Analysis of Puumala hantavirus genome in patients with nephropathia epidemica and rodent carriers from the sites of infection

Citation
A. Plyusnin et al., Analysis of Puumala hantavirus genome in patients with nephropathia epidemica and rodent carriers from the sites of infection, J MED VIROL, 59(3), 1999, pp. 397-405
Citations number
41
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Microbiology
Journal title
JOURNAL OF MEDICAL VIROLOGY
ISSN journal
01466615 → ACNP
Volume
59
Issue
3
Year of publication
1999
Pages
397 - 405
Database
ISI
SICI code
0146-6615(199911)59:3<397:AOPHGI>2.0.ZU;2-I
Abstract
Reverse transcription-polymerase chain reaction (RT-PCR) followed by sequen ce and phylogenetic analyses were used to study specimens from nine Finnish nephropathia epidemica (NE) patients admitted to hospital during the epide mic in winter 1996-1997. Blood samples from six patients were found to be p ositive for the partial M- and/or S-segment sequences of Puumala hantavirus (PUUV). Analyses of these sequences (nt 2168-2610 for the M segment, and n t 819-1082 for the S segment) revealed six distinct PUUV strains showing hi ghest similarity to previously described PUUV strains from Finland: 90-95% for the S segment, and 90-99% for the M segment. Accordingly, on the phylog enetic trees calculated for both viral segments, all six human strains were placed within the Finnish genetic lineage of PUUV. Attempts were made to t race five RT-PCR-positive patients to local bank voles (Clethrionomys glare olus) infected with wildtype PUUV, and for two patients a comparative analy sis of human- and rodent-originated viral sequences was undertaken. Whereas in the first case the differences between the sequences were substantial ( 5.7% for the S segment, and 10.8%, for the M segment), in the other case th e M segment sequence recovered from the clinical specimen was 100% identica l to three sequences recovered from rodent lungs, and the S sequences diffe red by one silent substitution only. This is the first finding of virtually identical PUUV sequences in an NE patient and a natural rodent host from t he site of infection. (C) 1999 Wiley-Liss, Inc.