Microtine Rodent-Borne Hantavirus from Poland and Korea: Molecular Characterization and Phylogenetic Analysis.
- Author:
Jin Won SONG
;
Jae Kyung YOON
;
Sang Hyun KIM
;
Jong Hun KIM
;
Young Eun LEE
;
Ki Joon SONG
;
Luck Ju BAEK
;
Yong Ju LEE
;
Radzislaw KORDEK
;
Pawel P LIBERSKI
;
Richard YANAGIHARA
- Publication Type:Original Article
- MeSH:
Arvicolinae*;
Austria;
Enzyme-Linked Immunosorbent Assay;
Genetic Variation;
Gyeonggi-do;
Hantavirus*;
Hemorrhagic Fever with Renal Syndrome;
Humans;
Immunoglobulin M;
Korea*;
Lung;
Poland*;
RNA;
Rodentia;
Russia;
Seoul;
Yugoslavia
- From:Journal of the Korean Society of Virology
1998;28(3):275-285
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Based on the geographic range and distribution of its rodent reservoir host, the European common vole (Microtus arvalis), Tula virus is likely to be widespread throughout Eurasia. Tula virus-infected voles have been captured in Central Russia, Austria, Czech and Slovak Republics, and the former Yugoslavia. Although serologic evidence for Hantaan (HTN) or Seoul (SEO) virus infection can be found in the vast majority of the more than 300 cases of hemorrhagic fever with renal syndrome (HFRS) occurring annually in Korea, approximately 4% of Korean patients with HFRS show a more than 4-fold higher antibody titer to Puumala (PUU) virus than to HTN or SEO virus by double-sandwich IgM ELISA, suggesting the existence of pathogenic Puumala-related hantaviruses in Korea. To further define the geographic distribution and genetic diversity of Tula virus in Eurasia and to investigate the existence of previously unrecognized Microtus-borne hantavirus in Korea, arvicolid rodents were captured in Lodz, Poland in 1995 and in Yunchon-kun, Kyungki-do during April to May, 1998. In addition, sera from 18 Korean HFRS patients who showed higher (or the same) antibody titer to Tula virus than HTN and SEO viruses were examined for hantavirus RNA by RT-PCR. Hantaviral sequences were not detected in any of the 18 patients or in 35 reed voles (Microtus fortis) in Korea. Alignment and comparison of a 208-nucleotide region of the S segment, amplified from lung tissues of two hantavirus-seropositive M. arvalis captured in Poland, revealed 80.8~83.2% sequence similarity, respectively, with Tula virus strains from Central Russia and the Czech and Slovak Republics. Phylogenetic analysis indicated that the newfound Tula virus strains from Poland were closely related to other Tula hantaviruses from Eurasia.
