Methodological basics for differential detection of EBV1/EBV2 and HHV6A/HHV6B

Cover Page


Cite item

Full Text

Abstract

Among a whole variety of EBV- and HHV6-linked diseases only infectious mononucleosis is subject to official statistical reporting in Russia that substantially complicates objective assessment of etiological structure, incidence rate, characteristics of developing epidemic process. Currently, the data on the genetic EBV heterogeneity, even at the level of the main types (EBV1 and EBV2), as well as HHV6A and HHV6B, prevalence and clinical importance are mainly limited to foreign research publications. Few publications assessing this issue are available in Russian scientific papers. At the same time, examining circulation of virus genetic types (variants) and use of such data in implementing epidemiological surveillance after some other infections have been commonly practiced. One of the key issues is the level of developed laboratory support for molecular genetic monitoring. The goal of the study was to improve methodological basics for differential detection of HHV6A/B and the major EBV types. There were used samples of peripheral blood leukocytes collected from children aged 1–15 years with acute (n = 50) and asymptomatic infectious mononucleosis (n = 29). The detection and quantification of EBV and HHV6 DNA was performed by using real-time PCR. For differential determination of EBV1/EBV2 and HHV6A/HHV6B, an optimized one-round PCR with electrophoretic agarose gel detection amplification products was used. The data from our own study showed that frequency of detected EBV and HHV6 DNA in acute infectious mononucleosis patients comprised 74 and 72% compared to control group reaching 35 and 74%, respectively. It was found that among the examined children of Nizhny Novgorod Region, EBV1 and HHV6B prevailed in the viral population that agrees with existing insights about their geographical distribution in the adjacent territories. EBV2 was found in a single sample only in the control group. HHV6A was not detected in any of the groups. The methodological approach optimized in this study allows to separately detect HHV6A/HHV6B and the main EBV types according to a unified laboratory protocol, whereas combining it with additional stage of DNA enrichment increases the diagnostic sensitivity of PCR analysis, minimizes proportion of discordant and false negative results. Such an integrated approach can be applied for diagnostic, epidemiological and research purposes.

About the authors

M. I. Popkova

Academician I.N. Blokhina Nizhny Novgorod Scientific Research Institute of Epidemiology and Microbiology

Author for correspondence.
Email: popmarig@mail.ru
ORCID iD: 0000-0001-5864-5862

Mariia I. Popkova - PhD (Мedicine), Leading Researcher, Laboratory of Molecular Biology and Biotechnology, Academician I.N. Blokhina Nizhny Novgorod Scientific Research Institute of Epidemiology and Microbiology.

603950, Nizhny Novgorod, Malaya Yamskaya str., 71.

Phone: +7 (831) 469-79-46. Fax: +7 (831) 469-79-20.

SPIN: 4485-2459

Russian Federation

O. V. Utkin

Academician I.N. Blokhina Nizhny Novgorod Scientific Research Institute of Epidemiology and Microbiology

Email: utkino2004@mail.ru
ORCID iD: 0000-0002-7571-525X

PhD (Biology), Leading Researcher, Laboratory of Molecular Biology and Biotechnology, Academician I.N. Blokhina Nizhny Novgorod Scientific Research Institute of Epidemiology and Microbiology.

Nizhny Novgorod.

SPIN: 1174-6500

Russian Federation

E. A. Soboleva

Privolzhsky Research Medical University

Email: Fullofcarrot@pimunn.ru
ORCID iD: 0000-0003-3591-9618

Ifectologist, Assistant Professor, Department of Infectious Diseases, Privolzhsky Research Medical University.

Nizhny Novgorod.

Russian Federation

N. A. Sakharnov

Academician I.N. Blokhina Nizhny Novgorod Scientific Research Institute of Epidemiology and Microbiology

Email: saharnov@nniiem.ru
ORCID iD: 0000-0003-3965-2033

Researcher, Laboratory of Molecular Biology and Biotechnology, Academician I.N. Blokhina Nizhny Novgorod Scientific Research Institute of Epidemiology and Microbiology.

Nizhny Novgorod.

SPIN:8457-3501

Russian Federation

D. A. Bryzgalova

Academician I.N. Blokhina Nizhny Novgorod Scientific Research Institute of Epidemiology and Microbiology

Email: moskvinadara7@gmail.com
ORCID iD: 0000-0002-6663-8440

Junior Researcher, Laboratory of Molecular Biology and Biotechnology, Academician I.N. Blokhina Nizhny Novgorod Scientific Research Institute of Epidemiology and Microbiology.

Nizhny Novgorod.

SPIN: 5626-3491

Russian Federation

A. O. Senatskaia

Academician I.N. Blokhina Nizhny Novgorod Scientific Research Institute of Epidemiology and Microbiology

Email: seanna@bk.ru
ORCID iD: 0000-0003-2024-4283

Junior Researcher, Laboratory of Molecular Biology and Biotechnology, Academician I.N. Blokhina Nizhny Novgorod Scientific Research Institute of Epidemiology and Microbiology.

Nizhny Novgorod.

SPIN: 6891-2140

Russian Federation

E. A. Kulova

Privolzhsky Research Medical University

Email: dr_kulova@mail.ru
ORCID iD: 0000-0002-5207-1164

PhD (Medicine), Assistant Professor, Department of Infectious Diseases, Privolzhsky Research Medical University.

Nizhny Novgorod.

SPIN: 4331-6958

Russian Federation

References

  1. Гончарова Е.В., Сенюта Н.Б., Смирнова К.В., Щербак Л.Н., Гурцевич В.Э. Вирус Эпштейна–Барр (ВЭБ) в России: инфицированность населения и анализ вариантов гена LMP1 у больных ВЭБ-ассоциированными патологиями и здоровых лиц // Вопросы вирусологии. 2015. Т. 60, № 2. С. 11–17.
  2. Гурцевич В.Э., Смирнова К.В., Ботезату И.В., Душенькина Т.Е., Лубенская А.К., Дубар Э., Сенюта Н.Б., Лихтенштейн А.В., Петров С.В. Полиморфизм онкогена LMP1 вируса Эпштейна–Барр в двух этнических группах россии, татар и славян, и его влияние на развитие некоторых злокачественных опухолей // Инфекция и иммунитет. 2020. Т. 10, № 2. C. 347–358. doi: 10.15789/2220-7619-EBV-1162
  3. Львов Н.Д., Дудукина Е.А. Ключевые вопросы диагностики Эпштейна–Барр вирусной инфекции // Инфекционные болезни: новости, мнения, обучение. 2013. № 3. С. 24–32.
  4. Мелехина Е.В., Домонова Э.А., Гоптарь И.А., Шипулина О.Ю., Горелов А.В. Первый в России случай наследственной передачи хромосомно-интегрированного вируса герпеса человека 6В (Human betaherpesvirus 6B) // Вопросы практической педиатрии. 2019. Т. 14, № 1. C. 33–40. doi: 10.20953/1817-7646-2019-1-33-40
  5. Мелехина Е.В., Музыка А.Д., Калугина М.Ю., Горелов А.В., Чугунова О.Л. Современные представления об инфекции, вызванной вирусом герпеса человека 6 типа // Архивъ внутренней медицины. 2016. Т. 6, № 1. C. 13–19. doi: 10.20514/2226-6704-2016-6-1-13-19
  6. Никольский М.А., Вязовая А.А., Ведерников В.Е., Нарвская О.В., Лиознов Д.А., Смирнова Н.Н., Полунина А.В., Бурмистрова А.Г., Золотова М.А. Молекулярно-биологическая характеристика вируса герпеса человека 6-го типа у пациентов с различными вариантами течения заболевания // Педиатрия. 2019. Т. 98, № 1. С. 53–56. doi: 10.24110/0031-403X-2019-98-1-53-56
  7. О состоянии санитарно-эпидемиологического благополучия населения в Российской Федерации в 2018 году: государственный доклад. М.: Роспотребнадзор, 2019. 254 с.
  8. Смирнова К.В., Дидук С.В., Гурцевич В.Э. Полиморфизм онкогена LMP1 вируса Эпштейна–Барр у представителей коренного малочисленного народа Дальнего Востока России // Эпидемиология и инфекционные болезни. 2017. Т. 22, № 5. С. 239–247. doi: 10.18821/1560-9529-2017-22-5-239-247
  9. Соломай Т.В. Динамика заболеваемости и территориальное распространение инфекционного мононуклеоза // Здравоохранение Российской Федерации. 2019. Т. 63, № 4. C. 186–192. doi: 10.18821/0044-197Х-2019-63-4-186-192
  10. Тимченко В.Н., Баннова С.Л., Павлова Н.В., Павлова Е.Б., Каплина Т.А., Федорова А.В., Булина О.В., Балашов А.Л., Хакизимана Ж.-К. ВЭБ-мононуклеоз на госпитальном этапе: клиническая характеристика и этиотропная терапия у детей различного возраста // Педиатр. 2018. Т. 9, № 6. С. 77–82.
  11. Хакизимана Ж.К., Тимченко В.Н., Шакмаева М.А., Каплина Т.А., Субботина М.Д., Баннова С.Л., Федорова А.В., Суховецкая В.Ф., Павлова Е.Б., Павлов Н.В. ВЭБ-мононуклеоз у детей в современных условиях // Детские инфекции. 2020. Т. 19, № 2. C. 23–28. doi: 10.22627/2072-8107-2020-19-2-23-28
  12. Хафизов К.Ф., Сперанская А.С., Мацвай А.Д., Шипулин Г.А., Дедков В.Г. Передовые технологии в диагностике вирусных заболеваний неясной этиологии // Инфекция и иммунитет. 2020. Т. 10, № 1. C. 9–25. doi: 10.15789/2220-7619-ATI-824
  13. Шарипова Е.В., Бабаченко И.В. Герпесвирусные инфекции и инфекционный мононуклеоз (обзор литературы) // Журнал инфектологии. 2013. Т. 5, № 2. C. 5–12. doi: 10.22625/2072-6732-2013-5-2-
  14. Ablashi D., Agut H., Alvarez-Lafuente R., Clark D.A., Dewhurst S., DiLuca D., Flamand L., Frenkel N., Gallo R., Gompels U.A., Höllsberg P., Jacobson S., Luppi M., Lusso P., Malnati M., Medveczky P., Mori Y., Pellett P.E., Pritchett J.C., Yamanishi K., Yoshikawa T. Classification of HHV-6A and HHV-6B as distinct viruses. Arch. Virol., 2014, vol. 159, pp. 863–870. doi: 10.1007/s00705-013-1902-5
  15. Adams M.J., Carstens E.B. Ratification vote on taxonomic proposals to the International Committee on Taxonomy of Viruses. Arch. Virol., 2012, vol. 157, no. 7, pp. 1411–1422. doi: 10.1007/s00705-012-1299-6
  16. Babcock G.J., Decker L.L., Volk M., Thorley-Lawson D.A. EBV persistence in memory B cells in vivo. Immunity, 1998, vol. 9, no. 3, pp. 395–404. doi: 10.1016/s1074-7613(00)80622-6
  17. Bhatia K., Raj A., Guitierrez M.I., Judde J.G., Spangler G., Venkatesh H., Magrath I.T. Variation in the sequence of Epstein–Barr virus nuclear antigen 1 in normal peripheral blood lymphocytes and in Burkitt’s lymphomas. Oncogene, 1996, vol. 13, pp. 177–181.
  18. Dambaugh T., Hennessy K., Chamnankit L., Kieff E. U2 region of Epstein–Barr virus DNA may encode Epstein–Barr nuclear antigen 2. Proc. Natl. Acad. Sci. USA, 1984, vol. 81, pp. 7632–7636. doi: 10.1073/pnas.81.23.7632
  19. Edwards R.H., Seillier-Moiseiwitsch F., Raab-Traub N. Signature amino acid changes in latent membrane protein 1 distinguish Epstein–Barr virus strains. Virology, 1999, vol. 261, pp. 79–95. doi: 10.1006/viro.1999.9855
  20. Eliassen E., Lum E., Pritchett J., Ongradi J., Krueger G., Crawford J.R., Phan T.L., Ablashi D., Hudnall S.D. Human Herpesvirus 6 and malignancy: a review. Front. Oncol., 2018, vol. 8: 512. doi: 10.3389/fonc.2018.00512
  21. Fafi-Kremer S., Brengel-Pesce K., Barguès G., Bourgeat M.J., Genoulaz O., Seigneurin J.M., Morand P. Assessment of automated DNA extraction coupled with real-time PCR for measuring Epstein–Barr virus load in whole blood, peripheral mononuclear cells and plasma. J. Clin. Virol., 2004, vol. 30, no. 2, pp. 157–164. doi: 10.1016/j.jcv.2003.10.002
  22. Greninger A.L., Roychoudhury P., Makhsous N., Hanson D., Chase J., Krueger G., Xie H., Huang M.-L., Saunders L., Ablashi D., Koelle D.M., Cook L., Jerome K.R. Copy number heterogeneity, large origin tandem repeats, and interspecies recombination in human herpesvirus 6A (HHV-6A) and HHV-6B reference strains. J. Virol., 2018, vol. 92, no. 10: e00135-18. doi: 10.1128/JVI.00135-18
  23. Hu L.F., Zabarovsky E.R., Chen F., Cao S.L., Ernberg I. Isolation and sequencing of the Epstein–Barr virus BNLF-1 gene (LMP1) from a Chinese nasopharyngeal carcinoma. J. Gen. Virol., 1991, vol. 72, pp. 2399–2409. doi: 10.1099/0022-1317-72-10-2399
  24. Hudnall S.D., Chen T., Allison P., Tyring S.K., Heath A. Herpesvirus prevalence and viral load in healthy blood donors by quantitative real-time polymerase chain reaction. Transfusion, 2008, vol. 48, no. 6, pp. 1180–1187. doi: 10.1111/j.1537-2995.2008.01685.x
  25. Kanda Т., Yajima М., Ikuta К. Epstein–Barr virus strain variation and cancer. Cancer Sci., 2019, vol. 110, no. 4, pp. 1132–1139. doi: 10.1111/cas.13954
  26. Kondo K., Kondo T., Okuno T., Takahashi M., Yamanishi K. Latent human herpesvirus 6 infection of human monocytes/macrophages. J. Gen. Virol., 1991, vol. 72, no. 6, pp. 1401–1408. doi: 10.1099/0022-1317-72-6-1401
  27. Mendes T.M., Oliveira L.C., Yamamoto L., Del Negro G.M., Okay T.S. Epstein–Barr virus nuclear antigen-2 detection and typing in immunocompromised children correlated with lymphoproliferative disorder biopsy findings. Braz. J. Infect. Dis., 2008, vol. 12, no. 3, pp. 186–191. doi: 10.1590/s1413-86702008000300005
  28. Monteiro T.A.F., Costa I.B., Costa I.B., Corrêa T.L.D.S., Coelho B.M.R., Silva A.E.S., Ramos F.L.P., Filh A.J.M., Monteiro J.L.F., Siqueira J.A.M., Gabbay Y.B., Sousa R.C.M. Genotypes of Epstein–Barr virus (EBV1/EBV2) in individuals with infectious mononucleosis in the metropolitan area of Belém, Brazil, between 2005 and 2016. Braz. J. Infect. Dis., 2020, vol. 24, no. 4, pp. 322–329. doi: 10.1016/j.bjid.2020.06.004
  29. Packham G., Brimmell M., Cook D., Sinclair A.J., Farrell P.J. Strain variation in Epstein–Barr virus immediate early genes. Virology, 1993, vol. 192, no. 2, pp. 541–550. doi: 10.1006/viro.1993.1070
  30. Reddy S., Manna P. Quantitative detection and differentiation of human herpesvirus 6 subtypes in bone marrow transplant patients by using a single real-time polymerase chain reaction assay. Biol. Blood Marrow Transplant., 2005, vol. 11, pp. 530–541. doi: 10.1016/j.bbmt.2005.04.010
  31. Smatti M.K., Yassine H.M., Abu Odeh R., Al Marawani A., Taleb S.A., Althani A.A., Nasrallah G.K. Prevalence and molecular profiling of Epstein–Barr virus (EBV) among healthy blood donors from different nationalities in Qatar. PLoS One, 2017, vol. 12, no. 12: e0189033. doi: 10.1371/journal.pone.0189033
  32. Traore L., Tao I., Bisseye C., Diarra B., Compaore T.R., Nebie Y., Assih M., Ouedraogo A., Zohoncon T., Djigma F., Ouermi D., Barro N., Sanou M., Ouedraogo R.T., Simpore J. Molecular diagnosis of cytomegalovirus, Epstein–Barr virus and herpes virus 6 among blood donors in Ouagadougou, Burkina Faso. BMC Infectious Diseases, 2014, vol. 14, no. 2: P99. doi: 10.1186/1471-2334-14-s2-p99
  33. Tzellos S., Farrell P.J. Epstein–Barr virus sequence variation-biology and disease. Pathogens, 2012, vol. 1, no. 2, pp. 156–174. doi: 10.3390/pathogens1020156
  34. Walling D.M., Shebib N., Weaver S.C., Nichols C.M., Flaitz C.M., Webster-Cyriaque J. The molecular epidemiology and evolution of Epstein–Barr virus: Sequence variation and genetic recombination in the latent membrane protein-1 gene. J. Infect. Dis., 1999, vol. 179, pp. 763–774. doi: 10.1086/314672
  35. Yalcin S., Karpuzglu T., Suleymanlar G., Mutlu G., Mukai T., Yamamoto T., Isegawa Y., Yamanishi K. Human herpesvirus 6 and human herpesvirus 7 infections in renal transplant recipients and healthy adults in Turkey. Arch. Virol., 1994, vol. 136, pp. 183– 190. doi: 10.1007/BF01538827
  36. Zimber U., Adldinger H.K., Lenoir G.M., Vuillaume M., Knebel-Doeberitz M.V., Laux G., Desgranges C., Wittmann P., Freese U.K., Schneider U., Bornkamm G.W. Geographical prevalence of two types of Epstein–Barr virus. Virology, 1986, vol. 154, pp. 56–66. doi: 10.1016/0042-6822(86)90429-0

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2021 Popkova M.I., Utkin O.V., Soboleva E.A., Sakharnov N.A., Bryzgalova D.A., Senatskaia A.O., Kulova E.A.

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.

СМИ зарегистрировано Федеральной службой по надзору в сфере связи, информационных технологий и массовых коммуникаций (Роскомнадзор).
Регистрационный номер и дата принятия решения о регистрации СМИ: серия ПИ № ФС 77 - 64788 от 02.02.2016.


This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies