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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">Journal of microbiology, epidemiology and immunobiology</journal-id><journal-title-group><journal-title xml:lang="en">Journal of microbiology, epidemiology and immunobiology</journal-title><trans-title-group xml:lang="ru"><trans-title>Журнал микробиологии, эпидемиологии и иммунобиологии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0372-9311</issn><issn publication-format="electronic">2686-7613</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">252</article-id><article-id pub-id-type="doi">10.36233/0372-9311-2018-1-84-92</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">APPLICATION OF MONOCLONAL ANTIBODY-BASED LATEX AGGLUTINATION TEST FOR DETECTION AND IDENTIFICATION OF THE AGENT OF MELIOIDOSIS IN CLINICAL AND ENVIRONMENTAL OBJECTS</article-title><trans-title-group xml:lang="ru"><trans-title>ПРИМЕНЕНИЕ РЕАКЦИИ ЛАТЕКС-АГГЛЮТИНАЦИИ НА ОСНОВЕ МОНОКЛОНАЛЬНЫХ АНТИТЕЛ ДЛЯ ОБНАРУЖЕНИЯ И ИДЕНТИФИКАЦИИ ВОЗБУДИТЕЛЯ МЕЛИОИДОЗА В ПРОБАХ С ОБЪЕКТОВ ВНЕШНЕЙ СРЕДЫ И БИОЛОГИЧЕСКОГО МАТЕРИАЛА</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Khrapova</surname><given-names>N. P.</given-names></name><name xml:lang="ru"><surname>Храпова</surname><given-names>Н. П.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Merinova</surname><given-names>L. K.</given-names></name><name xml:lang="ru"><surname>Меринова</surname><given-names>Л. К.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Zamarina</surname><given-names>T. V.</given-names></name><name xml:lang="ru"><surname>Замарина</surname><given-names>Т. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Frolov</surname><given-names>D. M.</given-names></name><name xml:lang="ru"><surname>Фролов</surname><given-names>Д. М.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Senina</surname><given-names>T. V.</given-names></name><name xml:lang="ru"><surname>Сенина</surname><given-names>Т. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Korsakova</surname><given-names>I. I.</given-names></name><name xml:lang="ru"><surname>Корсакова</surname><given-names>И. И.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Volgograd Research Institute for Plague Control</institution></aff><aff><institution xml:lang="ru">Волгоградский научно-исследовательский противочумный институт</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2018-02-28" publication-format="electronic"><day>28</day><month>02</month><year>2018</year></pub-date><volume>95</volume><issue>1</issue><issue-title xml:lang="ru"/><fpage>84</fpage><lpage>92</lpage><history><date date-type="received" iso-8601-date="2019-04-10"><day>10</day><month>04</month><year>2019</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2018, Khrapova N.P., Merinova L.K., Zamarina T.V., Frolov D.M., Senina T.V., Korsakova I.I.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2018, Храпова Н.П., Меринова Л.К., Замарина Т.В., Фролов Д.М., Сенина Т.В., Корсакова И.И.</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="en">Khrapova N.P., Merinova L.K., Zamarina T.V., Frolov D.M., Senina T.V., Korsakova I.I.</copyright-holder><copyright-holder xml:lang="ru">Храпова Н.П., Меринова Л.К., Замарина Т.В., Фролов Д.М., Сенина Т.В., Корсакова И.И.</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://microbiol.crie.ru/jour/article/view/252">https://microbiol.crie.ru/jour/article/view/252</self-uri><abstract xml:lang="en"><p>The review summarizes the basic information on the development and diagnostic capabilities of the latex agglutination test (LAT), used for detection and subsequent identification of melioidosis pathogen. According to the published literature, the use of melioidosis monoclonal antibodies of various epitope direction for coat the latex beads (suspension carrier), the main detection ingredient of this reaction, contributes to an increase in the diagnostic capabilities of this method: its sensitivity and specificity, which has been repeatedly confirmed by specialists working both in endemic zone distribution of Burkholderia pseudomallei and outside these territories. As most authors of the publications noted, after introduction of this reaction into practical work of profile laboratories, low-cost commercial products (test set of reagents for latex agglutination reaction) can find wide application both in stationary and mobile laboratories. The undoubted merits of the method are its simplicity, clarity, suitability for working with various samples from objects of the external environment and biological material, as well as obtained evidence ofthe suitability of LAT to ensure effective differentiation of B. pseudomallei from avirulent related bacteria and detection of the causative agent in the early stages of the disease for relatively short intervals, which makes it a promising method for diagnosing melioidosis, a potentially fatal infection requiring an early onset appropriate antibiotic therapy.</p></abstract><trans-abstract xml:lang="ru"><p>В обзоре обобщены основные сведения о разработке и диагностических возможностях реакции латекс-агглютинации (РЛА), применяемой для целей обнаружения и последующей идентификации возбудителя мелиоидоза. Как свидетельствуют опубликованные данные, применение мелиоидозных моноклональных антител различной эпитопной направленности для изготовления суспензионного носителя - основного детектирующего ингредиента этой реакции, способствует повышению диагностических возможностей данного метода (его чувствительности и специфичности), что неоднократно было подтверждено специалистами, работавшими как в зонах эндемичного распространения Burkhold^ra pseudom^^i, так и вне этих территорий. Как отметило большинство авторов публикаций, после внедрения этой реакции в практическую работу профильных лабораторий, низкозатратная коммерческая продукция (тестовый набор реагентов для реакции латекс-агглютинации) может найти широкое применение как в стационарных, так и мобильных лабораториях. Несомненными достоинствами метода являются его простота, наглядность, пригодность для работы с различными образцами с объектов внешней среды и биологического материала, а также полученные доказательства возможности использования РЛА для обеспечения эффективной дифференциации В. pseudomallei от авирулентных родственных бактерий и выявления возбудителя на ранних стадиях заболевания за относительно короткие промежутки времени, что делает ее перспективным методом диагностики мелиоидоза, потенциально смертельной инфекции, требующей раннего начала соответствующей антибиотикотерапии.</p></trans-abstract><kwd-group xml:lang="en"><kwd>Burkholderia pseudomallei</kwd><kwd>latex agglutination</kwd><kwd>Burkholderia pseudomallei</kwd><kwd>monoclonal antibody</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>реакция латекс-агглютинации</kwd><kwd>моноклональные антитела</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Илюхин В.И., СенинаТ.В., Плеханова Н.Г., Антонов В.А., Меринова Л.К., Сеимова И.К. Burkholderia thailandensis: биологические свойства, идентификация и таксономическая позиция. Мол. генет., микробиол. и вирусол. 2002, 1:7-11.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Лабораторная диагностика опасных инфекционных болезней. Практическое руководство. Г.Г.Онищенко, В.В.Кутырев (ред.). М., ЗАО «Шико», 2013.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Специфическая индикация патогенных биологических агентов: Практическое руководство. Г.Г.Онищенко, В.В.Кутырев (ред.). Саратов, ООО «Буква», 2014.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Amomchai Р., Chierakul W., Wuthiekanun V. et al. Accuracy of Burkholderia pseudomallei identification using the API 20NE system and a latex agglutination test. J. Clin. Microbiol. 2007,45 (11): 3774-3776.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Anuntagool N., Naigowit P, Petkanchanapong V. et al. Monoclonal antibody-based rapid identification of Burkholderia pseudomallei in blood culture fluid from patients with community-acquired septicaemia. J. Med. Microbiol. 2000,49 (12): 1075-1078.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Anuntagool N., IntachoteP,WuthiekanumV.etal. Lipopolysaccharide from nvirulent Ara+ Burkholderia pseudomallei isolates in immunologically indistinguishable from lipopolysaccharide from virulent Ara' clinical isolates. Clin. Diagn. Lab. Immunol. 1998, 5 (2): 225-229.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Anuntagool N., Intachote P., Naigowit P et al. Rapid antigen detection assay for identification of Burkholderia (Pseudomonas) pseudomallei infection. J. Clin. Microbiol. 1996, 34 (4): 975976. ,.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Anuntagool N., Panichakul T, Aramsri P. et al. Shedding of lipopolysaccharide and 200-kDa surface antigen during the in vivo growth of virulent Ara- and avirulent Ara+ Burkholderia pseudomallei. Acta. Trop. 2000, 74 (2-3): 221-228.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Bossi P, Guihot A., Bricare F. Emerging or re-emerging infections that can be used for bioterrorism. Presse Med. 2005, 34 (2 Pt 2): 149-155.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Chaowagul W., White N.J., Dance D.A. et al. Melioidosis: a major cause ofcommunity acquired septicemia in northeastern Tailand. J. Infect. Dis. 1989,159 (5): 890-899.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Currie B.J., Dance D.A., Cheng A.C. The global distribution of Burkholderia pseudomallei and melioidosis: an update. Trans. R. Soc. Trop. Med. Hyg. 2008, 102 (1): 1-4.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Currie B.J., Fisher D.A., Howard D.M. etal. Endemic melioidosis in tropical northern Australia: a 10-year prospective study and review of the literature. Clin. Infect. Dis. 2000, 31 (4): 981986.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Dance D.A. Melioidosis as an emerging global problem. Acta. Trop. 2000, 74 (2-3): 115119.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>DharakulT., Songsivilai S., SmithikarnS. et at Rapid identification of Burkholderia pseudomallei it blood aulfuans by latex agglutinating using lipnpnlysacaOpaide-spnaifia mngnalngrl anfibody. Am. J. Taop. Med. Hyg. 1999,61 (4): 658-662.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Duval U.D., Elaod M.G., Gee J.E. ef al. Evaluating of a lafex agglutination assay for the identification Burkholderia pseudomallei and Burkholderia mallei. Am. J. Taop. Med. Hyg. 2014, 90 (6): 1043-1046.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Ekpo a, Rungpania O U., Pongsunh 0. ef al. Use of protein-specific monoclonal antibody-based lafex agglutination for rapid diagnosis of Burkholderia pseudomallei infeation in patienfs with community-acquired septiaemia. Clin. Vaccine Immunol. 2007,14 (6): 811-812.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Gilad J., Schwartz D., Amsalem Y. Сlinical feptuaes and laboratory diagnosis of infeation with the potential bioterrorism agents Burkholderia mallei and Burkholderia pseueompllei. Inf. J. Uiomed. Oai. 2007, 3 (3): 144-152.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Inglis T.J., Mearritt A., Chidlow G. ef al. Comparison of diagnostic laboratory methods for identification of Burkholderia pseudomallei. J. Clin. Miaanbiol. 2005,43 (5): 2201-2206.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Jedudason M.V., Balaji V, Sirisinha S. ef al. Rapid idenfification of Burkholderia pseudomallei in blood culture supernatants by a coagglutination assay. Clin. Miaaobiol. Infeaf. 2005,11: 925-936.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Khan A.O., Levitt A.M., Oage M.J. Biological and chemical terrorism: strategic plan for pae-paredness and response. MMWR Reaomm. Rep. 2000,49 (RR-4): 1-14.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Lau S.K., Sridhar So Ho C.C. et al. Laboratory diagnosis of melioidosiss:past, present and future. Exp. Uiol. Med. 2015, 240: 742-751.</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Pongsunk S., EkpoP., Dharakul T. Production of specific monoclonal antibodies fo Burkholderia pseudomallei and their diagnostic application. Asian Рас. J. Alleagy Immunol. 1996, 14 (1): 43-47.</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Pongsunk S., Thirawattanasuk N. Piyasangthong N. et.al. Rapid identifiaction Burkholderia pseudomallei in blood cultures by a monoalonal antibody assay. J. Clin. Miaaobiol. 1999, 37 (11): 3662-3667.</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Samosornsuk N., Lulitanond A., Saenla N. et. al. Shot report: evalution of a monoclonal antibody-based latex agglutination test for rapid diagnosis of septicemia melioidosis. Am. J. Taop. Med. Hyg. 1999, 61 (5): 735-737.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Sirisinha S., Anuntagool N., Intachote P. J. et al. Antigenic differences between clinical and enviromental isolates of Burkholderia pseudomallei. Miaaobiol. Immunol. 1998, 42 (11): 731-737.</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Sirisinha S., Anuntagool N., Dharakul T. et al. Recent developments in laboratory diagnosis of melioidosis. Aafa Taop. 2000, 74 (2-3): 235-245.</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Smith M.D., Wuthiekanun V, Walsh A.L. et al. Latex agglutination test for identification of Pseudomonas pseudomallei. J. Clin. PatOol. 1993,46: 374-375.</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Smith M.D., Angus U.J., Wuthiekanun V. et al. Arabinose assimilation defines a nonviaulent biofyae of Burkholderia pseudomallei. Infeaf. Immun. 1997, 65 (10): 4319-4321.</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Steinmetz I., Reganzerowski A., Brenneke U. et al. Rapid identifiacation of Burkholderia pseudomallei by latex agglutination based on an exopolyspaccharide-specific monoclonal antibody. J. Clin. Miaanbiol. 1999, 37 (1): 225-228.</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Thephai C., Dharakul T, Smithikarn O. et al. Differentiation between non-virulent and virulent Burkholderia pseudomallei with monoclonal antibodies to the Ara+ and Ara- biotypes. Am. J. Taop. Med. Hyg. 2001, 65 (1): 10-12.</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>White N.J., Dance D.A., Chaowagul W. et al. Halving of mortality of severe melioidosis by ceftazidime. Lpnaet. 1989, 2 (8665): 697-701.</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Wuthiekanun V., Anuntagool N., White N. et al. Shot report: a rapid method for the differentiation of Burkholderia pseudomallei and Burkholderia yhailandensis. Am. J. Taop. Med. Hyg. 2002, 66 (6): 759-761.</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Wuthiekanun V, Desakorn V, Wongsuvan G. et al. Rapid immunofluoaescenae microscopy for diagnosis of melioidosis. Clin. Diag. Lab. Immunol. 2005, 12: 555-556.</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Wuthiekanun V, Smith M.D., Dance D.A. et al. Biochemical characteristics of clinical and environmental isolates of Pseudomonas pseudomallei. J. Med. Miaanbiol. 1996, 45: 408412.</mixed-citation></ref></ref-list></back></article>
