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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">vestib</journal-id><journal-title-group><journal-title xml:lang="ru">Известия Национальной  академии наук Беларуси. Серия биологических наук</journal-title><trans-title-group xml:lang="en"><trans-title>Proceedings of the National Academy of Sciences of Belarus, Biological Series</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1029-8940</issn><issn pub-type="epub">2524-230X</issn><publisher><publisher-name>The Republican Unitary Enterprise Publishing House "Belaruskaya Navuka"</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.29235/1029-8940-2026-71-2-144-156</article-id><article-id custom-type="elpub" pub-id-type="custom">vestib-1013</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>Статьи</subject></subj-group></article-categories><title-group><article-title>Определение вирусной нагрузки TTV в биологическом материале целевых групп пациентов с использованием молекулярно-генетического метода</article-title><trans-title-group xml:lang="en"><trans-title>Determination of TTV viral load in biological material of target patient groups using a molecular genetic method</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1931-4224</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Осипкина</surname><given-names>О. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Osipkina</surname><given-names>O. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Осипкина Ольга Викторовна – заведующий научно- исследовательской лабораторией</p><p>ул. Ланге, 5, 246000, г. Гомель</p></bio><bio xml:lang="en"><p>Olga V. Osipkina – Head of the Research Laboratory</p><p>5, Lange Str., 246000, Gomel</p></bio><email xlink:type="simple">olvik197@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Гомельский государственный медицинский университет</institution></aff><aff xml:lang="en"><institution>Gomel State Medical University</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2026</year></pub-date><pub-date pub-type="epub"><day>30</day><month>04</month><year>2026</year></pub-date><volume>71</volume><issue>2</issue><fpage>144</fpage><lpage>156</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Осипкина О.В., 2026</copyright-statement><copyright-year>2026</copyright-year><copyright-holder xml:lang="ru">Осипкина О.В.</copyright-holder><copyright-holder xml:lang="en">Osipkina O.V.</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://vestibio.belnauka.by/jour/article/view/1013">https://vestibio.belnauka.by/jour/article/view/1013</self-uri><abstract><p>В результате проведенных исследований выбрана мишень генома Torque Teno Virus (TTV), разработан набор праймеров и TaqMan-зонда, фланкирующих консервативный регион длиной 111 п. н. (позиции нуклеотидов 103–213 референсного генома TTV TA278 GenBank: AB017610.1), ставший основой молекулярно-генетического метода диагностики TTV-инфекции, позволяющего выявлять и рассчитывать вирусную нагрузку TTV в биологическом материале человека. С помощью разработанного молекулярно-генетического метода обнаружена высокая частота выявления ДНК TTV в плазме (71,4–90,4 %) и в лейкоцитарной фракции крови (81,0–97,1 %) как в контрольной группе, так и у пациентов со вторичным иммунодефицитом, с ВИЧ-инфекцией и тяжелым течением инфекции COVID-19. Определена вирусная нагрузка TTV в целевых группах. Выявлена значимо более низкая медиана вирусной нагрузки TTV в лейкоцитарной фракции крови контрольной группы – 2,58 [1,66; 3,25] log10 копий ДНК TTV/105 клеток, чем в группе пациентов со вторичным иммунодефицитом – 3,67 [1,88; 4,47] log10 копий ДНК TTV/105 клеток (р = 0,0014), пациентов с ВИЧ-инфекцией – 3,84 [3,09; 4,20] log10 копий ДНК TTV/105 клеток (р &lt; 0,001) и в группе пациентов с тяжелым течением инфекции COVID-19, точка 1 – 3,67 [3,09; 3,91] log10 копий ДНК TTV/105 клеток (р &lt; 0,001).</p></abstract><trans-abstract xml:lang="en"><p>As a result of the conducted research, a target of the Torque Teno Virus (TTV) genome was selected, a set of primers and a TaqMan probe were developed flanking a conserved region of 111 nucleotide pairs (nucleotide positions 103–213 of the TTV reference genome TA278 GenBank: AB017610.1). This probe formed the basis of a molecular genetic method for diagnosing TTV infection, allowing for the detection and calculation of TTV viral load in human biological material. Using the developed molecular genetic method, a high frequency of TTV DNA detection was detected in plasma (71.4–90.4 %) and in the leukocyte fraction of blood (81.0–97.1 %), in both in the control group and in patients afflicted with secondary immunodeficiency, with HIV infection, and severe COVID-19 infection. The TTV viral load in the target groups was determined. A significantly lower median TTV viral load was found in the leukocyte fraction of blood in the control group – 2.58 [1.66; 3.25] log10 TTV DNA copies/105 cells, than in the group of patients with secondary immunodeficiency – 3.67 [1.88; 4.47] log10 TTV DNA copies/105 cells (p = 0.0014), patients with HIV infection – 3.84 [3.09; 4.20] log10 TTV DNA copies/105 cells (p &lt; 0.001) and in the group of patients with severe COVID-19 infection, point 1 – 3.67 [3.09; 3.91] log10 TTV DNA copies/105 cells (p &lt; 0.001).</p></trans-abstract><kwd-group xml:lang="ru"><kwd>TTV</kwd><kwd>молекулярно-генетический метод</kwd><kwd>праймеры</kwd><kwd>ПЦР</kwd><kwd>вирусная нагрузка</kwd></kwd-group><kwd-group xml:lang="en"><kwd>TTV</kwd><kwd>molecular genetic method</kwd><kwd>primers</kwd><kwd>PCR</kwd><kwd>viral load</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">Virus Taxonomy: 2024 Release // International Committee on Taxonomy of Viruses. – URL: https://ictv.global/taxonomy (date of access: 10.02.2026).</mixed-citation><mixed-citation xml:lang="en">Virus Taxonomy: 2024 Release. 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