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Вопросы вирусологии. 2018; 63: 275-280

МОНОКЛОНАЛЬНЫЕ АНТИТЕЛА К ГЕМАГГЛЮТИНИНУ ВИРУСОВ ГРИППА В ВИКТОРИАНСКОЙ ЭВОЛЮЦИОННОЙ ЛИНИИ

Сорокин Е. В., Царёва Т. Р., Желтухина А. И.

https://doi.org/10.18821/0507-4088-2018-63-6-275-280

Аннотация

Социркуляция двух эволюционных линий (ЭЛ) вируса гриппа В в один эпидемический сезон определяет необходимость создания специфичных реагентов для быстрой идентификации и типирования новых изолятов. С этой целью была разработана панель моноклональных антител (МКА) к гемагглютинину (ГА) вируса гриппа В/Брисбен/46/15 Викторианской ЭЛ. Установлено, что все полученные МКА реагировали в иммуноферментном анализе только с вирусами Викторианской ЭЛ при полном отсутствии взаимодействия с гетерологичными вирусами гриппа В Ямагатской группы, сезонными и потенциально пандемическими вирусами гриппа А. МКА обладали выраженной антигемагглютинирующей и вируснейтрализующей активностью. Показано, что все МКА взаимодействовали в реакции торможения гемагглютинации (РТГА) только с вирусами Викторианской ветви, но не связывались с В/Ямагата-подобными штаммами. При анализе МКА с вирусами ранних лет выделения было обнаружено, что МКА 6E11, 9G5, 9B5 и 6A4 обладали способностью взаимодействовать с вирусом В/Россия/69, что может быть связано с наличием общего эпитопа у вирусов гриппа В еще до разделения на две независимые филогенетические ветви и современных штаммов гриппа В Викторианской ветви. Показано, что МКА 7C8, 7G9, 7H8 и 8D11 направлены к консервативному эпитопу (или эпитопам), специфичным для ГА вирусов гриппа В Викторианской линии. Наличие различий в эффективности взаимодействия МКА 6A9, 7G9 и 8A8 в РТГА позволяет выявлять и дифференцировать изоляты, выделенные в куриных эмбрионах и культуре клеток MDCK. Таким образом, разработанные МКА могут быть успешно применены для идентификации и антигенного анализа В/Виктория-подобных штаммов.
Список литературы

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4. Lin Y.P., Gregory V., Bennett M., Hay A. Recent changes among human influenza viruses. Virus Res. 2004; 103(1-2): 47-52.

5. Paiva T.M., Benega M.A., Silva D.B., Santos K.C., Cruz A.S., Hortenci M.F., et al. Evolutionary pattern of reemerging influenza B/Victoria lineage viruses in São Paulo, Brazil, 1996-2012: Implications for vaccine composition strategy. J. Med. Virol. 2013; 85(11): 1983-9.

6. Osterhaus A.D., Rimmelzwaan G.F., Martina B.E., Bestebroer T.M., Fouchier R.A. Influenza B virus in seals. Science. 2000; 288(5468): 1051-3.

7. Bodewes R., Morick D., de Mutsert G., Osinga N., Bestebroer T., van der Vliet S., et al. Recurring influenza B virus infections in seals. Emerg. Infect. Dis. 2013; 19(3): 511-2.

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17. Лобова Т.Г., Прокопец А.В., Комиссаров А.Б., Даниленко Д.М., Паянкова В.Ф., Суховецкая В.Ф. и др. Эволюционная изменчивость вирусов гриппа В, циркулировавших в Российской Федерации с 2005 по 2012 г. Вопросы вирусологии. 2012; 54(6): 22-6

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19. Lugovtsev V.Y., Vodeiko G.M., Levandowski R.A. Mutational pattern of influenza B viruses adapted to high growth replication in embryonated eggs. Virus Res. 2005; 109(2): 149-57.

20. Govorkova E.A., Matrosovich M.N., Tuzikov A.B., Bovin N.V., Gerdil C., Fanget B., et al. Selection of receptor-binding variants of human influenza A and B viruses in baby hamster kidney cells. Virology. 1999; 262(1): 31-8.

21. Nerome R., Hiromoto Y., Sugita S., Tanabe N., Ishida M., Matsumoto M., et al. Evolutionary characteristics of influenza B virus since its first isolation in 1940: dynamic circulation of deletion and insertion mechanism. Arch. Virol. 1998; 143(8): 1569-83.

22. Chen J.M., Guo Y.J., Wu K.Y., Guo J.F., Wang M., Dong J., et al. Exploration of the emergence of the Victoria lineage of influenza B virus. Arch. Virol. 2007; 152(2): 415-22.

23. Kanegae Y., Sugita S., Endo A., Ishida M., Senya S., Osako K., et al. Evolutionary pattern of the hemagglutinin gene of influenza B viruses isolated in Japan: cocirculating lineages in the same epidemic season. J. Virol. 1990; 64(6): 2860-5.

24. Lin Y.P., Gregory V., Bennett M., Hay A. Recent changes among human influenza viruses. Virus Res. 2004; 103(1-2): 47-52.

25. Paiva T.M., Benega M.A., Silva D.B., Santos K.C., Cruz A.S., Hortenci M.F., et al. Evolutionary pattern of reemerging influenza B/Victoria lineage viruses in São Paulo, Brazil, 1996-2012: Implications for vaccine composition strategy. J. Med. Virol. 2013; 85(11): 1983-9.

26. Osterhaus A.D., Rimmelzwaan G.F., Martina B.E., Bestebroer T.M., Fouchier R.A. Influenza B virus in seals. Science. 2000; 288(5468): 1051-3.

27. Bodewes R., Morick D., de Mutsert G., Osinga N., Bestebroer T., van der Vliet S., et al. Recurring influenza B virus infections in seals. Emerg. Infect. Dis. 2013; 19(3): 511-2.

28. Ran Z., Shen H., Lang Y., Kolb E.A., Turan N., Zhu L., et al. Domestic pigs are susceptible to infection with influenza B viruses. J. Virol. 2015; 89(9): 4818-26.

29. Glezen W., Schmier J.K., Kuehn C.M., Ryan K.J., Oxford J. The burden of influenza B: a structured literature review. Am. J. Public Health. 2013; 103(3): e43-5. doi: 10.2105/AJPH.2012.301137.

30. Caini S., Huang Q.S., Ciblak M.A., Kusznierz G., Owen R., Wangchuk S., et al. Epidemiological and virological characteristics of influenza B: results of the Global Influenza B Study. Influenza Other Respir. Viruses. 2015; 9(Suppl. 1): 3-12.

31. Kohler G., Milstein C. Derivation of specific antibody-producing tissue culture and tumor lines by cell fusion. Eur. J. Immunol. 1976; 6(7): 511-9.

32. Sominina A.A., Burtseva E.I., Lobova T.G., Konovalova N.I., Gudkova T.M., Litvinova O.M., et al. MR «Isolation of influenza viruses in cell cultures and chicken embryos and their identification». Moscow; 2006. (in Russian)

33. Recommended composition of influenza virus vaccines for use in the 2016-2017 northern hemisphere influenza season. Wkly Epidemiol. Rec. 2016; 91(10): 121-32.

34. Recommended composition of influenza virus vaccines for use in the 2017-2018 northern hemisphere influenza season. Wkly Epidemiol. Rec. 2017; 92(11): 117-28.

35. Rota P.A., Wallis T.R., Harmon M.W., Rota J.S., Kendal A.P., Nerome K. Cocirculation of two distinct evolutionary lineages of influenza type B virus since 1983. Virology. 1990; 175(1): 65-8.

36. Ambrose C.S., Levin M.J. The rationale for quadrivalent influenza vaccines. Hum. Vaccin. Immunother. 2012; 8(1): 81-8.

37. Lobova T.G., Prokopets A.V., Komissarov A.B., Danilenko D.M., Payankova V.F., Sukhovetskaya V.F., et al. Evolutionary variability of influenza B viruses in Russian Federation in 2005-2012. Voprosy virusologii. 2012; 54(6): 22-6. (in Russian)

38. Lugovtsev V.Y., Vodeiko G.M, Strupczewski C.M., Ye Z., Levandowski R.A. Generation of the influenza B viruses with improved growth phenotype by substitution of specific amino acids of Hemagglutinin. Virology. 2007; 365(2): 315-23.

39. Lugovtsev V.Y., Vodeiko G.M., Levandowski R.A. Mutational pattern of influenza B viruses adapted to high growth replication in embryonated eggs. Virus Res. 2005; 109(2): 149-57.

40. Govorkova E.A., Matrosovich M.N., Tuzikov A.B., Bovin N.V., Gerdil C., Fanget B., et al. Selection of receptor-binding variants of human influenza A and B viruses in baby hamster kidney cells. Virology. 1999; 262(1): 31-8.

Problems of Virology. 2018; 63: 275-280

MONOCLONAL ANTIBODIES TO HEMAGGLUTININ OF INFLUENZA B VIRUSES VICTORIA EVOLUTIONARY LINEAGE

Sorokin E. V., Tsareva T. R., Zheltukhina A. I.

https://doi.org/10.18821/0507-4088-2018-63-6-275-280

Abstract

Co-circulation of two evolutionary distinct lineages of influenza virus in one epidemic season has led to development specific reagents for rapid identification and typing of new isolates. Panel of MAbs to hemagglutinin of influenza virus B/Brisbane/46/15 belonging to Victoria evolutionary lineage was developed. All MAbs reacted in ELISA with B/Victoria-like strains only. There were no interactions with heterologous influenza viruses of B/Yamagata lineage, seasonal and potentially pandemic influenza A viruses. All MAbs reacted in hemagglutination inhibition and virus neutralization. MAbs interacted in hemagglutination inhibition only with B/Victoria-like viruses, but did not interacted B/Yamagata-like strains. Neutralization and hemagglutination inhibition studies of viruses isolated before 1983 with MAbs revealed that MAbs 6E11, 9G5, 9B5 and 6A4 had the ability to interact with the virus B/ Russia/69 which may evidence that B strains of early isolation period (before lineage separation) have common epitope with recent Victoria lineage viruses. MAbs 7C8, 7G9, 7H8 and 8D11 were directed to a conserved epitope (or epitopes) specific for influenza hemagglutinin viruses of B/Victoria group. The presence of differences in the effectiveness of the interaction of MAbs 6A9, 7G9 and 8A8 in hemagglutination inhibition test allows the identification and differentiation of strains isolated in chicken embryos and MDCK cell culture. Thus, the developed MAbs can be successfully used for identification and antigenic analysis of B/Victoria-like strains.
References

1. Nerome R., Hiromoto Y., Sugita S., Tanabe N., Ishida M., Matsumoto M., et al. Evolutionary characteristics of influenza B virus since its first isolation in 1940: dynamic circulation of deletion and insertion mechanism. Arch. Virol. 1998; 143(8): 1569-83.

2. Chen J.M., Guo Y.J., Wu K.Y., Guo J.F., Wang M., Dong J., et al. Exploration of the emergence of the Victoria lineage of influenza B virus. Arch. Virol. 2007; 152(2): 415-22.

3. Kanegae Y., Sugita S., Endo A., Ishida M., Senya S., Osako K., et al. Evolutionary pattern of the hemagglutinin gene of influenza B viruses isolated in Japan: cocirculating lineages in the same epidemic season. J. Virol. 1990; 64(6): 2860-5.

4. Lin Y.P., Gregory V., Bennett M., Hay A. Recent changes among human influenza viruses. Virus Res. 2004; 103(1-2): 47-52.

5. Paiva T.M., Benega M.A., Silva D.B., Santos K.C., Cruz A.S., Hortenci M.F., et al. Evolutionary pattern of reemerging influenza B/Victoria lineage viruses in São Paulo, Brazil, 1996-2012: Implications for vaccine composition strategy. J. Med. Virol. 2013; 85(11): 1983-9.

6. Osterhaus A.D., Rimmelzwaan G.F., Martina B.E., Bestebroer T.M., Fouchier R.A. Influenza B virus in seals. Science. 2000; 288(5468): 1051-3.

7. Bodewes R., Morick D., de Mutsert G., Osinga N., Bestebroer T., van der Vliet S., et al. Recurring influenza B virus infections in seals. Emerg. Infect. Dis. 2013; 19(3): 511-2.

8. Ran Z., Shen H., Lang Y., Kolb E.A., Turan N., Zhu L., et al. Domestic pigs are susceptible to infection with influenza B viruses. J. Virol. 2015; 89(9): 4818-26.

9. Glezen W., Schmier J.K., Kuehn C.M., Ryan K.J., Oxford J. The burden of influenza B: a structured literature review. Am. J. Public Health. 2013; 103(3): e43-5. doi: 10.2105/AJPH.2012.301137.

10. Caini S., Huang Q.S., Ciblak M.A., Kusznierz G., Owen R., Wangchuk S., et al. Epidemiological and virological characteristics of influenza B: results of the Global Influenza B Study. Influenza Other Respir. Viruses. 2015; 9(Suppl. 1): 3-12.

11. Kohler G., Milstein C. Derivation of specific antibody-producing tissue culture and tumor lines by cell fusion. Eur. J. Immunol. 1976; 6(7): 511-9.

12. Sominina A.A., Burtseva E.I., Lobova T.G., Konovalova N.I., Gudkova T.M., Litvinova O.M. i dr. MR «Vydelenie virusov grippa v kletochnykh kul'turakh i kurinykh embrionakh i ikh identifikatsiya». M.; 2006

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15. Rota P.A., Wallis T.R., Harmon M.W., Rota J.S., Kendal A.P., Nerome K. Cocirculation of two distinct evolutionary lineages of influenza type B virus since 1983. Virology. 1990; 175(1): 65-8.

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18. Lugovtsev V.Y., Vodeiko G.M, Strupczewski C.M., Ye Z., Levandowski R.A. Generation of the influenza B viruses with improved growth phenotype by substitution of specific amino acids of Hemagglutinin. Virology. 2007; 365(2): 315-23.

19. Lugovtsev V.Y., Vodeiko G.M., Levandowski R.A. Mutational pattern of influenza B viruses adapted to high growth replication in embryonated eggs. Virus Res. 2005; 109(2): 149-57.

20. Govorkova E.A., Matrosovich M.N., Tuzikov A.B., Bovin N.V., Gerdil C., Fanget B., et al. Selection of receptor-binding variants of human influenza A and B viruses in baby hamster kidney cells. Virology. 1999; 262(1): 31-8.

21. Nerome R., Hiromoto Y., Sugita S., Tanabe N., Ishida M., Matsumoto M., et al. Evolutionary characteristics of influenza B virus since its first isolation in 1940: dynamic circulation of deletion and insertion mechanism. Arch. Virol. 1998; 143(8): 1569-83.

22. Chen J.M., Guo Y.J., Wu K.Y., Guo J.F., Wang M., Dong J., et al. Exploration of the emergence of the Victoria lineage of influenza B virus. Arch. Virol. 2007; 152(2): 415-22.

23. Kanegae Y., Sugita S., Endo A., Ishida M., Senya S., Osako K., et al. Evolutionary pattern of the hemagglutinin gene of influenza B viruses isolated in Japan: cocirculating lineages in the same epidemic season. J. Virol. 1990; 64(6): 2860-5.

24. Lin Y.P., Gregory V., Bennett M., Hay A. Recent changes among human influenza viruses. Virus Res. 2004; 103(1-2): 47-52.

25. Paiva T.M., Benega M.A., Silva D.B., Santos K.C., Cruz A.S., Hortenci M.F., et al. Evolutionary pattern of reemerging influenza B/Victoria lineage viruses in São Paulo, Brazil, 1996-2012: Implications for vaccine composition strategy. J. Med. Virol. 2013; 85(11): 1983-9.

26. Osterhaus A.D., Rimmelzwaan G.F., Martina B.E., Bestebroer T.M., Fouchier R.A. Influenza B virus in seals. Science. 2000; 288(5468): 1051-3.

27. Bodewes R., Morick D., de Mutsert G., Osinga N., Bestebroer T., van der Vliet S., et al. Recurring influenza B virus infections in seals. Emerg. Infect. Dis. 2013; 19(3): 511-2.

28. Ran Z., Shen H., Lang Y., Kolb E.A., Turan N., Zhu L., et al. Domestic pigs are susceptible to infection with influenza B viruses. J. Virol. 2015; 89(9): 4818-26.

29. Glezen W., Schmier J.K., Kuehn C.M., Ryan K.J., Oxford J. The burden of influenza B: a structured literature review. Am. J. Public Health. 2013; 103(3): e43-5. doi: 10.2105/AJPH.2012.301137.

30. Caini S., Huang Q.S., Ciblak M.A., Kusznierz G., Owen R., Wangchuk S., et al. Epidemiological and virological characteristics of influenza B: results of the Global Influenza B Study. Influenza Other Respir. Viruses. 2015; 9(Suppl. 1): 3-12.

31. Kohler G., Milstein C. Derivation of specific antibody-producing tissue culture and tumor lines by cell fusion. Eur. J. Immunol. 1976; 6(7): 511-9.

32. Sominina A.A., Burtseva E.I., Lobova T.G., Konovalova N.I., Gudkova T.M., Litvinova O.M., et al. MR «Isolation of influenza viruses in cell cultures and chicken embryos and their identification». Moscow; 2006. (in Russian)

33. Recommended composition of influenza virus vaccines for use in the 2016-2017 northern hemisphere influenza season. Wkly Epidemiol. Rec. 2016; 91(10): 121-32.

34. Recommended composition of influenza virus vaccines for use in the 2017-2018 northern hemisphere influenza season. Wkly Epidemiol. Rec. 2017; 92(11): 117-28.

35. Rota P.A., Wallis T.R., Harmon M.W., Rota J.S., Kendal A.P., Nerome K. Cocirculation of two distinct evolutionary lineages of influenza type B virus since 1983. Virology. 1990; 175(1): 65-8.

36. Ambrose C.S., Levin M.J. The rationale for quadrivalent influenza vaccines. Hum. Vaccin. Immunother. 2012; 8(1): 81-8.

37. Lobova T.G., Prokopets A.V., Komissarov A.B., Danilenko D.M., Payankova V.F., Sukhovetskaya V.F., et al. Evolutionary variability of influenza B viruses in Russian Federation in 2005-2012. Voprosy virusologii. 2012; 54(6): 22-6. (in Russian)

38. Lugovtsev V.Y., Vodeiko G.M, Strupczewski C.M., Ye Z., Levandowski R.A. Generation of the influenza B viruses with improved growth phenotype by substitution of specific amino acids of Hemagglutinin. Virology. 2007; 365(2): 315-23.

39. Lugovtsev V.Y., Vodeiko G.M., Levandowski R.A. Mutational pattern of influenza B viruses adapted to high growth replication in embryonated eggs. Virus Res. 2005; 109(2): 149-57.

40. Govorkova E.A., Matrosovich M.N., Tuzikov A.B., Bovin N.V., Gerdil C., Fanget B., et al. Selection of receptor-binding variants of human influenza A and B viruses in baby hamster kidney cells. Virology. 1999; 262(1): 31-8.