Methodological basics for differential detection of EBV1/EBV2 and HHV6A/HHV6B
- Authors: Popkova M.I.1, Utkin O.V.1, Soboleva E.A.2, Sakharnov N.A.1, Bryzgalova D.A.1, Senatskaia A.O.1, Kulova E.A.2
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Affiliations:
- Academician I.N. Blokhina Nizhny Novgorod Scientific Research Institute of Epidemiology and Microbiology
- Privolzhsky Research Medical University
- Issue: Vol 11, No 6 (2021)
- Pages: 1057-1066
- Section: ORIGINAL ARTICLES
- Submitted: 28.12.2020
- Accepted: 30.05.2021
- Published: 12.07.2021
- URL: https://iimmun.ru/iimm/article/view/1661
- DOI: https://doi.org/10.15789/2220-7619-MBF-1661
- ID: 1661
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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.
Keywords
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
РоссияO. 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
РоссияE. 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.
РоссияN. 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
РоссияD. 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
РоссияA. 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
РоссияE. 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
РоссияReferences
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