Hostname: page-component-cd9895bd7-dk4vv Total loading time: 0 Render date: 2024-12-22T16:28:12.677Z Has data issue: false hasContentIssue false
  • English
  • Français

Antigenic and genetic analyses of eight influenza C strains isolated in various areas of Japan during 1985–9

Published online by Cambridge University Press:  15 May 2009

S. Ohyama ,
K. Adachi ,
K. Sugawara ,
S. Hongo ,
H. Nishimura ,
F. Kitame  and
K. Nakamura
S. Ohyama
Affiliation:
Yamagata Prefectural Institute of Public Health, Yamagata 990, Japan
K. Adachi
Affiliation:
Department of Bacteriology, Yamagata University School of Medicine, Yamagata 990-23, Japan
K. Sugawara
Affiliation:
Department of Bacteriology, Yamagata University School of Medicine, Yamagata 990-23, Japan
S. Hongo
Affiliation:
Department of Bacteriology, Yamagata University School of Medicine, Yamagata 990-23, Japan
H. Nishimura
Affiliation:
Department of Bacteriology, Yamagata University School of Medicine, Yamagata 990-23, Japan
F. Kitame
Affiliation:
Department of Bacteriology, Yamagata University School of Medicine, Yamagata 990-23, Japan
K. Nakamura*
Affiliation:
Department of Bacteriology, Yamagata University School of Medicine, Yamagata 990-23, Japan
*
*K. Nakamura. Department of Bacteriology, Yamagata University School of Medicine. Iida-Nishi. Yamagata 990–23, Japan.
Rights & Permissions [Opens in a new window]

Summary

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Eight strains of influenza C virus isolated in various areas of Japan between January 1985 and January 1989 were compared using monoclonal antibodies to the haemagglutinin-esterase (HE) glycoproteins and by oligonucleotide mapping of total vRNA. Five of six strains isolated during 1986–9 were closely related to one another and also resembled the virus, C/Aichi/1/81, isolated in 1981 in Aichi prefecture. This suggests that the C/Aichi/l/81-related viruses had an epidemiological advantage over any co-circulating viruses at least during that period. One of two 1985 isolates (C/Nara/1/85) was antigenically indistinguishable from the C/Mississippi/1/80 strain though their oligonucleotide patterns were markedly different from each other. This raises the possibility that C/Nara/1/85 may be a recombinant virus which receives its HE gene from the C/Mississippi/l/80-related parent.

Type
Research Article
Information
Epidemiology & Infection , Volume 108 , Issue 2 , April 1992 , pp. 353 - 365
Copyright
Copyright © Cambridge University Press 1992

References

REFERENCES

1.Homma, M, Ohyama, S, Katagiri, S. Age distribution of the antibody to type C influenza virus. Microbiol Immunol 1982; 26: 639–42.CrossRefGoogle ScholarPubMed
2.Nishimura, H, Sugawara, K, Kitame, F, Nakamura, K, Sasaki, H. Prevalence of the antibody to influenza C virus in a northern Luzon highland village, Phillippines. Microbiol Immunol 1987; 31: 1137–43.CrossRefGoogle Scholar
3.Katagiri, S, Ohizumi, A, Homma, M. An outbreak of type C influenza in a children's home. J Infect Dis 1983; 148: 51–6.CrossRefGoogle Scholar
4.Katagiri, S, Ohizumi, A, Ohyama, S, Homma, M. Follow-up study of type C influenza outbreak in a children's home. Microbiol Immunol 1987; 31: 337–43.CrossRefGoogle Scholar
5.Racaniello, VR, Palese, P. Isolation of influenza C virus recombinants. J Virol 1979; 32: 1006–14.CrossRefGoogle ScholarPubMed
6.Guo, Y, Desselberger, U. Genome analysis of influenza C viruses isolated in 1981/82 from pigs in China. J Gen Virol 1984; 65: 1857–72.Google Scholar
7.Nakada, S, Greager, RS, Krystal, M, Aaronson, RP, Palese, P. Influenza C virus hemagglutinin: Comparison with influenza A and B virus hemagglutinins. J Virol 1984; 50: 118–24.CrossRefGoogle ScholarPubMed
8.Pfeifer, JB, Compans, RW. Structure of the influenza C glycoprotein gene as determined from cloned DNA. Virus Res 1984; 1: 281–96.CrossRefGoogle ScholarPubMed
9.Sugawara, K, Nishimura, H, Kitame, F, Nakamura, K. Antigenic variation among human strains of influenza C virus detected with monoclonal antibodies to gp88 glycoprotein. Virus Res 1986; 6: 27–32.Google ScholarPubMed
10.Both, GW, Sleigh, MJ, Cox, NJ, Kendal, AP. Antigenic drift in influenza virus H3 hemagglutinin from 1968 to 1980. Multiple evolutionary pathways and sequential amino acid changes at key antigenic sites. J Virol 1983; 48: 52–60.CrossRefGoogle ScholarPubMed
11.Raymond, FL, Caton, AJ, Cox, NJ, Kendal, AP, Brownlee, GG. The antigenicity and evolution of influenza H1 haemagglutinin, from 1950–1957 and 1977–1983: Two pathways from one gene. Virology 1986; 148: 275–87.CrossRefGoogle ScholarPubMed
12.Buonagurio, DA, Nakada, S, Desselberger, U, Krystal, M, Palese, P. Noncumulative sequence changes in the hemagglutinin genes of influenza C virus isolates. Virology 1985; 146: 221–32.CrossRefGoogle ScholarPubMed
13.Buonagurio, DA, Nakada, S, Fitchi, WM, Palese, P. Epidemiology of influenza C virus in man: Multiple evolutionary linages and low rates of change. Virology 1986; 153: 12–21.CrossRefGoogle Scholar
14.Kawamura, H, Tashiro, M, Kitame, F, Homma, M, Nakamura, K. Genetic variation among human strains of influenza C virus isolated in Japan. Virus Res 1986; 4: 275–88.CrossRefGoogle ScholarPubMed
15.Adachi, K, Kitame, F, Sugawara, K, Nishimura, H, Nakamura, K. Antigenic and genetic characterization of three influenza C strains isolated in the Kinki district of Japan in 1982–1983. Virology 1989; 172: 125–33.CrossRefGoogle ScholarPubMed
16.Hongo, S, Sugawara, K, Homma, M, Nakamura, K. The functions of oligosaccharide chains associated with influenza C viral glycoproteins. II. The role of carbohydrates in the antigenic properties of influenza C viral glycoproteins. Arch Virol 1986; 89: 189–201.CrossRefGoogle ScholarPubMed
17.Sugawara, K, Kitame, F, Nishimura, H, Nakamura, K. Operational and topological analyses of antigenic sites on influenza C virus glycoprotein and their dependence on glycosylation. J Gen Virol 1988; 69: 537–47.CrossRefGoogle ScholarPubMed
18.Hongo, S, Sugawara, K, Homma, M, Nakamura, K. The functions of oligosaccharide chains associated with influenza C viral glycoproteins. I. The formation of influenza C virus particles in the absence of glycosylation. Arch Virol 1986; 89: 171–87.CrossRefGoogle ScholarPubMed
19.Palese, P, Schulman, JL. Differences in RNA patterns of influenza A virus. J Virol 1976; 17: 876–84.CrossRefGoogle Scholar
20.Nakajima, K, Desselberger, U, Palese, P. Recent human influenza A (H1N1) viruses are closely related genetically to strains isolated in 1950. Nature 1978; 274: 334–9.CrossRefGoogle ScholarPubMed
21.Sanger, F, Nicklen, S, Coulson, AR. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci USA 1977; 74: 5463–7.CrossRefGoogle ScholarPubMed
22.Czekalowski, JW, Prasad, AK. Studies of influenza C virus I. Antigenic variation in influenza virus type C. Arch Ges Virusforsch 1973; 42: 215–27.CrossRefGoogle Scholar
23.Meier-Ewert, H, Petri, T, Bishop, DHL. Oligonucleotide fingerprint analyses of influenza C virion RNA recovered from five different isolates. Arch Virol 1981; 67: 141–7.CrossRefGoogle ScholarPubMed