Literature DB >> 18635048

Analyses of Patois group bunyaviruses: evidence for naturally occurring recombinant bunyaviruses and existence of immune precipitable and nonprecipitable nonvirion proteins induced in bunyavirus-infected cells.

H Ushijima1, C M Clerx-Van Haaster, D H Bishop.   

Abstract

Shark River (SR) and Pahayokee (PAH) bunyaviruses (Patois serogroup, Bunyavirus genus, family Bunyaviridae) have almost identical L and S RNA oligonucleotide fingerprints, but M RNA fingerprints that are different, suggesting that the two viruses may represent naturally occurring reassortant viruses. These observations are in agreement with serological studies (B. N. Fields, B. E. Henderson, P. H. Coleman, and T. H. Work, 1969, Amer. J. Epidemiol., 89, 222-226) which have distinguished these two viruses by neutralization of infectivity tests (presumably reflecting differences in M RNA gene products, J. R. Gentsch, E. J. Rozhon, R. A. Klimas, L. H. El Said, R. E. Shope, and D. H. L. Bishop, 1980, Virology102, 190-204), but not by complement fixation tests (which probably relate to the viral N polypeptide coded by the S RNA, J. Gentsch, L. R. Wynne, J. P. Clewley, R. E. Shope, and D. H. L. Bishop, 1977b, J. Virol. 24,893-902). The 3' terminal 11 nucleotides of PAH S RNA (3' (HO)OUCAUCAAAUGA ... 5') are identical in sequence to those of the S RNA species of snowshoe hare (SSH) and La Crosse (LAC) viruses, except for a position 7A residue which is a C residue in the SSH and LAC sequences. The major virion polypeptides of SR and PAH viruses include a nucleocapsid polypeptide (N, 22 x 10(3)) and two glycoproteins (PAH: G1 118 x 10(3), G2, 35 x 10(3); SR: G1 113 x 10(3), G2, 35 x 10(3)). In SR-infected cells several immune precipitable polypeptides have been detected. These include 11-, 54-, 64-, 93-, and 104 x 10(3)-dalton polypeptides. In addition, both SR and PAH viruses induce a 74 x 10(3)-dalton polypeptide (p74) that has not been detected in actinomycin D-treated infected cells, and is not immune precipitated from infected cell extracts.

Entities:  

Year:  1981        PMID: 18635048

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


  6 in total

1.  Electron microscopic and antigenic studies of uncharacterized viruses. II. Evidence suggesting the placement of viruses in the family Bunyaviridae.

Authors:  H G Zeller; N Karabatsos; C H Calisher; J P Digoutte; C B Cropp; F A Murphy; R E Shope
Journal:  Arch Virol       Date:  1989       Impact factor: 2.574

2.  Genetic reassortment of mammalian reoviruses in mice.

Authors:  E A Wenske; S J Chanock; L Krata; B N Fields
Journal:  J Virol       Date:  1985-11       Impact factor: 5.103

3.  Analysis of reassortment of genome segments in mice mixedly infected with rotaviruses SA11 and RRV.

Authors:  J L Gombold; R F Ramig
Journal:  J Virol       Date:  1986-01       Impact factor: 5.103

4.  Seasonal Dynamics of Mosquito-Borne Viruses in the Southwestern Florida Everglades, 2016, 2017.

Authors:  John F Anderson; Durland Fish; Philip M Armstrong; Michael J Misencik; Angela Bransfield; Francis J Ferrandino; Theodore G Andreadis; Mark D Stenglein; Marylee L Kapuscinski
Journal:  Am J Trop Med Hyg       Date:  2022-01-10       Impact factor: 2.345

5.  Genetic Characterization of the Patois Serogroup (Genus Orthobunyavirus; Family Peribunyaviridae) and Evidence That Estero Real Virus is a Member of the Genus Orthonairovirus.

Authors:  Patricia V Aguilar; William Marciel de Souza; Jesus A Silvas; Thomas Wood; Steven Widen; Marcílio Jorge Fumagalli; Márcio Roberto Teixeira Nunes
Journal:  Am J Trop Med Hyg       Date:  2018-06-07       Impact factor: 2.345

6.  Combinatorial Minigenome Systems for Emerging Banyangviruses Reveal Viral Reassortment Potential and Importance of a Protruding Nucleotide in Genome "Panhandle" for Promoter Activity and Reassortment.

Authors:  Fuli Ren; Min Zhou; Fei Deng; Hualin Wang; Yun-Jia Ning
Journal:  Front Microbiol       Date:  2020-04-08       Impact factor: 5.640

  6 in total

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