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Journal of Clinical Microbiology, January 1999, p. 122-126, Vol. 37, No. 1
The Department of Medicine1
and
the Department of Molecular Genetics and
Microbiology,5 Stony Brook University, Stony
Brook, New York 11794, Department of Pathology, University of
New Mexico, Albuquerque, New Mexico,2
The Northport VA Medical Center, Northport, New York
11768,4 and
USAMRIID, Fort Detrick,
Maryland3
Received 24 July 1998/Returned for modification 17 September
1998/Accepted 30 September 1998
New York 1 virus (NY-1) and Sin Nombre virus (SN) are associated
with hantavirus pulmonary syndrome (HPS). NY-1 and SN are derived from
unique mammalian hosts and geographic locations but have similar G1 and
G2 surface proteins (93 and 97% identical, respectively). Focus
reduction neutralization assays were used to define the serotypic
relationship between NY-1 and SN. Sera from NY-1-positive
Peromyscus leucopus neutralized NY-1 and SN at titers of
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
New York 1 and Sin Nombre Viruses Are Serotypically
Distinct Viruses Associated with Hantavirus Pulmonary
Syndrome
1/3,200 and
1/400, respectively (n = 12).
Conversely, SN-specific rodent sera neutralized NY-1 and SN at titers
of <1/400 and 1/6,400, respectively (n = 13).
Acute-phase serum from a New York HPS patient neutralized NY-1 (1/640)
but not SN (<1/20), while sera from HPS patients from the southwestern
United States had 4- to >16-fold-lower neutralizing titers to NY-1
than to SN. Reference sera to Hantaan, Seoul, and Prospect Hill viruses
also failed to neutralize NY-1. These results indicate that SN and NY-1
define unique hantavirus serotypes and implicate the presence of
additional HPS-associated hantavirus serotypes in the Americas.
*
Corresponding author. Mailing address: Department of
Medicine/GI, Stony Brook University, HSC T17, Rm. 60, Stony Brook, N.Y. 11794. Phone: 516-444-2120. Fax: 516-444-8886. E-mail:
EMackow{at}mail.som.sunysb.edu.
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