Literature DB >> 2508317

Determination of the coding capacity of the M genome segment of nephropathia epidemica virus strain Hällnäs B1 by molecular cloning and nucleotide sequence analysis.

L B Giebel1, R Stohwasser, L Zöller, E K Bautz, G Darai.   

Abstract

The M genome RNA segment of nephropathia epidemica virus (NEV) strain Hällnäs B1 was characterized by molecular cloning and DNA nucleotide sequencing of the corresponding cDNA clones. The size of the M RNA segment is 3682 nucleotides. The 3' and 5' terminal sequences are complementary for 21 bases and their predicted secondary structure is very stable. The viral complementary messenger RNA possesses a single long open reading frame with a coding capacity of 1148 amino acids (polypeptide of 126 kDa). A comparison of the NEV M segment to that of Hantaan virus strain 76-118 reveals 61% sequence homology at the nucleotide level and 53% at the deduced amino acid level. Four out of five potential asparagine-linked glycosylation sites of the encoded glycoproteins have been conserved between NEV and Hantaan M. The isoelectric points (IEP) are nearly identical. Furthermore it was found that 90% of all cysteine residues have been conserved. Putative NEV G1 and G2 are preceded by a short hydrophobic sequence as shown for G1 and G2 of Hantaan virus. Hydrophilicity profiles of the two segments are of striking similarity. These data indicate that NEV- and Hantaan virus M-encoded polypeptides seem to be very similar in structure and function despite the relatively low amino acid sequence homology.

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Year:  1989        PMID: 2508317     DOI: 10.1016/0042-6822(89)90192-x

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  13 in total

1.  Nucleotide sequence of the M genome segment of hemorrhagic fever with renal syndrome virus strain B-1.

Authors:  Y Isegawa; Y Fujiwara; A Ohshima; R Fukunaga; H Murakami; K Yamanishi; Y Sokawa
Journal:  Nucleic Acids Res       Date:  1990-08-25       Impact factor: 16.971

2.  A major antigenic domain of hantaviruses is located on the aminoproximal site of the viral nucleocapsid protein.

Authors:  P Gött; L Zöller; G Darai; E K Bautz
Journal:  Virus Genes       Date:  1997       Impact factor: 2.332

3.  Coding strategy of the S and M genomic segments of a hantavirus representing a new subtype of the Puumala serotype.

Authors:  A Reip; B Haring; C Sibold; R Stohwasser; E K Bautz; G Darai; H Meisel; D H Krüger
Journal:  Arch Virol       Date:  1995       Impact factor: 2.574

4.  Molecular evolution of Puumala hantavirus.

Authors:  T Sironen; A Vaheri; A Plyusnin
Journal:  J Virol       Date:  2001-12       Impact factor: 5.103

5.  A newly recognized virus associated with a fatal case of hantavirus pulmonary syndrome in Louisiana.

Authors:  S P Morzunov; H Feldmann; C F Spiropoulou; V A Semenova; P E Rollin; T G Ksiazek; C J Peters; S T Nichol
Journal:  J Virol       Date:  1995-03       Impact factor: 5.103

6.  Antigenic properties and diagnostic potential of puumala virus nucleocapsid protein expressed in insect cells.

Authors:  O Vapalahti; A Lundkvist; H Kallio-Kokko; K Paukku; I Julkunen; H Lankinen; A Vaheri
Journal:  J Clin Microbiol       Date:  1996-01       Impact factor: 5.948

7.  Genetic analysis of the diversity and origin of hantaviruses in Peromyscus leucopus mice in North America.

Authors:  S P Morzunov; J E Rowe; T G Ksiazek; C J Peters; S C St Jeor; S T Nichol
Journal:  J Virol       Date:  1998-01       Impact factor: 5.103

Review 8.  New ecological aspects of hantavirus infection: a change of a paradigm and a challenge of prevention--a review.

Authors:  Martin Zeier; Michaela Handermann; Udo Bahr; Baldur Rensch; Sandra Müller; Roland Kehm; Walter Muranyi; Gholamreza Darai
Journal:  Virus Genes       Date:  2005-03       Impact factor: 2.332

9.  The Hantaan virus M-segment glycoproteins G1 and G2 can be expressed independently.

Authors:  M N Pensiero; J Hay
Journal:  J Virol       Date:  1992-04       Impact factor: 5.103

10.  Identification and characterization of a Hantavirus strain of unknown origin by nucleotide sequence analysis of the cDNA derived from the viral S RNA segment.

Authors:  L B Giebel; K Raab; L Zöller; E K Bautz; G Darai
Journal:  Virus Genes       Date:  1991-04       Impact factor: 2.332

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