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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">sredob</journal-id><journal-title-group><journal-title xml:lang="ru">Здоровье населения и среда обитания – ЗНиСО</journal-title><trans-title-group xml:lang="en"><trans-title>Public Health and Life Environment – PH&amp;LE</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2219-5238</issn><issn pub-type="epub">2619-0788</issn><publisher><publisher-name>ФБУЗ ФЦГиЭ Роспотребнадзора</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.35627/2219-5238/2024-32-3-63-69</article-id><article-id custom-type="elpub" pub-id-type="custom">sredob-1879</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ЭПИДЕМИОЛОГИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>EPIDEMIOLOGY</subject></subj-group></article-categories><title-group><article-title>Геномный мониторинг вируса SARS-CоV-2, циркулировавшего на территории Кыргызской Республики в 2020–2021 гг.</article-title><trans-title-group xml:lang="en"><trans-title>Genome Monitoring of SARS-CoV-2 Circulating in the Kyrgyz Republic in 2020–2021</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0005-9065-6744</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Джумаканова</surname><given-names>А. Б</given-names></name><name name-style="western" xml:lang="en"><surname>Dzhumakanova</surname><given-names>A. B.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Джумаканова Айгуль Бейшебаевна – начальник Центра лабораторных испытаний Департамента профилактики заболеваний и Госсанэпиднадзора МЗ КР.</p><p>ул. Фрунзе, д. 535, Бишкек, 720033</p></bio><bio xml:lang="en"><p>Aigul B. Dzhumakanova - Head of the Testing Laboratory Center, Department of Disease Prevention and State Sanitary and Epidemiological Surveillance of the Ministry of Health of the Kyrgyz Republic.</p><p>535 Frunze Street, Bishkek, 720033</p></bio><email xlink:type="simple">aigul.dzumakanova.dgsn@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Департамент профилактики заболеваний и государственного санитарно-эпидемиологического надзора Министерства здравоохранения Кыргызской Республики</institution><country>Кыргызстан</country></aff><aff xml:lang="en"><institution>Department of Disease Prevention and State Sanitary and Epidemiological Surveillance of the Ministry of Health of the Kyrgyz Republic</institution><country>Kyrgyzstan</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>29</day><month>03</month><year>2024</year></pub-date><volume>32</volume><issue>3</issue><fpage>63</fpage><lpage>69</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Джумаканова А.Б., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Джумаканова А.Б.</copyright-holder><copyright-holder xml:lang="en">Dzhumakanova A.B.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://zniso.fcgie.ru/jour/article/view/1879">https://zniso.fcgie.ru/jour/article/view/1879</self-uri><abstract><sec><title> </title><p> </p></sec><sec><title>Введение</title><p>Введение. РНК-содержащий вирус тяжелого острого респираторного заболевания SARS-CoV-2 быстро распространился по миру вследствие адаптации к хозяину путем генетической эволюции. Появление геновариантов с мутациями, повышающими контагиозность и трансмиссивность, могут негативно влиять на эффективность программ борьбы с заболеванием и снизить эффективность вакцинации.</p></sec><sec><title>Цель исследования</title><p>Цель исследования: выявление доминирующих геновариантов вируса SARS-CoV-2, циркулирующих на территории Кыргызской Республики в 2020–2021 гг.</p></sec><sec><title>Материалы и методы</title><p>Материалы и методы. Геномный мониторинг был проведен на положительных мазках из носоглотки. Диагностику COVID-19 проводили методом ПЦР в реальном времени с обратной транскрипцией (ОТ-ПЦР) на различных коммерческих тест-системах.</p><p>Определение геновариантов (n = 15) проводилось методом высокопроизводительного секвенирования на приборе MiSeq по протоколу ARTIC v3. Изучение мутационной изменчивости вируса SARS-CoV-2 проводили посредством кластерного анализа аминокислотных замен в S-белке по методу Уорда. Нуклеотидные последовательности из Кыргызстана (n = 15), России (n = 16), Индии (n = 2) и Китая (n = 2) выравнивали с помощью MAFFT. Филогенетическое дерево было создано с помощью метода максимального правдоподобия (ML) в IQ-TREE v1.6.12 с использованием</p></sec><sec><title>процессов Nextstrain</title><p>процессов Nextstrain. Корнем дерева считались образцы SARS-CoV-2 Wuhan/Hu-1/2019 и Wuhan/WH01/2019, загруженными из базы данных GenBank®.</p></sec><sec><title>Результаты</title><p>Результаты. Филогенетический анализ полученных данных выявил, что доминирующим геновариантом VOC был В.1.1.7 (Alpha), на долю которого приходилось 36,4 % (12/33), также был выявлен B.1.351 (Веtа) VOC, на долю которого приходилось 6,1 % (2/33). При исследовании образцов на наличие аминокислотных замен в S-белке обнаружено, что изоляты B.1.1.7 Alpha (Британский) кластеризуются на две отдельные ветви.</p></sec><sec><title>Заключение</title><p>Заключение. Изучение частоты и влияния мутаций на патогенетические свойства вируса, а также анализ преобладающих геновариантов вируса позволят своевременно принимать меры по противодействию распространению вируса SARS-CoV-2 в стране. В связи с этим необходим постоянный геномный мониторинг за циркулирующими геновариантами COVID-19.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Introduction</title><p>Introduction: The RNA-containing severe acute respiratory syndrome virus SARS-CoV-2 has spread rapidly around the world by adaptation to the host through genetic evolution. The emergence of variants with genetic mutations that increase contagiousness and transmission may hamper the effectiveness of disease control programs and efficacy of vaccination.</p></sec><sec><title>Objective</title><p>Objective: To establish dominant SARS-CoV-2 variants circulating in the Kyrgyz Republic in 2020–2021.</p></sec><sec><title>Materials and methods</title><p>Materials and methods: Genomic monitoring was carried out based on positive results of testing nasopharyngeal swabs. SARS-CoV-2 was detected by a real-time reverse transcription –polymerase chain reaction (RT-PCR) assay using registered commercial test kits. Genetic variants (n = 15) were determined by high-throughput sequencing on a MiSeq device (Illumina, USA) using the COVID-19 ARTIC v3 protocol. Mutational variability of SARS-CoV-2 was examined using a cluster analysis of amino acid substitutions in the S protein applying Ward’s method. Nucleotide sequences from Kyrgyzstan (n = 15), Russia (n = 16), India (n = 2), and China (n = 2) were aligned using MAFFT. IQ-TREE v1.6.12 was used to infer the phylogenetic tree by maximum likelihood applying Nextstrain processes. Isolates Wuhan/Hu-1/2019 and Wuhan/WH01/2019 downloaded from the GenBank® database were considered to be the root of the tree (reference).</p></sec><sec><title>Results</title><p>Results: Phylogenetic data analysis revealed that SARS-CoV-2 B.1.1.7 (Alpha) was the dominant VOC variant, the proportion of which was as high as 36.4 % (12/33); B.1.351 (Beta) was also found (6.1 % or 2/33). When samples were examined for amino acid substitutions in the S-protein, B.1.1.7 Alpha (British) isolates were found to cluster into two distinct branches.</p></sec><sec><title>Conclusion</title><p>Conclusion: The study of the frequency and influence of mutations on pathogenetic properties of the virus, as well as the analysis of the predominant variants of the virus will allow timely measures to be taken to counteract the spread of SARS-CoV-2 in the country. In this regard, continuous genome monitoring of circulating COVID-19 variants is necessary.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>SARS-CoV-2</kwd><kwd>COVID-19</kwd><kwd>ПЦР в реальном времени</kwd><kwd>новая коронавирусная инфекция</kwd></kwd-group><kwd-group xml:lang="en"><kwd>SARS-CoV-2</kwd><kwd>COVID-19</kwd><kwd>real-time PCR</kwd><kwd>novel coronavirus disease</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Li Q, Tang B, Bragazzi NL, Xiao Y, Wu J. Modeling the impact of mass influenza vaccination and public health interventions on COVID-19 epidemics with limited detection capability. Math Biosci. 2020;325:108378. doi: 10.1016/j.mbs.2020.108378</mixed-citation><mixed-citation xml:lang="en">Li Q, Tang B, Bragazzi NL, Xiao Y, Wu J. 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