Hantaviruses are NIH category A pathogens. New World hantaviruses cause hantavirus cardiopulmonary syndrome (HCPS), a disease case with fatality rates that approach 40% in both North and South America. Although first recognized in North America, HCPS is a much larger problem in South America where cumulative numbers of cases and deaths from HCPS in Chile, Argentina and Brazil far exceed those in the United States. In a population one-twentieth that of the US, more total cases (604) have been in reported in Chile than in the US (~500 cases), and more cases and deaths occur each year in Chile than in the US. Humans acquire Andes virus (ANDV), the etiologic agent of HCPS in Chile, from virus-infected rodents, but ANDV is the only hantavirus that may then be transmitted from person to person. In Chile, this results in household case clusters, particularly among sex partners. In this second competitive renewal, the first aim is to refine the study of index cases with HCPS and prospectively study their close household contacts to evaluate risk factors for person to person transmission. Risk factors will be assessed through a questionnaire and through testing saliva, gingival crevicular fluid, respiratory and genital secretions, blood and urine for the presence of ANDV by RT-PCR and by viral culture in RT-PCR positive samples.
The second aim i s to enhance ANDV isolation and characterization using deep sequencing to evaluate the spectrum of viral variants from patients and rodents and use complementary approaches to facilitate recovery of replication-competent virus. The first goal is to determine whether there are physiological and genetic bottlenecks influencing the selection of particular ANDV variants in transmission from rodents to humans and from human to human. The second is to identify tractable approaches that lead to more efficient virus propagation and facilitate virus characterization.
The third aim i s to establish anti-ANDV vaccine evaluation capacity by a) developing test sites and b) developing and validating a high throughput assay for measurement of neutralizing antibody. Test sites will be established in rural, high-risk areas where both seroprevalence and vaccine acceptability will be determined. Validation of the BSL-2 assay will include transfer of an assay developed by Doms and colleagues and comparison results from the more laborious BSL-3 focus reduction assay.

Public Health Relevance

Andes virus is a hantavirus that causes a serious disease that kills almost 40% of those who become infected. This research is designed to help us learn how the virus is transmitted, information that could be used for education and prevention. The research will also develop test sites where a vaccine to prevent Andes virus infection could be tested and a blood test to see whether people respond to vaccination.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01AI045452-15
Application #
8651848
Study Section
Special Emphasis Panel (ZAI1)
Program Officer
Cassetti, Cristina
Project Start
1999-09-15
Project End
2015-04-30
Budget Start
2014-05-01
Budget End
2015-04-30
Support Year
15
Fiscal Year
2014
Total Cost
Indirect Cost
Name
University of New Mexico Health Sciences Center
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
City
Albuquerque
State
NM
Country
United States
Zip Code
87131
Valdivieso, Francisca; Gonzalez, Claudia; Najera, Manuel et al. (2017) Knowledge, attitudes, and practices regarding hantavirus disease and acceptance of a vaccine trial in rural communities of southern Chile. Hum Vaccin Immunother 13:808-815
Vial, Cecilia; Martinez-Valdebenito, Constanza; Rios, Susana et al. (2016) Molecular method for the detection of Andes hantavirus infection: validation for clinical diagnostics. Diagn Microbiol Infect Dis 84:36-39
Angulo, Jenniffer; Pino, Karla; Echeverría-Chagas, Natalia et al. (2015) Association of Single-Nucleotide Polymorphisms in IL28B, but Not TNF-?, With Severity of Disease Caused by Andes Virus. Clin Infect Dis 61:e62-9
Martinez-Valdebenito, Constanza; Calvo, Mario; Vial, Cecilia et al. (2014) Person-to-person household and nosocomial transmission of andes hantavirus, Southern Chile, 2011. Emerg Infect Dis 20:1629-36
Palma, R Eduardo; Polop, Jaime J; Owen, Robert D et al. (2012) Ecology of rodent-associated hantaviruses in the Southern Cone of South America: Argentina, Chile, Paraguay, and Uruguay. J Wildl Dis 48:267-81
Vera-Otarola, Jorge; Solis, Loretto; Soto-Rifo, Ricardo et al. (2012) The Andes hantavirus NSs protein is expressed from the viral small mRNA by a leaky scanning mechanism. J Virol 86:2176-87
Brocato, Rebecca; Josleyn, Matthew; Ballantyne, John et al. (2012) DNA vaccine-generated duck polyclonal antibodies as a postexposure prophylactic to prevent hantavirus pulmonary syndrome (HPS). PLoS One 7:e35996
Schountz, Tony; Acuña-Retamar, Mariana; Feinstein, Shira et al. (2012) Kinetics of immune responses in deer mice experimentally infected with Sin Nombre virus. J Virol 86:10015-27
Palma, R Eduardo; Boric-Bargetto, Dusan; Torres-Pérez, Fernando et al. (2012) Glaciation effects on the phylogeographic structure of Oligoryzomys longicaudatus (Rodentia: Sigmodontinae) in the southern Andes. PLoS One 7:e32206
Marsac, Delphine; Garcia, Stephanie; Fournet, Alexandra et al. (2011) Infection of human monocyte-derived dendritic cells by ANDES Hantavirus enhances pro-inflammatory state, the secretion of active MMP-9 and indirectly enhances endothelial permeability. Virol J 8:223

Showing the most recent 10 out of 12 publications