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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">biob</journal-id><journal-title-group><journal-title xml:lang="ru">Биобезопасность и Биотехнология</journal-title><trans-title-group xml:lang="en"><trans-title>Biosafety and Biotechnology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2707-7241</issn><issn pub-type="epub">2957-5702</issn><publisher><publisher-name>Научно-исследовательский институт проблем биологической безопасности</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.58318/2957-5702-2022-9-6-13</article-id><article-id custom-type="elpub" pub-id-type="custom">biob-20</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>БИОЛОГИЧЕСКАЯ БЕЗОПАСНОСТЬ И БИОЗАЩИТА</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>BIOLOGICAL SAFETY AND BIOSECURITY</subject></subj-group></article-categories><title-group><article-title>ПРОВЕДЕНИЕ ПОЛИМЕРАЗНОЙ ЦЕПНОЙ РЕАКЦИИ В РЕАЛЬНОМ ВРЕМЕНИ С ПРИМЕНЕНИЕМ ФЛУОРЕСЦЕНТНОГО КРАСИТЕЛЯ SYBR GREEN I ДЛЯ ДИАГНОСТИКИ ЧУМЫ ПЛОТОЯДНЫХ</article-title><trans-title-group xml:lang="en"><trans-title>REAL-TIME POLYMERASE CHAIN REACTION USING SYBR GREEN I FLUORESCENT DYE TO DIAGNOSE CANINE DISTEMPER VIRUS</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Исакеев</surname><given-names>М. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Isakeev</surname><given-names>M. K.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Орозов</surname><given-names>Ж. Ч.</given-names></name><name name-style="western" xml:lang="en"><surname>Orozov</surname><given-names>Zh. Ch.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ахмеджанов</surname><given-names>М. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Ahmedjanov</surname><given-names>M. A.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Джээнбаева</surname><given-names>С. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Dzheenbaeva</surname><given-names>S. A.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Кыргызский научно-исследовательский институт им. А. Дуйшеева<country>Кыргызстан</country></aff><aff xml:lang="en">Kyrgyz Scientific-Research Institute of Veterinary Medicine named after A. Duisheeva<country>Kyrgyzstan</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>27</day><month>11</month><year>2022</year></pub-date><volume>0</volume><issue>10</issue><fpage>6</fpage><lpage>13</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Исакеев М.К., Орозов Ж.Ч., Ахмеджанов М.А., Джээнбаева С.А., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Исакеев М.К., Орозов Ж.Ч., Ахмеджанов М.А., Джээнбаева С.А.</copyright-holder><copyright-holder xml:lang="en">Isakeev M.K., Orozov Z.C., Ahmedjanov M.A., Dzheenbaeva S.A.</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://journal.biosafety.kz/jour/article/view/20">https://journal.biosafety.kz/jour/article/view/20</self-uri><abstract><p>Проведена диагностика чумы плотоядных с применением полимеразной цепной реакции в реальном времени (ПЦР-РВ). Для проведения ПЦР-РВ применялся флуоресцентный краситель SYBR Green I. С помощью ПЦР-РВ проверяли 106 собак в окрестностях города Бишкек. Из 106 собак, 10 были здоровыми и использовались в качестве контроля. Из 96 собак получены клинические образцы, из 87 выявлен возбудитель чумы плотоядных и 9 дали отрицательный результат. Метод ПЦР в последние годы успешно применяется в ветеринарной практике и в научных центрах страны для диагностирования инфекционных заболеваний сельскохозяйственных и домашних животных. В ветеринарной практике и науке при определении инфекционных заболеваний ПЦР является стандартной процедурой, которая позволяет определить наличие гена возбудителя. При чуме плотоядных применение метода ПЦР, считается необходимой процедурой, так как другие методы менее чувствительны и мало эффективны. Применение ПЦР-РВ упрощает диагностику, и экономит время проведения анализа, чем ПЦР в классическом варианте. Поэтому на сегодня, в нашей стране считается актуальной внедрение ПЦР-РВ в практическую ветеринарную диагностику.</p></abstract><trans-abstract xml:lang="en"><p>The canine distemper virus was diagnosed using real-time polymerase chain reaction (RT-PCR). For diagnostics with RT-PCR, the fluorescent dye SYBR Green I was used. Using RT-PCR, 106 dogs were tested in the vicinity of Bishkek and c. Bishkek. Of 106 dogs, 10 healthy dogs were used for controls. Clinical samples were obtained from 96 dogs, from 87 the causative agent of canine distemper virus was identified and 9 gave a negative result. In recent years, the PCR method has been successfully used in veterinary practice and in scientific centers of the our country to diagnose infectious diseases of agricultural and domestic animals. In veterinary practice and science, when determining infectious diseases, PCR is a standard procedure that allows you to determine the presence of the pathogen gene. With canine distemper virus, the use of the PCR method is considered a necessary procedure, since other methods are less sensitive and not very effective. The use of RT-PCR simplifies diagnostics and saves time for the analysis than PCR in the classic version. Therefore, today, the introduction of RT-PCR into practical veterinary medicine is considered relevant in our country.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>чума плотоядных</kwd><kwd>диагностика</kwd><kwd>ПЦР-РВ</kwd><kwd>SYBR Green I</kwd><kwd>вирус</kwd><kwd>собака</kwd></kwd-group><kwd-group xml:lang="en"><kwd>canine distemper virus</kwd><kwd>diagnostics</kwd><kwd>RT-PCR</kwd><kwd>SYBR Green I</kwd><kwd>virus</kwd><kwd>dog</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">Сюрин В.Н., Самуйленко А.Я., Соловьев Б.В., Фомин Н.В. 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