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Public release date: 22-Apr-2013[ | E-mail |
Share ] Contact: Timothy S. Paul
tp2111@columbia.edu
212-305-2676
Columbia University's Mailman School of Public Health
Discovery opens avenues to developing new treatments
As many as one in 50 people around the world is infected with some type of hepacivirus or pegivirus, including up to 200 million with hepatitis C virus (HCV), a leading cause of liver failure and liver cancer. There has been speculation that these agents arose in wildlife and jumped species to infect humans; however, little was known about their distribution in other species.
In two new papers published in the journals mBio and Proceedings of the National Academy of Sciences, investigators at the Center for Infection and Immunity (CII) at Columbia University's Mailman School of Public Health report the discovery of hepaciviruses and pegivirusesclose relatives of HCVin rodents and bats. The viruses are similar to those that infect humans and may therefore provide insights into the origins of HCV, as well as the mechanisms behind animal-to-human transmission. It may also enable development of new animal systems with which to model HCV pathogenesis, vaccine design, and treatment.
Both discoveries were made using high-throughput sequencing and other molecular methods for pathogen discovery pioneered at CII. Both represented multicenter global efforts.
As reported in mBio, Amit Kapoor, PhD, and colleagues screened more than 400 wild-caught rodents. Molecular analysis revealed the presence of hepaciviruses and pegiviruses closely related to those found in humans. "Importantly, the rodent hepaviviruses contained sequences that are thought to play a role in liver infection in HCV," says Dr. Kapoor, lead author of the study and assistant professor of Pathology and Cell Biology at Columbia University Medical Center. "We also found instances of a single animal infected with multiple hepaciviruses."
Such co-infections have also been observed with HCV in humans, suggesting that the immune response to HCV is different than with most viral infectionsa finding that has implications for vaccine design. "It also supports the potential use of rodent hepaciviruses in developing models for human disease," says W. Ian Lipkin, MD, John Snow Professor of Epidemiology and director of the CII.
Researchers from Rockefeller University, University of Edinburgh, University of Copenhagen, University of New Mexico, North Carolina College of Veterinary Medicine, Pennsylvania State University and the National Institutes of Health contributed to the study. Results appear online in mBio.
In a second study led by P. Lan Quan, PhD, molecular assays of 1,615 bats collected worldwide led to the identification of 83 novel hepaciviruses and pegiviruses, representing an infection rate of nearly 5%. "The broad prevalence, unprecedented diversity, and worldwide distribution of these novel viruses suggest that bats are a major and ancient reservoir for both hepaciviruses and pegiviruses, and provide insights into the evolutionary history of HCV and human pegiviruses," says Dr. Quan, associate research scientist at the Center for Infection and Immunity.
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Researchers from EcoHealth Alliance, Centers for Disease Control, University of Pretoria, University of Kinshasa, Universidad Nacional Autnoma de Mxico, Ahmadu Bello University, Universidad del Valle de Guatemala, University of Kisangani, National Museum of Kenya, and the University of Sydney contributed to the study. Results appear online in the Proceedings of the National Academy of Sciences.
The work reported in these two papers was supported by awards from the National Institute of Allergy and Infectious Diseases of the National Institutes of Health, U.S. Agency for International Development (PREDICT), the Centers for Disease Control, and the Department of Defense.
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AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.
Public release date: 22-Apr-2013[ | E-mail |
Share ] Contact: Timothy S. Paul
tp2111@columbia.edu
212-305-2676
Columbia University's Mailman School of Public Health
Discovery opens avenues to developing new treatments
As many as one in 50 people around the world is infected with some type of hepacivirus or pegivirus, including up to 200 million with hepatitis C virus (HCV), a leading cause of liver failure and liver cancer. There has been speculation that these agents arose in wildlife and jumped species to infect humans; however, little was known about their distribution in other species.
In two new papers published in the journals mBio and Proceedings of the National Academy of Sciences, investigators at the Center for Infection and Immunity (CII) at Columbia University's Mailman School of Public Health report the discovery of hepaciviruses and pegivirusesclose relatives of HCVin rodents and bats. The viruses are similar to those that infect humans and may therefore provide insights into the origins of HCV, as well as the mechanisms behind animal-to-human transmission. It may also enable development of new animal systems with which to model HCV pathogenesis, vaccine design, and treatment.
Both discoveries were made using high-throughput sequencing and other molecular methods for pathogen discovery pioneered at CII. Both represented multicenter global efforts.
As reported in mBio, Amit Kapoor, PhD, and colleagues screened more than 400 wild-caught rodents. Molecular analysis revealed the presence of hepaciviruses and pegiviruses closely related to those found in humans. "Importantly, the rodent hepaviviruses contained sequences that are thought to play a role in liver infection in HCV," says Dr. Kapoor, lead author of the study and assistant professor of Pathology and Cell Biology at Columbia University Medical Center. "We also found instances of a single animal infected with multiple hepaciviruses."
Such co-infections have also been observed with HCV in humans, suggesting that the immune response to HCV is different than with most viral infectionsa finding that has implications for vaccine design. "It also supports the potential use of rodent hepaciviruses in developing models for human disease," says W. Ian Lipkin, MD, John Snow Professor of Epidemiology and director of the CII.
Researchers from Rockefeller University, University of Edinburgh, University of Copenhagen, University of New Mexico, North Carolina College of Veterinary Medicine, Pennsylvania State University and the National Institutes of Health contributed to the study. Results appear online in mBio.
In a second study led by P. Lan Quan, PhD, molecular assays of 1,615 bats collected worldwide led to the identification of 83 novel hepaciviruses and pegiviruses, representing an infection rate of nearly 5%. "The broad prevalence, unprecedented diversity, and worldwide distribution of these novel viruses suggest that bats are a major and ancient reservoir for both hepaciviruses and pegiviruses, and provide insights into the evolutionary history of HCV and human pegiviruses," says Dr. Quan, associate research scientist at the Center for Infection and Immunity.
###
Researchers from EcoHealth Alliance, Centers for Disease Control, University of Pretoria, University of Kinshasa, Universidad Nacional Autnoma de Mxico, Ahmadu Bello University, Universidad del Valle de Guatemala, University of Kisangani, National Museum of Kenya, and the University of Sydney contributed to the study. Results appear online in the Proceedings of the National Academy of Sciences.
The work reported in these two papers was supported by awards from the National Institute of Allergy and Infectious Diseases of the National Institutes of Health, U.S. Agency for International Development (PREDICT), the Centers for Disease Control, and the Department of Defense.
[ | E-mail | Share ] ?
AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.
Source: http://www.eurekalert.org/pub_releases/2013-04/cums-hcv041713.php
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