Abstract
In order to provide an easy and powerful analysis of influenza C viral HEF RNA segment of a recent strain, a combination of reverse transcription and the polymerase chain reaction was used. We amplified the entire coding region of the HEF gene of a laboratory strain of virus called C/Johannesburg/1/66, widely used for binding and esterase activity studies as well as that of a strain isolated in 1991 (C/Paris/145/91) from a patient suffering from severe flu syndrome. The sequences we amplified were about 2 kilobases long. In this work, we show that the forward ‘universal primer’ Unil, which has been used for influenza A and B viruses cDNA syntheses can also be used for influenza C virus. The PCR primers were designed to contain restriction sites to make the PCR products ready to be used for further purposes. A restriction analysis of the PCR products combined with analyses of all the human influenza C virus HEF gene sequences published so far permitted the design of sets of oligonucleotides which can prime PCR on cDNA of unknown influenza C virus for cloning.
Keywords: Influenza C virus, Reverse transcription, Polymerase chain reaction, Detection, HEF protein
References
- Andrews B.E., McDonald J.C. Influenza virus C infection in England. Br. Med. J. 1955;2:992–993. doi: 10.1136/bmj.2.4946.992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Compans R.W., Bishop D.H.L., Meier-Ewert H. Structural components of influenza C virions. J. Virol. 1977;21(2):658–665. doi: 10.1128/jvi.21.2.658-665.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Davies H.D., Appleyard G., Cuningham P., Pereira M.S. The use of a continuous cell line for the isolation of influenza viruses. Bull. World Hlth Org. 1978;56:991–993. [PMC free article] [PubMed] [Google Scholar]
- Desselberger U., Racaniello V.R., Z.J.J., Palese P. The 3' and 5' sequences of influenza A, B and C virus RNA segments are highly conserved and show partial inverted complementary sequences. Gene. 1980;8(3):315–328. doi: 10.1016/0378-1119(80)90007-4. [DOI] [PubMed] [Google Scholar]
- Dowdle W.A., Kendal A.P., Noble G.R. Influenza viruses. In: Lennette E., Schmidt N., editors. Diagnostic procedures for viral, rickettsial and chlamydial infections. 5th edn. American Public Health Association; Washington D.C: 1979. pp. 585–606. [Google Scholar]
- Dyke A.C., Cherry J.D., Nolan C.E. A clinical, epidemiologic, serologic and virologic study of influenza C virus infection. Arch. Int. Med. 1980;140:1295–1298. [PubMed] [Google Scholar]
- Gerber P., Woolridge R.L., Seal J.R., Ziegra S.R. Vol. 81. 1952. Epidemic influenza B and C in Navy recruits during winter 1951–1952; pp. 624–628. (Proc. Exp. Biol. Med.). [DOI] [PubMed] [Google Scholar]
- Gerth H.J., Bauer K.H., Steinitz H. Gibt es Hinweise für Antigendrift der Influenza-C-Viren? Zbl. Bakt. Hyg. I. Abt. Orig. A. 1975;231:47–56. [PubMed] [Google Scholar]
- Hannoun C., Dab W., Cohen J.-M. A new Influenza surveillance system in France: the Ile-de-France ‘GROG’ I. Principles and methodology. Eur. J. Epidemiol. 1989;5(3):285–293. doi: 10.1007/BF00144828. [DOI] [PubMed] [Google Scholar]
- Herrler G., Klenk H.-D. The surface receptor is a major determinant of the cell tropism of influenza C virus. Virol. 1987;159(1):102–108. doi: 10.1016/0042-6822(87)90352-7. [DOI] [PubMed] [Google Scholar]
- Herrler G., Dürkop H., Becht H., Klenk H.-D. The glycoprotein of influenza C virus is the haemagglutinin, esterase and fusion factor. J. Gen. Virol. 1988;69:839–846. doi: 10.1099/0022-1317-69-4-839. [DOI] [PubMed] [Google Scholar]
- Homma M., Ohyama S., Katagiri S. Age distribution of the antibody to type C influenza virus. Microbiol. Immunol. 1982;26(7):639–642. doi: 10.1111/mim.1982.26.7.639. [DOI] [PubMed] [Google Scholar]
- Jennings R. Respiratory viruses in Jamaica: a virologic study, hemagglutination inhibition antibody to type B and C virus in the sera of Jamaicans. Am. J. Epidemiol. 1968;87:440–445. doi: 10.1093/oxfordjournals.aje.a120834. [DOI] [PubMed] [Google Scholar]
- Katagiri S., Ohizumi A., Homma M. An outbreak of type C influenza in a children's home. J. Infect. Dis. 1983;148:51–56. doi: 10.1093/infdis/148.1.51. [DOI] [PubMed] [Google Scholar]
- Librach I.M. Pneumonia due to infection with influenza C virus. Practitioner. 1956;177:617–618. [PubMed] [Google Scholar]
- Luytjes W., Bredenbeek P.J., Noten A.F.H., Horzinek M.C., Spaan W.J.M. Sequence of mouse hepatitis virus A59 mRNA2: indications for RNA recombination between coronaviruses and influenza C virus. Virol. 1988;166:415–422. doi: 10.1016/0042-6822(88)90512-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Manuguerra J.-C., Hannoun C., Aymard M. Influenza C virus infection in France. J. Infect. 1992;24:91–99. doi: 10.1016/0163-4453(92)91150-a. [DOI] [PubMed] [Google Scholar]
- Manuguerra J.C., Dubois C., Hannoun C. Analytical detection of 9(4)-O-acetylated sialoglycoproteins and gangliosides using influenza-C virus. Anal. Biochem. 1991;194(2):425–432. doi: 10.1016/0003-2697(91)90252-O. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Minuse E., Quilligan J.J., Francis T. Type C influenza virus. J. Lab. Clin. Med. 1954;43:31–42. [PubMed] [Google Scholar]
- Nakada S., Greager R.S., Krystal M., Aaronson R.P., Palese P. Influenza C virus hemagglutinin: comparison with influenza A and B virus hemagglutinins. J. Virol. 1984;50(1):118–124. doi: 10.1128/jvi.50.1.118-124.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nishimura H., Sagawara K., Kitame F. Prevalence of the antibody to influenza C virus in a Northern Luzon highland village, Philippines. Microbiol. Immunol. 1987;31(11):1137–1143. doi: 10.1111/j.1348-0421.1987.tb01348.x. [DOI] [PubMed] [Google Scholar]
- Nishimura H., Sugawara K., Kitame F., Nakamura K., Katsushima N., Moriuchi H., Numazaki Y. A human melanoma cell line highly susceptible to influenza C virus. J. Gen. Virol. 1989;70:1653–1661. doi: 10.1099/0022-1317-70-7-1653. [DOI] [PubMed] [Google Scholar]
- O'Callaghan R.J., Gohd R.S., Labat D.D. Human antibody to influenza C virus: its age-related distribution and distinction from receptor analogs. Inf. Immunity. 1980;30(2):500–505. doi: 10.1128/iai.30.2.500-505.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pead P.J., Saeed A.A., Pomeroy M. Influenza C virus in the United Kingdom. J. Infect. 1985;10:78–79. doi: 10.1016/s0163-4453(85)80018-9. [DOI] [PubMed] [Google Scholar]
- Pfeiffer J.B., Compans R.W. Structure of the influenza C glycoprotein gene as determined from cloned DNA. Virus Res. 1984;1:281–296. doi: 10.1016/0168-1702(84)90017-0. [DOI] [PubMed] [Google Scholar]
- Pothier P., Bour B.B., Lhuillier M., Hannoun C. Detection rapide des antigènes grippaux dans les produits pathologiques à 1'aide d'anticorps monoclonaux. Rev. Franc. Laborat. 1988;169:7–10. [Google Scholar]
- Robertson J.S. 5' and 3' terminal nucleotide sequences of the RNA genome segments of influenza virus. Nucl. Acid Res. 1979;6:3745–3757. doi: 10.1093/nar/6.12.3745. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Robertson J.S., Bootman J.S., Newman R., Oxford J.S., Daniels R.S., Webster R.G., Schild G.C. Structural changes in the haemagglutinin which accompany egg adaptation of an influenza A (H1N1) virus. Virol. 1987;160:31–37. doi: 10.1016/0042-6822(87)90040-7. [DOI] [PubMed] [Google Scholar]
- Robertson J.S., Nicolson C., Bootman J.S., Major D., Robertson E.W., Wood J.M. Sequence analysis of the haemagglutinin (HA) of influenza A(H1N1) viruses present in clinical material and comparison with the HA of laboratory-derived virus. J. Gen. Virol. 1991;72:2671–2677. doi: 10.1099/0022-1317-72-11-2671. [DOI] [PubMed] [Google Scholar]
- Robertson R.J., Naeve C.W., Webster R.G., Bootman J.S., Newman R., Schild G.C. Alterations in the hemagglutinin associated with adaptation of influenza B virus to growth in eggs. Virol. 1985;143:166–174. doi: 10.1016/0042-6822(85)90105-9. [DOI] [PubMed] [Google Scholar]
- Saiki R.K., Gelfand D.H., Stoffel S., Scharf S.J., Higuchi R., Horn G.T., Mullis K.B., Ehrlich H.A. Primer directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science. 1988;239:487–491. doi: 10.1126/science.2448875. [DOI] [PubMed] [Google Scholar]
- Schaffer H.E., Sederoff R.R. Improved estimation of DNA fragment lengths from agarose gels. Anal. Biochem. 1981;115:113–122. doi: 10.1016/0003-2697(81)90533-9. [DOI] [PubMed] [Google Scholar]
- Szepanski S., Gross H.J., Brossmer R., Klenk H.-D., Herrler G. A single point mutation of the influenza C virus glycoprotein (HEF) changes the viral receptor-binding activity. Virol. 1992;188:85–92. doi: 10.1016/0042-6822(92)90737-A. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Troisi C.L., Monto A.S. Comparison of enzyme-linked immunosorbent assay and hemagglutination inhibition in a seroepidemiological study of influenza type C infection. J. Clin. Microbiol. 1981;14(5):516–521. doi: 10.1128/jcm.14.5.516-521.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vlasak R., Krystal M., Nacht M., Palese P. The influenza C virus glycoprotein (HE) exhibits receptor-binding (hemagglutinin) and receptor-destroying (esterase) activities. Virol. 1987;160:419–425. doi: 10.1016/0042-6822(87)90013-4. [DOI] [PubMed] [Google Scholar]
- Vlasak R., Luytjes W., Span W., Palese P. Vol. 85. 1988. Human and bovine coronaviruses recognize sialic acid-containing receptors similar to those of influenza C viruses; pp. 4526–4529. (Proc. Natl. Acad. Sci. USA). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Winter G., Fields S., Brownlee G.G. Nucleotide sequence of the haemagglutinin gene of a human influenza virus H1 subtype. Nature. 1981;292:72–75. doi: 10.1038/292072a0. [DOI] [PubMed] [Google Scholar]
