the genome is simply an evolutionary relic that has no real function in protecting the bird,鈥 Delany said.
Collaborators and funding
Collaborating on the study with Delany were lead author Marla C. McPherson, a doctoral candidate at 新澳门六合彩内幕信息 Davis, and Hans H. Cheng of the USDA Avian Disease and Oncology Laboratory in East Lansing, Michigan.
Funding for the study was provided by the U.S. Department of Agriculture鈥檚 National Institute of Food and Agriculture.
Media Resources
Mary Delany, 新澳门六合彩内幕信息 Davis Animal Science, 530-752-0233, medelany@ucdavis.edu
Pat Bailey, 新澳门六合彩内幕信息 Davis News and Media Relations, 530-219-9640, pjbailey@ucdavis.edu