This grant proposes collaborative studies between investigators at Baylor College of Medicine (BCM) and The University of Rochester Medical School to develop new diagnostic assays for the Norwalk group of viruses. Norwalk virus is one of the most important viral pathogens causing acute epidemic gastroenteritis. Epidemiology studies indicate that transmission of Norwalk virus is through water-borne, food-borne or person-to-person routes. Norwalk virus is a 27-nm virus and virus particles reportedly contain a single structural polypeptide with an apparent molecular weight of 59,000. The morphology of some virions and the presence of a single structural protein are features similar to viruses in the Caliciviridae family. Based on recent studies with cDNAs made in the last year at BCM, the nucleic acid of Norwalk virus has been shown to be single-stranded RNA. We will use molecular approaches to completely characterize the Norwalk virus genome and develop new diagnostic assays for Norwalk virus. Characterization of the Norwalk virus genome will be done using specific cloned DNA made at BCM in libraries of pUC-13 or in the lambda ZAPII vector. Specific cDNAs identified by nucleic acid hybridization (and new ones to be identified) will be characterized until cDNA clones representing the entire genome are found. These clones will be used for nucleotide sequencing to determine the genome organization of this virus. Furthermore, cDNA clones encoding immunoreactive proteins will be identified, subcloned and expressed using a baculovirus expression system. Each expressed protein will be used as an immunogen to produce immunologic reagents. Methods of virus detection based on diagnostic assays using prepared hyperimmune antiserum and monoclonal antibodies or based on detection of nucleic acid by polymerase chain reaction (PCR) will be developed and compared.
We aim to determine what assay(s) will be (1) the most rapid, sensitive and specific for detection of Norwalk virus and (2) capable of detecting Norwalk virus only or Norwalk virus and Norwalk-like viruses [Snow Mountain agent (SMA), Hawaii agent] and possibly human caliciviruses.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01AI030448-03
Application #
3547693
Study Section
Special Emphasis Panel (SRC (66))
Project Start
1990-07-01
Project End
1995-06-30
Budget Start
1992-07-01
Budget End
1993-06-30
Support Year
3
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Type
Schools of Medicine
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
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Hutson, Anne M; Atmar, Robert L; Graham, David Y et al. (2002) Norwalk virus infection and disease is associated with ABO histo-blood group type. J Infect Dis 185:1335-7
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Hardy, M E; Kramer, S F; Treanor, J J et al. (1997) Human calicivirus genogroup II capsid sequence diversity revealed by analyses of the prototype Snow Mountain agent. Arch Virol 142:1469-79
Prasad, B V; Hardy, M E; Jiang, X et al. (1996) Structure of Norwalk virus. Arch Virol Suppl 12:237-42
Hardy, M E; Estes, M K (1996) Completion of the Norwalk virus genome sequence. Virus Genes 12:287-90
Kogawa, K; Nakata, S; Ukae, S et al. (1996) Dot blot hybridization with a cDNA probe derived from the human calicivirus Sapporo 1982 strain. Arch Virol 141:1949-59

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