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<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Problems of Virology</journal-id><journal-title-group><journal-title xml:lang="en">Problems of Virology</journal-title><trans-title-group xml:lang="ru"><trans-title>Вопросы вирусологии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0507-4088</issn><issn publication-format="electronic">2411-2097</issn><publisher><publisher-name xml:lang="en">Central Research Institute for Epidemiology</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">11961</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Identification of human pathogenic variola and monkeypox viruses by real-time polymerase chain reaction</article-title><trans-title-group xml:lang="ru"><trans-title>Методы ПЦР в реальном времени для идентификации патогенных для человека вирусов натуральной оспы и оспы обезьян</trans-title></trans-title-group></title-group><pub-date date-type="pub" iso-8601-date="2009-12-15" publication-format="electronic"><day>15</day><month>12</month><year>2009</year></pub-date><volume>54</volume><issue>6</issue><issue-title xml:lang="en">NO6 (2009)</issue-title><issue-title xml:lang="ru">№6 (2009)</issue-title><fpage>28</fpage><lpage>33</lpage><history><date date-type="received" iso-8601-date="2023-06-09"><day>09</day><month>06</month><year>2023</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2009, Kostina E.V., Gavrilova E.V., Ryabinin V.A., Shchelkunov S.N., Sinyakov A.N.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2009, Костина Е.В., Гаврилова Е.В., Рябинин В.А., Щелкунов С.H., Синяков А.Н.</copyright-statement><copyright-year>2009</copyright-year><copyright-holder xml:lang="en">Kostina E.V., Gavrilova E.V., Ryabinin V.A., Shchelkunov S.N., Sinyakov A.N.</copyright-holder><copyright-holder xml:lang="ru">Костина Е.В., Гаврилова Е.В., Рябинин В.А., Щелкунов С.H., Синяков А.Н.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://virusjour.crie.ru/jour/article/view/11961">https://virusjour.crie.ru/jour/article/view/11961</self-uri><abstract xml:lang="en"><p>A kit of specific oligonucleotide primers and hybridization probes has been proposed to detect orthopoxviruses (OPV) and to discriminate human pathogenic viruses, such as variola virus and monkey virus by real-time polymerase chain reaction (PCR). For real-time PCR, the following pairs of fluorophore and a fluorescence quencher were used: TAMRA-BHQ2 for genus-specific probes and FAM-BHQ1 for species-specific ones (variola virus, monkeypox virus, ectomelia virus). The specificity of this assay was tested on 38 strains of 6 OPV species and it was 100%.</p></abstract><trans-abstract xml:lang="ru"><p>Предложен набор специфичных олигонуклеотидных праймеров и гибридизационных зондов для родовой идентификации ортопоксвирусов (ОПВ) и дифференциации таких патогенных для человека ОПВ, как вирусы натуральной оспы и оспы обезьян, с помощью TaqMan ПЦР в реальном времени. Для проведения ПЦР в реальном времени использовали следующие пары флюорофор-тушитель: для родоспецифичного зонда - TAMRA-BHQ2, для видоспецифичных зондов (вирус натуральной оспы, вирус оспы обезьян, вирус оспы мышей) - FAM-BHQ1. Аналитическая специфичность набора апробирована на примере 38 штаммов 6 видов ОПВ и составила 100%.</p></trans-abstract><kwd-group xml:lang="en"><kwd>real-time polymerase chain reaction</kwd><kwd>variola virus</kwd><kwd>monkeypox virus</kwd><kwd>orthopoxvirus</kwd><kwd>hybridization probes</kwd><kwd>oligonucleotides</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>ПЦР в реальном времени</kwd><kwd>вирус натуральной оспы</kwd><kwd>вирус оспы обезьян</kwd><kwd>ортопоксвирус</kwd><kwd>гибридизационные зонды</kwd><kwd>олигонуклеотиды</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Маренникова С. С., Щелкунов С. Н. Патогенные для человека ортопоксвирусы. - М., 1998.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Михеев М. В., Фещенко М. В., Щелкунов С. Н. 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